Creatine nitrate supplementation strengthens energy status and delays glycolysis of broiler muscle via inhibition of LKB1/AMPK pathway
文献类型: 外文期刊
作者: Duan, B. B. 1 ; Xu, J. W. 1 ; Xing, T. 1 ; Li, J. L. 2 ; Zhang, L. 1 ; Gao, F. 1 ;
作者机构: 1.Nanjing Agr Univ, Jiangsu Prov Key Lab Gastrointestinal Nutr & Anim, Jiangsu Prov Key Lab Anim Origin Food Prod & Safe, Coll Anim Sci & Technol,Jiangsu Prov Collaborat I, Nanjing 210095, Jiangsu, Peoples R China
2.Jiangsu Acad Agr Sci, Inst Agr Prod Proc, Nanjing 210014, Peoples R China
关键词: broiler; creatine nitrate; meat quality; energy status; glycolysis
期刊名称:POULTRY SCIENCE ( 影响因子:4.014; 五年影响因子:4.192 )
ISSN:
年卷期: 2022 年 101 卷 3 期
页码:
收录情况: SCI
摘要: This study aimed to evaluate the effects of dietary creatine nitrate (CrN) on growth performance, meat quality, energy status, glycolysis, and related gene expression of liver kinase B1/AMP-activated protein kinase (LKB1/AMPK) pathway in Pectoralis major (PM) muscle of broilers. A total of 240 male Arbor Acres broilers (28-day-old) were randomly allocated to one of 5 dietary treatments: the basal diet (control group), and the basal diets supplemented with 600 mg/kg guanidinoacetic acid (GAA), 300, 600, or 900 mg/kg CrN (identified as GAA(600), CrN300, CrN600, or CrN900, respectively). We found that dietary GAA and CrN supplementation for 14 d from d 28 to 42 did not affect broiler growth performance, carcass traits, and textural characteristics of breast muscle. GAA(600), CrN600, and CrN900 treatments increased pH(24h) and decreased drip loss of PM muscle compared with the control (P < 0.05). The PM muscles of CrN600 and CrN900 groups showed higher glycogen concentration and lower lactic acid concentration accompanied by lower activities of phosphofructokinase (PFK), pyruvate kinase (PK), and lactate dehydrogenase (LDH) (P < 0.05). Simultaneously, GAA(600) and all CrN treatments increased concentration of muscle creatine, phosphocreatine (PCr) and ATP, and decreased AMP concentration and AMP/ATP ratio (P < 0.05). Meanwhile, the concentrations of muscle creatine, PCr, and ATP were increased linearly, while muscle AMP concentration and AMP/ATP ratio were decreased linearly and quadratic as the dose of CrN increased (P < 0.05). GAA(600), CrN600, and CrN900 treatments upregulated mRNA expression of CreaT in PM muscle, and CrN600 and CrN900 treatments downregulated GAMT expression in liver and PM muscle compared with the control or GAA(600) groups (P < 0.05). The mRNA expression of muscle LKB1, AMPK alpha 1, and AMPK alpha 2 was downregulated linearly in response to the increasing CrN level (P < 0.05). Overall, CrN showed better efficacy on strengthening muscle energy status and improve meat quality than GAA at the some dose. These results indicate that CrN may be a potential replacement for GAA as a new creatine supplement.
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