4.7 Article

Ghrelin directly interacts with neuropeptide-Y-containing neurons in the rat arcuate nucleus Ca2+ signalling via protein kinase A and N-type channel-dependent mechanisms and cross-talk with leptin and orexin

期刊

DIABETES
卷 52, 期 4, 页码 948-956

出版社

AMER DIABETES ASSOC
DOI: 10.2337/diabetes.52.4.948

关键词

-

向作者/读者索取更多资源

Ghrelin is a newly discovered peptide that is released from the stomach and from neurons in the hypothalamic arcuate nucleus (ARC) and potently stimulates growth hormone release and food intake. Neuropeptide-Y (NPY) neurons in the ARC play an important role in the stimulation of food intake. The present study aimed to determine whether ghrelin directly activates NPY neurons and, if so, to explore its. signaling mechanisms. Whether the neurons that respond to ghrelin could be regulated by orexin and leptin was also examined. We isolated single neurons from the ARC. of rats and measured the cytosolic Cg(2+) concentration ([Ca2+](i)) with fara-4 fluorescence imaging. Ghrelin (10(-12) to 10(-8) mol/l) concentration-dependently increased [Ca2+](i), which occurred in 35% of the ARC neurons. Approximately 80% of these ghrelin-responsive neurons were proved to be NPY-containing by immunocytochemical staining, and 58% of them were glucose-sensitive neurons as judged by their responses to lowering glucose concentrations. The [Ca2+](i) responses to. ghrelin were markedly attenuated by inhibitors of protein kinase A (PKA) but not protein kinase C And by a blocker of N-type but not L-type Ca2+ channels. Orexin increased [Ca2+](i) and leptin attenuated ghrelin-induced [Ca2+](i) increases in the majority (80%) of ghrelin-responsive NPY neurons. These-results demonstrate that ghrelin directly interacts with NPY neurons in the ARC to induce Ca2+ Signaling via PKA and N-type Ca2+ channel-dependent mechanisms. The integration of stimulatory effects of ghrelin and orexin and inhibitory effect of leptin may play An important role in the regulation of the activity of NPY neurons and thereby feeding.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据