1. Introduction
As one of the most numerous and ubiquitous domestic animals, chickens (
Gallus gallus domesticus) provide abundant, high-quality, and affordable meat and egg protein for humans [
1]. Numerous studies have demonstrated that housing systems can impact the welfare, physiology, health, productivity, and product quality of poultry by modifying their physical activity, such as through the provision of perches, addition of ramps, implementation of barriers between food and water, or changing the rearing system [
2,
3]. Due to variations in factors such as species, age, nutrition, density, etc., the effects of different housing systems on poultry performance and product quality indicators remain controversial.
Recently, Guo et al. (2019) and Wang et al. (2021) used pedometers to track and measure the walking steps of chickens in a free-range setting to assess the effect of exercise on growth, carcass yield, meat quality, muscle mRNA expression profiles, and tibial strength [
4,
5]. Their findings provide fresh perspectives on the effects of exercise on chickens, indicating that increased exercise led to higher body weight, enhanced meat quality through increased water-holding capacity and reduced shear force values, decreased percentage of breast muscle weight, and improved tibial strength. However, the differences in exercise profiles among birds under different rearing systems and the specific effect of housing systems on poultry from the perspective of variations in physical activity levels remain largely unknown.
Previous reports have demonstrated that slow-growing poultry breeds are the ones that can derive maximum benefits from a free-range housing system, as fast-growing birds exhibit a significantly lower level of adaptability [
6,
7,
8,
9]. Traditionally, Chinese indigenous chickens are selected not primarily for the meat yield capacity but for organic qualities, high meat quality, and intense flavor [
10]. Therefore, Jiuyuan Black chickens, a typical slow-growing breed extensively raised in southwestern China, were selected for this study.
In the present study, a pedometer was used to record the daily step counts of Jiuyuan Black chickens under different housing systems. The main purpose of this study was to investigate the effects of different housing systems on the body conformation, carcass traits, meat quality, and serum biochemical parameters of slow-growing chickens from the perspective of differences in exercise levels.
2. Materials and Methods
2.1. Animals and Experimental Design
In this study, 30-day-old Jiuyuan Black male chickens (a Chinese indigenous chicken breed) were randomly housed in conventional cages and a free-range environment reared with 1500 individuals each. At an age ranging from 30 to 60 days, the chickens were housed in triple-layered, three-dimensional cages of 70 cm × 70 cm × 40 cm (length × width × height) with a density of 10 birds per cage. At 60 d of age, 300 chickens with similar body weights in each housing system were further randomly divided into 3 groups of 100 individuals each: from 60 to 90 d of age, from 90 to 120 d of age, and from 120 to 150 d of age, and the stocking density was adjusted to 1 cage per bird. In the free-range model, chickens were maintained in the hills at a density of 150 birds per 667 m2. The daily step counts of all experimental chickens in each group were recorded individually by an intelligent pedometer system consisting of a smart ankle bracelet (pedometer), a signal receiving device, and a data storage system (Shenzhen Lianwen Intelligent Technology Co., Ltd., Shenzhen, China). The daily step counts of all experimental chickens in each group were recorded by the pedometer (Shenzhen Lianwen Intelligent Technology Co., Ltd., Shenzhen, China). Based on the average daily step counts, the chickens of each group mentioned above were further chosen as the high-steps group (the top 20 birds) and low-steps group (the last 20 birds). Therefore, based on the difference of the housing system and exercise volume, this study was finally divided into four experimental groups: the cage high-steps group (CHS), the cage low-steps group (CLS), the free-range high-steps group (FHS), and the free-range low-steps group (FLS). All birds were raised with free access to feed and water in the Poultry Breeding Farm of Wan yuan Hengkang Agricultural Development Co., Ltd., Wanyuan, China.
2.2. Sample Collection and Measurement
At 90, 120, and 150 d of age, 20 chickens of each experimental group were randomly selected for live body conformation measurement after a 12 h fast. After the individual live body weight (LBW) was recorded, live body conformation measurements, which included body slope length (BSL, the body surface distance from shoulder joint to ischial tuberosity), keel length (KL, the body surface distance from the front to the end of the keel), breast width (BW, the distance between two shoulder joints), breast depth (BD, the distance from the first thoracic vertebra to the front of the keel), and shank length (SL, the distance from the hind corner of the hock joint to the first scale of the third toe), were measured with a digital vernier caliper and flexible measuring tape [
5,
11,
12]. To avoid individual variations in measurements, all the indicators above were measured by the same trained person.
In addition, 15 birds of each experimental group were randomly selected, and blood samples were collected from the wing vein. The blood collection tubes were centrifuged at 3000 rpm for 15 min to separate the serum [
13], and the serum samples were stored at −20 °C until further use. The levels of lactate dehydrogenase (LDH) and creatine kinase (CK) in the serum were detected by using the enzyme-linked immunosorbent assay (ELISA) kit, following the manufacturer’s instructions (Enzyme-linked Biotechnology Co., Ltd., Shanghai, China).
The above 20 birds of each experimental group with measured live body conformation were electrically stunned and killed by exsanguination, and then scalded, defeathered, weighed (carcass weight, CW), eviscerated, and divided. The dressing percentage was calculated as the ratio between CW and LBW. Carcass traits were measured using the method called performance terms and measurement for poultry by the Agricultural Ministry of China (NY/T 823-2004 [
14]) as follows:
Half-eviscerated weight (HEW) refers to the carcass after subtracting the weight of the trachea, esophagus, full crop, intestines, spleen, pancreas, gallbladder, and reproductive organs. Eviscerated weight (EW) was calculated by subtracting the weight of the heart, liver, glandular stomach, gizzard, lung, abdominal fat, head, and legs from the half-eviscerated weight. The proportion of the HEW and EW in the LBW, the percentage of the leg muscle and breast muscle of the EW, and the percentage of abdominal fat of the weight (EW + abdominal fat weight) were calculated, respectively. Additionally, heart weight (HW), liver weight (LW), glandular stomach weight (GSW), gizzard weight (GW), and abdominal fat weight (AFW) were measured. The percentages of heart weight (PHW), liver weight (PLW), glandular stomach weight (PGSW), gizzard weight (PGW), and abdominal fat weight (PAFW) were calculated, respectively.
After the carcass parameters were determined, the breast and leg muscle samples of all individuals above were further collected for meat quality analyses. The pH values were measured at 24 h (pH
24h) postmortem (stored at 4 °C) at 1 cm depth in triplicate using a pH-Star meter (Orion Co., Ltd., Boston, MA, USA). By hanging the whole piece of meat (1.0 cm × 1.0 cm × 2.0 cm) in a sealed pocket at 4 °C for 24 h, drip loss was calculated as the percentage of weight loss during storage. Muscle shear force was measured by using the C-LM3 digital meat tenderness meter (North-east Agricultural University, Harbin, China) with the methods described by [
4]. Dry matter (DM) was measured by oven drying, and intramuscular fat (IMF) was determined using Soxhlet petroleum–ether extraction [
15]. The content of inosinic acid (IMP) was measured by Agilent 1100 High-Performance Liquid Chromatography (Agilent, Co., Ltd., Palo Alto, CA, USA).
2.3. Statistical Analysis
All values were expressed as the means ± standard deviation (SD), and statistical significance was analyzed using a one-way analysis of variance (ANOVA) followed by Duncan’s multiple range analysis by the SPSS version 19.0 software (SPSS Inc., Chicago, IL, USA). Differences were considered significant at p < 0.05.
4. Discussion
The results show that the ADS or TS of all birds decreased from 60 d to 150 d. This result is inconsistent with that of Wang et al. (2021), who reported that sex and environmental factors, but not age, could affect the amount of exercise during the adolescent stage of Chinese indigenous chickens [
5]. The reasons for this discrepancy could be attributed to the differences of breed and test period. Clearly, the TS of the CHS and CLS groups were significantly lower than those in the FHS and FLS groups with the increase in age (from D60 to D90), which implied that the reduction in the amount of exercise in cage birds may be affected by the continuous decrease in activity space. Compared to traditional studies on the effects of different feeding models on animal welfare and production performance [
16,
17,
18], this research offers a new perspective for similar studies. The findings indicate that feeding models, age, and individual differences may influence the amount of exercise observed in chickens.
The present study showed that increased exercise volume results in reduced shank length (90 d), breast width (90 d), and keel length (150 d), which suggested that increased exercise may have a negative impact on partial body measurements. This is partly in accordance with the finding of Wang et al. (2021), who reported that birds with a higher exercise volume showed a shorter shank length [
5]. Additionally, previous studies showed that chicken reared in a free-range system or with a high number of step counts displayed a higher shank strength, bone density, and total bone mineral content than birds from conventional cages [
5,
19], which implied that increased exercise volume or free-range systems could have positive effects on the chicken bone characteristics.
In the present study, only birds at 90 d of age from the FHS and FLS groups exhibited lower live body weight, carcass weight, half-eviscerated weight, eviscerated weight, breast muscle weight, leg muscle weight, and percentage of eviscerated weight than the CLS group, inconsistent with previous studies [
5,
20,
21], and indicated that no difference observed in the carcass and parts yields between conventional and free-range or high exercise group and low exercise group. The indigenous chicken breed selected in this study is still not at somatic maturity at 90 d of age, and the difference in exercise volume caused by the housing systems and individual differences at this age stage may lead to this phenomenon. Interestingly, birds from the FHS group showed the highest heart weight values but the lowest abdominal fat weight values among these four groups. Our study suggested that increased exercise can effectively increase heart weight and reduce abdominal fat in poultry, which were consistent with previous studies [
5,
20,
22].
The breeds that are indigenous to China are not primarily selected for their meat yield capacity but for organic purposes, high meat quality, and intense flavor [
10]. Both the dry matter and shear force are important meat quality characteristics. The dry matter refers to everything in the meat, except for the water content. Shear force is an important parameter of tenderness, with lower values indicating greater tenderness [
23,
24]. The present study showed that both the breast and leg muscle samples from the FHS group displayed a higher dry matter and shear force than those from the CHS and CLS groups, and similar findings have been reported by Castellini et al. (2002), who demonstrated that the housing system affected the shear force that was higher in either the breast or leg of the organic birds [
7]. In addition, Jin et al. (2019) reported that shear force increased linearly with the increase in free-range days [
25]. These findings might be due to the increased motor activity under the free-range system, which could contribute to development of the skeletal muscle, and thus might affect the shear force. However, Guo et al. (2019) and Wang et al. (2021) stated that increased exercise decreased the shear force [
4,
5], and Wang et al. (2009) reported that the raising system had no effect on the shear force [
20]. These discrepancies may be due to differences in breed, age, environmental factors, and farming systems. It is important to acknowledge that, out of consideration for animal welfare, consumers in certain countries may be willing to accept a slightly lower quality in free-range systems. Intramuscular fat is another important evaluation index of meat quality, which is positively correlated with tenderness and flavor [
26,
27]. Our data indicated that the FHS group displayed the lowest intramuscular fat among the four groups, which showed a similar trend to the abdominal fat weight results. Similarly, previous studies indicated that non-caged chickens showed thinner subcutaneous fat and lower abdominal fat and intramuscular fat contents [
28,
29]. The increased activity of chickens in the free-range system may be a contributing factor to this phenomenon, resulting in a greater dietary energy consumption and correspondingly less fat deposition.
In 1958, the first reported increase in serum enzyme activity following exercise in humans marked the beginning of subsequent studies that have established the multifactorial nature of the degree to which the serum activities of various enzymes increase during and after exercise [
30]. Increased serum concentrations of creatine kinase (CK) and lactate dehydrogenase (LDH) are used as indicators of damage to muscle membrane and other tissue structures, as these molecules are fragments of the myosin heavy chain and are unable to cross the sarcoplasmic membrane barrier [
31,
32,
33]. Generally, the serum CK concentration has been considered to be the best indirect index of human skeletal muscle damage, particularly for the diagnosis of some diseases [
34], and showed large variability between subjects [
35]. Moreover, both CK, closely associated with intracellular energy metabolism and muscle contraction, and LDH, responsible for catalyzing the interconversion of pyruvate and lactate, have been shown to physiologically increase in humans with rising levels of physical activity [
36,
37,
38]. Interestingly, our study indicates that the CK and LDH levels in chickens of all age stages almost have been observed to rise with increased physical activity, which suggests that serum CK and LDH levels can be used to indirectly reflect the actual level of physical activity in chickens.