Pub Date : 2025-03-15eCollection Date: 2025-01-01DOI: 10.2141/jpsa.2025013
Phuong V Tran
Regulation of food intake, especially during the neonatal period, is important to ensure optimal nutrition and meet the metabolic requirements of growing and healthy animals. However, many problems associated with neonatal chicks remain unsolved. Feeding behavior during the neonatal stage is characterized by short resting periods between very brief times spent taking up food. Accordingly, neuropeptides, which take time to synthesize and release, as well as nutrients that are taken up via feeding, may be involved in feeding regulation. The present review summarizes current knowledge about the role of amino acids and their interaction with neuropeptides on the regulation of food intake in neonatal chicks with special emphasis on L-arginine metabolism and neuropeptide Y. Fasting and subsequent short-term refeeding influence amino acid metabolism in the brain. Short-term refeeding induces a rapid increase in the concentrations of several amino acids, which may contribute to satiety signals in the neonatal chick brain. The function of L-arginine is related to its metabolite, L-ornithine, which acts as an innate satiety signal in the control of food intake. Co-injection with L-ornithine attenuates the orexigenic effect of neuropeptide Y in a dose-dependent manner. This implies a potent interaction in the brain between the regulation of food intake by neuropeptide Y and acute satiety signals by L-ornithine. The roles of other amino acids in feeding and their relationship with the stress response are also discussed in this review. In conclusion, endogenous neuropeptides and endogenous and/or exogenous nutrients such as amino acids are believed to coordinate the feeding behavior of neonatal chicks.
{"title":"Function of Amino Acids and Neuropeptides in Feeding Behavior in Chicks.","authors":"Phuong V Tran","doi":"10.2141/jpsa.2025013","DOIUrl":"https://doi.org/10.2141/jpsa.2025013","url":null,"abstract":"<p><p>Regulation of food intake, especially during the neonatal period, is important to ensure optimal nutrition and meet the metabolic requirements of growing and healthy animals. However, many problems associated with neonatal chicks remain unsolved. Feeding behavior during the neonatal stage is characterized by short resting periods between very brief times spent taking up food. Accordingly, neuropeptides, which take time to synthesize and release, as well as nutrients that are taken up via feeding, may be involved in feeding regulation. The present review summarizes current knowledge about the role of amino acids and their interaction with neuropeptides on the regulation of food intake in neonatal chicks with special emphasis on L-arginine metabolism and neuropeptide Y. Fasting and subsequent short-term refeeding influence amino acid metabolism in the brain. Short-term refeeding induces a rapid increase in the concentrations of several amino acids, which may contribute to satiety signals in the neonatal chick brain. The function of L-arginine is related to its metabolite, L-ornithine, which acts as an innate satiety signal in the control of food intake. Co-injection with L-ornithine attenuates the orexigenic effect of neuropeptide Y in a dose-dependent manner. This implies a potent interaction in the brain between the regulation of food intake by neuropeptide Y and acute satiety signals by L-ornithine. The roles of other amino acids in feeding and their relationship with the stress response are also discussed in this review. In conclusion, endogenous neuropeptides and endogenous and/or exogenous nutrients such as amino acids are believed to coordinate the feeding behavior of neonatal chicks.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025013"},"PeriodicalIF":1.8,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11903097/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143649440","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-10eCollection Date: 2025-01-01DOI: 10.2141/jpsa.2025012
Santosh Haunshi, Shanmugam Murugesan, Prince L L Leslie, Rajkumar Ullengala, Chatterjee R Nath
The present study aimed to determine the inheritance and effect of dwarfism, which occurs naturally in the Nicobari chicken breed, on various growth and production traits. The dwarf character did not affect body weight for up to 4 weeks; but had a negative impact from 8 weeks onward, with body weight declining by 5.5%-9.0% in males and 9.0%-16% in females. Shank length was 22% and 27% shorter in male and female dwarf birds, respectively, than in full-size birds. The average age at first egg was 3.08% higher in dwarf hens than in their normal counterparts, and was accompanied by a non-significant decline (5.63%) in 40 weeks egg production. Egg weights were 2.23% and 2.64% lower at 32 and 40 weeks, respectively, in dwarf hens. Instead, the shape index and shell thickness were better in dwarf hens. The eggs of dwarf hens were darker and red, with less hue than those of normal hens; whereas internal egg quality was the same. Fertility and hatchability were lower in dwarf dams mated with dwarf sires than in crosses or reciprocal crosses between normal and dwarf birds. Breeding experiments and sequencing of transmembrane protein 263 ruled out the sex-linked (dw) and autosomal dwarfism (adw), as the genetic causes of dwarfism in the Nicobari breed, which instead appears to follow a novel pattern and has a unique effect on growth traits.
{"title":"Effect of a Unique Dwarfism on Growth, Production, and Reproduction Performance of the Nicobari Chicken Breed.","authors":"Santosh Haunshi, Shanmugam Murugesan, Prince L L Leslie, Rajkumar Ullengala, Chatterjee R Nath","doi":"10.2141/jpsa.2025012","DOIUrl":"10.2141/jpsa.2025012","url":null,"abstract":"<p><p>The present study aimed to determine the inheritance and effect of dwarfism, which occurs naturally in the Nicobari chicken breed, on various growth and production traits. The dwarf character did not affect body weight for up to 4 weeks; but had a negative impact from 8 weeks onward, with body weight declining by 5.5%-9.0% in males and 9.0%-16% in females. Shank length was 22% and 27% shorter in male and female dwarf birds, respectively, than in full-size birds. The average age at first egg was 3.08% higher in dwarf hens than in their normal counterparts, and was accompanied by a non-significant decline (5.63%) in 40 weeks egg production. Egg weights were 2.23% and 2.64% lower at 32 and 40 weeks, respectively, in dwarf hens. Instead, the shape index and shell thickness were better in dwarf hens. The eggs of dwarf hens were darker and red, with less hue than those of normal hens; whereas internal egg quality was the same. Fertility and hatchability were lower in dwarf dams mated with dwarf sires than in crosses or reciprocal crosses between normal and dwarf birds. Breeding experiments and sequencing of transmembrane protein 263 ruled out the sex-linked (dw) and autosomal dwarfism (adw), as the genetic causes of dwarfism in the Nicobari breed, which instead appears to follow a novel pattern and has a unique effect on growth traits.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025012"},"PeriodicalIF":1.8,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11885934/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143597246","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-07eCollection Date: 2025-01-01DOI: 10.2141/jpsa.2025010
Heng Wang, Lin Liu, Xi He, Guozhi Bian
Betaine has been proposed as a low-cost source of methyl groups in poultry feed, replacing methionine and choline. The present study aimed to investigate the effect of betaine on growth performance, methionine metabolism, and methyl transfer in broilers aged 1 to 21 days fed a low-methionine diet. A total of 960 one-day-old male broilers were randomly divided into four groups: positive control (0.62% methionine in the diet), negative control (0.37% methionine in the diet), and two treatment groups (0.37% methionine in the diet plus either 1500 or 3000 mg betaine/kg diet). Chicks fed the 1500 mg betaine/kg diet had the highest feed-to-gain ratio (P < 0.05), but no significant difference in final body weight, average daily gain, average daily feed intake, or mortality. Serum S-adenosyl-L-methionine and total homocysteine were higher at 1500 mg betaine/kg diet; whereas serum S-adenosylhomocysteine exhibited the opposite trend. Except for DNA methyltransferase 1, key enzymes and metabolites involved in the hepatic single-carbon pathway showed the highest levels at 1500 mg betaine/kg diet and declined thereafter. Furthermore, betaine promoted dose-dependent mRNA and protein expression of enzymes involved in the hepatic single-carbon metabolic cycle and methyl transferase pathways in chicks fed methionine-deficient diets. In conclusion, while the addition of betaine did not significantly improve the growth performance of chicks aged 1-21 days, inclusion of 1500 mg betaine/kg diet effectively stabilized methionine metabolism and methyl transfer in methionine-deficient diets.
{"title":"Effect of betaine on growth performance, methionine metabolism, and methyl transfer in broilers aged 1 to 21 days and fed a low-methionine diet.","authors":"Heng Wang, Lin Liu, Xi He, Guozhi Bian","doi":"10.2141/jpsa.2025010","DOIUrl":"10.2141/jpsa.2025010","url":null,"abstract":"<p><p>Betaine has been proposed as a low-cost source of methyl groups in poultry feed, replacing methionine and choline. The present study aimed to investigate the effect of betaine on growth performance, methionine metabolism, and methyl transfer in broilers aged 1 to 21 days fed a low-methionine diet. A total of 960 one-day-old male broilers were randomly divided into four groups: positive control (0.62% methionine in the diet), negative control (0.37% methionine in the diet), and two treatment groups (0.37% methionine in the diet plus either 1500 or 3000 mg betaine/kg diet). Chicks fed the 1500 mg betaine/kg diet had the highest feed-to-gain ratio (<i>P</i> < 0.05), but no significant difference in final body weight, average daily gain, average daily feed intake, or mortality. Serum S-adenosyl-L-methionine and total homocysteine were higher at 1500 mg betaine/kg diet; whereas serum S-adenosylhomocysteine exhibited the opposite trend. Except for DNA methyltransferase 1, key enzymes and metabolites involved in the hepatic single-carbon pathway showed the highest levels at 1500 mg betaine/kg diet and declined thereafter. Furthermore, betaine promoted dose-dependent mRNA and protein expression of enzymes involved in the hepatic single-carbon metabolic cycle and methyl transferase pathways in chicks fed methionine-deficient diets. In conclusion, while the addition of betaine did not significantly improve the growth performance of chicks aged 1-21 days, inclusion of 1500 mg betaine/kg diet effectively stabilized methionine metabolism and methyl transfer in methionine-deficient diets.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025010"},"PeriodicalIF":1.8,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11879611/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143586061","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Freedom from thirst is an undeniable requirement of the poultry industry. However, the regulatory mechanisms underlying water intake in chicks are not yet fully understood. In humans, increased blood osmolality is probably the strongest signal for drinking. Angiotensin II, a hyperosmotic signal, induces water intake in chickens; this effect is attenuated by an opioid receptor antagonist. Vasotocin and mesotocin appear to have osmoregulatory functions in chicken. Dehydration activates brain corticotrophin-releasing factor (CRF) neurons in rats, and the central administration of CRF induces water intake in rabbits. This study aimed to clarify the effects of neuropeptides such as opioid peptides, vasotocin, mesotocin, and CRF on water intake to identify thirst-inducing neuropeptides in chicks. Eight-day-old male chicks were intracerebroventricularly injected with saline or the peptides. Water intake was measured 120 min after the injection under feed-deprived conditions. Intracerebroventricular administration of Met-enkephalin (a δ-opioid receptor agonist), β-endorphin (a δ-opioid receptor agonist), and nociception (a κ-opioid receptor and opioid receptor-like protein agonist) significantly suppressed water intake in chicks, whereas dynorphin B (a κ-opioid receptor agonist) and endomorphin-1 and 2 (μ-opioid receptor agonists) did not affect water intake. Intracerebroventricular administration of vasotocin, mesotocin, and CRF significantly suppressed water intake in chicks. Our findings suggest that none of the neuropeptides used in this study function as thirst-inducing peptides in the central nervous system of chicks.
{"title":"Effects of Central Administration of Opioid Peptides, Vasotocin, Mesotocin, and Corticotrophin-Releasing Factor on Water Intake in Chicks.","authors":"Yuhui Zhang, Kaoruko Murata, Junya Takegaki, Takaoki Saneyasu, Kazuhisa Honda","doi":"10.2141/jpsa.2025011","DOIUrl":"10.2141/jpsa.2025011","url":null,"abstract":"<p><p>Freedom from thirst is an undeniable requirement of the poultry industry. However, the regulatory mechanisms underlying water intake in chicks are not yet fully understood. In humans, increased blood osmolality is probably the strongest signal for drinking. Angiotensin II, a hyperosmotic signal, induces water intake in chickens; this effect is attenuated by an opioid receptor antagonist. Vasotocin and mesotocin appear to have osmoregulatory functions in chicken. Dehydration activates brain corticotrophin-releasing factor (CRF) neurons in rats, and the central administration of CRF induces water intake in rabbits. This study aimed to clarify the effects of neuropeptides such as opioid peptides, vasotocin, mesotocin, and CRF on water intake to identify thirst-inducing neuropeptides in chicks. Eight-day-old male chicks were intracerebroventricularly injected with saline or the peptides. Water intake was measured 120 min after the injection under feed-deprived conditions. Intracerebroventricular administration of Met-enkephalin (a δ-opioid receptor agonist), β-endorphin (a δ-opioid receptor agonist), and nociception (a κ-opioid receptor and opioid receptor-like protein agonist) significantly suppressed water intake in chicks, whereas dynorphin B (a κ-opioid receptor agonist) and endomorphin-1 and 2 (μ-opioid receptor agonists) did not affect water intake. Intracerebroventricular administration of vasotocin, mesotocin, and CRF significantly suppressed water intake in chicks. Our findings suggest that none of the neuropeptides used in this study function as thirst-inducing peptides in the central nervous system of chicks.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025011"},"PeriodicalIF":1.8,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11879654/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143586078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-07eCollection Date: 2025-01-01DOI: 10.2141/jpsa.2025009
Andrea Pietruska, Kenneth S Macklin, Xu Wang, James T Krehling, Teresa Dormitorio, Rüdiger Hauck
Salmonella enterica and coccidia (Eimeria spp.) are important intestinal pathogens in broiler production. Salmonella has high zoonotic potential, and coccidia are responsible for large economic losses. Live vaccines reduce shedding of Salmonella and minimize the impact of coccidial infections on broiler performance. This study investigated the interaction between both vaccines on the intestinal health of broilers. The 2 × 2 experimental design included vaccination against Salmonella Typhimurium (ST) (no vaccination or vaccination on day 14) and vaccination against coccidiosis (no vaccination or vaccination on day 1). On day 28, all groups were challenged with a ST marker strain resistant to nalidixic acid. Re-isolation of ST from the liver and ceca on day 42 indicated higher susceptibility to systemic infection with ST in birds vaccinated against coccidiosis than that in unvaccinated birds. On day 42, cecal immunoglobulin A (IgA) levels against ST decreased in the group vaccinated against ST and coccidia compared to those in all other groups. IgG antibodies in the cecal contents significantly decreased in the group vaccinated against coccidiosis compared to that of the group vaccinated against ST. There was no difference in systemic IgG levels among groups. Analysis of the cecal microbiota revealed a significant difference in beta diversity on days 28 and 42 between the groups vaccinated against coccidiosis and unvaccinated groups. Functional pathway profiling showed increased activity of pathways associated with carbohydrate and arachidonic acid metabolism in the group vaccinated against ST compared to that in other groups. Gene expression of claudin 1, claudin 4, E-cadherin, β-catenin, and zonula occludens 2 in the cecal wall differed between the groups on days 28 and 42. These findings indicated the significant influence of ST and coccidiosis vaccines on the intestinal health of broilers; however, further studies are required to clarify the implications for health and performance.
肠炎沙门氏菌和球虫(Eimeria spp.)是肉鸡生产中重要的肠道病原体。沙门氏菌具有很高的人畜共患可能性,而球虫则会造成巨大的经济损失。活疫苗可减少沙门氏菌的脱落,并将球虫感染对肉鸡生产性能的影响降至最低。本研究调查了两种疫苗对肉鸡肠道健康的相互作用。2 × 2 试验设计包括接种鼠伤寒沙门氏菌 (ST) 疫苗(不接种或在第 14 天接种)和球虫病疫苗(不接种或在第 1 天接种)。第 28 天,所有组别都接种了对萘啶酸耐药的 ST 标记菌株。第 42 天,从肝脏和盲肠中再次分离出 ST,结果表明接种球虫病疫苗的禽类比未接种疫苗的禽类更容易全身感染 ST。第 42 天,接种 ST 和球虫疫苗组的鸟类盲肠中针对 ST 的免疫球蛋白 A (IgA) 含量比其他各组都要低。与接种 ST 疫苗组相比,接种球虫疫苗组盲肠内容物中的 IgG 抗体明显降低。各组之间的全身 IgG 水平没有差异。对盲肠微生物群的分析表明,在第28天和第42天,接种球虫病疫苗组和未接种疫苗组在β多样性方面存在显著差异。功能通路分析表明,接种球虫病疫苗组与其他组相比,与碳水化合物和花生四烯酸代谢相关的通路活性增加。第28天和第42天,各组间盲肠壁上的Claudin 1、Claudin 4、E-cadherin、β-catenin和zonula occludens 2的基因表达量有所不同。这些研究结果表明,ST 和球虫病疫苗对肉鸡的肠道健康有重大影响;然而,还需要进一步的研究来阐明其对健康和生产性能的影响。
{"title":"Investigation of Intestinal Health in Broiler Chickens Following <i>Salmonella</i> Typhimurium and Coccidiosis Vaccination and Challenge with <i>Salmonella</i> Typhimurium.","authors":"Andrea Pietruska, Kenneth S Macklin, Xu Wang, James T Krehling, Teresa Dormitorio, Rüdiger Hauck","doi":"10.2141/jpsa.2025009","DOIUrl":"10.2141/jpsa.2025009","url":null,"abstract":"<p><p><i>Salmonella enterica</i> and coccidia (<i>Eimeria</i> spp.) are important intestinal pathogens in broiler production. <i>Salmonella</i> has high zoonotic potential, and coccidia are responsible for large economic losses. Live vaccines reduce shedding of <i>Salmonella</i> and minimize the impact of coccidial infections on broiler performance. This study investigated the interaction between both vaccines on the intestinal health of broilers. The 2 × 2 experimental design included vaccination against <i>Salmonella</i> Typhimurium (ST) (no vaccination or vaccination on day 14) and vaccination against coccidiosis (no vaccination or vaccination on day 1). On day 28, all groups were challenged with a ST marker strain resistant to nalidixic acid. Re-isolation of ST from the liver and ceca on day 42 indicated higher susceptibility to systemic infection with ST in birds vaccinated against coccidiosis than that in unvaccinated birds. On day 42, cecal immunoglobulin A (IgA) levels against ST decreased in the group vaccinated against ST and coccidia compared to those in all other groups. IgG antibodies in the cecal contents significantly decreased in the group vaccinated against coccidiosis compared to that of the group vaccinated against ST. There was no difference in systemic IgG levels among groups. Analysis of the cecal microbiota revealed a significant difference in beta diversity on days 28 and 42 between the groups vaccinated against coccidiosis and unvaccinated groups. Functional pathway profiling showed increased activity of pathways associated with carbohydrate and arachidonic acid metabolism in the group vaccinated against ST compared to that in other groups. Gene expression of claudin 1, claudin 4, E-cadherin, β-catenin, and zonula occludens 2 in the cecal wall differed between the groups on days 28 and 42. These findings indicated the significant influence of ST and coccidiosis vaccines on the intestinal health of broilers; however, further studies are required to clarify the implications for health and performance.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025009"},"PeriodicalIF":1.8,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11879612/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143586079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
From the perspective of animal welfare, freedom from hunger and thirst is an undeniable requirement for the poultry industry. Regulatory mechanisms underlying drinking behavior have not yet been identified in chickens; however, the regulation of osmolality and water intake appears to be closely related. This study clarified whether wet feeding affects appetite, osmolality, and stress-related gene expression in the hypothalami of chicks. In Experiment 1, the effects of different wet feed percentages on the growth of broiler chicks were examined. Wet feeds were prepared by mixing either 0.25 g (20% wet feed), 0.667 g (40% wet feed), or 1.5 g (60% wet feed) of distilled water per g of commercial feed. Then, the wet feeds were offered to 4-day-old broiler chicks until 42 d of age. Forty percent wet feed significantly increased body, breast, and leg weights. In Experiment 2, 7-day-old broiler chicks were given either commercial starter feed or 40% wet feed until 21 d of age. Again, weights of the body, breasts, and legs were significantly increased by wet feeding. The total amount of water loss in the individual waterers was significantly decreased by wet feeding. No significant changes were observed in mRNA levels of the genes encoding appetite-regulatory peptides (neuropeptide Y and α melanocyte-stimulating hormone), osmoregulatory peptides (vasotocin and mesotocin), or stress-related peptides (corticotrophin-releasing factor) in the chicken hypothalamus. Overall, 40% wet feed improved growth without inducing thirst or hunger in broiler chicks. These findings suggest that wet feeding contributes to both meat yield and animal welfare during broiler production.
{"title":"Wet Feeding Promotes Growth without Affecting Hypothalamic Peptide Gene Expression in Growing Broiler Chicks.","authors":"Tomoya Matsunami, Yuhui Zhang, Yuji Taniguchi, Sei-Ichi Hinomoto, Takaoki Saneyasu, Hiroshi Kamisoyama, Kazuhisa Honda","doi":"10.2141/jpsa.2025008","DOIUrl":"10.2141/jpsa.2025008","url":null,"abstract":"<p><p>From the perspective of animal welfare, freedom from hunger and thirst is an undeniable requirement for the poultry industry. Regulatory mechanisms underlying drinking behavior have not yet been identified in chickens; however, the regulation of osmolality and water intake appears to be closely related. This study clarified whether wet feeding affects appetite, osmolality, and stress-related gene expression in the hypothalami of chicks. In Experiment 1, the effects of different wet feed percentages on the growth of broiler chicks were examined. Wet feeds were prepared by mixing either 0.25 g (20% wet feed), 0.667 g (40% wet feed), or 1.5 g (60% wet feed) of distilled water per g of commercial feed. Then, the wet feeds were offered to 4-day-old broiler chicks until 42 d of age. Forty percent wet feed significantly increased body, breast, and leg weights. In Experiment 2, 7-day-old broiler chicks were given either commercial starter feed or 40% wet feed until 21 d of age. Again, weights of the body, breasts, and legs were significantly increased by wet feeding. The total amount of water loss in the individual waterers was significantly decreased by wet feeding. No significant changes were observed in mRNA levels of the genes encoding appetite-regulatory peptides (neuropeptide Y and α melanocyte-stimulating hormone), osmoregulatory peptides (vasotocin and mesotocin), or stress-related peptides (corticotrophin-releasing factor) in the chicken hypothalamus. Overall, 40% wet feed improved growth without inducing thirst or hunger in broiler chicks. These findings suggest that wet feeding contributes to both meat yield and animal welfare during broiler production.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025008"},"PeriodicalIF":1.8,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11795110/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143382783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-06eCollection Date: 2025-01-01DOI: 10.2141/jpsa.2025007
Sadequllah Ahmadi, Takeshi Ohkubo
Leptin, a key regulator of reproductive physiology, influences various processes in vertebrates, including oocyte proliferation, embryogenesis, the onset of puberty, ovarian function, and follicle development. In mammals, leptin affects steroidogenesis, folliculogenesis, and hormonal regulation through the hypothalamic-pituitary-gonadal axis. Instead, in avian species, leptin-controlled mechanisms are poorly understood, because birds do not produce leptin in adipocytes. In birds, leptin is expressed in the brain, pituitary glands, and gonads, where it enhances ovarian function and egg-laying performance, particularly during feed deprivation. In this review, we discuss and summarize the recently discovered role of leptin in regulating ovarian function during different life stages in birds and compare it with its function in mammals.
{"title":"A Bird's-Eye Overview of Leptin and Female Reproduction -with Mammalian Comparisons.","authors":"Sadequllah Ahmadi, Takeshi Ohkubo","doi":"10.2141/jpsa.2025007","DOIUrl":"10.2141/jpsa.2025007","url":null,"abstract":"<p><p>Leptin, a key regulator of reproductive physiology, influences various processes in vertebrates, including oocyte proliferation, embryogenesis, the onset of puberty, ovarian function, and follicle development. In mammals, leptin affects steroidogenesis, folliculogenesis, and hormonal regulation through the hypothalamic-pituitary-gonadal axis. Instead, in avian species, leptin-controlled mechanisms are poorly understood, because birds do not produce leptin in adipocytes. In birds, leptin is expressed in the brain, pituitary glands, and gonads, where it enhances ovarian function and egg-laying performance, particularly during feed deprivation. In this review, we discuss and summarize the recently discovered role of leptin in regulating ovarian function during different life stages in birds and compare it with its function in mammals.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025007"},"PeriodicalIF":1.8,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11794366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143364465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plumage color in birds is determined by melanin, whose synthesis and transport are affected by many genes, including specific solute carriers (SLCs). The main objective of this study was to detect polymorphisms in the SLC24A5 gene of the Chinese yellow quail (Coturnix japonica) and analyze their effect on tyrosinase activity in skin tissue and melanin content in down feathers. The cDNA of the SLC24A5 gene was cloned by RT-PCR and subjected to Sanger sequencing. Potential single-nucleotide polymorphisms (SNPs) were screened using multiple sequence alignment. The screened nonsynonymous SNPs were genotyped across 265 Chinese yellow quails using the kompetitive allele-specific PCR method. The association of genotypes with tyrosinase activity in the skin and melanin content in down feathers was analyzed. The g.8884145A/G SNP was identified in exon 9 of the SLC24A5 gene, resulting in an Asp396Ala mutation. The mutant residue was predicted to be located inside the eighth transmembrane helix of the SLC24A5 protein, which is primarily responsible for recognizing Na+/Ca2+ ions. Mutant individuals had significantly lower total melanin content in the feathers and tyrosinase activity in dorsal skin, in spite of no significant difference in SLC24A5 mRNA expression in the same tissues. This study indicates that the g.8884145A/G mutation reduced tyrosinase activity by affecting the function of the SLC24A5 protein, which in turn decreased melanin content of down feathers in Chinese yellow quail.
{"title":"A Nonsynonymous Single-nucleotide Polymorphism in <i>SLC24A5</i> Regulates Feather Pigment Deposition in Chinese Yellow Quail.","authors":"Xiaohui Zhang, Fanghu Wu, Yanxia Qi, Yuanyuan Shang, Lingyun Fan, Yifei Wang","doi":"10.2141/jpsa.2025006","DOIUrl":"10.2141/jpsa.2025006","url":null,"abstract":"<p><p>Plumage color in birds is determined by melanin, whose synthesis and transport are affected by many genes, including specific solute carriers (SLCs). The main objective of this study was to detect polymorphisms in the <i>SLC24A5</i> gene of the Chinese yellow quail (<i>Coturnix japonica</i>) and analyze their effect on tyrosinase activity in skin tissue and melanin content in down feathers. The cDNA of the <i>SLC24A5</i> gene was cloned by RT-PCR and subjected to Sanger sequencing. Potential single-nucleotide polymorphisms (SNPs) were screened using multiple sequence alignment. The screened nonsynonymous SNPs were genotyped across 265 Chinese yellow quails using the kompetitive allele-specific PCR method. The association of genotypes with tyrosinase activity in the skin and melanin content in down feathers was analyzed. The g.8884145A/G SNP was identified in exon 9 of the <i>SLC24A5</i> gene, resulting in an Asp396Ala mutation. The mutant residue was predicted to be located inside the eighth transmembrane helix of the SLC24A5 protein, which is primarily responsible for recognizing Na<sup>+</sup>/Ca<sup>2+</sup> ions. Mutant individuals had significantly lower total melanin content in the feathers and tyrosinase activity in dorsal skin, in spite of no significant difference in <i>SLC24A5</i> mRNA expression in the same tissues. This study indicates that the g.8884145A/G mutation reduced tyrosinase activity by affecting the function of the SLC24A5 protein, which in turn decreased melanin content of down feathers in Chinese yellow quail.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025006"},"PeriodicalIF":1.8,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11779592/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143080455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Trehalose (Tre) is composed of two molecules of D-glucose joined by an α,α-1,1 glucosidic linkage. Because Tre is utilized by the gut microbiome and enhances gut immunity in chickens, it is used as a feed ingredient. However, taste preference and metabolic dynamics of Tre in chickens are not fully understood. Therefore, in this study, we investigated the taste preference in chickens for Tre and the metabolism of this disaccharide. In a short-term drinking test, chickens preferred low concentrations of Tre solution while avoiding high concentrations. Instead, in a conditioned taste aversion test, chickens did not show taste aversion to Tre, implying that chickens do not have a sufficient taste for Tre. The initial feed intake rate increased when 0.5% Tre was added. Respiratory gas analysis revealed that intragastric administration of 1.0 M Tre weakly increased the respiratory quotient. Furthermore, approximately 50% of Tre was metabolized in chickens. These results suggest that chickens slightly taste the sweetness of Tre. Moreover, adding Tre to feed increases the chickens' initial appetite, and they use approximately 50% of Tre as an energy source. This information is relevant for using Tre alone or as a supplement in poultry feed.
海藻糖(Tre)由两个d -葡萄糖分子通过α,α-1,1糖苷键连接而成。由于tre3被肠道微生物群利用并增强鸡的肠道免疫力,因此它被用作饲料成分。然而,鸡的味觉偏好和tre3的代谢动力学尚不完全清楚。因此,在本研究中,我们研究了鸡对tre3的味觉偏好和这种双糖的代谢。在短期饮水试验中,鸡更喜欢低浓度的三硫溶液,而避免高浓度的三硫溶液。相反,在条件厌恶味觉测试中,鸡没有表现出对三的厌恶,这意味着鸡对三没有足够的味觉。添加0.5% tre3可提高初始采食量。呼吸气体分析显示,灌胃1.0 M tre3可微弱增加呼吸商。此外,约50%的Tre在鸡体内代谢。这些结果表明,鸡能轻微品尝到糖的甜味。此外,在饲料中添加三氧化二氮增加了鸡的初始食欲,它们使用大约50%的三氧化二氮作为能量来源。这一信息与单独使用tre3或在家禽饲料中作为补充剂有关。
{"title":"Taste Preference and Metabolic Rate of Trehalose in Chickens.","authors":"Fuminori Kawabata, Misako Sakai, Hiroki Murasawa, Yu Komine, Kazuhisa Mukai, Yuko Kawabata","doi":"10.2141/jpsa.2025005","DOIUrl":"10.2141/jpsa.2025005","url":null,"abstract":"<p><p>Trehalose (Tre) is composed of two molecules of D-glucose joined by an α,α-1,1 glucosidic linkage. Because Tre is utilized by the gut microbiome and enhances gut immunity in chickens, it is used as a feed ingredient. However, taste preference and metabolic dynamics of Tre in chickens are not fully understood. Therefore, in this study, we investigated the taste preference in chickens for Tre and the metabolism of this disaccharide. In a short-term drinking test, chickens preferred low concentrations of Tre solution while avoiding high concentrations. Instead, in a conditioned taste aversion test, chickens did not show taste aversion to Tre, implying that chickens do not have a sufficient taste for Tre. The initial feed intake rate increased when 0.5% Tre was added. Respiratory gas analysis revealed that intragastric administration of 1.0 M Tre weakly increased the respiratory quotient. Furthermore, approximately 50% of Tre was metabolized in chickens. These results suggest that chickens slightly taste the sweetness of Tre. Moreover, adding Tre to feed increases the chickens' initial appetite, and they use approximately 50% of Tre as an energy source. This information is relevant for using Tre alone or as a supplement in poultry feed.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025005"},"PeriodicalIF":1.8,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11737969/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007137","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-17eCollection Date: 2025-01-01DOI: 10.2141/jpsa.2025004
Md Al Amin, Md Badiul Alam, Kohzy Hiramatsu
This study clarified the histological changes in the mucosal epithelium of the chicken intestine during the pre- and post-hatching stages. The duodenum, jejunum, ileum, and colorectum were collected from embryos at 15, 17, 18, 19, and 21 days of incubation and from chicks at 1 and 3 days after hatching. Paraffin sections prepared from tissue samples were stained with periodic acid-Schiff followed by alcian blue for histological analysis and to detect goblet cells. Villin and β-actin were detected using double immunofluorescence. Villi with finger-like shape were already observed in embryos after 15 days of incubation, and no obvious change in shape was observed even after hatching. Villous height increased in all intestinal regions as the developmental stage progressed, particularly a few days before and after hatching. Goblet cells first appeared in the epithelium of all intestinal regions after 18 days of incubation. The density of goblet cells rapidly increased from 18 to 21 days of incubation. Both villin and β-actin immunoreactivities were detected at the apical surface of the villous epithelium in all intestinal regions, and villin immunopositivity was stronger in the jejunum and ileum after hatching. These findings indicate that the villi and microvilli of the intestine of broiler chickens show histological changes during few days just before and after hatching. Additionally, the density of goblet cells rapidly increased for a few days before hatching.
{"title":"Histological Changes of the Mucosal Epithelium in the Chicken Intestine during Pre- and Post-Hatching Stages.","authors":"Md Al Amin, Md Badiul Alam, Kohzy Hiramatsu","doi":"10.2141/jpsa.2025004","DOIUrl":"https://doi.org/10.2141/jpsa.2025004","url":null,"abstract":"<p><p>This study clarified the histological changes in the mucosal epithelium of the chicken intestine during the pre- and post-hatching stages. The duodenum, jejunum, ileum, and colorectum were collected from embryos at 15, 17, 18, 19, and 21 days of incubation and from chicks at 1 and 3 days after hatching. Paraffin sections prepared from tissue samples were stained with periodic acid-Schiff followed by alcian blue for histological analysis and to detect goblet cells. Villin and β-actin were detected using double immunofluorescence. Villi with finger-like shape were already observed in embryos after 15 days of incubation, and no obvious change in shape was observed even after hatching. Villous height increased in all intestinal regions as the developmental stage progressed, particularly a few days before and after hatching. Goblet cells first appeared in the epithelium of all intestinal regions after 18 days of incubation. The density of goblet cells rapidly increased from 18 to 21 days of incubation. Both villin and β-actin immunoreactivities were detected at the apical surface of the villous epithelium in all intestinal regions, and villin immunopositivity was stronger in the jejunum and ileum after hatching. These findings indicate that the villi and microvilli of the intestine of broiler chickens show histological changes during few days just before and after hatching. Additionally, the density of goblet cells rapidly increased for a few days before hatching.</p>","PeriodicalId":16883,"journal":{"name":"Journal of Poultry Science","volume":"62 ","pages":"2025004"},"PeriodicalIF":1.8,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11733151/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143006807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}