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缺氧诱导的厌食大鼠模型中胃饥饿素、胆囊收缩素、胰高血糖素样肽-1及过氧化物酶体增殖物激活受体的变化

Changes in ghrelin, CCK, GLP-1, and peroxisome proliferator-activated receptors in a hypoxia-induced anorexia rat model.

作者信息

Duraisamy Arul Joseph, Bayen Susovan, Saini Supriya, Sharma Alpesh Kumar, Vats Praveen, Singh Shashi Bala

机构信息

Endocrinology & Metabolism Division, Defence Institute of Physiology and Allied Sciences, Lucknow Road, Timarpur, Delhi - 110054, India.

出版信息

Endokrynol Pol. 2015;66(4):334-41. doi: 10.5603/EP.2015.0043.

DOI:10.5603/EP.2015.0043
PMID:26323471
Abstract

INTRODUCTION

A high-altitude environment causes appetite loss in unacclimatised humans, leading to weight reduction. Ghrelin, cholecystokinin (CCK), and glucagon like peptide-1 (GLP-1), are gut hormones involved in the regulation of food intake and energy metabolism. The liver is an important site of metabolic regulation, and together with the gut it plays a role in food intake regulation. This study intends to study the time-dependent changes occurring in plasma gut hormones, PPARα, PPARδ, and PGC1α, in the stomach and liver during hypoxia.

MATERIAL AND METHODS

Male Sprague Dawley rats were exposed to hypobaric hypoxia in a decompression chamber at 7620 m for different durations up to seven days.

RESULTS

Hypoxia increased circulating ghrelin from the third day onwards while CCK and GLP-1 decreased immediately. An increase in ghrelin, ghrelin receptor protein levels, and GOAT mRNA levels in the stomach was observed. Stomach cholecystokinin receptor (CCKAR), PPARα, and PPARδ decreased. Liver CCKAR decreased during the first day of hypoxia and returned to normal levels from the third day onwards. PPARα and PGC1α expression increased while PPARδ protein levels reduced in the liver on third day.

CONCLUSION

Hypoxia alters the expression of ghrelin and ghrelin receptor in the stomach, CCKAR in the liver, and PPAR and its cofactors, which might be possible role players in the contribution of gut and liver to anorexia at high altitude.

摘要

引言

高海拔环境会导致未适应的人食欲减退,进而体重减轻。胃饥饿素、胆囊收缩素(CCK)和胰高血糖素样肽-1(GLP-1)是参与食物摄入和能量代谢调节的肠道激素。肝脏是代谢调节的重要场所,它与肠道一起在食物摄入调节中发挥作用。本研究旨在探讨低氧状态下血浆肠道激素、过氧化物酶体增殖物激活受体α(PPARα)、过氧化物酶体增殖物激活受体δ(PPARδ)和过氧化物酶体增殖物激活受体γ共激活因子1α(PGC1α)在胃和肝脏中随时间的变化。

材料与方法

将雄性斯普拉格-道利大鼠置于减压舱中,暴露于7620米的低压低氧环境中不同时长,最长达7天。

结果

从第三天起,低氧使循环中的胃饥饿素增加,而CCK和GLP-1立即减少。观察到胃中胃饥饿素、胃饥饿素受体蛋白水平和GOAT mRNA水平增加。胃胆囊收缩素受体(CCKAR)、PPARα和PPARδ减少。低氧第一天肝脏CCKAR减少,从第三天起恢复到正常水平。第三天肝脏中PPARα和PGC1α表达增加,而PPARδ蛋白水平降低。

结论

低氧改变了胃中胃饥饿素及其受体、肝脏中CCKAR以及PPAR及其辅因子的表达,这可能是肠道和肝脏导致高原厌食的潜在作用因素。

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