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胃饥饿素以一氧化氮依赖的方式增强食物摄入和碳水化合物氧化。

Ghrelin enhances food intake and carbohydrate oxidation in a nitric oxide dependent manner.

作者信息

Abtahi Shayan, Mirza Aaisha, Howell Erin, Currie Paul J

机构信息

Department of Psychology, Reed College, Portland, OR, USA.

Department of Psychology, Reed College, Portland, OR, USA.

出版信息

Gen Comp Endocrinol. 2017 Sep 1;250:9-14. doi: 10.1016/j.ygcen.2017.05.017. Epub 2017 May 26.

Abstract

In the present study we sought to investigate interactions between hypothalamic nitric oxide (NO) and ghrelin signaling on food intake and energy substrate utilization as measured by the respiratory exchange ratio (RER). Guide cannulae were unilaterally implanted in either the arcuate (ArcN) or paraventricular (PVN) nuclei of male Sprague-Dawley rats. Animals were pretreated with subcutaneous (2.5-10mg/kg/ml) or central (0-100pmol) N-nitro-l-Arginine methyl ester (l-NAME) followed by 50pmol of ghrelin administered into either the ArcN or PVN. Both l-NAME and ghrelin were microinjected at the onset of the active cycle and food intake and RER were assessed 2h postinjection. RER was measured as the ratio of the volume of carbon dioxide expelled relative to the volume of oxygen consumed (VCO/VO) using an open-circuit indirect calorimeter. Our results demonstrated that peripheral and central l-NAME pretreatment dose-dependently attenuated ghrelin induced increases in food intake and RER in either the ArcN or PVN. In fact the 100pmol dose largely reversed the metabolic effects of ghrelin in both anatomical regions. These findings suggest that ghrelin enhancement of food intake and carbohydrate oxidation in the rat ArcN and PVN is NO-dependent.

摘要

在本研究中,我们试图通过呼吸交换率(RER)来研究下丘脑一氧化氮(NO)与胃饥饿素信号传导之间对食物摄入和能量底物利用的相互作用。将引导套管单侧植入雄性Sprague-Dawley大鼠的弓状核(ArcN)或室旁核(PVN)。动物先皮下注射(2.5 - 10mg/kg/ml)或脑室内注射(0 - 100pmol)N-硝基-L-精氨酸甲酯(L-NAME)进行预处理,随后向ArcN或PVN注射50pmol胃饥饿素。L-NAME和胃饥饿素均在活跃期开始时微量注射,并在注射后2小时评估食物摄入量和RER。使用开路间接热量计测量RER,其为呼出二氧化碳体积与消耗氧气体积之比(VCO₂/VO₂)。我们的结果表明,外周和中枢L-NAME预处理均剂量依赖性地减弱了胃饥饿素诱导的ArcN或PVN中食物摄入量和RER的增加。实际上,100pmol剂量在很大程度上逆转了胃饥饿素在两个解剖区域的代谢作用。这些发现表明,大鼠ArcN和PVN中胃饥饿素对食物摄入和碳水化合物氧化的增强作用是依赖NO的。

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