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过氧化物酶体增殖物激活受体调控幼龄反刍动物瘤胃的生酮作用及其机制 被引量:4

Peroxisome Proliferator-Activated Receptors:Regulation in Ketogenesis of Young Ruminants and Its Mechanisms
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摘要 发育良好的瘤胃对于幼龄反刍动物至关重要,不仅关乎其自身的健康,也与其成年后生产性能的发挥息息相关。对于刚出生的幼龄反刍动物,其瘤胃不具有生酮功能,随日龄的增加,瘤胃形态与功能逐渐发育成熟,逐渐具备了该功能。生酮作用是瘤胃发育成熟的关键因素,β-羟丁酸(BHBA)被认为是瘤胃发育成熟的标志。近十几年来,许多学者针对影响瘤胃生酮作用的因素进行了大量研究,发现过氧化物酶体增殖物激活受体(PPARs)对于瘤胃生酮和上皮细胞增殖十分重要,转录因子PPARs可以影响到生酮作用关键酶3-羟基-3-甲基戊二酰辅酶A合成酶2(HMGCS2)的表达。但目前对于PPARs调控瘤胃生酮作用分子机制的了解仍然十分有限,因此本文针对PPARs调控幼龄反刍动物瘤胃发育的研究进展进行了综述。 A well-developed rumen is critical for young ruminants,not only for the health,but also for the production performance after grow up.There is no ketogenic function in rumen of new born young ruminants,the rumen morphology and function gradually mature with increasing of the days of age,and ketogenic function occurs.Ketogenesis is a key factor in rumen development and maturation,and beta-hydroxybutyric acid(BHBA)is thought to be a mark of rumen development and maturation.Over the past decade,researchers have done a lot of researches on the factors that affect rumen ketogenesis,it has been found that peroxisome proliferator-activated receptors(PPARs)are important for the proliferation of epithelial cells and ketogenesis.The expression of 3-hydroxy-3-methylglutaryl coenzyme A synthase 2(HMGCS2)can be influenced by PPARs.But the current understanding of the mechanism of PPARs regulating ketogenesis remains unclear.This paper reviewed the progress of PPARs regulating rumen development in young ruminants.
作者 吕小康 王杰 刁其玉 张乃锋 LYU Xiaokang ;WANG Jie;DIAO Qiyu;ZHANG Naifeng(Key Laboratory of Feed Biotechnology of the Ministry of Agriculture,Feed Research Institute of Chinese Academy of Agricultural Sciences,Beijing 100081,China)
出处 《动物营养学报》 CAS CSCD 北大核心 2018年第4期1238-1244,共7页 CHINESE JOURNAL OF ANIMAL NUTRITION
基金 国家公益性行业(农业)科研专项(201303143) 国家肉羊产业技术体系建设专项(CARS-39)
关键词 过氧化物酶体增殖物激活受体 幼龄反刍动物 瘤胃 生酮作用 分子机制 peroxisome proliferator-activated receptors young ruminants rumen ketogenesis molecular mechanism
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  • 1Teayoun Kim,Qinglin Yang.Peroxisome-proliferator-activated receptors regulate redox signaling in the cardiovascular system[J].World Journal of Cardiology,2013,5(6):164-174. 被引量:14
  • 2谢洁琼,吕秋军,温利青,赵金红,叶棋浓,陈振花.基于报告基因和PPARγ信号通路的药物筛选模型的建立[J].中国药理学通报,2005,21(4):504-507. 被引量:16
  • 3Zerehdaran S,Vereijken AL,van Arendonk JA,van der Waaijt EH.Estimation of genetic parameters for fat deposition and carcass traits in broilers.Poult Sci,2004,83(4):521–525.
  • 4Bray GA,Bouchard C.Handbook of obesity-clinical applications.3rd ed.New York:Informa Health Care,2008:1–2.
  • 5Lefterova MI,Lazar MA.New developments in adipogenesis.Trends Endocrinol Metab,2009,20(3):107–114.
  • 6Issemann I,Green S.Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators.Nature,1990,347(6294):645–650.
  • 7Ferré P.The biology of peroxisome proliferator-activated receptors:relationship with lipid metabolism and insulin sensitivity.Diabetes,2004,53(Suppl.1):S43–S50.
  • 8Lehrke M,Lazar MA.The many faces of PPARγ.Cell,2005,123(6):993–999.
  • 9El-Jack AK,Hamm JK,Pilch PF,Farmer SR.Reconstitution of insulin-sensitive glucose transport in fibroblasts requires expression of both PPARγ and C/EBPα.J Biol Chem,1999,274(12):7946–7951.
  • 10MacDougald OA,Mandrup S.Adipogenesis:forces that tip the scales.Trends Endocrinol Metab,2002,13(1):5–11.

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