Effects of Rumen-Protected β-Alanine on Hepatic Gluconeogenesis-Related Indices and Muscle Energy Metabolism in Transported Cattle.

IF 3.2 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Animals Pub Date : 2026-09-29 DOI:10.3390/ani16193074
Boya Fu, Yitian Zang, Haoxiang Xu, Daci Fu, Guwei Lu, Kang Mao, Qinghua Qiu, Xianghui Zhao, Mingren Qu, Kehui Ouyang, Yanjiao Li
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引用次数: 0

Abstract

Preslaughter nutritional strategies that preserve energy reserves in transported beef cattle may help maintain normal post-mortem muscle metabolism and meat quality. β-alanine, a carnosine precursor, enhances glucose metabolism and glycogen reserves. This study evaluated the effects of rumen-protected β-alanine (RP-β-Ala) on meat quality, hepatic gluconeogenesis-related indices, and muscle energy metabolism in long-distance transported cattle. Thirty-six healthy 18-month-old Simmental crossbred bulls (627 ± 41 kg) were randomly assigned diets containing 0 (control) or 96 g/head/d RP-β-Ala. After 28 days of feeding, serum was sampled from six bulls per group. Following a 2-day rest (RP-β-Ala supplementation continued), these twelve bulls were transported, slaughtered, and sampled. Transport significantly increased serum lactate dehydrogenase (LDH) and creatine kinase (CK). The transport × RP-β-Ala interaction significantly affected serum superoxide dismutase (SOD). Post-slaughter tissue indices were analyzed solely for the effect of RP-β-Ala supplementation, as all slaughtered bulls underwent transportation. Compared to controls, the RP-β-Ala group exhibited significantly higher muscle pH45 min and an accelerated pH decline rate within 24 h post-mortem in both M. longissimus dorsi (LD) and M. semitendinosus (ST) muscles. In LD muscle, hardness, shear force, gumminess, and chewiness significantly decreased, while ATP content and HK, PFK, PK, and LDH activities significantly increased. In ST muscle, lactate content and GP, HK, PFK, and LDH activities significantly increased. In the liver, glucose, lactate, ATP, and ADP contents significantly increased, alongside enhanced G-6-Pase and pyruvate carboxylase (PC) activities. Dietary RP-β-Ala supplementation may regulate energy metabolism in transported cattle by enhancing muscle glycolytic activity and indices associated with hepatic gluconeogenic capacity, thereby improving selected meat-quality traits.

保护瘤胃β-丙氨酸对运输牛肝脏糖异生相关指标和肌肉能量代谢的影响
在运输肉牛中保存能量储备的笑前营养策略可能有助于维持正常的死后肌肉代谢和肉质。β-丙氨酸,肌肽前体,增强葡萄糖代谢和糖原储备。本研究旨在研究保瘤胃β-丙氨酸(RP-β-Ala)对长途运输牛肉质、肝脏糖异生相关指标和肌肉能量代谢的影响。选取36头健康18月龄西蒙塔尔杂交公牛(627±41 kg),随机分配饲粮中RP-β-Ala含量分别为0(对照)和96 g/头/d。饲喂28 d后,每组抽取6头公牛的血清。在休息2天后(继续补充RP-β-Ala),这12头公牛被运输、屠宰并取样。转运显著增加血清乳酸脱氢酶(LDH)和肌酸激酶(CK)。转运与RP-β-Ala相互作用显著影响血清超氧化物歧化酶(SOD)。屠宰后的组织指标仅分析RP-β-Ala补充的影响,因为所有屠宰的公牛都经过运输。与对照组相比,RP-β-Ala组在死后24 h内,背最长肌(LD)和半腱肌(ST)肌肉的pH值均显著升高,pH值下降速度加快。LD肌肉硬度、剪切力、胶性、嚼劲显著降低,ATP含量和HK、PFK、PK、LDH活性显著升高。ST肌乳酸含量和GP、HK、PFK、LDH活性显著升高。肝脏中葡萄糖、乳酸、ATP和ADP含量显著升高,G-6-Pase和丙酮酸羧化酶(PC)活性增强。饲粮中添加RP-β-Ala可能通过提高肌肉糖酵解活性和肝脏糖异生能力相关指标来调节运输牛的能量代谢,从而改善部分肉质性状。
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来源期刊
Animals
Animals Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍: Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).
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