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Roux-en-Y胃旁路术后下丘脑基因表达的变化

Alterations in hypothalamic gene expression following Roux-en-Y gastric bypass.

作者信息

Barkholt Pernille, Pedersen Philip J, Hay-Schmidt Anders, Jelsing Jacob, Hansen Henrik H, Vrang Niels

机构信息

Gubra, Agern Alle 1, 2970 Hørsholm, Denmark; Department of Neuroscience and Pharmacology, University of Copenhagen, Blegdamsvej 3, 2200 Copenhagen N, Denmark.

Gubra, Agern Alle 1, 2970 Hørsholm, Denmark.

出版信息

Mol Metab. 2016 Jan 25;5(4):296-304. doi: 10.1016/j.molmet.2016.01.006. eCollection 2016 Apr.

DOI:10.1016/j.molmet.2016.01.006
PMID:27069869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4811984/
Abstract

OBJECTIVE

The role of the central nervous system in mediating metabolic effects of Roux-en-Y gastric bypass (RYGB) surgery is poorly understood. Using a rat model of RYGB, we aimed to identify changes in gene expression of key hypothalamic neuropeptides known to be involved in the regulation of energy balance.

METHODS

Lean male Sprague-Dawley rats underwent either RYGB or sham surgery. Body weight and food intake were monitored bi-weekly for 60 days post-surgery. In situ hybridization mRNA analysis of hypothalamic AgRP, NPY, CART, POMC and MCH was applied to RYGB and sham animals and compared with ad libitum fed and food-restricted rats. Furthermore, in situ hybridization mRNA analysis of dopaminergic transmission markers (TH and DAT) was applied in the midbrain.

RESULTS

RYGB surgery significantly reduced body weight and intake of a highly palatable diet but increased chow consumption compared with sham operated controls. In the arcuate nucleus, RYGB surgery increased mRNA levels of orexigenic AgRP and NPY, whereas no change was observed in anorexigenic CART and POMC mRNA levels. A similar pattern was seen in food-restricted versus ad libitum fed rats. In contrast to a significant increase of orexigenic MCH mRNA levels in food-restricted animals, RYGB did not change MCH expression in the lateral hypothalamus. In the VTA, RYGB surgery induced a reduction in mRNA levels of TH and DAT, whereas no changes were observed in the substantia nigra relative to sham surgery.

CONCLUSION

RYGB surgery increases the mRNA levels of hunger-associated signaling markers in the rat arcuate nucleus without concomitantly increasing downstream MCH expression in the lateral hypothalamus, suggesting that RYGB surgery puts a brake on orexigenic hypothalamic output signals. In addition, down-regulation of midbrain TH and DAT expression suggests that altered dopaminergic activity also contributes to the reduced intake of palatable food in RYGB rats.

摘要

目的

中枢神经系统在介导胃旁路术(RYGB)代谢效应中的作用尚不清楚。我们利用RYGB大鼠模型,旨在确定已知参与能量平衡调节的关键下丘脑神经肽基因表达的变化。

方法

将雄性瘦型Sprague-Dawley大鼠进行RYGB手术或假手术。术后每两周监测一次体重和食物摄入量,持续60天。对接受RYGB手术和假手术的动物进行下丘脑刺鼠肽相关蛋白(AgRP)、神经肽Y(NPY)、可卡因-安非他明调节转录肽(CART)、阿黑皮素原(POMC)和黑色素浓集激素(MCH)的原位杂交mRNA分析,并与自由采食和限食大鼠进行比较。此外,对中脑进行多巴胺能传递标志物(酪氨酸羟化酶(TH)和多巴胺转运体(DAT))的原位杂交mRNA分析。

结果

与假手术对照组相比,RYGB手术显著降低了体重和对美味食物的摄入量,但增加了普通饲料的消耗量。在弓状核中,RYGB手术增加了促食欲的AgRP和NPY的mRNA水平,而厌食的CART和POMC的mRNA水平未观察到变化。限食大鼠与自由采食大鼠也呈现类似模式。与限食动物中促食欲的MCH mRNA水平显著增加相反,RYGB手术并未改变下丘脑外侧区的MCH表达。在腹侧被盖区(VTA),RYGB手术导致TH和DAT的mRNA水平降低,而相对于假手术,黑质未观察到变化。

结论

RYGB手术增加了大鼠弓状核中与饥饿相关信号标志物的mRNA水平,但未同时增加下丘脑外侧区下游MCH的表达,这表明RYGB手术抑制了下丘脑促食欲输出信号。此外,中脑TH和DAT表达的下调表明,多巴胺能活性的改变也导致了RYGB大鼠对美味食物摄入量的减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/8e0ebb33357c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/dbba5ff8ea7e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/b50fcf20cc59/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/53d36f17925c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/4d3c47a7bf38/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/e1429ba59d34/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/8e0ebb33357c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/dbba5ff8ea7e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/b50fcf20cc59/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/53d36f17925c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/4d3c47a7bf38/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/e1429ba59d34/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ee/4811984/8e0ebb33357c/gr6.jpg

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