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中枢胰高血糖素诱导的高血糖是由肾上腺髓质和交感神经末梢的联合激活介导的。

Central glucagon-induced hyperglycemia is mediated by combined activation of the adrenal medulla and sympathetic nerve endings.

作者信息

Amir S

出版信息

Physiol Behav. 1986;37(4):563-6. doi: 10.1016/0031-9384(86)90286-6.

Abstract

Intracerebroventricular (ICV) microinjection of glucagon (0.0025-2.5 micrograms) produced significant dose-dependent hyperglycemia in mice. This hyperglycemic effect was prevented by pretreatment with the sympathetic ganglionic blocker chlorisondamine chloride or bilateral adrenalectomy plus chemical sympathectomy with 6-hydroxydopamine. Similar pretreatments had no effect on the plasma glucose responses to systemic glucagon administration. Pretreatment with somatostatin, which blocks pancreatic glucagon secretion had no effect on the hyperglycemic response to central glucagon administration. The results suggest that the increase in plasma glucose following central glucagon administration is mediated by combined action of adrenal and sympathetic amines to stimulate hepatic glucose production, or additionally to inhibit insulin release from the pancreas. The possible involvement of glucagon in the central nervous system in systemic glucoregulation is discussed.

摘要

向小鼠脑室内(ICV)微量注射胰高血糖素(0.0025 - 2.5微克)可产生显著的剂量依赖性高血糖。交感神经节阻滞剂氯筒箭毒碱预处理或双侧肾上腺切除术加用6 - 羟基多巴胺进行化学性交感神经切除术可预防这种高血糖效应。类似的预处理对全身给予胰高血糖素后的血糖反应没有影响。用抑制胰腺胰高血糖素分泌的生长抑素预处理对中枢给予胰高血糖素后的高血糖反应没有影响。结果表明,中枢给予胰高血糖素后血浆葡萄糖的升高是由肾上腺和交感胺联合作用介导的,以刺激肝脏葡萄糖生成,或者另外抑制胰腺胰岛素释放。本文讨论了胰高血糖素在中枢神经系统中可能参与全身葡萄糖调节的情况。

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