Next Article in Journal
Effect of Breed on Hematological and Biochemical Parameters of Apparently Healthy Dogs Infected with Zoonotic Pathogens Endemic to the Mediterranean Basin
Previous Article in Journal
Trace Elements in Stenella coeruleoalba: Assessment of Marine Environmental Pollution and Dolphin Health Status
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Plant Polysaccharides Combined with Boric Acid on Digestive Function, Immune Function, Harmful Gas and Heavy Metal Contents in Faeces of Fatteners

1
College of Animal Science, Anhui Science and Technology University, Chuzhou 233100, China
2
Anhui Province Key Laboratory of Animal Nutrition Regulation and Health, Chuzhou 233100, China
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Animals 2024, 14(11), 1515; https://doi.org/10.3390/ani14111515
Submission received: 1 March 2024 / Revised: 29 April 2024 / Accepted: 16 May 2024 / Published: 21 May 2024
(This article belongs to the Section Pigs)

Abstract

:

Simple Summary

With the transformation of the breeding industry towards a healthy breeding model, the application of green feed additives in pig production is gradually increasing. Many plant polysaccharides are widely used as safe and green additives in animal production. Boron may be a necessary trace element for animals and its application in animal husbandry is also increasing. The study on the application effect of the combined addition of plant polysaccharides and boron in fatteners production performance, immune function, antioxidant function, digestive function and harmful substance emissions is of great significance for the rational use of both. This study added boron and different types of plant polysaccharides to the diet in the form of boric acid and found that the combined addition of boric acid and plant polysaccharides can improve the production performance and antioxidant function of fatteners by enhancing the activity of intestinal digestive enzymes and reducing the content of harmful substances such as heavy metals and harmful gases in feces and urine, thereby effectively improving healthy growth and reducing environmental pollution today.

Abstract

The experiment aimed to investigate the effects of plant polysaccharides combined with boric acid on digestive function, immune function and harmful gas and heavy metal contents in the faeces of fatteners. For this study, 90 healthy crossbred fatteners were selected and randomly divided into five groups: the control group was fed with a basal diet (Con); experimental group I was fed with basal diet + 40 mg/kg boric acid (BA); experimental group II was fed with basal diet + 40 mg/kg boric acid + 400 mg/kg Astragalus polysaccharides (BA+APS); experimental group III was fed with basal diet + 40 mg/kg boric acid + 200 mg/kg Ganoderma lucidum polysaccharides (BA+GLP); and experimental group IV was fed with basal diet + 40 mg/kg boric acid + 500 mg/kg Echinacea polysaccharides (BA+EPS). Compared with Con, the average daily gain (ADG), the trypsin activities in the duodenum and jejunum, the IL-2 levels in the spleen, the T-AOC activities and GSH-Px contents in the lymph node of fattening were increased in the BA group (p < 0.05), but malondialdehyde content in the lymph and spleen, and the contents of NH3, H2S, Hg, Cu, Fe and Zn in the feces and urine were decreased (p < 0.05). Compared with the BA, the ADG, gain-to-feed ratio (G/F), the trypsin and maltase activities in the duodenum and jejunum were increased in the BA+APS (p < 0.05), and the T-SOD activities in the spleen and T-AOC activities in the lymph node were also increased (p < 0.05), but the H2S level was decreased in the feces and urine (p < 0.05). Compared with the BA, the ADG, G/F and the trypsin and maltase activities in the duodenum were increased in the BA+GLP and BA+EPS (p < 0.05), the activities of maltase and lipase in the duodenum of fatteners in the BA+GLP and the activities of trypsin, maltase and lipase in the BA+EPS were increased (p < 0.05). Gathering everything together, our findings reveal that the combined addition of boric acid and plant polysaccharides in the diet of fatteners synergistically improved their growth performance and immune status. That may be achieved by regulating the activity of intestinal digestive enzymes, improving the antioxidant function and then promoting the digestion and absorption of nutrients. Furthermore, the above results reduce the emission of harmful gases and heavy metals in feces and urine.

1. Introduction

Antibiotics, as a drug that can inhibit and kill bacteria, are widely used in the livestock and poultry industry, playing a crucial role in preventing and treating animal diseases and promoting animal growth. Research has confirmed that the unreasonable use of veterinary antibiotics can lead to increased resistance to pathogenic bacteria, increased drug residues in animal products, decreased meat and egg quality and intensified environmental pollution [1]. In this situation, many countries have issued “anti-antibiotic orders” to reduce the application of antibiotics in animal husbandry production. Antibiotic substitution has gradually become a hot topic of concern. Under the trend of healthy and green development in animal husbandry, the utilization of antibiotic alternatives has become crucial for sustainable development in the field of livestock husbandry [2]. More and more literature reports that some organic trace elements, medicinal plants and fungi and their extracts can be ideal alternatives to antibiotics. This is because most medicinal plants, fungi and their extracts not only have a significant immune-enhancing effect but also have a certain promoting effect on animal growth. Many organic trace elements not only have antioxidant and immune-enhancing effects but also have the effect of improving the quality of meat and eggs [3]. In addition, medicinal plants, fungi and their extracts share common advantages with organic trace elements, such as low toxicity, no residue and no drug resistance [4]. Therefore, the application of medicinal plants, their extracts and organic trace elements in the healthy breeding of livestock and poultry is becoming increasingly widespread.
Plant and fungal polysaccharides are common plant or fungi extracts that are the main active ingredient for plants and fungi to exert physiological regulatory effects on animal bodies. Astragalus membranaceus, Echinacea purpurea and Ganoderma lucidum are common medicinal plants and fungi. Their extracts (polysaccharides) have broad biological activities, which can enhance the antioxidant and immune functions of animal bodies, improve digestive enzyme activity, promote animal cell growth and improve production performance. Research has found that adding 800 mg/kg Astragalus polysaccharides to the diet can increase the average daily weight gain and feed conversion rate of LPS-infected weaned piglets, promote cytokine expression, enhance antioxidant enzyme activity and thereby improve immune and digestive functions [5,6]. There are also reports pointing out that the addition of Echinacea at an appropriate level can enhance macrophage bactericidal ability, thereby regulating host defense against pathogen invasion and enhancing immune function in mice [7].
Boric acid is a weak inorganic acid and its boron element is an essential mineral element in animal bodies. Research has found that, like many organic trace elements, boron has lower toxicity to animal bodies. Supplementing boron elements in the form of boric acid in an appropriate amount can improve gastrointestinal pH and intestinal tissue structure and regulate intestinal microbiota and pepsin activity, thereby promoting nutrient digestibility [8]. In addition, boric acid can improve growth performance and enhance immunity and antioxidant function, while reducing the release of toxic and harmful substances from the body [9]. Furthermore, the results of previous experiments conducted by our lab have revealed that the addition of appropriate amounts of boric acid could mediate the apoptosis and immune function response of splenic lymphocytes in rats, indicating that boric acid could be added in appropriate amounts as an immunomodulatory agent in animal foods [10,11,12].
With the continuous improvement of people’s living standards, countries around the world are paying more and more attention to environmental pollution. The production of manure and harmful gases from pig farms is one of the main sources of environmental pollution, which not only has adverse effects on the healthy growth environment of animals but also poses a threat to human health [13]. How to effectively reduce environmental pollution caused by pig farming is gradually becoming a hot research topic. Research has found that adding green feed additives can improve animal digestive function, increase nutrient utilization and feed conversion rates, effectively reduce the emission of toxic and harmful substances in feces and urine, and thereby reduce environmental pollution, adding non-starch polysaccharides to the diet can improve the absorption rate of nutrients by fatteners, effectively control fecal excretion, reduce CO2 and other harmful gas emissions and further reduce environmental pollution [14,15].
However, as an ideal alternative to antibiotics and beneficial trace elements, it is still unclear whether Astragalus polysaccharides, Echinacea polysaccharides, Ganoderma lucidum polysaccharides and Boric acid can effectively reduce the emission of toxic and harmful substances in the feces and urine of fatteners. Moreover, it is not known whether the combined addition of Boric acid and plant polysaccharides can have a more effective effect on the production performance, digestive function, antioxidant function and immune function of fatteners, which hurts the scientific and rational use of these additives in pig production and the improvement of breeding efficiency. Therefore, we investigated the effects of the combined addition of Boric acid and plant polysaccharides on the production performance, digestive enzyme activity, immune and antioxidant functions, as well as harmful gas and heavy metal emissions in feces and urine of fatteners, to determine whether the combined addition can further improve the application effect and reduce the emission of harmful substances in pig feces and urine, thereby achieving better overall results.

2. Materials and Methods

The experimental protocol was reviewed and approved by the Animal Care and Use Committee of Anhui Science and Technology University.

2.1. Experimental Products

In this study, boric acid (analytical purity, 99.5% purity) is provided by China National Pharmaceutical Group Chemical Reagent Co., Ltd. (Shanghai, China) Astragalus polysaccharides, Ganoderma lucidum polysaccharides (brownish yellow powder) and Echinacea polysaccharides have purities of 50%, 70% and 10%, respectively, and provided by Xi’an Aosai Biotechnology Co., Ltd. (Xi’an, China) and Ningshan Guosheng Biotechnology Co., Ltd. (Shanxi, China).

2.2. Animals, Dietary Treatments and Experimental Design

A total of 90 crossbred fatteners (Duroc × Landrace × Yorkshire, 90 days old, from the same farm origin) with an initial body weight (IBW) of 41.25 ± 3.07 kg, were evenly divided into five groups, three replicate pens per group and six fatteners per pen. The five treatment groups were as follows: the control group was fed with a basal diet without boric acid and plant polysaccharides (Con), the experimental group I was fed with a basal diet + 40 mg/kg of boric acid (BA) [16], the experimental group II was fed with a basal diet + 40 mg/kg of boric acid + 400 mg/kg of 50% Astragalus polysaccharides (BA+APS) [17]; the experimental group III was fed with a basal diet + 40 mg/kg of boric acid + 200 mg/kg of 70% Ganoderma lucidum polysaccharides (BA+GLP) [18,19]; the experimental group IV was fed with a basal diet + 40 mg/kg of boric acid + 500 mg/kg of 10% Echinacea polysaccharides (BA+EPS) [20]. The whole experiment lasted for 90 days. The basal diet was formulated to meet the nutrient requirements according to the National Research Council (NRC 2012), as shown in Table 1. The basal diet used in the experiment is powder, produced by the feed processing plant of Anhui Hefeng Agriculture and Animal Husbandry Co., Ltd. (Bozhou, China). Before adding to the basal diet, boric acid and plant polysaccharides are weighed separately, first mixed with 1 kg of basal diet, then mixed with 10 kg of basal diet and finally mixed with 100 kg of basal diet.
Pigs were obtained and reared in fattening houses of the Wu Zifeng Experimental Farm at the Anhui Hefeng Agriculture and Animal Husbandry Co., Ltd. and six pigs per pen (18 m2 per pen and 3.0 m2 per piglet) were raised in the same area for suitable pig density during the whole experiment. Per pig per pen is kept separately with a metal fence on the partially slatted floor, with separate drinking water and feeding trough provided. There was 1 automatic stainless steel nipple drinker and 1 cement feeder (6 slots) per pig. The study was conducted from September to November 2022 in Lixin, Bozhou, Anhui Province. The conditions (temperature, humidity and so on) of the farm were, in real-time, monitored and controlled, and all fatteners were vaccinated following the farm’s routine vaccination program.

2.3. Sample Collection

Animals were weighed and labeled before the start of the experiment, and the initial weight measurements were recorded. The per-pen feed intake and uneaten feed were recorded to calculate the average daily feed intake at a fixed time every day. Three days before the end of the experiment, fresh feces and urine were randomly collected from 2 pigs per pen every morning. At the end of the experiment, the pigs were fasted for 12 h, and blood samples were taken from the ear vein, which were stored at 4 °C. The samples were centrifuged at 3000 r/min to obtain serum samples, which were stored at −80 °C. Tissue samples from the duodenum, jejunum, spleen and lymph nodes were collected from pigs after anesthesia [21]. Two pigs per pen were randomly selected for sample collection (30 samples), and the samples were frozen in liquid nitrogen and stored at −80 °C in an ultrafreezer.

2.4. Determination of Indices

2.4.1. Growth Performance

Individual pigs were weighed on an empty stomach at 7:00 a.m. on the 28th, 56th and 84th day of the experiment and before slaughter to determine the Average-day-gain (ADG). In addition, the amount of feed provided, uneaten feed and feed intake per pig per day were used to determine the average daily feed intake (ADFI), and gain-to-feed ratio (G/F) of the pig during the developmental stage.

2.4.2. Determination of Intestinal Digestive Enzyme Activity

The thawed duodenum and jejunum tissues was weighed on an electronic balance (accuracy up to 1000th of a gram), homogenized in an ice bath and centrifuged at 3000 revolutions per minute (rpm) for 15 min at 4 °C. The supernatants were obtained and stored at −80 °C for later use. The total protein content in the duodenum and jejunum homogenates was determined using the Total Protein Assay Kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). The activities of trypsin, maltase and lipase were measured with the corresponding Enzyme Activity Detection Kits as per the instructions of the manufacturer (Nanjing Jiancheng Bioengineering Institute).

2.4.3. Determination of Cytokine Contents

After thawing the supernatants of spleen and lymph node tissue at room temperature, tumor necrosis factor (TNF-α), interleukin-2 (IL-2), interleukin-6 (IL-6) and interferon-gamma (IFN-γ) in serum samples, spleen and lymph node tissues were measured. The measurement was performed according to the manufacturer’s instructions for the kit (Beijing Dacome Technology Co., Beijing, China).

2.4.4. Determination of Antioxidant Function

After thawing the supernatants of spleen and lymph node tissue at room temperature, the content or activity of malondialdehyde (MDA), superoxide dismutase (T-SOD), glutathione peroxidase (GSH-Px) and total antioxidant capacity (T-AOC) in the spleen and lymph node were measured using Antioxidant Function Assay Kit based on the manufacturer’s instructions (Nanjing Jiancheng Bioengineering Institute).

2.4.5. Determination of Harmful Gases and Metallic Elements in Faeces

Freshly collected 50 g feces and 50 g urine are mixed in an 845 mL plastic bottle for fermentation at room temperature (20 °C) for 24 h. Gas emissions of NH3 and H2S from feces and urine samples were continuously measured for three days. A portable gas sampling pump (ZC500; suction flow rate at 500 mL/min; Henan Kailu Electronic, Anyang, China) was used to extract gas from 2 cm above the mixture of feces and urine through a small hole at the bottle mouth. The gas values were recorded by the composite multi-gas detector (K-400A; Henan Kailu Electronic Co., Ltd.) [22].
The detection of metal ions and NH3-N contents in feces was performed by Qingdao Science and Technology Innovation Quality Testing Co., Ltd. (Qingdao, China)

2.5. Statistical Analysis

The normality of the distribution of the data was analyzed using Kolmogorov–Smirnov and the Shapiro–Wilk test (p > 0.05). Data following a normal parametric distribution underwent analysis of variance using the General Linear Model (GLM), with the model considering block, time and treatment effects. Tukey’s post hoc test was employed to analyze the significant differences between treatment groups. A p-value less than 0.05 was considered statistically significant. Non-normally distributed data were analyzed using the non-parametric Kruskal–Wallis test, the significance level of p < 0.05 was considered statistically significant. Designating treatment as the fixed factor and per pen as the experimental units. The dosage and type of additives are the main factors. The initial body weight was included as a covariate in the growth performance analysis. The statistical analyses were conducted using the IBM SPSS Statistics 23.0 software (SPSS Inc., Chicago, IL, USA). Correlations were assessed using Pearson correlation analysis of the Euclidean distance. All the data were presented as mean ± SD.

3. Results

3.1. Effects of Plant Polysaccharides Combined with Boric Acid on Growth Performance of Fatteners

Compared to the Con (Figure 1), the ADG was increased in BA, BA+APS, BA+GLP and BA+EPS (p = 0.042, p = 0.011, p = 0.022, p = 0.027), the ADFI was increased in BA+APS (p = 0.033) and the G/F were also increased in BA+APS, BA+GLP and BA+EPS (p = 0.031, p = 0.041, p = 0.046). Compared with BA, the ADG were increased in BA+APS, BA+GLP and BA+EPS (p = 0.025, p = 0.0342, p = 0.044), and the G/F were also increased in BA+APS, BA+GLP and BA+EPS (p = 0.031, p = 0.039, p = 0.046).

3.2. Effects of Plant Polysaccharides Combined with Boric Acid on Digestive Enzyme Activities of Fatteners

Compared with the Con (Figure 2), the trypsin activities were increased in the duodenum of fatteners in other groups (p = 0.039, p = 0.002, p = 0.023, p = 0.011), and increased in the jejunum of fatteners in other groups (p = 0.027, p = 0.014, p = 0.040, p = 0.005). Compared with the Con, the maltase activities were increased by 68.16%, 65.68% and 157.54% in the duodenum of fatteners in the BA+APS, BA+GLP and BA+EPS, respectively (p = 0.021, p = 0.020, p = 0.002), and also increased by 47.19%, 70.05% and 166.36% in the jejunum of fatteners in the BA, BA+APS and BA+EPS (p = 0.025, p = 0.014, p = 0.005), respectively, but decreased in the jejunum of fatteners in the BA+GLP (p = 0.034). Compared with the Con, the lipase activities were increased in the duodenum of fatteners in the BA+APS and BA+GLP (p = 0.021, p = 0.012), and also increased in the jejunum of fatteners in the BA+EPS (p = 0.011) but decreased in the duodenum of fatteners in the BA+EPS (p = 0.019). Compared with the BA, the trypsin activities were increased in the duodenum of fatteners in the BA+APS, BA+GLP and BA+EPS (p = 0.007, p = 0.027, p = 0.018), and also increased in the jejunum of fatteners in the BA+APS and BA+EPS (p = 0.021, p = 0.010). Compared with the BA, the maltase activities were increased in the duodenum of fatteners in the BA+APS, BA+GLP and BA+EPS (p = 0.024, p = 0.027, p = 0.007), and also increased in the jejunum of fatteners in the BA+APS and BA+EPS (p = 0.038, p = 0.011). Compared with the BA, the lipase activities were increased in the duodenum of fatteners in the BA+APS and BA+GLP (p = 0.019, p = 0.010), and also increased in the jejunum fatteners in the BA+EPS (p = 0.019, p = 0.010).

3.3. Effects of Plant Polysaccharides Combined with Boric Acid on Immune Function of Fatteners

Compared with the Con (Figure 3), the IL-2 levels were decreased in the serum of fatteners in the BA+APS (p = 0.034) but increased in the spleen of fatteners in the BA and BA+EPS (p = 0.028, p = 0.041). Compared with the Con, the IL-6 levels were decreased in the serum of fatteners in BA+APS (p = 0.032), and the IFN-γ levels were increased in the lymph node of fatteners in the BA+EPS (p = 0.033). Compared with the BA, the IL-2 levels were decreased in the spleen of fatteners in the BA+APS (p = 0.027), the IFN-γ levels were decreased in the serum of fatteners in the BA+APS (p = 0.046) and the IL-6 levels were also decreased in the serum of fatteners in BA+APS (p = 0.039).

3.4. Effects of Plant Polysaccharides Combined with Boric Acid on Antioxidant Activity of Fatteners

Compared with the Con (Figure 4), the T-AOC activities were increased in the lymph node of fatteners in BA (p = 0.016) and also increased in the spleen of fatteners in the BA+APS and BA+GLP (p = 0.012, p = 0.041). Compared with the Con, the T-SOD activities were decreased in the lymph node of fatteners in other groups (p < 0.01) but increased in the spleen of fatteners in other groups (p = 0.014, p = 0.031, p = 0.038, p = 0.016). Compared with the Con, the GSH-Px contents were increased in the lymph node of fatteners in other groups (p < 0.05), and the MDA contents were decreased in the lymph node of fatteners in other groups (p < 0.01) and also decreased in the spleen of fatteners in the BA (p = 0.026). Compared with the BA, the T-AOC activities were increased in the spleen of fatteners in the BA+APS (p = 0.027) and the MDA contents were increased in the lymph node and spleen of fatteners in the BA+EPS (p = 0.019, p = 0.034).

3.5. Effects of Plant Polysaccharides Combined with Boric Acid on the Contents of Harmful Substances in Feces and Urine of Fatteners

Compared with the Con (Figure 5), the contents of NH3 were decreased in the feces and urine of fatteners in other groups (p = 0.024, p = 0.026, p = 0.024, p = 0.012), and the contents of H2S were also decreased in the feces and urine of fatteners in other groups (p = 0.036, p = 0.002, p = 0.023, p = 0.025). No difference was found in NH3-N contents of the feces and urine in other groups. Compared with BA, the contents of NH3 were decreased by 9.33% in the feces and urine of fatteners in the BA+EPS (p = 0.041), and the contents of H2S were also decreased by 50.00% in the feces and urine of fatteners in the BA+APS (p = 0.015), while no change in NH3-N contents was observed.
Compared with the Con (Figure 6), no differences were observed in the contents of metal manganese (Mn) in the feces and urine of fatteners in other groups, but the contents of hydrargyrum (Hg), copper (Cu), ferrum (Fe) and zinc (Zn) were decreased in the feces and urine of fatteners in the BA (p = 0.036, p = 0.037, p = 0.008, p = 0.009), and the contents of Fe were decreased in the feces and urine of fatteners in the BA+APS, BA+GLP and BA+EPS (p = 0.028, p = 0.035, p = 0.008), and the contents of Zn were also decreased in the feces and urine of fatteners in the BA+APS, BA+GLP and BA+EPS (p = 0.032, p = 0.039, p = 0.009). Compared with the BA, the contents of Fe were increased in the feces and urine of fatteners in the BA+APS and BA+GLP (p = 0.024, p = 0.013), and the contents of Zn were also increased in the feces and urine of fatteners in the BA+APS and BA+GLP (p = 0.027, p = 0.015).

3.6. Correlation Analysis

3.6.1. The Correlation Analyses between Intestinal Digestive Enzymes and the Contents of Harmful Substances

In the duodenum, the intestinal digestive enzymes were significantly negatively correlated with NH3 and H2S (Figure 7). In the jejunum, the intestinal digestive enzymes were significantly negatively correlated with NH3, Fe and Zn.

3.6.2. The Correlation Analyses between Serum Immune Proteins and the Contents of Harmful Substances

As shown in Figure 8, the IL-2 was significantly positively correlated with H2S, the IL-6 was significantly positively correlated with NH3-N, the INF-γ was significantly negatively correlated with NH3, Fe and Zn, the TNF-α was significantly negatively correlated with Cu.

3.6.3. The Correlation Analyses between Antioxidant Function and the Contents of Harmful Substances

In the lymph node, the T-AOC was significantly negatively correlated with Fe and Zn (Figure 9). The T-SOD was significantly positively correlated with NH3, H2S, Mn, Fe and Zn. The MDA was significantly positively correlated with NH3, H2S and Mn. In the spleen, the T-AOC was significantly negatively correlated with H2S. The T-SOD was significantly negatively correlated with NH3, Mn, Fe and Zn. The GSH-Px was significantly positively correlated with Hg, Mn, Fe and Zn. The NH3 was significantly positively correlated with Mn, Fe and Zn.
The results of correlation analysis support the hypothesis that boric acid and plant polysaccharides have a significant correlation (p < 0.05 or p < 0.01) with intestinal digestive enzymes, serum cytokines and antioxidant indicators in the process of dealing with harmful gas and heavy metal emissions in the health fatteners. It may be that the response of intestinal digestive enzymes promotes the body to digest and absorb nutrients, improves the immune function of the body, increases the utilization rate of animal feed and reduces the emission of harmful gases and the emission of feces containing various heavy metal elements.

4. Discussion

Plant polysaccharides have various biological activities, which can regulate animal nutritional requirements and potentially improve their digestive capacity, thereby effectively reducing the use of antibiotics in animal husbandry [23]. Studies have shown that the feed supplemented with Astragalus polysaccharides effectively enhanced their immunity and growth performance in broiler chickens [24]. Similarly, compared to the control group, fed Echinacea polysaccharides increased weight gain and feed conversion ratio during the growing period of broiler chickens [25]. Additionally, it has been shown that providing an appropriate amount of boric acid can increase ADG and ADFI during the growth period of pigs [26].
The functioning of digestive enzymes in the animal intestine is crucial for breaking down and absorbing ingested nutrients. Supplementing exogenous digestive enzymes in the diet can improve animal production performance, feed conversion rate and digestion rate, thereby enhancing intestinal immune function [27] and promoting animal health. Luo et al. found that adding protease and glucoamylase to the diet of broiler chickens can significantly increase trypsin activity, increase digestion emptying time and reduce FCR (F/G) and visible water in feces, thereby alleviating diarrhea caused by newly harvested corn diets [28]. Yi et al. reported that adding enzyme complexes containing amylase, protease and xylanase to the diet can improve nutrient digestibility, increase the concentration of volatile fatty acids and the proportion of Escherichia coli, thereby promoting intestinal health and improve piglet production performance [29]. Previous studies have fully confirmed that increasing the activity of digestive enzymes can promote the absorption of nutrients, increase nutrient digestibility, enhance immune function and thereby enhance animal production performance, promoting body health. However, the secretion and activity of these digestive enzymes can be influenced by various factors, such as the parts of the intestine and cells, the amount and composition of amino acids and the digestion products of ingested proteins [30,31]. Previous studies have shown that supplementation with Astragalus polysaccharides in feed can effectively enhance digestive enzyme activity and improve secretion in the chicken intestine [32]. Additionally, it has been reported that feeding Ganoderma lucidum polysaccharides to freshwater shrimp (Macrobrachium rosenbergii) promoted growth and digestive enzyme activity, thus promoting digestive function [33].
In this study, the combination of different plant polysaccharides and boric acid can enhance the activities of trypsin, maltase and lipase in the duodenum and jejunum of fatteners when compared to the control group and the group supplemented with only boric acid. These results suggest that the combination of different plant polysaccharides and boric acid can improve the ability of the animals to chemically digest nutrients in the intestine. One possible mechanism is that Astragalus polysaccharides and Echinacea extract can improve the balance of intestinal micro-organisms, thus maintaining intestinal function and promoting overall growth performance and health levels [34,35].
Several studies have highlighted that Echinacea can stimulate T-cell phagocytosis and enhance lymphocyte activity in broilers, as well as improve cell antioxidant, anti-inflammatory and antimicrobial activities [36]. Therefore, Echinacea can be considered a recommended alternative to antibiotics [37,38,39]. Moreover, Echinacea polysaccharides have been shown to improve immune indices and increase levels of INF-α, IFN-γ and IL-2 in sera [40], as well as an increase in the total levels of lgG and γ-interferon along with an increase of important cytokine genes expression in calves [41]. Similarly, feeding Astragalus polysaccharides to mice with lung cancer resulted in improvements in white blood cell count, thymus index, spleen index and cytokine levels, thus effectively regulating immune function [42]. Moreover, Ganoderma lucidum polysaccharides have been shown to produce immunomodulatory effects by increasing the levels of serum IL-2, TNF-α and IFN-γ, then enhancing the activity of NK cells and T-cells and regulating the immune response [43].
Immune function and spleen lymphocyte proliferation were improved by administering 0.4 mmol/L of boron in mice [10]. The beneficial effects of the combinations of plant polysaccharides and boric acid were observed possibly due to the effect of individual immune-enhancing effects of boric acid in this study because its addition produced a more pronounced improvement in antibody levels and cytokine production in fatteners.
Research focused on the antioxidant function of Echinacea has revealed that the addition of 0.5–2.0% Echinacea into animal feed could increase the Trolox equivalent antioxidant capacity, as well as catalase (CAT) and SOD activity in the serum and spleen of broilers [26]. Similarly, adding Echinacea into the diet of crucian carp could stimulate their growth performance and elicit an antioxidant response [44]. Feeding a large yellow croaker with 150 mg/kg of Astragalus polysaccharides increased liver T-AOC, GSH-Px and lysozyme activities [45]. Furthermore, supplementation with Ganoderma lucidum polysaccharides has been shown to alleviate oxidative stress and inflammation in rats by up-regulating SOD, CAT and GSH-Px contents, increasing IL-10 levels and preventing excess production of MDA [46]. The addition of 160 mg/kg of boric acid positively affected the development of ostrich kidneys, inhibited cell apoptosis, regulated enzyme activity, improved the antioxidant system and enhanced overall antioxidant capacity [47]. This enhanced antioxidant effect can be attributed to the antioxidant properties of Astragalus polysaccharides, Ganoderma lucidum polysaccharides and Echinacea extract individually. When combined with boric acid, their effects are synergistically enhanced, further promoting their effects.
Animal feces can produce harmful gases, such as NH3 and H2S. If harmful gases are emitted excessively, they will pollute the air and threaten human health. NH3 can cause respiratory diseases, while H2S can damage the nervous system [48]. Plant secondary metabolites have been shown to improve the composition of animal rumen bacterial communities, leading to a reduction in methane emissions and influencing rumen fermentation [49]. Previous studies showed that adding a mixture of plant extracts can reduce the emissions of harmful gases (NH3 and H2S) in the feces of growing and fatteners [50].
In this study, the addition of boric acid alone decreased the contents of NH3 and H2S. However, the combined use of boric acid and plant polysaccharides further reduced NH3 and H2S emissions. When boric acid was combined with Echinacea polysaccharides, the NH3 contents were decreased, while its combination with Astragalus polysaccharides led to a reduction of H2S contents. The results can be attributed to that boric acid can improve animal digestion and promote protein absorption in the feed, while plant polysaccharides enhance the intestinal microbial community and improve intestinal function [51]. The addition of polysaccharides can regulate rumen microbial populations, promoting the growth of beneficial micro-organisms while inhibiting methanogenic bacteria, thus helping to reduce methane production [52,53]. Thus, the combined supplementation of boric acid and plant polysaccharides enhances gastrointestinal digestion, leading to a reduction in the emission of harmful gases in feces.
Excessive emissions of heavy metal substances from feces can have detrimental effects on the environment and food safety. Moreover, the long-term accumulation of metals in the soil can lead to risks for both the atmosphere and agricultural products Common metal residues found in livestock and poultry feces include Zn, Fe, lead, chromium, cadmium, arsenic, Hg and others. In this study, the addition of boric acid alone led to a reduction of contents of Cu, Fe and Zn, when compared to the control group. However, when boric acid was combined with plant polysaccharides—particularly Echinacea polysaccharides—further reductions in the contents of Fe and Zn were noted. The reason may be that a series of effects of boron on the metabolism of minerals in animal organisms [54], at the same time, the addition of polysaccharides may also have a series of beneficial effects on the absorption and utilization of minerals by the body [55]. By combining the two, the body can enhance its absorption and utilization of minerals, thereby reducing the excretion of heavy metals through feces and urine [56].
As one of the most common substrates in biogas production, cow and pig faces are often considered to provide necessary nutrients and trace elements to stabilize the biogas process [57], and the harmful gases can have a huge impact on the environment and seriously pollute human health. Research reports indicate that supplementing with lipase in diet can promote the digestion rate of nutrients, thereby having a beneficial effect on intestinal proteases and reducing NH3 emissions in pigs. This is consistent with our research findings, which indicate that NH3 decreases with the increase of digestive enzymes [58]. When livestock faces are used as fertilizer, metal elements present as common pollutants in livestock manure may cause terrestrial ecological toxicity. Research has found that zinc and copper are the main factors affecting the overall soil quality [59]. Research has reported that there is a correlation between Fe, Mn and Al elements in the body and the inflammatory response in humans and animals [60], which is consistent with this conclusion. Previous results showed that a diet with a copper level of 20 mg·kg−1 significantly increased TNF-α of serum in piglets [61,62]. This is consistent with our results. Further studies have pointed out that heavy metals or toxic elements are one of the interfering factors affecting the absorption process of trace elements from the intestine [63].
This study analyzed the correlation between the harmful gas and element content and intestinal digestive enzymes, serum immune proteins and antioxidant function. It was found that intestinal digestive enzyme activity, serum cytokines and antioxidant function showed a certain correlation with the contents of harmful gases, which may affect the emission of harmful gases and heavy metals by animals, thereby reducing their environmental pollution.
However, in our experiment, choosing fattening pigs as the research object has certain limitations. Different animals have different sensitivities to the added doses of boron and plant polysaccharides [64,65]. Broilers and ostriches have significantly different sensitivities to boron compared to rats. Broilers and ostriches need to supplement higher doses of boron to have beneficial effects. Moreover, environmental conditions have a direct impact on the application effect of boron and plant polysaccharides. Therefore, further research is needed to confirm the application effect of the results of this study in other animals.

5. Conclusions

In this study, the combined use of boric acid and plant polysaccharides in the diets of fatteners led to favorable effects, when compared to the use of boric acid alone. In particular, the combined use of boric acid and plant polysaccharides increased ADG and G/F and increased the trypsin activity in the duodenum and jejunum and GSH-Px content of lymph nodes, but decreased MDA content in lymph nodes. So, the combination of boric acid and plant polysaccharides can improve the digestion and absorption of nutrients by enhancing intestinal digestive enzyme activity and antioxidant function. With the increase of digestive enzyme activity, the body can effectively utilize various nutrients, which can reduce the release of harmful gases such as NH3 and H2S and reduce the content of harmful heavy metals in feces and urine. Based on the above results, the combination of boric acid and Echinacea polysaccharides presented the most pronounced benefits. This study provided a basis for future research on boric acid and plant polysaccharides as a feed additive in pigs.

Author Contributions

Conceptualization, J.D., F.Z., H.F., Y.Z., C.Z., M.R., E.J. and Y.G.; methodology, J.D., F.Z. and E.J.; formal analysis, J.D., F.Z. and C.Z.; resources, J.D. and F.Z.; data curation, J.D., H.F. and M.R.; writing—original draft preparation, J.D.; writing—review and editing, J.D., F.Z. and E.J.; project administration, J.D., Y.Z. and Y.G.; funding acquisition, J.D. and E.J. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (32172816, 32002160), the Anhui Natural Science Foundation Project (2108085MC117, 2208085MC77), the Natural Science Key Foundation of Anhui Education Department (2022AH040032). Anhui Province Key Research and Development Program Project (202204c06020055), the Anhui Province Graduate Innovation and Entrepreneurship Practice (2022cxcysj196) and the Innovation Project for College Students in Anhui Province (S202310879058). Anhui Province Graduate Innovation and Entrepreneurship Practice (2023cxcysj176).

Institutional Review Board Statement

This study was conducted according to the guidelines of the Guide for the Care and Use of Laboratory Animals and approved by the Institutional Animal Care and Use Committee of the Anhui Science and Technology University (permission number: No. SYXK2020-0053, 20 August 2020).

Informed Consent Statement

Not applicable.

Data Availability Statement

Raw data collected and presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Du, D.; Zhou, J.; Zhang, K.; Zhi, S. Seasonal pollution characteristics of antibiotics on pig farms of different scales. Int. J. Environ. Res. Public Health 2022, 19, 8264. [Google Scholar] [CrossRef] [PubMed]
  2. Pu, H.; Li, X.; Du, Q.; Cui, H.; Xu, Y. Research progress in the application of chinese herbal medicines in aquaculture: A Review. Engineering 2017, 3, 731–737. [Google Scholar] [CrossRef]
  3. Yang, C.M.; Han, Q.J.; Wang, K.L.; Xu, Y.L.; Lan, J.H.; Cao, G.T. Astragalus and ginseng polysaccharides improve developmental, intestinal morphological, and immune functional characters of weaned piglets. Front. Physiol. 2019, 10, 418. [Google Scholar] [CrossRef] [PubMed]
  4. Zhao, R.-H.; Yang, F.-X.; Bai, Y.-C.; Zhao, J.-Y.; Hu, M.; Zhang, X.-Y.; Dou, T.-F.; Jia, J.-J. Research progress on the mechanisms underlying poultry immune regulation by plant polysaccharides. Front. Vet. Sci. 2023, 10, 1175848. [Google Scholar] [CrossRef] [PubMed]
  5. Zhuge, Z.-Y.; Zhu, Y.-H.; Liu, P.-Q.; Yan, X.-D.; Yue, Y.; Weng, X.-G.; Zhang, R.; Wang, J.-F. Effects of astragalus polysaccharide on immune responses of porcine PBMC stimulated with PRRSV or CSFV. PLoS ONE 2012, 7, e29320. [Google Scholar] [CrossRef]
  6. Wang, K.L.; Zhang, H.R.; Han, Q.J.; Lan, J.H.; Chen, G.Y.; Cao, G.T.; Yang, C.M. Effects of astragalus and ginseng polysaccharides on growth performance, immune function and intestinal barrier in weaned piglets challenged with lipopolysaccharide. J. Anim. Physiol. Anim. Nutr. 2020, 104, 1096–1105. [Google Scholar] [CrossRef]
  7. Fu, A.K.; Wang, Y.; Wu, Y.P.; Chen, H.L.; Zheng, S.S.; Li, Y.L.; Xu, X.; Li, W.F. Echinacea purpurea extract polarizes M1 macrophages in murine bone marrow-derived macrophages through the activation of JNK. J. Cell. Biochem. 2017, 118, 2664–2671. [Google Scholar] [CrossRef]
  8. Pearlin, B.V.; Muthuvel, S.; Govidasamy, P.; Villavan, M.; Alagawany, M.; Ragab Farag, M.; Dhama, K.; Gopi, M. Role of acidifiers in livestock nutrition and health: A review. J. Anim. Physiol. Anim. Nutr. 2020, 104, 558–569. [Google Scholar] [CrossRef]
  9. Haseeb, K.; Wang, J.; Xiao, K.; Yang, K.L.; Peng, K.M. Effects of boron supplementation on expression of hsp70 in the spleen of african ostrich. Biol. Trace Elem. Res. 2018, 182, 317–327. [Google Scholar] [CrossRef]
  10. Wang, C.F.; Jin, E.H.; Deng, J.; Pei, Y.Q.; Ren, M.; Hu, Q.Q.; Gu, Y.F.; Li, S.H. GPR30 mediated effects of boron on rat spleen lymphocyte proliferation, apoptosis, and immune function. Food Chem. Toxicol. 2020, 146, 8. [Google Scholar] [CrossRef]
  11. Jin, E.; Ren, M.; Liu, W.; Liang, S.; Hu, Q.; Gu, Y.; Li, S. Effect of boron on thymic cytokine expression, hormone secretion, antioxidant functions, cell proliferation, and apoptosis potential via the ERK1/2 signaling pathway. J. Agric. Food Chem. 2017, 65, 11280–11291. [Google Scholar] [CrossRef]
  12. Jin, E.; Li, S.; Ren, M.; Hu, Q.; Gu, Y.; Li, K. Boron affects immune function through modulation of splenic T lymphocyte subsets, cytokine secretion, and lymphocyte proliferation and apoptosis in rats. Biol. Trace Elem. Res. 2017, 178, 261–275. [Google Scholar] [CrossRef] [PubMed]
  13. Lan, R.; Kim, I.H. Effects of bacillus licheniformis and bacillus subtilis complex on growth performance and faecal noxious gas emissions in growing-finishing pigs. J. Sci. Food Agric. 2018, 99, 1554–1560. [Google Scholar] [CrossRef] [PubMed]
  14. Chen, Y.; Shen, D.; Zhang, L.; Zhong, R.; Liu, Z.; Liu, L.; Chen, L.; Zhang, H. Supplementation of non-starch polysaccharide enzymes cocktail in a corn-miscellaneous meal diet improves nutrient digestibility and reduces carbon dioxide emissions in finishing pigs. Animals 2020, 10, 232. [Google Scholar] [CrossRef] [PubMed]
  15. Clark, O.G.; Moehn, S.; Edeogu, I.; Price, J.; Leonard, J. Manipulation of dietary protein and nonstarch polysaccharide to control swine manure emissions. J. Environ. Qual. 2005, 34, 1461–1466. [Google Scholar] [CrossRef] [PubMed]
  16. Liao, S.F.; Monegue, J.S.; Lindemann, M.D.; Cromwell, G.L.; Matthews, J.C. Dietary supplementation of boron differentially alters expression of borate transporter (NaBCl) mRNA by jejunum and kidney of growing pigs. Biol. Trace Elem. Res. 2011, 143, 901–912. [Google Scholar] [CrossRef]
  17. Lai, X.; Xia, W.; Wei, J.; Ding, X. Therapeutic effect of astragalus polysaccharides on hepatocellular carcinoma H22-bearing mice. Dose-Response 2017, 15, 3517–3524. [Google Scholar] [CrossRef]
  18. Huang, Q.; Li, L.; Chen, H.; Liu, Q.; Wang, Z. GPP (composition of Ganoderma iucidum poly-saccharides and Polyporus umbellatus poly-saccharides) enhances innate immune function in mice. Nutrients 2019, 11, 1480. [Google Scholar] [CrossRef] [PubMed]
  19. Li, X.L.; He, L.P.; Yang, Y.; Liu, F.J.; Cao, Y.; Zuo, J.J. Effects of extracellular polysaccharides of Ganoderma lucidum supplementation on the growth performance, blood profile, and meat quality in finisher pigs. Livest. Sci. 2015, 178, 187–194. [Google Scholar] [CrossRef]
  20. Gu, D.; Wang, H.; Yan, M.; Li, Y.; Yang, S.; Shi, D.; Guo, S.; Wu, L.; Liu, C. Echinacea purpurea (L.) moench extract suppresses inflammation by inhibition of C3a/C3aR signaling pathway in TNBS-induced ulcerative colitis rats. J. Ethnopharmacol. 2023, 307, 116221. [Google Scholar] [CrossRef]
  21. Barbosa, K.A.; Genova, J.L.; Pazdziora, M.L.; Hennig, J.F.; Azevedo, L.B.d.; Veiga, B.R.d.M.; Rodrigues, G.d.A.; Carvalho, S.T.; Paiano, D.; Saraiva, A.; et al. The role of dietary monoglycerides and tributyrin in enhancing performance and intestinal health function in nursery piglets. Ital. J. Anim. Sci. 2023, 22, 626–638. [Google Scholar] [CrossRef]
  22. Philippe, F.-X.; Canart, B.; Vandenheede, M.; Nicks, B. Comparison of ammonia and greenhouse gas emissions during the fattening of pigs, kept either on fully slatted floor or on deep litter. Livest. Sci. 2007, 111, 144–152. [Google Scholar] [CrossRef]
  23. Mohan, K.; Rajan, D.K.; Muralisankar, T.; Ganesan, A.R.; Marimuthu, K.; Sathishkumar, P. The potential role of medicinal mushrooms as prebiotics in aquaculture: A review. Rev. Aquac. 2022, 14, 1300–1332. [Google Scholar] [CrossRef]
  24. Wu, S.J. Effect of dietary Astragalus membranaceus polysaccharide on the growth performance and immunity of juvenile broilers. Poult. Sci. 2018, 97, 3489–3493. [Google Scholar] [CrossRef] [PubMed]
  25. Lee, T.T.; Chen, C.L.; Wang, C.C.; Yu, B. Growth performance and antioxidant capacity of broilers supplemented with Echinacea purpurea L. in the diet. J. Appl. Poult. Res. 2012, 21, 484–491. [Google Scholar] [CrossRef]
  26. Armstrong, T.A.; Spears, J.W. Effect of dietary boron on growth performance, calcium and phosphorus metabolism, and bone mechanical properties in growing barrows. J. Anim. Sci. 2001, 79, 3120–3127. [Google Scholar] [CrossRef] [PubMed]
  27. Liu, S.; Feng, L.; Jiang, W.-D.; Liu, Y.; Jiang, J.; Wu, P.; Zeng, Y.-Y.; Xu, S.-D.; Kuang, S.-Y.; Tang, L.; et al. Impact of exogenous lipase supplementation on growth, intestinal function, mucosal immune and physical barrier, and related signaling molecules mRNA expression of young grass carp (Ctenopharyngodon idella). Fish Shellfish Immunol. 2016, 55, 88–105. [Google Scholar] [CrossRef] [PubMed]
  28. Luo, C.; Wang, L.; Yuan, J. Supplemental enzymes and probiotics on the gut health of broilers fed with a newly harvested corn diet. Poult. Sci. 2023, 102, 102740. [Google Scholar] [CrossRef]
  29. Yi, J.Q.; Piao, X.S.; Li, Z.C.; Zhang, H.Y.; Chen, Y.; Li, Q.Y.; Liu, J.D.; Zhang, Q.; Ru, Y.J.; Dong, B. The Effects of Enzyme Complex on Performance, Intestinal Health and Nutrient Digestibility of Weaned Pigs. Asian-Australas. J. Anim. Sci. 2013, 26, 1181–1188. [Google Scholar] [CrossRef]
  30. Ren, M.; Liu, C.; Zeng, X.; Yue, L.; Mao, X.; Qiao, S.; Wang, J. Amino acids modulates the intestinal proteome associated with immune and stress response in weaning pig. Mol. Biol. Rep. 2014, 41, 3611–3620. [Google Scholar] [CrossRef]
  31. Kyoung, H.; Lee, J.J.; Cho, J.H.; Choe, J.; Kang, J.; Lee, H.; Liu, Y.H.; Kim, Y.; Kim, H.B.; Song, M. Dietary glutamic acid modulates immune responses and gut health of weaned pigs. Animals 2021, 11, 15. [Google Scholar] [CrossRef] [PubMed]
  32. Ma, Y.H.; Liu, C.Y.; Qu, D.; Chen, Y.; Huang, M.M.; Liu, Y.P. Antibacterial evaluation of sliver nanoparticles synthesized by polysaccharides from Astragalus membranaceus roots. Biomed. Pharmacother. 2017, 89, 351–357. [Google Scholar] [CrossRef] [PubMed]
  33. Li, K.K.; Zhuo, C.; Teng, C.Y.; Yu, S.M.; Wang, X.; Hu, Y.; Ren, G.M.; Yu, M.; Qu, J.J. Effects of Ganoderma lucidum polysaccharides on chronic pancreatitis and intestinal microbiota in mice. Int. J. Biol. Macromol. 2016, 93, 904–912. [Google Scholar] [CrossRef] [PubMed]
  34. Matthias, A.; Banbury, L.; Bone, K.M.; Leach, D.N.; Lehmann, R.P. Echinacea alkylamides modulate induced immune responses in T-cells. Fitoterapia 2008, 79, 53–58. [Google Scholar] [CrossRef] [PubMed]
  35. Rahimi, S.; Zadeh, Z.T.; Torshizi, M.; Omidbaigi, R.; Rokni, H. Effect of the three herbal extracts on growth performance, immune system, blood factors and lntestinal selected bacterial population in broiler chickens. J. Agric. Sci. Technol. 2011, 13, 527–539. [Google Scholar] [CrossRef]
  36. Gh, G.; Toghyani, M.; Moattar, F. The effects of Echinacea purpurea L. (purple coneflower) as an antibiotic growth promoter substitution on performance, carcass characteristics and humoral immune response in broiler chickens. J. Med. Plants Res. 2011, 5, 2332–2338. [Google Scholar] [CrossRef]
  37. Tierra, M. Echinacea: An effective alternative to antibiotics. J. Herb. Pharmacother 2008, 7, 78–89. [Google Scholar]
  38. Fu, R.; Zhang, P.; Deng, Z.; Jin, G.; Guo, Y.; Zhang, Y. Diversity of antioxidant ingredients among Echinacea species. Ind. Crop. Prod. 2021, 170, 113699. [Google Scholar] [CrossRef] [PubMed]
  39. Ogal, M.; Johnston, S.L.; Klein, P.; Schoop, R. Echinacea reduces antibiotic usage in children through respiratory tract infection prevention: A randomized, blinded, controlled clinical trial. Eur. J. Med. Res. 2021, 26, 33. [Google Scholar] [CrossRef]
  40. Lin, R.Z.; Zhi, C.P.; Su, Y.L.; Chen, J.X.; Gao, D.B.; Li, S.H.; Shi, D.Y. Effect of echinacea on gut microbiota of immunosuppressed ducks. Front. Microbiol. 2023, 13, 12. [Google Scholar] [CrossRef]
  41. Seckin, C.; Kalayci, G.A.; Turan, N.; Yilmaz, A.; Yilmaz, H. Immunomodulatory effects of echinacea and pelargonium on the innate and adoptive immunity in calves. Food Agric. Immunol. 2018, 29, 744–761. [Google Scholar] [CrossRef]
  42. Zhou, X.; Liu, Z.J.; Long, T.T.; Zhou, L.J.; Bao, Y.X. Immunomodulatory effects of herbal formula of astragalus polysaccharide (APS) and polysaccharopeptide (PSP) in mice with lung cancer. Int. J. Biol. Macromol. 2018, 106, 596–601. [Google Scholar] [CrossRef] [PubMed]
  43. Wang, C.H.; Shi, S.S.; Chen, Q.; Lin, S.Q.; Wang, R.; Wang, S.Z.; Chen, C.M. Antitumor and immunomodulatory activities of Ganoderma lucidum polysaccharides in glioma-bearing rats. Integr. Cancer Ther. 2018, 17, 674–683. [Google Scholar] [CrossRef] [PubMed]
  44. Tang, X.-L.; Fu, J.-H.; Li, Z.-H.; Fang, W.-P.; Yang, J.-Y.; Zou, J.-X. Effects of a dietary administration of purple coneflower (Echinacea purpurea) on growth, antioxidant activities and 8 miRNAs expressions in crucian carp (Carassius auratus). Aquac. Res. 2016, 47, 1631–1638. [Google Scholar] [CrossRef]
  45. Sun, Y.; Wang, X.; Zhou, H.; Mai, K.; He, G. Dietary astragalus polysaccharides ameliorates the growth performance, antioxidant capacity and immune responses in turbot (Scophthalmus maximus L.). Fish Shellfish Immunol. 2020, 99, 603–608. [Google Scholar] [CrossRef] [PubMed]
  46. Jiang, G.Y.; Lei, A.T.; Chen, Y.; Yu, Q.; Xie, J.H.; Yang, Y.; Yuan, T.J.; Su, D. The protective effects of the Ganoderma atrum polysaccharide against acrylamide-induced inflammation and oxidative damage in rats. Food Funct. 2021, 12, 397–407. [Google Scholar] [CrossRef]
  47. Khaliq, H.; Wang, J.; Xiao, K.; Yang, K.L.; Sun, P.P.; Lei, C.; Qiu, W.W.; Lei, Z.X.; Liu, H.Z.; Song, H.; et al. Boron affects the development of the kidney through modulation of apoptosis, antioxidant capacity, and Nrf2 pathway in the african ostrich chicks. Biol. Trace Elem. Res. 2018, 186, 226–237. [Google Scholar] [CrossRef] [PubMed]
  48. Wang, Y.; Chen, Y.J.; Cho, J.H.; Yoo, J.S.; Huang, Y.; Kim, H.J.; Shin, S.O.; Zhou, T.X.; Kim, I.H. Effect of soybean hull supplementation to finishing pigs on the emission of noxious gases from slurry. Anim. Sci. J. 2009, 80, 316–321. [Google Scholar] [CrossRef] [PubMed]
  49. Joch, M.; Mrazek, J.; Skrivanova, E.; Cermak, L.; Marounek, M. Effects of pure plant secondary metabolites on methane production, rumen fermentation and rumen bacteria populations in vitro. J. Anim. Physiol. Anim. Nutr. 2018, 102, 869–881. [Google Scholar] [CrossRef]
  50. Yan, L.; Lim, S.U.; Kim, I.H. Effect of fermented chlorella supplementation on growth performance, nutrient digestibility, blood characteristics, fecal microbial and fecal noxious gas content in growing pigs. Asian-Australas. J. Anim. Sci. 2012, 25, 1742–1747. [Google Scholar] [CrossRef]
  51. Liu, C.; Jiang, W.H.; Yang, F.W.; Cheng, Y.L.; Guo, Y.H.; Yao, W.R.; Zhao, Y.; Qian, H. The combination of microbiome and metabolome to analyze the cross-cooperation mechanism of echinacea purpurea polysaccharide with the gut microbiota in vitro and in vivo. Food Funct. 2022, 13, 10069–10082. [Google Scholar] [CrossRef] [PubMed]
  52. Cheong, K.-L.; Zhang, Y.; Li, Z.; Li, T.; Ou, Y.; Shen, J.; Zhong, S.; Tan, K. Role of Polysaccharides from Marine Seaweed as Feed Additives for Methane Mitigation in Ruminants: A Critical Review. Polymers 2023, 15, 3153. [Google Scholar] [CrossRef]
  53. Sun, X.; Cheng, L.; Jonker, A.; Munidasa, S.; Pacheco, D. A review: Plant carbohydrate types—The potential impact on ruminant methane emissions. Front. Vet. Sci. 2022, 9, 880115. [Google Scholar] [CrossRef]
  54. Hunt, C.D.; Herbel, J.L.; Idso, J.P. Dietary boron modifies the effects of vitamin D3 nutrition on indices of energy substrate utilization and mineral metabolism in the chick. J. Bone Miner. Res. 1994, 9, 171–182. [Google Scholar] [CrossRef]
  55. Na, Y.; Lee, J.; Lee, S.H.; Kumar, P.; Kim, J.H.; Patel, R. Removal of heavy metals by polysaccharide: A review. Polym.-Plast. Tech. Mat. 2020, 59, 1770–1790. [Google Scholar] [CrossRef]
  56. Yu, Q.L.; Sun, X.H.; Zhao, J.L.; Zhao, L.; Chen, Y.F.; Fan, L.N.; Li, Z.X.; Sun, Y.Z.; Wang, M.Q.; Wang, F. The effects of zinc deficiency on homeostasis of twelve minerals and trace elements in the serum, feces, urine and liver of rats. Nutr. Metab. 2019, 16, 8. [Google Scholar] [CrossRef]
  57. Nordell, E.; Nilsson, B.; Nilsson Påledal, S.; Karisalmi, K.; Moestedt, J. Co-digestion of manure and industrial waste—The effects of trace element addition. Waste Manag. 2016, 47, 21–27. [Google Scholar] [CrossRef] [PubMed]
  58. Liu, J.B.; Cao, S.C.; Liu, J.; Pu, J.; Chen, L.; Zhang, H.F. Effects of dietary energy and lipase levels on nutrient digestibility, digestive physiology and noxious gas emission in weaning pigs. Asian-Australas. J. Anim. Sci. 2018, 31, 1963–1973. [Google Scholar] [CrossRef]
  59. Sydow, M.; Chrzanowski, Ł.; Leclerc, A.; Laurent, A.; Owsianiak, M. Terrestrial ecotoxic impacts stemming from emissions of Cd, Cu, Ni, Pb and Zn from manure: A spatially differentiated assessment in europe. Sustainability 2018, 10, 4094. [Google Scholar] [CrossRef]
  60. So, K.-M.; Lee, Y.; Bok, J.D.; Kim, E.B.; Chung, M.I. Analysis of ionomic profiles of canine hairs exposed to lipopolysaccharide (LPS)-induced stress. Biol. Trace Elem. Res. 2016, 172, 364–371. [Google Scholar] [CrossRef]
  61. Zhang, F.; Zheng, W.; Guo, R.; Yao, W. Effect of dietary copper level on the gut microbiota and its correlation with serum inflammatory cytokines in Sprague-Dawley rats. J. Microbiol. 2017, 55, 694–702. [Google Scholar] [CrossRef] [PubMed]
  62. Zhang, F.; Zheng, W.; Xue, Y.; Yao, W. Suhuai suckling piglet hindgut microbiome-metabolome responses to different dietary copper levels. Appl. Microbiol. Biotechnol. 2019, 103, 853–868. [Google Scholar] [CrossRef] [PubMed]
  63. Xu, Z.R.; Han, X.Y.; Wang, Y.Z. Effects on growth and cadmium residues from feeding cadmium-added diets with and without montmorillonite nanocomposite to growing pigs. Vet. Human Toxicol. 2004, 46, 238–241. [Google Scholar] [CrossRef] [PubMed]
  64. Jin, E.; Gu, Y.; Wang, J.; Jin, G.; Li, S. Effect of Supplementation of Drinking Water with Different Levels of Boron on Performance and Immune Organ Parameters of Broilers. Ital. J. Anim. Sci. 2014, 13, 3152. [Google Scholar] [CrossRef]
  65. Sun, P.; Luo, Y.; Wu, X.T.; Ansari, A.R.; Wang, J.; Yang, K.; Xiao, K.; Peng, K. Effects of Supplemental Boron on Intestinal Proliferation and Apoptosis in African Ostrich Chicks. Int. J. Morphol 2016, 34, 830–835. [Google Scholar] [CrossRef]
Figure 1. Effects of adding different plant polysaccharides combined with boric acid in the diet on growth performance of fatteners (n = 3): ADG: Average daily weight gain; ADFI: Average daily feed intake; G/F: Gain-to-feed ratios. Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum polysaccharides; EPS: Echinacea polysaccharides. a,b,c,d Different letters indicate differences (p < 0.05).
Figure 1. Effects of adding different plant polysaccharides combined with boric acid in the diet on growth performance of fatteners (n = 3): ADG: Average daily weight gain; ADFI: Average daily feed intake; G/F: Gain-to-feed ratios. Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum polysaccharides; EPS: Echinacea polysaccharides. a,b,c,d Different letters indicate differences (p < 0.05).
Animals 14 01515 g001
Figure 2. Effects of Adding different plant polysaccharides combined with boric acid in the diet on intestinal digestive enzyme activities of fatteners (n = 6): Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum polysaccharides; EPS: Echinacea polysaccharides. a,b,c,d,e Different letters indicate differences (p < 0.05).
Figure 2. Effects of Adding different plant polysaccharides combined with boric acid in the diet on intestinal digestive enzyme activities of fatteners (n = 6): Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum polysaccharides; EPS: Echinacea polysaccharides. a,b,c,d,e Different letters indicate differences (p < 0.05).
Animals 14 01515 g002
Figure 3. Effects of Adding different plant polysaccharides combined with boric acid in the diet on cytokines of fatteners (n = 6): TNF-α: Tumor necrosis factor; IL-2: Interleukin-2; IL-6: Interleukin-6; IFN-γ: Interferon-gamma; Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum poly-saccharides; EPS: Echinacea polysaccharides. a,b Different letters indicate differences (p < 0.05).
Figure 3. Effects of Adding different plant polysaccharides combined with boric acid in the diet on cytokines of fatteners (n = 6): TNF-α: Tumor necrosis factor; IL-2: Interleukin-2; IL-6: Interleukin-6; IFN-γ: Interferon-gamma; Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum poly-saccharides; EPS: Echinacea polysaccharides. a,b Different letters indicate differences (p < 0.05).
Animals 14 01515 g003
Figure 4. Effects of Adding different plant polysaccharides combined with boric acid in the diet on the antioxidant function of fatteners (n = 6): T-AOC: Total antioxidant capacity; T-SOD: Superoxide dismutase; GSH-Px: Glutathione peroxidase; MDA: Malondialdehyde. Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum poly-saccharides; EPS: Echinacea polysaccharides. a,b,c Different letters indicate differences (p < 0.05).
Figure 4. Effects of Adding different plant polysaccharides combined with boric acid in the diet on the antioxidant function of fatteners (n = 6): T-AOC: Total antioxidant capacity; T-SOD: Superoxide dismutase; GSH-Px: Glutathione peroxidase; MDA: Malondialdehyde. Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum poly-saccharides; EPS: Echinacea polysaccharides. a,b,c Different letters indicate differences (p < 0.05).
Animals 14 01515 g004
Figure 5. Effects of Adding different plant polysaccharides combined with boric acid in the diet on harmful gas emissions in feces and urine of fatteners (n = 6): Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum polysaccharides; EPS: Echinacea polysaccharides. a,b,c Different letters indicate differences (p < 0.05).
Figure 5. Effects of Adding different plant polysaccharides combined with boric acid in the diet on harmful gas emissions in feces and urine of fatteners (n = 6): Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum polysaccharides; EPS: Echinacea polysaccharides. a,b,c Different letters indicate differences (p < 0.05).
Animals 14 01515 g005
Figure 6. Effects of adding different plant polysaccharides combined with boric acid in the diet on metal elements in feces and urine of fatteners (n = 6): Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum poly-saccharides; EPS: Echinacea polysaccharides. a,b,c Different letters indicate differences (p < 0.05).
Figure 6. Effects of adding different plant polysaccharides combined with boric acid in the diet on metal elements in feces and urine of fatteners (n = 6): Con: Control; AB: Boric acid; APS: Astragalus polysaccharides; GLP: Ganoderma lucidum poly-saccharides; EPS: Echinacea polysaccharides. a,b,c Different letters indicate differences (p < 0.05).
Animals 14 01515 g006
Figure 7. Heatmap describing variables horizontally and vertically for the levels of harmful gases and heavy metals in feces and urine and intestinal digestive enzyme activity. Orange and brown represent a significant positive correlation, blue and light blue represent a significant negative correlation and white represents no correlation. * Indicates p < 0.05.
Figure 7. Heatmap describing variables horizontally and vertically for the levels of harmful gases and heavy metals in feces and urine and intestinal digestive enzyme activity. Orange and brown represent a significant positive correlation, blue and light blue represent a significant negative correlation and white represents no correlation. * Indicates p < 0.05.
Animals 14 01515 g007
Figure 8. Heatmap describing variables horizontally and vertically for the levels of harmful gases and heavy metals in feces, urine and serum immune proteins. Orange and brown represent a significant positive correlation, blue and light blue represent a significant negative correlation and white represents no correlation. * Indicates p < 0.05.
Figure 8. Heatmap describing variables horizontally and vertically for the levels of harmful gases and heavy metals in feces, urine and serum immune proteins. Orange and brown represent a significant positive correlation, blue and light blue represent a significant negative correlation and white represents no correlation. * Indicates p < 0.05.
Animals 14 01515 g008
Figure 9. Heatmap describing variables horizontally and vertically for the levels of harmful gases and heavy metals in feces and urine and antioxidant function. Orange and brown represent a significant positive correlation, blue and light blue represent a significant negative correlation and white represents no correlation. * Indicates p < 0.05.
Figure 9. Heatmap describing variables horizontally and vertically for the levels of harmful gases and heavy metals in feces and urine and antioxidant function. Orange and brown represent a significant positive correlation, blue and light blue represent a significant negative correlation and white represents no correlation. * Indicates p < 0.05.
Animals 14 01515 g009
Table 1. Diet composition and nutrient level of basal diet (air-dried basis).
Table 1. Diet composition and nutrient level of basal diet (air-dried basis).
IngredientsContent (%)NutrientsContent
Corn25.75ME, kcal/kg3055.00
Wheat24.00DM, %87.77
Wheat middlings mix18.50CP, %13.51
Wheat flour15.00EE, %2.97
Rice bran meal12.50CF, %3.68
Limestone (40)1.03Ca, %0.75
Calcium hydrogen phosphate0.95Avail P, %0.30
Soybean oil0.80Total AA, %12.15
Sodium bicarbonate0.28Total Lys, %0.81
NaCl0.20Total Met, %0.25
L-Lysine HCl0.56
L-threonine0.10
Ethoxyquin0.03
Vitamins and minerals Premix a0.30
Total100.00
This feed formula comes from Anhui Hefeng Animal Husbandry Co. Ltd., and the nutritional level is calculated. ME: Metabolizable Energy; DM: Dry Matter (air dried); CP: Crude Protein; EE: Crude Ether Extract; CF: Crude Fiber; Avail P: Available Phosphorus; AA: Amino Acid; Lys: Lysine; Met: Methionine. a Provided the following per kg of diet: Vitamin A, 12,500 IU; Vitamin D, 1250 IU; Vitamin E, 125 IU; Vitamin B12, 90 µg; Vitamin B2, 10 mg; Pantothenic acid, 48 mg; Niacin, 35 mg; Folic acid, 4.5 mg; Biotin, 0.25 mg; Fe, 130 mg as iron sulfate; Zn, 180 mg as zinc sulfate; Cu, 15 mg as copper sulfate; Mn, 30 mg as manganese sulfate; I, 0.60 mg as calcium iodate; Se, 0.25 mg as selenate.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Deng, J.; Zhang, F.; Fan, H.; Zheng, Y.; Zhao, C.; Ren, M.; Jin, E.; Gu, Y. Effects of Plant Polysaccharides Combined with Boric Acid on Digestive Function, Immune Function, Harmful Gas and Heavy Metal Contents in Faeces of Fatteners. Animals 2024, 14, 1515. https://doi.org/10.3390/ani14111515

AMA Style

Deng J, Zhang F, Fan H, Zheng Y, Zhao C, Ren M, Jin E, Gu Y. Effects of Plant Polysaccharides Combined with Boric Acid on Digestive Function, Immune Function, Harmful Gas and Heavy Metal Contents in Faeces of Fatteners. Animals. 2024; 14(11):1515. https://doi.org/10.3390/ani14111515

Chicago/Turabian Style

Deng, Juan, Feng Zhang, Haoran Fan, Yuxuan Zheng, Chunfang Zhao, Man Ren, Erhui Jin, and Youfang Gu. 2024. "Effects of Plant Polysaccharides Combined with Boric Acid on Digestive Function, Immune Function, Harmful Gas and Heavy Metal Contents in Faeces of Fatteners" Animals 14, no. 11: 1515. https://doi.org/10.3390/ani14111515

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop