4.6 Review

Glucose Sensing Neurons in the Ventromedial Hypothalamus

期刊

SENSORS
卷 10, 期 10, 页码 9002-9025

出版社

MDPI
DOI: 10.3390/s101009002

关键词

glucose-excited neurons; glucose-inhibited neurons; insulin; leptin; obesity; diabetes; hypoglycemia; hypoglycemia-associated autonomic failure; fasting

资金

  1. National Institute of Health [2RO1DK55619, 1RO1DK81358]
  2. Juvenile Diabetes Research Foundation [1-2007-13]
  3. NATIONAL CANCER INSTITUTE [R21CA139063] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK055619, R01DK064566, R01DK081538, R01DK081358, R56DK055619] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Neurons whose activity is regulated by glucose are found in a number of brain regions. Glucose-excited (GE) neurons increase while glucose-inhibited (GI) neurons decrease their action potential frequency as interstitial brain glucose levels increase. We hypothesize that these neurons evolved to sense and respond to severe energy deficit (e.g., fasting) that threatens the brains glucose supply. During modern times, they are also important for the restoration of blood glucose levels following insulin-induced hypoglycemia. Our data suggest that impaired glucose sensing by hypothalamic glucose sensing neurons may contribute to the syndrome known as hypoglycemia-associated autonomic failure in which the mechanisms which restore euglycemia following hypoglycemia become impaired. On the other hand, increased responses of glucose sensing neurons to glucose deficit may play a role in the development of Type 2 Diabetes Mellitus and obesity. This review will discuss the mechanisms by which glucose sensing neurons sense changes in interstitial glucose and explore the roles of these specialized glucose sensors in glucose and energy homeostasis.

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

4.6
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