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补充胍基乙酸对安格斯阉牛生长性能、瘤胃发酵、血液指标、养分消化及氮代谢的影响

Effect of Guanidinoacetic Acid Supplementation on Growth Performance, Rumen Fermentation, Blood Indices, Nutrient Digestion, and Nitrogen Metabolism in Angus Steers.

作者信息

Yi Simeng, Hu Sanlong, Wang Jinze, Abudukelimu Abudusaimijiang, Wang Yao, Li Xiang, Wu Hao, Meng Qingxiang, Zhou Zhenming

机构信息

State Key Laboratory of Animal Nutrition and Feeding, College of Animal Science and Technology, China Agricultural University, Beijing 100193, China.

出版信息

Animals (Basel). 2024 Jan 26;14(3):401. doi: 10.3390/ani14030401.

DOI:10.3390/ani14030401
PMID:38338043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10854538/
Abstract

Guanidinoacetic acid (GAA) functions as a precursor for creatine synthesis in the animal body, and maintaining ample creatine reserves is essential for fostering rapid growth. This study aimed to explore the impact of GAA supplementation on growth performance, rumen fermentation, blood indices, nutrient digestion, and nitrogen metabolism in Angus steers through two experiments: a feeding experiment (Experiment 1) and a digestive metabolism experiment (Experiment 2). In Experiment 1, thirty-six Angus steers (485.64 ± 39.41 kg of BW) at 16 months of age were randomly assigned to three groups: control (CON), a conventional dose of GAA (CGAA, 0.8 g/kg), and a high dose of GAA (HGAA, 1.6 g/kg), each with twelve steers. The adaptation period lasted 14 days, and the test period was 130 days. Weighing occurred before morning feeding on days 0, 65, and 130, with rumen fluid and blood collected before morning feeding on day 130. Experiment 2 involved fifteen 18-month-old Angus steers (575.60 ± 7.78 kg of BW) randomly assigned to the same three groups as in Experiment 1, with a 7-day adaptation period and a 3-day test period. Fecal and urine samples were collected from all steers during this period. Results showed a significantly higher average daily gain (ADG) in the CGAA and HGAA groups compared to the CON group ( = 0.043). Additionally, the feed conversion efficiency (FCE) was significantly higher in the CGAA and HGAA groups than in the CON group ( = 0.018). The concentrations of acetate and the acetate:propionate ratio were significantly lower in the CGAA and HGAA groups, while propionate concentration was significantly higher ( < 0.01). Serum concentration of urea (UREA), blood ammonia (BA), GAA, creatine, and catalase (CAT) in the CGAA and HGAA groups were significantly higher than in the CON group, whereas malondialdehyde (MDA) concentrations were significantly lower ( < 0.05). Digestibility of dry matter (DM) and crude protein (CP) and the nitrogen retention ratio were significantly higher in the CGAA and HGAA groups than in the CON group ( < 0.05). In conclusion, dietary addition of both 0.8 g/kg and 1.6 g/kg of GAA increased growth performance, regulated rumen fermentation and blood indices, and improved digestibility and nitrogen metabolism in Angus steers. However, higher doses of GAA did not demonstrate a linear stacking effect.

摘要

胍基乙酸(GAA)在动物体内作为肌酸合成的前体,维持充足的肌酸储备对于促进快速生长至关重要。本研究旨在通过两项实验探讨补充GAA对安格斯阉牛生长性能、瘤胃发酵、血液指标、养分消化和氮代谢的影响:一项饲养实验(实验1)和一项消化代谢实验(实验2)。在实验1中,将36头16月龄的安格斯阉牛(体重485.64±39.41千克)随机分为三组:对照组(CON)、常规剂量GAA组(CGAA,0.8克/千克)和高剂量GAA组(HGAA,1.6克/千克),每组12头阉牛。适应期持续14天,试验期为130天。在第0、65和130天早晨喂食前称重,在第130天早晨喂食前采集瘤胃液和血液。实验2涉及15头18月龄的安格斯阉牛(体重575.60±�.78千克),随机分为与实验1相同的三组,适应期为7天,试验期为3天。在此期间从所有阉牛采集粪便和尿液样本。结果显示,CGAA组和HGAA组的平均日增重(ADG)显著高于CON组(P = 0.043)。此外,CGAA组和HGAA组的饲料转化效率(FCE)显著高于CON组(P = 0.018)。CGAA组和HGAA组的乙酸浓度和乙酸:丙酸比值显著较低,而丙酸浓度显著较高(P < 0.01)。CGAA组和HGAA组的血清尿素(UREA)、血氨(BA)、GAA、肌酸和过氧化氢酶(CAT)浓度显著高于CON组,而丙二醛(MDA)浓度显著较低(P < 0.05)。CGAA组和HGAA组的干物质(DM)和粗蛋白(CP)消化率以及氮保留率显著高于CON组(P < 0.05)。总之,日粮中添加0.8克/千克和1.б克/千克的GAA均可提高安格斯阉牛的生长性能,调节瘤胃发酵和血液指标,并改善消化率和氮代谢。然而,较高剂量的GAA并未表现出线性叠加效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/86dceb6a051d/animals-14-00401-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/5b7cd9eae166/animals-14-00401-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/189989e32281/animals-14-00401-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/d82ddf196051/animals-14-00401-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/86dceb6a051d/animals-14-00401-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/5b7cd9eae166/animals-14-00401-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/189989e32281/animals-14-00401-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/d82ddf196051/animals-14-00401-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bf/10854538/86dceb6a051d/animals-14-00401-g004.jpg

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