Ashford M L, Boden P R, Treherne J M
Department of Pharmacology, University of Cambridge, UK.
Pflugers Arch. 1990 Jan;415(4):479-83. doi: 10.1007/BF00373626.
Intracellular recordings were made from neurones located in the ventromedial hypothalamic nucleus (VMHN) of slices from rat hypothalamus. These neurones were hyperpolarized on removal of extracellular glucose, resulting in an inhibition of firing, actions which were reversed on the re-introduction of glucose. No reversal of the inhibition of firing was observed when 10 mM mannoheptulose, an inhibitor of glucose metabolism, was present in addition to glucose. Increasing the mannoheptulose concentration to 20 mM resulted in further hyperpolarization. Cell-attached recordings from isolated neurones revealed that an increase in extracellular glucose inhibited a K+ channel and increased action current activity. ATP induced closure of this K+ channel when applied to inside-out membrane patches. Closure was also induced by Mg-free ATP or the non-hydrolysable ATP-analogue, adenylylimidodiphosphate indicating no requirement for ATP metabolism. We suggest that the closure of ATP-sensitive potassium channels underlies increased hypothalamic firing following an increase in extracellular glucose.
对取自大鼠下丘脑切片腹内侧下丘脑核(VMHN)的神经元进行细胞内记录。去除细胞外葡萄糖后,这些神经元发生超极化,导致放电受到抑制,重新加入葡萄糖后这些作用逆转。当除葡萄糖外还存在10 mM甘露庚酮糖(一种葡萄糖代谢抑制剂)时,未观察到放电抑制的逆转。将甘露庚酮糖浓度增加到20 mM导致进一步超极化。对分离神经元进行的细胞贴附式记录显示,细胞外葡萄糖增加会抑制钾通道并增加动作电流活性。当应用于内向外膜片时,ATP可诱导该钾通道关闭。无镁ATP或不可水解的ATP类似物腺苷酰亚胺二磷酸也可诱导关闭,表明不需要ATP代谢。我们认为,细胞外葡萄糖增加后下丘脑放电增加的基础是ATP敏感性钾通道的关闭。