Next Article in Journal
Limosilactobacillus reuteri Alleviates Anxiety-like Behavior and Intestinal Symptoms in Two Stressed Mouse Models
Previous Article in Journal
Multifactorial Analysis of Influences on Quality of Life in Cancer Patients
Previous Article in Special Issue
Effect of Selenium and Selenoproteins on Radiation Resistance
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Nutrients
Volume 16
Issue 18
10.3390/nu16183208
nutrients-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Alleviation of Lipid Disorder and Liver Damage in High-Fat Diet-Induced Obese Mice by Selenium-Enriched Cardamine violifolia with Cadmium Accumulation

by
Junying Zhu
1,†,
Qingqing Lv
1,†,
Fengna Li
1,†,
Ping Xu
1,
Ziyu Han
1,
Aolin Yang
1,
Zhan Shi
1,
Chao Wang
2,
Jie Jiang
2,
Yunfen Zhu
3,
Xiaofei Chen
3,
Lvhui Sun
4,
Xin Gen Lei
5,* and
Ji-Chang Zhou
1,6,7,*
1
School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen 518107, China
2
Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, China
3
Enshi Autonomous Prefecture Academy of Agricultural Sciences, Enshi 445000, China
4
Hubei Hongshan Laboratory, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan 430070, China
5
Department of Animal Science, Cornell University, Ithaca, NY 14853, USA
6
Guangdong Province Engineering Laboratory for Nutrition Translation, Shenzhen 518107, China
7
Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou 510080, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Nutrients 2024, 16(18), 3208; https://doi.org/10.3390/nu16183208
Submission received: 30 August 2024 / Revised: 18 September 2024 / Accepted: 20 September 2024 / Published: 22 September 2024
(This article belongs to the Special Issue Selenium-Rich Products: Their Development and Regulation of Human Health)
Browse Figures
Review Reports Versions Notes

Abstract

:
Background/Objectives: As a hyperaccumulator of selenium (Se), Cardamine violifolia (Cv) and its peptide extract could ameliorate the negative effects of a high-fat diet (HFD). However, the effects of the coaccumulation of cadmium (Cd) in Se-enriched Cv (Cv2) and the potential confounding effect on the roles of enriched Se remain unknown. We aimed to investigate whether Cv2 could alleviate HFD-induced lipid disorder and liver damage. Methods: Three groups of 31-week-old female mice were fed for 41 weeks (n = 10–12) with a control Cv-supplemented diet (Cv1D, 0.15 mg Se/kg, 30 µg Cd/kg, and 10% fat calories), a control Cv-supplemented HFD (Cv1HFD, 45% fat calories), and a Cv2-supplemented HFD (Cv2HFD, 1.5 mg Se/kg, 0.29 mg Cd/kg, and 45% fat calories). Liver and serum were collected to determine the element concentrations, markers of liver injury and lipid disorder, and mRNA and/or protein expression of lipid metabolism factors, heavy metal detoxification factors, and selenoproteins. Results: Both Cv1HFD and Cv2HFD induced obesity, and Cv2HFD downregulated Selenoi and upregulated Dio3 compared with Cv1D. When comparing Cv2HFD against Cv1HFD, Cv2 increased the liver Se and Cd, the protein abundance of Selenoh, and the mRNA abundance of 10 selenoproteins; reduced the serum TG, TC, and AST; reduced the liver TG, lipid droplets, malondialdehyde, and mRNA abundance of Mtf1 and Mt2; and differentially regulated the mRNA levels of lipid metabolism factors. Conclusions: Cv2 alleviated HFD-induced lipid dysregulation and liver damage, which was probably associated with its unique Se speciation. However, further research is needed to explore the interaction of plant-coenriched Se and Cd and its effects on health.

1. Introduction

As one of the trace essential elements for both humans and animals, selenium (Se) serves as a critical and unique constitutive part of selenocysteine (Sec) in 25 human and 24 rodent selenoproteins [1]. Both organic and inorganic forms of Se from external sources can be efficiently absorbed via the gastrointestinal tract. Organic forms of Se generally exhibit lower toxicity, higher bioavailability, and better antioxidant properties than inorganic forms [2]. Plants can serve as carriers of beneficial elements for the maintenance of body health and are major sources of Se supplementation, as they are capable of biotransforming selenate and selenite into organic Se forms [3].
Cardamine violifolia (Cv) is a medicinal and edible plant, characterized by being a hyperaccumulator of Se [4]. Moreover, by enriching Se in the major forms of selenocystine and methylselenocystine [5], Se-enriched Cv is being developed as a promising Se-rich source. Concerningly, soils in Se-rich areas in the Enshi region of China often contain high levels of cadmium (Cd) [6,7]. In addition to Se, Cv could also accumulate the harmful heavy metal Cd [8], and the accumulation of Cd by Cv increases with the level of Se fertilization [8,9], thus yielding Se-enriched Cv (Cv2). The most common type of Cd exposure in non-smoking populations occurs through food and water contaminated with Cd [10], and Cd continuously accumulates in tissue due to the absence of effective excretory mechanisms. As exemplified by the severe Cd poisoning-induced itai-itai disease [11], the long-term accumulation of Cd can eventually cause damage to the functions of various organs in the body, including the liver, kidneys, bones, testes, and others [12]. Interestingly, recent studies have shown that Cv2-derived endogenous Se has the potential to antagonize Cd-induced renal damage, skeletal metabolism disorders, and hepatotoxicity [8,9]. Furthermore, reports of Cd-related toxicity are uncommon in areas with high geologic backgrounds of Se and Cd, which may be attributed to the interaction between Se and Cd in plants, leading to alterations in the forms of Cd present in plants that enter the human body, thereby reducing the toxicity of Cd [13,14]. On the other hand, Se can partially alleviate the body health damage caused by Cd exposure [14,15].
It is important to note that obesity has also progressively become one of the most important public health problems in the world [16] and is a significant risk factor for the development and progression of multiple diseases, such as type 2 diabetes, hypertension, hyperlipidemia, non-alcoholic fatty liver disease, and immune disorders [17,18,19]. Many animal studies have found that Se plays a beneficial role in improving lipid metabolic disorder and liver damage [20,21,22], and Cv-derived Se-enriched peptides (CSP) could alleviate those phenotypes induced by a high-fat diet (HFD) [23]. However, combined exposure to a HFD and Cd often results in stronger toxic effects on the body [24,25,26], while the effect of Se in the presence of plant-derived Cd accumulation on the adverse health consequences induced by a HFD in Se–Cd-rich areas remains unknown.
Thus, by applying Cv2 to feed adult female mice with varied dietary fat for more than 40 weeks, our study was to investigate the effect of Cv2-derived endogenous Se, in the presence of Cd accumulation, on the lipid metabolic disorders and liver injuries caused by the long-term exposure to HFD. Additionally, we hope to provide some new insights into the effects of Se on ameliorating adverse effects of HFD and Cd caused by consuming foods in naturally Se–Cd-rich areas.

2. Materials and Methods

2.1. Diets and Animals

The control Cv (Cv1) and Cv2 powders used in this study were provided by the Enshi Academy of Agricultural Sciences. Regarding the cultivation methods and conditions of Cv, briefly, Cv1 was cultivated in soil with Se and Cd concentrations of 1.22 mg/kg and 0.61 mg/kg, respectively. On a field adjacent to that for Cv1 planting, during the same season, Cv2 was obtained by cultivating the same strain of Cv1 with Se fertilizer-treated soil (Enshi Zhonghui Selenium Enriched Agricultural Technology Development Co., Ltd., Enshi, China) at a concentration of ≥200 mg Se/kg and with sodium selenite (purity of 97%) applied through foliar spraying. After the two types of whole plants were harvested, they were rinsed, dried, ground, and sieved to obtain a Cv1 powder (total Se: 7.24 mg/kg; total Cd: 1.4 mg/kg) and a Cv2 powder (total Se: 76.95 mg/kg; total Cd: 14.5 mg/kg). Over 80% of the Se in these powders existed in the forms of selenocystine and methylselenocystine [5].
The three types of feed used during the experiment were prepared by the Trophic Animal Feed High-Tech Co., Ltd., Nantong, China. For the Se-deficient diet used in all three types of feed, except for Se, all components of this diet met the standards of AIN93. The Cv1 powder was supplemented into the Se-deficient diet to contain 0.15 mg Se/kg and 0.03 mg Cd/kg, with fat providing 10% or 45% of the energy, to obtain the Cv1-supplemented control diet (Cv1D) or the Cv1-supplemented HFD (Cv1HFD), respectively. The Cv2 powder was used to replace the same amount of Cv1 powder in Cv1HFD to obtain the Cv2-supplemented HFD (Cv2HFD), containing 1.5 mg Se/kg and 0.29 mg Cd/kg.
All animal experiments reported in this manuscript were approved by the Animal Care and Use Committee of the Institute of Sun Yat-sen University and adhered to the criteria outlined in the ‘Guide of the Care and Use of Laboratory Animals’. Thirty-four female C57BL/6J mice aged 31 weeks, purchased from the Guangdong Medical Laboratory Animal Center, were randomly divided into three groups and fed Cv1D (n = 12), Cv1HFD (n = 12), and Cv2HFD (n = 10) based on the baseline body weight (BW). The animals were maintained under standard conditions, including 4–5 mice per cage, a temperature of 25 ± 2 °C, 70–75% humidity, and a light/dark cycle of 12 h, with free access to food and water during the experimentation. The experimental period was 41 weeks, and the BW was monitored every four weeks for each mouse. At the end of the experiment, all mice were fasted overnight and anesthetized with sodium pentobarbital to minimize pain before being euthanized by heart bleeding.

2.2. Oral Glucose Tolerance Test (OGTT) and Insulin Tolerance Test (ITT)

At the 40th week of the animal experiment, all mice were fasted for 6 h. Tail vein blood glucose was measured with a glucometer (ACCU-CHEK Performa, Roche Diagnostics GmbH, Mannheim, Germany). The OGTT was performed using an oral gavage of 2 g/kg BW of glucose, and blood glucose was measured at 0, 15, 30, 60, and 120 min after glucose loading. In the middle of the 41st week of the experiment, all mice were fasted for 4 h. Then, the ITT was performed using an intraperitoneal injection of 1 U/kg BW of insulin, and blood glucose was measured at 0, 15, 30, 60, 90, and 120 min after insulin loading with a glucometer. Prior to measuring the tail vein blood glucose and administering insulin via intraperitoneal injection, mild and non-irritating disinfection with an iodine tincture was performed on the local area to minimize animals’ pain and stress and to reduce the risk of infection.

2.3. Sample Preparation and Biochemical Analysis

Blood and tissue samples were collected promptly for analysis or cryopreservation. The serum samples were isolated by centrifugation at 12,000× g for 10 min at 4 °C. Approximately 50 mg liver samples were homogenized and centrifugated at 2500× g for 10 min at 4 °C to collect the supernatant. For the prepared serum and liver homogenate samples, commercial kits were used to measure the concentrations of TG (Fujifilm Wako Pure Chemical Co., Osaka, Japan), total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C) (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). The serum activity of alanine aminotransferase (ALT) and aspartate transaminase (AST) was measured by a HITACHI Automatic Analyzer 3100 at the Laboratory Animal Center of Sun Yat-sen University.

2.4. Elemental Analysis

Element quantification in the Cv1, Cv2, Cv1D, Cv1HFD, Cv2HFD, and liver tissue was performed using an Agilent 7850 Inductively Coupled Plasma Mass Spectrometer (Agilent Technologies, Santa Clara, CA, USA). Briefly, for sample digestion using an oven, 5 mL of nitric acid was added to a fluoroplastic liner containing an individual sample, and the samples in the insert were pre-incubated for 30 min at 80 °C. Subsequently, they were incubated for 2 h at 110 °C, followed by an additional incubation step for 4 h at 160 °C. Then, the dissolved samples were allowed to cool down to room temperature and quantitatively transferred to test tubes. Finally, a specific volume of deionized water was added to the test tubes, which were then vortexed and further assayed.

2.5. Malondialdehyde (MDA) Levels and Total Antioxidant Capacity (T-AOC)

To analyze the MDA levels, 20 mg liver samples were homogenized with phosphate-buffered saline using a tissue grinder. The homogenate was centrifuged at 3000× g for 10 min at 4 °C, and the supernatant was collected for analysis using an MDA assay kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). For T-AOC measurement, the liver homogenate was centrifuged at 12,000× g for 5 min at 4 °C. Then, the supernatant was collected for analysis using a T-AOC assay kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).

2.6. Histological Analysis

Six mice were randomly selected from each group and the histopathology of hepatic steatosis was evaluated by determining the average number, size, and area of hepatic lipid droplets. The freshly isolated livers of the mice were fixed in 10% neutral buffered formalin and then embedded in paraffin and sliced at 5 μm. After this, sections of the liver were stained with hematoxylin and eosin (H&E). The quantitative analysis of the number and size of the lipid droplets was performed using the ImageJ software 1.52v with three fields per slide, and the mean values were calculated.

2.7. RNA Extraction and Quantitative Real-Time PCR (qPCR)

Total RNA was extracted from the liver tissue using a total RNA extraction reagent (Yeasen Biotech (Shanghai) Co., Ltd., Shanghai, China), according to the manufacturer’s instructions. The concentration and purity of the RNA were determined by measuring the absorbance at 260/280 nm using a spectrophotometer (NanoDrop, Thermo Fisher Scientific, Waltham, MA, USA). The RNA integrity was checked by agarose gel electrophoresis. cDNA was synthesized using a reverse transcription kit (Takara Biomedical Technology (Beijing) Co., Ltd., Beijing, China), and then qPCR was performed. All primers for the selenoprotein genes and lipid metabolism-related genes used in the qPCR are listed in Table S1. Relative quantification was performed using the 2−ΔΔCT method normalized to the control Actb.

2.8. Western Blot Assay

The Western blotting experiment was performed according to a protocol previously described [27]. Briefly, 20 mg liver samples were homogenized in ice-cold RIPA lysis buffer (Beyotime Biotechnology, Shanghai, China) containing complete protease inhibitor using a tissue grinder. The homogenate was centrifuged at 12,000× g for 15 min at 4 °C, and the supernatant was collected. The protein concentration was determined using the BCA Protein Assay Kit (Thermo Fisher Scientific). After this, equal amounts of protein (usually 20 μg) from each sample were separated by SDS-PAGE and transferred onto a PVDF membrane (0.22 or 0.45 μm, Millipore, Burlington, MA, USA). Then, the membrane was blocked with 5% non-fat milk in a Tris–Tween-buffered saline buffer (TBST) for 2 h and was incubated with primary antibodies (Table S2) overnight at 4 °C. After washing with TBST, the membrane was incubated with horseradish peroxidase-conjugated secondary antibodies (dilution: 1:5000) for 1 h at room temperature. Finally, blots were developed on the membrane using MiniChemiTM910 reagents (Beijing SinSage Technology Co., Ltd., Beijing, China). We digitally quantified the resultant signals and normalized the data to the Actb abundance.

2.9. Statistical Analysis

All data were presented as the mean ± SEM. Statistical analysis was performed using GraphPad Prism 9.51 (GraphPad Software Inc., San Diego, CA, USA) and SPSS 26.0 (SPSS Inc., Chicago, IL, USA). The differences between the groups were determined using one-way or two-way ANOVA with Tukey’s multiple comparison test. The results were considered statistically significant at p < 0.05.

3. Results

3.1. Growth Performance

Over the 41 weeks of HFD administration, we found that Cv2 did not significantly alleviate HFD-induced weight gain in female mice. As shown in Figure 1, there was no significant difference in BW between the Cv1HFD and Cv2HFD groups (p ≥ 0.05).

3.2. Concentrations of Trace Elements in the Liver

Compared with those of the Cv1D or Cv1HFD group, the accumulation of Se significantly increased by ~22% in the livers of the Cv2HFD group (p < 0.0001; Figure 2A), while the accumulation of Cd significantly increased by 360% or 500%, respectively (p < 0.0001; Figure 2B). However, there was no difference in either Se or Cd between the Cv1D and Cv1HFD groups (p ≥ 0.05). We also observed a significant association between the Se and Cd levels in the Cv1D group (R2 = 0.4822, p = 0.0379) and all mice (R2 = 0.5612, p < 0.0001; Figure 2C). Furthermore, no differences were observed in the concentrations of copper, iron, and zinc among the Cv1D, Cv1HFD, and Cv2HFD groups (p ≥ 0.05; Figure S1A–C).

3.3. Glucose Metabolism

After the mice were fasted for 12 h before the OGTT test, the blood glucose levels in the Cv1HFD group and Cv2HFD group were both significantly higher than those in the Cv1D group at 60 min (p < 0.05; Figure S2A). Interestingly, although differences were not observed at other time points or in the glucose area under the curve (AUC) of OGTT among the three groups, there was a trend toward lower blood glucose levels in the Cv2HFD group compared with the Cv1HFD group (Figure S2B). For the ITT assessment, the fast plasma glucose level and the blood glucose level at 30 min after the injection of insulin in the mice in the Cv1HFD and Cv2HFD groups were significantly higher than those in the Cv1D group (p < 0.05; Figure S2C). However, no difference in the glucose AUC was observed among the three groups (p ≥ 0.05; Figure S2D).

3.4. Lipid Disorder and Liver Injury

Compared with the Cv1HFD group, Cv2 significantly decreased the serum levels of TG (20%, p < 0.05; Figure 3A) and TC (210%, p < 0.05; Figure 3B), as well as liver TG (69%, p < 0.05; Figure 3D), in the Cv2HFD group, without a significant effect on the serum LDL-C (p ≥ 0.05; Figure 3C) and liver TC and LDL-C (p ≥ 0.05; Figure 3E,F). Furthermore, although no difference was observed in the serum ALT activity (p ≥ 0.05; Figure 3G), Cv2 alleviated HFD-induced liver injuries, characterized by a ~33% decrease in serum AST activity in the Cv2HFD group compared with the Cv1HFD group (p < 0.05; Figure 3H).

3.5. Regulating Gene and Protein Expression in Lipid Metabolism

In the Cv1HFD group, unclear intercellular boundaries, shrinking nuclei squeezed to the edges of the cell, and the disordered arrangement of hepatic cords were observed (Figure 4A). In the Cv2HFD group, hepatic lipid droplets were significantly fewer and smaller, with clearer boundaries of liver cells than those in the Cv1HFD group (p < 0.05). However, there was no significant difference in the liver weight among the Cv1D, Cv1HFD, and Cv2HFD groups (p ≥ 0.05; Figure 4B).
The mRNA levels of key genes (Gpat1, Gpat2, Dgat1, and Dgat2) involved in TG synthesis showed no significant differences in the livers of Cv1HFD-fed female mice compared with Cv1D-fed female mice (p ≥ 0.05), but a gene involved in TG hydrolysis (Lipc) was significantly downregulated (p < 0.05; Figure 4C). In contrast, in the livers of Cv2HFD-fed mice, genes involved in TG synthesis (Gpat1 and Dgat2) and genes involved in TG hydrolysis (Atgl and Hsl) were significantly downregulated compared to the Cv1HFD group, while the mRNA levels of Lipc and Lpl were significantly upregulated (p < 0.05).
Regarding cholesterol homeostasis in the livers of Cv1HFD-fed mice, a key gene involved in cholesterol synthesis, Hmgcr, was significantly downregulated compared to Cv1D-fed mice, and a gene involved in cholesterol transport, Abcg1, was upregulated (p < 0.05; Figure 4D). In the livers of Cv2HFD-fed mice, the mRNA levels of Hmgcr, Sqle, and Ldlr were significantly upregulated compared to the Cv1HFD and/or Cv1D group(s), while the mRNA levels of Abca1, Abcg1, and Abcg8 were significantly downregulated (p < 0.05).

3.6. Hepatic Oxidative Stress and Antioxidant Defense Capacity

Compared with those of the Cv1HFD group, Cv2 significantly downregulated the elevated mRNA expression levels of metal regulatory transcription factor 1 (Mtf1) and metallothionein 2 (Mt2) caused by the HFD in the livers of the Cv2HFD group (p < 0.05; Figure 5A,C). Furthermore, no differences in the relative protein levels of Mtf1, Mt, and Sod1, as well as the T-AOC level, were observed among the Cv1D, Cv1HFD, and Cv2HFD groups (p ≥ 0.05; Figure 5E–H). However, we found that, compared with the Cv1HFD group, Cv2 significantly decreased the liver MDA level in the Cv2HFD group by ~75% (p < 0.05; Figure 5I).

3.7. Relative mRNA and Protein Expression of Selenoproteins

The mRNA abundance of all selected selenoprotein genes showed no differences (p ≥ 0.05) between the Cv1D and Cv1HFD groups (Figure 6A,B; Figure S3). However, compared with those in the Cv1D and/or Cv1HFD group(s), the expression of 12 selenoprotein genes (Dio1, Dio3, Gpx4, Msrb1, Selenof, Selenoo, Selenos, Selenow, Sephs2, Txnrd1, Txnrd2, and Txnrd3) was significantly upregulated, while Selenoi was significantly downregulated in the livers of the Cv2HFD group (p < 0.05; Figure 6A,B).
Compared with those of the Cv1D group, the relative protein levels of the ER-resident Selenoi and the non-ER-resident Dio3 were, respectively, downregulated and upregulated in the livers of the Cv2HFD group (p < 0.05; Figure 6C–F). Furthermore, compared with those of the Cv1HFD group, the relative protein level of Selenoh was upregulated in the livers of the Cv2HFD group (p < 0.05; Figure S3C,D). Although there were no differences in the relative protein levels of Selenoo and Txnrd2 among the Cv1D, Cv1HFD, and Cv2HFD groups, there was an upregulatory trend in the Cv2HFD group (p = 0.05).

4. Discussion

The potential of Se-rich plants as a source for the development of novel Se supplements has drawn attention from many researchers due to their ability to improve health [23,28,29]. Cv, as a hyperaccumulator of Se, serves as an ideal plant-derived Se source. Previous studies have found that CSP from Cv may alleviate HFD-induced disorder of lipid metabolism through potential mechanisms such as increased thermogenesis and reduced oxidative stress and inflammation, as well as the regulation of gene expression in lipid and cholesterol metabolism [23]. However, Cv is also able to hyperaccumulate Cd, which hinders its promotion as an ideal Se supplement and calls for further investigations of the health effects of Se–Cd coenrichment in this species, as well as other plants [14,15]. Zhang et al. [8,9] aquacultured three types of Se–Cd-coenriched Cvs by supplementing 0, 1, or 2 mg/L of sodium selenate and 35 mg/L of cadmium chloride (CdCl2) in the culturing solution and found that both Se (0.2–0.86 g/kg) and Cd (4.2–5.4 g/kg) in Cv positively increased with the Se supplementation. By gavage in mice with a purified water control or the same dosage of Cd (3.2 mg/kg BW) in the form of CdCl2 or any of the three Se–Cd-coenriched Cvs, the Cd-induced renal damage, skeletal metabolism disorder [9], and hepatotoxicity [8] were improved with the increased Se levels across the three Se–Cd-coenriched Cvs, in which selenocystine probably played a critical role.
Given the characteristic of Cv being able to accumulate Se and Cd, we observed the naturally increased enrichment of Cd from the soil with Se supplementation in our study, which was consistent with the findings from other studies [7,8]. In our studied animals, the Cd exposure levels were much lower than those reported to cause significant liver damage [8,9,24,30,31,32,33]. Additionally, in the intervention model, the Se/Cd ratio (1.5 mg/kg Se vs. 0.29 mg/kg Cd) in our study was 5.17, while, in other studies showing the protective effect of Se against Cd exposure, the ratios were 0.16 (0.5 mg/kg Se vs. 3.2 mg/kg Cd) [8,9] and 0.8 (1.6 mg/kg Se vs. 2 mg/kg Cd) [34], much lower than ours. Se supplementation has been shown to improve the adverse health effects induced by HFD or Cd exposure; however, combined exposure to Cd and HFD often exhibits a synergistic effect in terms of damage to the health of the body [24,33,35]. Meanwhile, the role of Se in the presence of Cd accumulation on long-term HFD-induced health outcomes remains unknown. Thus, we conducted this study to investigate the effects of Cv2 on metabolic disorder and liver damage induced by the long-term consumption of a HFD and to explore the role of Se in the plant-derived high background of Cd.
We found that, despite the tenfold increase in both the Se and Cd levels in Cv2HFD compared to Cv1D and Cv1HFD, there was a significant difference in the accumulation levels of Se and Cd in the livers. Indeed, under physiological conditions, there is a mechanism in the body to maintain Se homeostasis, primarily regulated through urinary excretion rather than absorption [36]. However, mammals lack effective regulatory mechanisms to control the balance of Cd levels in the body. Thus, the small amount of Cd entering the body through food or other pathways could be excreted in minute quantities through the urine, with the majority continuously accumulating in organs like the liver and eventually causing harm to the body [37]. Previous studies have revealed that combined exposure to a HFD and Cd could significantly disrupt the essential metal homeostasis in female mice, which could be associated with influencing the expression of metal transporters [24]. However, this phenomenon was not observed in our study. This could be explained by Se being capable of alleviating the effect of the HFD and Cd in terms of disrupting essential metal homeostasis by regulating metal transporters to some extent [24,38]. It is well known that a long-term HFD can disrupt lipid metabolism, leading to obesity, lipid metabolic disorder, and liver damage [39,40]. Furthermore, chronic low Cd exposure (150 μg/L CdCl2 or 92 μg/L Cd spiked in pure water) at food limitation-relevant levels is sufficient to cause significantly disrupted hepatic energy metabolism homeostasis [41]. Therefore, the presence of Cd in Cv2 may influence the protective effect of Se against the metabolic disorder induced by a long-term HFD, potentially exacerbating the health damage in synergy with the HFD. Although we found that Cv2 did not significantly influence glucose tolerance or insulin sensitivity in HFD-induced female obese mice, we observed that the supplementation of Cv2 could alleviate the increase in serum and hepatic lipid levels, as well as liver injury marker levels, induced by the HFD in mice, which may be attributed to the protective effects of Cv-derived endogenous Se on lipid metabolic disorder and liver injury induced by a HFD and Cd [23,29,42].
Lipid disorder is closely associated with abnormalities in lipid (including TG and TC) synthesis, transport, and metabolism. Previous studies have found that Cd can downregulate the expression of Atgl and Lpl [43], while, in HFD-fed mice, CSP increased the expression of Lpl and reduced the expression of Hmgcr [23]. Similarly, another study also demonstrated that, in normal diet-fed broilers, Se-enriched Cv could upregulate the expression of LPL and reduce the expression of HMGCR in the liver, without an effect on DGAT2. Obviously, Se, Cd, and HFD could affect lipid homeostasis by influencing the expression of lipid metabolism-related factors. In our study, Cv2 downregulated the gene expression of TG synthesis enzymes (Gpat1 and Dgat2) and upregulated TG hydrolytic enzymes (Lipc and Lpl), which are helpful in alleviating the HFD-induced elevation of TG levels [44]. Interestingly, some results in our study differed from previous research. We observed that the expression of the other two TG hydrolytic enzyme genes (Atgl and Hsl) was downregulated by Cv2 supplementation in HFD-fed mice. Furthermore, we observed that Cv2 upregulated Hmgcr in the Cv2HFD group compared with the Cv1HFD group. These findings, differing from previous research, suggest that the plant-derived Cd accumulation in the mouse liver affected Se’s antagonistic effect on the HFD. We also observed that Cv2 reduced the expression of cholesterol transport-related genes (Abca1, Abcg1) while increasing the expression levels of ldlr involved in cholesterol clearance in the Cv2HFD group, which are helpful in reducing cholesterol efflux and promoting its clearance [45]. This might have contributed to the lower serum TC level in the Cv2HFD group than in the Cv1HFD group [45,46,47]. Therefore, although its effectiveness was attenuated by the presence of plant-derived Cd, the endogenous Se in Cv2 still demonstrated beneficial improvements in lipid metabolic disorder in HFD-induced obese mice.
Mts, particularly Mt1 and Mt2, are widely present in the parenchymal organs, such as the liver and kidneys, of mice, while Mtf1 serves as a positive regulatory factor for the expression of Mts [48,49]. They mainly participate in the detoxification of heavy metals, free radical scavenging, and protection against oxidative damage and are capable of inhibiting the toxicity of Cd [49]. Consistent with previous studies, we observed the upregulation of the gene expression levels of Mtf1, Mt1, and Mt2 in the mouse liver induced by Cv1HFD; this may be a response of the body to HFD-induced oxidative stress [50,51]. Furthermore, we found that Cv2 supplementation reduced the expression of these genes. Previous studies have found that exposure to Cd could upregulate the expression of Mtf1, Mt1, and Mt2, while Se reversed this effect [52], and the observed phenomenon between the Cv1HFD and Cv2HFD groups in our study may be attributed to the antagonistic effects of Se against Cd and the HFD. However, we observed no difference in the relative protein levels of Mt and Mtf1 among the three groups. In fact, a study also found that a HFD significantly increased the mRNA expression of Mt2, and the protein expression levels of Mts showed no significant difference compared to the control group [24], while another study reported the opposite results [33]. In fact, Mts primarily participate in maintaining the homeostasis of essential trace elements such as copper and zinc in the body [53]. Cd exposure stimulates the synthesis of hepatic Mts, which bind with Cd2+ to form Cd–MT complexes to reduce the damage caused by free Cd2+ [53]. Previous studies have indicated that combined exposure to Se and Cd results in the formation of Cd–Se complexes or Cd–Se protein complexes [54,55]. Therefore, the presence of endogenous Se in Cv2 may have led to the formation of inert complexes with Cd2+, reducing the need for Mts in the organism.
Furthermore, selenoproteins partly participated in alleviating the negative effects of the HFD and Cd exposure. SELENOP is essential in maintaining the homeostasis of selenoproteins and is also associated with lipid metabolism [56]. Elevated circulating levels of SELENOP have been observed in obese individuals [57], and a deficiency in Selenof [58], Selenom [59], Selenos [60], Selenot [61], or Selenov [62] has been shown to lead to lipid metabolic disorder in established mouse models and usually exacerbates HFD-induced lipid accumulation in the body. At the same dietary Se level, the Cv1D and Cv1HFD groups had no differences in the mRNA abundance of the selenogenome, regardless of the dietary fat content. The supplementation of Cv2 not only significantly increased the Se concentrations in the livers of the Cv2HFD group but also differentially regulated the mRNA expression levels of some selenoproteins. Previous studies have indicated that selenoproteins, particularly some endoplasmic reticulum-resident selenoproteins, play crucial roles in mediating Se’s antagonism against Cd-induced hepatic toxicity [63]. Interestingly, we observed that the protein abundance of some selenoproteins in the liver was not consistent with their corresponding mRNA expression. This may be caused by Cd in Cv2 inhibiting the biosynthesis of selenoproteins and Se metabolites to weaken the beneficial effects of Se on the organism [63]. In addition, the suppression of selenoprotein synthesis by Cd may also be due to the formation of the above-mentioned Cd–Se complex [63,64]. Although the specific selenoproteins involved and their respective abilities to bind Cd are not yet clear, the significantly changed protein levels of Dio3, Selenoh, and Selenoi in the Cv2HFD group suggest that these selenoproteins may have specific roles in mediating Se’s effect in the interaction of the HFD and Cd.
Lastly, it should be noted that our study has certain limitations: although the Se content was higher and the Cd content was lower in Cv2HFD in our study than in previous studies [8,9], we were unable to evaluate in detail the impact of the interaction between Se and Cd on HFD-induced health damage due to a shortage of Cv with high Se as in Cv2, low Cd as in Cv1, low Se as in Cv1, or high Cd as in Cv2 without exogenous element supplementation. Furthermore, previous studies have reported that, in Se–Cd-coenriched plants, Se could alter the forms and toxicity of Cd to the body [13,14,64]. However, we did not identify the forms of Cd present in Cv2 or their different impacts on health. Therefore, future studies need to illuminate the interaction between Se and Cd in the soil–plant–organism system in Se–Cd-rich areas. It would also be worthwhile to further investigate the utilization and safety of Se, changes in Cd toxicity in Se–Cd-coenriched agricultural products, and the impact of the interaction between Se, Cd, and the HFD on overall health.

5. Conclusions

In summary, our study suggests that, in the presence of Cd accumulation, Cv2 still demonstrates effects in terms of alleviating the elevated levels of serum TC and TG, as well as liver lipid deposition, histological damage, and oxidative stress, in HFD mice. The observed beneficial effects of Cv2 on HFD-induced metabolic disorder were probably associated with its unique Se speciation to antagonize the combined exposure to the HFD and Cd via its regulation of the expression of specific lipid metabolic genes and selenoproteins. However, the current study suggests that, when considering the consumption of Se-enriched agricultural products as a means of Se supplementation, it is necessary to evaluate the potential toxicity caused by the coaccumulation of Cd. Further research is still needed to explore the interaction of Se, Cd, and the HFD and its effects on health to provide a better reference for the development of Se supplements and Se-enriched agricultural products originating from naturally Se–Cd-rich areas.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/nu16183208/s1, Figure S1: Accumulation of copper, iron, and zinc in the livers of adult female mice; Figure S2: Blood glucose changes in OGTT and ITT; Figure S3: The relative mRNA expression of three ER selenoproteins and three non-ER selenoproteins; Table S1: Primer sequences for qPCR; Table S2: Target protein, type, dilution, and source of primary antibodies used for the Western blot analyses.

Author Contributions

Conceptualization, J.-C.Z. and X.G.L.; Methodology, J.Z., Q.L., F.L., P.X., Z.H., A.Y., C.W. and J.J.; Resources, Y.Z., X.C., and L.S.; Formal analysis, J.Z., Q.L., F.L. and P.X.; Visualization, J.Z., Q.L., F.L. and P.X.; Supervision, J.-C.Z. and X.G.L.; Project administration, J.-C.Z. and X.G.L.; Writing—original draft preparation, J.Z.; Writing—review and editing, Q.L., F.L., P.X., Z.H., A.Y., Z.S., X.G.L. and J.-C.Z.; Funding acquisition, J.-C.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Science, Technology and Innovation Commission of Shenzhen Municipality, China (GJHZ20240218114600001) and the National Natural Science Foundation of China (81973038) to J.C.Z.

Institutional Review Board Statement

The experiments were approved by the Animal Care and Use Committee of the Institute of Sun Yat-sen University (SYSU-IACUC-2019-B505, 5 March 2019).

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Acknowledgments

We would like to acknowledge Zhoutian Wang, Aiping Liu, and Minning Chen for their technical support in the animal experiments.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Ramírez-Acosta, S.; Huertas-Abril, P.V.; Selma-Royo, M.; Prieto-Álamo, M.J.; Collado, M.C.; Abril, N.; García-Barrera, T. The role of selenium in shaping mice brain metabolome and selenoproteome through the gut-brain axis by combining metabolomics, metallomics, gene expression, and amplicon sequencing. J. Nutr. Biochem. 2023, 117, 109323. [Google Scholar] [CrossRef] [PubMed]
  2. Hadrup, N.; Ravn-Haren, G. Toxicity of repeated oral intake of organic selenium, inorganic selenium, and selenium nanoparticles: A review. J. Trace Elem. Med. Biol. Organ Soc. Miner. Trace Elem. (GMS) 2023, 79, 127235. [Google Scholar] [CrossRef] [PubMed]
  3. Somagattu, P.; Chinnannan, K.; Yammanuru, H.; Reddy, U.K.; Nimmakayala, P. Selenium dynamics in plants: Uptake, transport, toxicity, and sustainable management strategies. Sci. Total Environ. 2024, 949, 175033. [Google Scholar] [CrossRef] [PubMed]
  4. Liu, X.M.; Yuan, Z.G.; Rao, S.; Zhang, W.W.; Ye, J.B.; Cheng, S.Y.; Xu, F. Identification, characterization, and expression analysis of WRKY transcription factors in Cardamine violifolia reveal the key genes involved in regulating selenium accumulation. BMC Plant Biol. 2024, 24, 860. [Google Scholar] [CrossRef]
  5. Cui, L.; Zhao, J.; Chen, J.; Zhang, W.; Gao, Y.; Li, B.; Li, Y.-F. Translocation and transformation of selenium in hyperaccumulator plant Cardamine enshiensis from Enshi, Hubei, China. Plant Soil 2018, 425, 577–588. [Google Scholar] [CrossRef]
  6. Guo, R.; Ren, R.; Wang, L.; Zhi, Q.; Yu, T.; Hou, Q.; Yang, Z. Using machine learning to predict selenium and cadmium contents in rice grains from black shale-distributed farmland area. Sci. Total Environ. 2024, 912, 168802. [Google Scholar] [CrossRef]
  7. Feng, R.; Wei, C.; Tu, S.; Ding, Y.; Song, Z. A dual role of Se on Cd toxicity: Evidences from the uptake of Cd and some essential elements and the growth responses in paddy rice. Biol. Trace Elem. Res. 2013, 151, 113–121. [Google Scholar] [CrossRef]
  8. Zhang, L.; Shi, W.Y.; Xu, J.Y.; Liu, Y.; Wang, S.J.; Zheng, J.Y.; Li, Y.H.; Yuan, L.X.; Qin, L.Q. Protective effects and mechanism of chemical- and plant-based selenocystine against cadmium-induced liver damage. J. Hazard. Mater. 2024, 468, 133812. [Google Scholar] [CrossRef]
  9. Zhang, L.; Shi, W.Y.; Zhang, L.L.; Sha, Y.; Xu, J.Y.; Shen, L.C.; Li, Y.H.; Yuan, L.X.; Qin, L.Q. Effects of selenium-cadmium co-enriched Cardamine hupingshanensis on bone damage in mice. Ecotoxicol. Environ. Saf. 2024, 272, 116101. [Google Scholar] [CrossRef]
  10. Zhu, H.; Tang, X.; Gu, C.; Chen, R.; Liu, Y.; Chu, H.; Zhang, Z. Assessment of human exposure to cadmium and its nephrotoxicity in the Chinese population. Sci. Total Environ. 2024, 918, 170488. [Google Scholar] [CrossRef]
  11. Baba, H.; Tsuneyama, K.; Yazaki, M.; Nagata, K.; Minamisaka, T.; Tsuda, T.; Nomoto, K.; Hayashi, S.; Miwa, S.; Nakajima, T.; et al. The liver in itai-itai disease (chronic cadmium poisoning): Pathological features and metallothionein expression. Mod. Pathol. 2013, 26, 1228–1234. [Google Scholar] [CrossRef] [PubMed]
  12. Huang, N.; Wang, B.; Liu, S.; Wang, K.; Wang, R.; Liu, F.; Chen, C. Cadmium exposure in infants and children: Toxicity, health effects, dietary risk assessment and mitigation strategies. Crit. Rev. Food Sci. Nutr. 2024, 1–23. [Google Scholar] [CrossRef] [PubMed]
  13. Ismael, M.A.; Elyamine, A.M.; Moussa, M.G.; Cai, M.; Zhao, X.; Hu, C. Cadmium in plants: Uptake, toxicity, and its interactions with selenium fertilizers. Metallomics 2019, 11, 255–277. [Google Scholar] [CrossRef] [PubMed]
  14. Yang, R.; He, Y.; Luo, L.; Zhu, M.; Zan, S.; Guo, F.; Wang, B.; Yang, B. The interaction between selenium and cadmium in the soil-rice-human continuum in an area with high geological background of selenium and cadmium. Ecotoxicol. Environ. Saf. 2021, 222, 112516. [Google Scholar] [CrossRef] [PubMed]
  15. Chen, J.; He, W.; Zhu, X.; Yang, S.; Yu, T.; Ma, W. Epidemiological study of kidney health in an area with high levels of soil cadmium and selenium: Does selenium protect against cadmium-induced kidney injury? Sci. Total Environ. 2020, 698, 134106. [Google Scholar] [CrossRef]
  16. Boutari, C.; Mantzoros, C.S. A 2022 update on the epidemiology of obesity and a call to action: As its twin COVID-19 pandemic appears to be receding, the obesity and dysmetabolism pandemic continues to rage on. Metab. Clin. Exp. 2022, 133, 155217. [Google Scholar] [CrossRef]
  17. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019. Lancet 2020, 396, 1204–1222. [CrossRef]
  18. Loomba, R.; Friedman, S.L.; Shulman, G.I. Mechanisms and disease consequences of nonalcoholic fatty liver disease. Cell 2021, 184, 2537–2564. [Google Scholar] [CrossRef]
  19. Świątkiewicz, I.; Wróblewski, M.; Nuszkiewicz, J.; Sutkowy, P.; Wróblewska, J.; Woźniak, A. The role of oxidative stress enhanced by adiposity in cardiometabolic diseases. Int. J. Mol. Sci. 2023, 24, 6382. [Google Scholar] [CrossRef]
  20. Wang, P.; Lu, Z.; He, M.; Shi, B.; Lei, X.; Shan, A. The effects of endoplasmic-reticulum-resident selenoproteins in a nonalcoholic fatty liver disease pig model induced by a high-fat diet. Nutrients 2020, 12, 692. [Google Scholar] [CrossRef]
  21. Zhao, Z.; Kim, J.; Lei, X.G. High Dietary Fat and Selenium Concentrations Exert Tissue- and Glutathione Peroxidase 1-Dependent Impacts on Lipid Metabolism of Young-Adult Mice. J. Nutr. 2020, 150, 1738–1748. [Google Scholar] [CrossRef] [PubMed]
  22. Wang, X.; Wu, B.; Sun, G.; Gao, J.; Huang, T.; Liu, J.; Zhou, Q.; He, X.; Zhang, S.; Wang, C.Y.; et al. Dietary selenomethionine attenuates obesity by enhancing beiging process in white adipose tissue. J. Nutr. Biochem. 2023, 113, 109230. [Google Scholar] [CrossRef] [PubMed]
  23. Yu, T.; Guo, J.; Zhu, S.; Li, M.; Zhu, Z.; Cheng, S.; Wang, S.; Sun, Y.; Cong, X. Protective effects of selenium-enriched peptides from Cardamine violifolia against high-fat diet induced obesity and its associated metabolic disorders in mice. RSC Adv. 2020, 10, 31411–31424. [Google Scholar] [CrossRef] [PubMed]
  24. Zhou, W.; Young, J.L.; Men, H.; Zhang, H.; Yu, H.; Lin, Q.; Xu, H.; Xu, J.; Tan, Y.; Zheng, Y.; et al. Sex differences in the effects of whole-life, low-dose cadmium exposure on postweaning high-fat diet-induced cardiac pathogeneses. Sci. Total Environ. 2022, 809, 152176. [Google Scholar] [CrossRef]
  25. Young, J.L.; Yan, X.; Xu, J.; Yin, X.; Zhang, X.; Arteel, G.E.; Barnes, G.N.; States, J.C.; Watson, W.H.; Kong, M.; et al. Cadmium and High-Fat Diet Disrupt Renal, Cardiac and Hepatic Essential Metals. Sci. Rep. 2019, 9, 14675. [Google Scholar] [CrossRef]
  26. Liu, T.; Liang, X.; Lei, C.; Huang, Q.; Song, W.; Fang, R.; Li, C.; Li, X.; Mo, H.; Sun, N.; et al. High-Fat Diet Affects Heavy Metal Accumulation and Toxicity to Mice Liver and Kidney Probably via Gut Microbiota. Front. Microbiol. 2020, 11, 1604. [Google Scholar] [CrossRef]
  27. Wang, J.; Song, Y.; Elsherif, L.; Song, Z.; Zhou, G.; Prabhu, S.D.; Saari, J.T.; Cai, L. Cardiac metallothionein induction plays the major role in the prevention of diabetic cardiomyopathy by zinc supplementation. Circulation 2006, 113, 544–554. [Google Scholar] [CrossRef]
  28. Zhang, X.; Xia, H.; Wang, J.; Leng, R.; Zhou, X.; Gao, Q.; He, K.; Liu, D.; Huang, B. Effect of selenium-enriched kiwifruit on body fat reduction and liver protection in hyperlipidaemic mice. Food Funct. 2021, 12, 2044–2057. [Google Scholar] [CrossRef]
  29. Shang, L.; Li, F.; Zhu, J.; Sun, C.; Wang, Y. Selenium-enriched and ordinary black teas regulate the metabolism of glucose and lipid and intestinal flora of hyperglycemic mice. Plant Foods Hum. Nutr. 2023, 78, 61–67. [Google Scholar] [CrossRef]
  30. Gu, J.; Kong, A.; Guo, C.; Liu, J.; Li, K.; Ren, Z.; Zhou, Y.; Tang, M.; Shi, H. Cadmium perturbed lipid profile and induced liver dysfunction in mice through phosphatidylcholine remodeling and promoting arachidonic acid synthesis and metabolism. Ecotoxicol. Environ. Saf. 2022, 247, 114254. [Google Scholar] [CrossRef]
  31. Liu, Y.; Kang, W.; Liu, S.; Li, J.; Liu, J.; Chen, X.; Gan, F.; Huang, K. Gut microbiota-bile acid-intestinal Farnesoid X receptor signaling axis orchestrates cadmium-induced liver injury. Sci. Total Environ. 2022, 849, 157861. [Google Scholar] [CrossRef] [PubMed]
  32. Chen, Z.; Shi, K.; Kuang, W.; Huang, L. Exploration of the optimal strategy for dietary calcium intervention against the toxicity of liver and kidney induced by cadmium in mice: An in vivo diet intervention study. PLoS ONE 2021, 16, e0250885. [Google Scholar] [CrossRef] [PubMed]
  33. Young, J.L.; Cave, M.C.; Xu, Q.; Kong, M.; Xu, J.; Lin, Q.; Tan, Y.; Cai, L. Whole life exposure to low dose cadmium alters diet-induced NAFLD. Toxicol. Appl. Pharmacol. 2022, 436, 115855. [Google Scholar] [CrossRef] [PubMed]
  34. Hu, X.; Chandler, J.D.; Fernandes, J.; Orr, M.L.; Hao, L.; Uppal, K.; Neujahr, D.C.; Jones, D.P.; Go, Y.M. Selenium supplementation prevents metabolic and transcriptomic responses to cadmium in mouse lung. Biochim. Biophys. Acta Gen. Subj. 2018, 1862, 2417–2426. [Google Scholar] [CrossRef] [PubMed]
  35. Zhang, X.; Li, X.; Sheng, Z.; Wang, S.; Li, B.; Tao, S.; Zhang, Z. Effects of combined exposure to cadmium and high-fat diet on bone quality in male mice. Biol. Trace Elem. Res. 2020, 193, 434–444. [Google Scholar] [CrossRef]
  36. Navarro-Alarcon, M.; Cabrera-Vique, C. Selenium in food and the human body: A review. Sci. Total Environ. 2008, 400, 115–141. [Google Scholar] [CrossRef]
  37. Genchi, G.; Sinicropi, M.S.; Lauria, G.; Carocci, A.; Catalano, A. The Effects of Cadmium Toxicity. Int. J. Environ. Res. Public Health 2020, 17, 3782. [Google Scholar] [CrossRef]
  38. Xu, Y.R.; Talukder, M.; Li, C.X.; Zhang, C.; Ge, J.; Li, J.L. Nanoselenium alleviates cadmium-induced cerebral injury via regulating cerebral metal transporters and metal-regulatory transcription factor 1. J. Agric. Food Chem. 2023, 71, 9896–9907. [Google Scholar] [CrossRef]
  39. Wang, Y.; Hou, J.; Li, X.; Chen, P.; Chen, F.; Pan, Y.; Deng, Z.; Li, J.; Liu, R.; Luo, T. Tyrosol regulates hepatic lipid metabolism in high-fat diet-induced NAFLD mice. Food Funct. 2024, 15, 3752–3764. [Google Scholar] [CrossRef]
  40. Lv, C.; Liu, X.; Chen, S.; Yi, Y.; Wen, X.; Li, T.; Qin, S. Extract of Gardenia jasminoides Ellis Attenuates High-Fat Diet-Induced Glycolipid Metabolism Disorder in Rats by Targeting Gut Microbiota and TLR4/Myd88/NF-κB Pathway. Antioxidants 2024, 13, 293. [Google Scholar] [CrossRef]
  41. He, X.; Qi, Z.; Hou, H.; Gao, J.; Zhang, X.X. Effects of chronic cadmium exposure at food limitation-relevant levels on energy metabolism in mice. J. Hazard. Mater. 2020, 388, 121791. [Google Scholar] [CrossRef] [PubMed]
  42. Song, Y.; Zhang, J.; Li, Y.; Wang, Y.; Wan, Y. Potential Protective Effect of Selenium-Enriched Lactobacillus plantarum on Cadmium-Induced Liver Injury in Mice. J. Microbiol. Biotechnol. 2024, 34, 1328–1339. [Google Scholar] [CrossRef] [PubMed]
  43. Wan, X.M.; Chen, J.; Wang, M.; Zheng, C.; Zhou, X.L. Puerarin attenuates cadmium-induced hepatic lipid metabolism disorder by inhibiting oxidative stress and inflammation in mice. J. Inorg. Biochem. 2021, 222, 111521. [Google Scholar] [CrossRef] [PubMed]
  44. Zhou, Y.; Chen, X.; Su, T.; Yuan, M.; Sun, X. Kiwifruit Peel Extract Improves the Alterations in Lipid Metabolism in High-fat Diet-fed Model Rats. Plant Foods Hum. Nutr. 2024, 79, 113–119. [Google Scholar] [CrossRef] [PubMed]
  45. Luo, J.; Yang, H.; Song, B.L. Mechanisms and regulation of cholesterol homeostasis. Nat. Rev. Mol. Cell Biol. 2020, 21, 225–245. [Google Scholar] [CrossRef]
  46. Rezaei, F.; Farhat, D.; Gursu, G.; Samnani, S.; Lee, J.Y. Snapshots of ABCG1 and ABCG5/G8: A Sterol’s Journey to Cross the Cellular Membranes. Int. J. Mol. Sci. 2022, 24, 484. [Google Scholar] [CrossRef]
  47. Funes, A.K.; Avena, V.; Boarelli, P.V.; Monclus, M.A.; Zoppino, D.F.; Saez-Lancellotti, T.E.; Fornes, M.W. Cholesterol dynamics in rabbit liver: High-fat diet, olive oil, and synergistic dietary effects. Biochem. Biophys. Res. Commun. 2024, 733, 150675. [Google Scholar] [CrossRef]
  48. Ogushi, S.; Kimura, T. The difference in zinc concentrations required for induction among metallothionein isoforms can be explained by the different MTF1 affinities to MREs in its promoter. Int. J. Mol. Sci. 2023, 24, 283. [Google Scholar] [CrossRef]
  49. Nordberg, M.; Nordberg, G.F. Metallothionein and Cadmium Toxicology-Historical Review and Commentary. Biomolecules 2022, 12, 360. [Google Scholar] [CrossRef]
  50. Lindeque, J.Z.; Jansen van Rensburg, P.J.; Louw, R.; van der Westhuizen, F.H.; Florit, S.; Ramírez, L.; Giralt, M.; Hidalgo, J. Obesity and metabolomics: Metallothioneins protect against high-fat diet-induced consequences in metallothionein knockout mice. Omics A J. Integr. Biol. 2015, 19, 92–103. [Google Scholar] [CrossRef]
  51. Sato, M.; Kawakami, T.; Kondoh, M.; Takiguchi, M.; Kadota, Y.; Himeno, S.; Suzuki, S. Development of high-fat-diet-induced obesity in female metallothionein-null mice. FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol. 2010, 24, 2375–2384. [Google Scholar] [CrossRef] [PubMed]
  52. Banni, M.; Messaoudi, I.; Said, L.; El Heni, J.; Kerkeni, A.; Said, K. Metallothionein gene expression in liver of rats exposed to cadmium and supplemented with zinc and selenium. Arch. Environ. Contam. Toxicol. 2010, 59, 513–519. [Google Scholar] [CrossRef] [PubMed]
  53. Cirovic, A.; Cirovic, A.; Yimthiang, S.; Vesey, D.A.; Satarug, S. Modulation of Adverse Health Effects of Environmental Cadmium Exposure by Zinc and Its Transporters. Biomolecules 2024, 14, 650. [Google Scholar] [CrossRef] [PubMed]
  54. Gasiewicz, T.A.; Smith, J.C. Properties of the cadmium and selenium complex formed in rat plasma in vivo and in vitro. Chem.-Biol. Interact. 1978, 23, 171–183. [Google Scholar] [CrossRef] [PubMed]
  55. Gasiewicz, T.A.; Smith, J.C. Interaction between cadmium and selenium in rat plasma. Environ. Health Perspect. 1978, 25, 133–136. [Google Scholar] [CrossRef] [PubMed]
  56. Yu, R.; Wang, Z.; Ma, M.; Xu, P.; Liu, L.; Tinkov, A.A.; Lei, X.G.; Zhou, J.C. Associations between Circulating SELENOP Level and Disorders of Glucose and Lipid Metabolism: A Meta-Analysis. Antioxidants 2022, 11, 1263. [Google Scholar] [CrossRef]
  57. Chen, M.; Liu, B.; Wilkinson, D.; Hutchison, A.T.; Thompson, C.H.; Wittert, G.A.; Heilbronn, L.K. Selenoprotein P is elevated in individuals with obesity, but is not independently associated with insulin resistance. Obes. Res. Clin. Pract. 2017, 11, 227–232. [Google Scholar] [CrossRef]
  58. Zheng, X.; Ren, B.; Li, X.; Yan, H.; Xie, Q.; Liu, H.; Zhou, J.; Tian, J.; Huang, K. Selenoprotein F knockout leads to glucose and lipid metabolism disorders in mice. J. Biol. Inorg. Chem. 2020, 25, 1009–1022. [Google Scholar] [CrossRef]
  59. Cai, J.; Huang, J.; Yang, J.; Chen, X.; Zhang, H.; Zhu, Y.; Liu, Q.; Zhang, Z. The protective effect of selenoprotein M on non-alcoholic fatty liver disease: The role of the AMPKα1–MFN2 pathway and Parkin mitophagy. Cell. Mol. Life Sci. CMLS 2022, 79, 354. [Google Scholar] [CrossRef]
  60. Qiao, L.; Men, L.; Yu, S.; Yao, J.; Li, Y.; Wang, M.; Yu, Y.; Wang, N.; Ran, L.; Wu, Y.; et al. Hepatic deficiency of selenoprotein S exacerbates hepatic steatosis and insulin resistance. Cell Death Dis. 2022, 13, 275. [Google Scholar] [CrossRef]
  61. Li, K.; Feng, T.; Liu, L.; Liu, H.; Huang, K.; Zhou, J. Hepatic proteomic analysis of selenoprotein T knockout mice by TMT: Implications for the role of selenoprotein T in glucose and lipid metabolism. Int. J. Mol. Sci. 2021, 22, 8515. [Google Scholar] [CrossRef] [PubMed]
  62. Chen, L.-L.; Huang, J.-Q.; Wu, Y.-Y.; Chen, L.-B.; Li, S.-P.; Zhang, X.; Wu, S.; Ren, F.-Z.; Lei, X.-G. Loss of Selenov predisposes mice to extra fat accumulation and attenuated energy expenditure. Redox Biol. 2021, 45, 102048. [Google Scholar] [CrossRef] [PubMed]
  63. Ramírez-Acosta, S.; Uhlírová, R.; Navarro, F.; Gómez-Ariza, J.L.; García-Barrera, T. Antagonistic interaction of selenium and cadmium in human hepatic cells through selenoproteins. Front. Chem. 2022, 10, 891933. [Google Scholar] [CrossRef] [PubMed]
  64. Zhang, L.; Yang, F.; Li, Y.; Cao, H.; Huang, A.; Zhuang, Y.; Zhang, C.; Hu, G.; Mao, Y.; Luo, J.; et al. The protection of selenium against cadmium-induced mitophagy via modulating nuclear xenobiotic receptors response and oxidative stress in the liver of rabbits. Environ. Pollut. 2021, 285, 117301. [Google Scholar] [CrossRef] [PubMed]
Nutrients 16 03208 g001
Figure 1. Growth performance in adult female mice during the 41-week experiment. (A) Body weight. (B) Total weight gain. Data are means ± SEM (n = 10–12) and differ with ****, p < 0.0001. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg.
Figure 1. Growth performance in adult female mice during the 41-week experiment. (A) Body weight. (B) Total weight gain. Data are means ± SEM (n = 10–12) and differ with ****, p < 0.0001. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg.
Nutrients 16 03208 g001
Nutrients 16 03208 g002
Figure 2. Accumulation of selenium (Se) (A) and cadmium (Cd) (B) and their correlation (C) in the livers of adult female mice. Data are means ± SEM (n = 9–12) and differ with ****, p < 0.0001. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg.
Figure 2. Accumulation of selenium (Se) (A) and cadmium (Cd) (B) and their correlation (C) in the livers of adult female mice. Data are means ± SEM (n = 9–12) and differ with ****, p < 0.0001. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg.
Nutrients 16 03208 g002
Nutrients 16 03208 g003
Figure 3. Lipid levels in the serum and liver and hepatic injury in adult female mice. (A–C) Serum concentrations of TG, TC, and LDL-C. (D–F) Liver concentrations of TG, TC, and LDL-C. (G,H) Serum ALT and AST activity. Data are means ± SEM (n = 8–10) and differ with *, p < 0.05; **, p < 0.01; ***, p < 0.001; and ****, p < 0.0001. ALT, alanine aminotransferase; AST, aspartate transaminase; Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; LDL-C, low-density lipoprotein cholesterol; Se, selenium; TC, total cholesterol; TG, triglyceride.
Figure 3. Lipid levels in the serum and liver and hepatic injury in adult female mice. (A–C) Serum concentrations of TG, TC, and LDL-C. (D–F) Liver concentrations of TG, TC, and LDL-C. (G,H) Serum ALT and AST activity. Data are means ± SEM (n = 8–10) and differ with *, p < 0.05; **, p < 0.01; ***, p < 0.001; and ****, p < 0.0001. ALT, alanine aminotransferase; AST, aspartate transaminase; Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; LDL-C, low-density lipoprotein cholesterol; Se, selenium; TC, total cholesterol; TG, triglyceride.
Nutrients 16 03208 g003
Nutrients 16 03208 g004
Figure 4. Improvement due to selenium (Se)-enriched Cardamine violifolia (Cv) in hepatic lipid accumulation and related molecular mechanisms. (A) H&E staining of the liver tissue with scale bar = 100 μM; the average number and area of hepatic lipid droplets were quantified with three fields per slide by using the “Analyze particles” function of ImageJ, and the mean values were calculated. (B) Total liver weight. (C) Expression of metabolic genes of triglycerides. (D) Expression of metabolic genes of cholesterol. Data are means ± SEM (n = 6–12) and differ with *, p < 0.05; **, p < 0.01; and ***, p < 0.001. Abca1, ATP-binding cassette subfamily A member 1; Abcg1/5/8, ATP-binding cassette subfamily G member 1/5/8; Atgl, adipose triglyceride lipase; ATP, adenosine triphosphate; Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Dgat1/2, diacylglycerol O-acyltransferase 1/2; Gpat1/2, glycerol-3-phosphate acyltransferase 1/2; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; Hmgcr, 3-hydroxy-3-methylglutaryl coenzyme A reductase; Hsl, hormone-sensitive lipase; Ldlr, low-density lipoprotein receptor; Lipc, lipase C hepatic type; Lpl, lipoprotein lipase; No., number; Sqle, squalene epoxidase.
Figure 4. Improvement due to selenium (Se)-enriched Cardamine violifolia (Cv) in hepatic lipid accumulation and related molecular mechanisms. (A) H&E staining of the liver tissue with scale bar = 100 μM; the average number and area of hepatic lipid droplets were quantified with three fields per slide by using the “Analyze particles” function of ImageJ, and the mean values were calculated. (B) Total liver weight. (C) Expression of metabolic genes of triglycerides. (D) Expression of metabolic genes of cholesterol. Data are means ± SEM (n = 6–12) and differ with *, p < 0.05; **, p < 0.01; and ***, p < 0.001. Abca1, ATP-binding cassette subfamily A member 1; Abcg1/5/8, ATP-binding cassette subfamily G member 1/5/8; Atgl, adipose triglyceride lipase; ATP, adenosine triphosphate; Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Dgat1/2, diacylglycerol O-acyltransferase 1/2; Gpat1/2, glycerol-3-phosphate acyltransferase 1/2; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; Hmgcr, 3-hydroxy-3-methylglutaryl coenzyme A reductase; Hsl, hormone-sensitive lipase; Ldlr, low-density lipoprotein receptor; Lipc, lipase C hepatic type; Lpl, lipoprotein lipase; No., number; Sqle, squalene epoxidase.
Nutrients 16 03208 g004
Nutrients 16 03208 g005
Figure 5. Oxidative stress and antioxidant levels in the livers of adult female mice. (A–C) The relative mRNA expression of Mtf1, Mt1, and Mt2. (D) A representative immunoblot image for Mtf1, Mt, and Sod1. (E–G) The relative protein levels of Mtf1, Mt, and Sod1. (H) The T-AOC level. (I) The level of MDA in the liver. Data are means ± SEM (n = 8–12) and differ with *, p < 0.05; **, p < 0.01; and ***, p < 0.001. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; MDA, malondialdehyde; Mt1/2, metallothionein 1/2; Mtf1, metal regulatory transcription factor 1; Se, selenium; Sod1, superoxide dismutase 1; T-AOC, total antioxidant capacity.
Figure 5. Oxidative stress and antioxidant levels in the livers of adult female mice. (A–C) The relative mRNA expression of Mtf1, Mt1, and Mt2. (D) A representative immunoblot image for Mtf1, Mt, and Sod1. (E–G) The relative protein levels of Mtf1, Mt, and Sod1. (H) The T-AOC level. (I) The level of MDA in the liver. Data are means ± SEM (n = 8–12) and differ with *, p < 0.05; **, p < 0.01; and ***, p < 0.001. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; MDA, malondialdehyde; Mt1/2, metallothionein 1/2; Mtf1, metal regulatory transcription factor 1; Se, selenium; Sod1, superoxide dismutase 1; T-AOC, total antioxidant capacity.
Nutrients 16 03208 g005
Nutrients 16 03208 g006
Figure 6. Expression of selenoproteins in the livers of adult female mice. (A) The relative mRNA expression levels of Selenof, Selenoi, and Selenos. (B) The relative mRNA expression levels of Dio1, Dio3, Gpx4, Msrb1, Selenoo, Selenow, Sephs2, Txnrd1, Txnrd2, and Txnrd3. (C) A representative immunoblot image for Selenof, Selenoi, and Selenos. (D) A representative immunoblot image for Dio1, Dio3, Gpx4, Selenoo, Txnrd1, and Txnrd2. (E) The relative protein levels of Selenof, Selenoi, and Selenos. (F) The relative protein levels of Dio1, Dio3, Gpx4, Selenoo, Txnrd1, and Txnrd2. Data are means ± SEM (n = 8–12) and differ with *, p < 0.05 and **, p < 0.01. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Dio1/3, iodothyronine deiodinase 1/3; ER, endoplasmic reticulum; Gpx4, glutathione peroxidase 4; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; MsrB1, methionine sulfoxide reductase B1; Se, selenium; Selenof/i/o/s/w, selenoprotein F/I/O/S/W; Sephs2, selenophosphate synthetase 2; Txnrd1/2/3, thioredoxin reductase 1/2/3.
Figure 6. Expression of selenoproteins in the livers of adult female mice. (A) The relative mRNA expression levels of Selenof, Selenoi, and Selenos. (B) The relative mRNA expression levels of Dio1, Dio3, Gpx4, Msrb1, Selenoo, Selenow, Sephs2, Txnrd1, Txnrd2, and Txnrd3. (C) A representative immunoblot image for Selenof, Selenoi, and Selenos. (D) A representative immunoblot image for Dio1, Dio3, Gpx4, Selenoo, Txnrd1, and Txnrd2. (E) The relative protein levels of Selenof, Selenoi, and Selenos. (F) The relative protein levels of Dio1, Dio3, Gpx4, Selenoo, Txnrd1, and Txnrd2. Data are means ± SEM (n = 8–12) and differ with *, p < 0.05 and **, p < 0.01. Cv1D, control diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv, Cardamine violifolia; Dio1/3, iodothyronine deiodinase 1/3; ER, endoplasmic reticulum; Gpx4, glutathione peroxidase 4; Cv1HFD, high-fat diet with 0.15 mg Se and 0.03 mg Cd (in the form of control Cv)/kg; Cv2HFD, high-fat diet with 1.5 mg Se and 0.29 mg Cd (in the form of Se-enriched Cv)/kg; MsrB1, methionine sulfoxide reductase B1; Se, selenium; Selenof/i/o/s/w, selenoprotein F/I/O/S/W; Sephs2, selenophosphate synthetase 2; Txnrd1/2/3, thioredoxin reductase 1/2/3.
Nutrients 16 03208 g006
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

Zhu, J.; Lv, Q.; Li, F.; Xu, P.; Han, Z.; Yang, A.; Shi, Z.; Wang, C.; Jiang, J.; Zhu, Y.; et al. Alleviation of Lipid Disorder and Liver Damage in High-Fat Diet-Induced Obese Mice by Selenium-Enriched Cardamine violifolia with Cadmium Accumulation. Nutrients 2024, 16, 3208. https://doi.org/10.3390/nu16183208

AMA Style

Zhu J, Lv Q, Li F, Xu P, Han Z, Yang A, Shi Z, Wang C, Jiang J, Zhu Y, et al. Alleviation of Lipid Disorder and Liver Damage in High-Fat Diet-Induced Obese Mice by Selenium-Enriched Cardamine violifolia with Cadmium Accumulation. Nutrients. 2024; 16(18):3208. https://doi.org/10.3390/nu16183208

Chicago/Turabian Style

Zhu, Junying, Qingqing Lv, Fengna Li, Ping Xu, Ziyu Han, Aolin Yang, Zhan Shi, Chao Wang, Jie Jiang, Yunfen Zhu, and et al. 2024. "Alleviation of Lipid Disorder and Liver Damage in High-Fat Diet-Induced Obese Mice by Selenium-Enriched Cardamine violifolia with Cadmium Accumulation" Nutrients 16, no. 18: 3208. https://doi.org/10.3390/nu16183208

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