Iguchi A, Gotoh M, Matsunaga H, Yatomi A, Honmura A, Yanase M, Sakamoto N
Third Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Am J Physiol. 1988 Dec;255(6 Pt 1):E920-7. doi: 10.1152/ajpendo.1988.255.6.E920.
We quantitatively determined the relative contributions of hormonal factors and the nervous system to the total glucose response after stimulation of the cholinergic neurons in the central nervous system of fed rats. Hepatic venous plasma glucose, glucagon, insulin, epinephrine, and norepinephrine were measured during 120 min after injection of neostigmine (5 X 10(-8) mol) into the third cerebral ventricle in rats subjected to bilateral adrenodemedullation (ADMX) to prevent epinephrine secretion (observed insulin secretion), with and without intravenous infusion of somatostatin to prevent glucagon and insulin secretion. Injection of neostigmine in intact rats resulted in increases in glucose, glucagon, epinephrine, and norepinephrine. Comparison of glucose areas suggests that 22% of the hyperglycemic response is due to the glucagon effect, that 29% is due to the epinephrine effect, and that an unknown factor other than epinephrine or glucagon, which may include activation through direct neural innervation of the liver via alpha-adrenergic receptor, contributes 49%. The suppressive effect of epinephrine on insulin secretion, which is potentially stimulated by direct neural activation of the pancreas, contributes 18% of the net hyperglycemia.
我们定量测定了激素因素和神经系统对喂食大鼠中枢神经系统中胆碱能神经元刺激后总葡萄糖反应的相对贡献。在双侧肾上腺髓质切除(ADMX)以防止肾上腺素分泌(观察到胰岛素分泌)的大鼠第三脑室注射新斯的明(5×10⁻⁸摩尔)后的120分钟内,测量肝静脉血浆葡萄糖、胰高血糖素、胰岛素、肾上腺素和去甲肾上腺素,同时有无静脉输注生长抑素以防止胰高血糖素和胰岛素分泌。在完整大鼠中注射新斯的明导致葡萄糖、胰高血糖素、肾上腺素和去甲肾上腺素增加。葡萄糖面积比较表明,22%的高血糖反应归因于胰高血糖素效应,29%归因于肾上腺素效应,肾上腺素或胰高血糖素以外的未知因素(可能包括通过α-肾上腺素能受体对肝脏的直接神经支配激活)贡献了49%。肾上腺素对胰岛素分泌的抑制作用(可能由胰腺的直接神经激活刺激)对净高血糖贡献了18%。