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整合肝脏蛋白质组学和代谢组学鉴定北京鸭泛酸缺乏影响的代谢途径。

Integrated liver proteomics and metabolomics identify metabolic pathways affected by pantothenic acid deficiency in Pekin ducks.

作者信息

Tang Jing, Wu Yongbao, Zhang Bo, Liang Suyun, Guo Zhanbao, Hu Jian, Zhou Zhengkui, Xie Ming, Hou Shuisheng

机构信息

State Key Laboratory of Animal Nutrition, Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, 100193, Beijing, China.

出版信息

Anim Nutr. 2022 Jun 21;11:1-14. doi: 10.1016/j.aninu.2022.03.008. eCollection 2022 Dec.

Abstract

Pantothenic acid deficiency (PAD) in animals causes growth depression, fasting hypoglycemia and impaired lipid and glucose metabolism. However, a systematic multi-omics analysis of effects of PAD on hepatic function has apparently not been reported. We investigated liver proteome and metabolome changes induced by PAD to explain its effects on growth and liver metabolic disorders. Pekin ducks (1-d-old,  = 128) were allocated into 2 groups, with 8 replicates and 8 birds per replicate. For 16 d, all ducks had ad libitum access to either a PAD or a pantothenic acid adequate (control, CON) diet, formulated by supplementing a basal diet with 0 or 8 mg pantothenic acid/kg of diet, respectively. Liver enlargement, elevated liver glycogen concentrations and decreased liver concentrations of triglyceride and unsaturated fatty acids were present in the PAD group compared to the CON group. Based on integrated liver proteomics and metabolomics, PAD mainly affected glycogen synthesis and degradation, glycolysis and gluconeogenesis, tricarboxylic acid (TCA) cycle, peroxisome proliferator-activated receptor (PPAR) signaling pathway, fatty acid beta oxidation, and oxidative phosphorylation. Selected proteins were confirmed by Western blotting. Downregulation of proteins and metabolites involved in glycogen synthesis and degradation, glycolysis and gluconeogenesis implied that these processes were impaired in PAD ducks, which could have contributed to fasting hypoglycemia, liver glycogen storage, insufficient ATP production, and growth retardation. In contrast, PAD also upregulated proteins and metabolites involved in fatty acid beta oxidation, the TCA cycle, and oxidative phosphorylation processes in the liver; presumably compensatory responses to produce ATP. We inferred that PAD decreased liver triglyceride and unsaturated fatty acids by activating fatty acid beta oxidation and impairing unsaturated fatty acid synthesis. These findings contributed to our understanding of the mechanisms of PAD-induced changes in hepatic metabolism.

摘要

动物泛酸缺乏症(PAD)会导致生长发育迟缓、空腹低血糖以及脂质和葡萄糖代谢受损。然而,目前显然尚未见有关于PAD对肝功能影响的系统性多组学分析报道。我们研究了PAD诱导的肝脏蛋白质组和代谢组变化,以解释其对生长和肝脏代谢紊乱的影响。将1日龄北京鸭(n = 128)分为2组,每组8个重复,每个重复8只鸭。在16天内,所有鸭子均可自由采食PAD日粮或泛酸充足(对照,CON)日粮,这两种日粮是通过在基础日粮中分别添加0或8 mg泛酸/kg日粮配制而成。与CON组相比,PAD组出现肝脏肿大、肝糖原浓度升高以及肝脏甘油三酯和不饱和脂肪酸浓度降低的情况。基于整合的肝脏蛋白质组学和代谢组学分析,PAD主要影响糖原合成与降解、糖酵解和糖异生、三羧酸(TCA)循环、过氧化物酶体增殖物激活受体(PPAR)信号通路、脂肪酸β氧化以及氧化磷酸化。通过蛋白质印迹法对选定的蛋白质进行了验证。参与糖原合成与降解、糖酵解和糖异生的蛋白质和代谢物下调,这表明这些过程在PAD鸭中受损,这可能导致了空腹低血糖、肝糖原储存、ATP生成不足以及生长迟缓。相反,PAD还上调了肝脏中参与脂肪酸β氧化、TCA循环和氧化磷酸化过程的蛋白质和代谢物;推测这是产生ATP的代偿性反应。我们推断,PAD通过激活脂肪酸β氧化并损害不饱和脂肪酸合成,从而降低了肝脏甘油三酯和不饱和脂肪酸的含量。这些发现有助于我们理解PAD诱导肝脏代谢变化的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f59/9356036/de5915b2c8e3/gr1.jpg

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