John G W, Doxey J C, Walter D S, Reid J L
Glasgow University Department of Medicine and Therapeutics, Gardiner Institute, Western Infirmary, U.K.
Eur J Pharmacol. 1990 Oct 23;187(3):531-6. doi: 10.1016/0014-2999(90)90382-g.
An investigation has been made of the effects of the selective alpha 2-adrenoceptor antagonist, idazoxan, on the plasma immunoreactive insulin and glucose responses following a glucose stimulus in conscious euglycaemic rats. UK 14304 (100 micrograms/kg), a selective alpha 2-adrenoceptor agonist, reduced the insulin response and potentiated the hyperglycaemia elicited by an intra-arterial glucose load (0.25 g/kg), thereby confirming previous findings that alpha 2-adrenoceptors can influence pancreatic insulin secretion and glycaemia. The effects of UK 14304 were totally abolished by idazoxan (1.0 mg/kg), indicating that idazoxan, at the dose studied, effectively antagonized alpha 2-adrenoceptor-mediated responses. However, idazoxan (1.0 mg/kg) by itself did not significantly affect the plasma glucose and insulin responses to glucose challenge. The data indicate that selective alpha 2-adrenoceptor blockade per se does not potentiate glucose-evoked insulin secretion.
已经对选择性α2-肾上腺素能受体拮抗剂咪唑克生对清醒正常血糖大鼠葡萄糖刺激后血浆免疫反应性胰岛素和葡萄糖反应的影响进行了研究。UK 14304(100微克/千克),一种选择性α2-肾上腺素能受体激动剂,降低了胰岛素反应,并增强了动脉内葡萄糖负荷(0.25克/千克)引起的高血糖,从而证实了先前的发现,即α2-肾上腺素能受体可以影响胰腺胰岛素分泌和血糖水平。咪唑克生(1.0毫克/千克)完全消除了UK 14304的作用,表明在所研究的剂量下,咪唑克生有效地拮抗了α2-肾上腺素能受体介导的反应。然而,咪唑克生(1.0毫克/千克)本身对葡萄糖激发后的血浆葡萄糖和胰岛素反应没有显著影响。数据表明,选择性α2-肾上腺素能受体阻断本身不会增强葡萄糖诱发的胰岛素分泌。