Hillaire-Buys D, Gross R, Blayac J P, Ribes G, Loubatières-Mariani M M
Eur J Pharmacol. 1985 Nov 5;117(2):253-7. doi: 10.1016/0014-2999(85)90610-7.
The effects of alpha-adrenergic drugs were studied on glucose-induced insulin secretion and effluent flow rate on the same preparation: the isolated perfused rat pancreas. An alpha 1-adrenoceptor agonist, phenylephrine 0.05 microM slightly decreased insulin secretion (-25%); this inhibition was counteracted by an alpha 2-adrenoceptor antagonist, yohimbine 0.6 microM. Phenylephrine evoked a fall in liquid flow rate (-13%) which was reversed by an alpha 1-adrenoceptor antagonist, prazosin 6 microM, but not by yohimbine. An alpha 2-adrenoceptor agonist, clonidine 0.01 and 0.05 microM decreased insulin secretion (-80%). This inhibition was reversed by yohimbine 0.6 and 6 microM respectively. Only the concentration of 0.05 microM clonidine evoked a fall (-25%) in liquid flow rate; this fall was counteracted by yohimbine 0.6 microM. In conclusion our results show that adrenergic inhibition of insulin secretion is mediated only by alpha 2-receptors whereas both types of adrenoceptors are implicated in the vasoconstrictor effect. The insulin inhibitory effect of adrenoceptor agonists is not related to vasoconstriction.
在同一实验制剂(离体灌注大鼠胰腺)上研究了α-肾上腺素能药物对葡萄糖诱导的胰岛素分泌及流出液流速的影响。α1-肾上腺素能受体激动剂去氧肾上腺素0.05微摩尔可使胰岛素分泌略有减少(-25%);这种抑制作用可被α2-肾上腺素能受体拮抗剂育亨宾0.6微摩尔抵消。去氧肾上腺素使液体流速下降(-13%),这一作用可被α1-肾上腺素能受体拮抗剂哌唑嗪6微摩尔逆转,但不能被育亨宾逆转。α2-肾上腺素能受体激动剂可乐定0.01和0.05微摩尔可使胰岛素分泌减少(-80%)。这种抑制作用分别被育亨宾0.6和6微摩尔逆转。仅0.05微摩尔浓度的可乐定可使液体流速下降(-25%);这一下降可被育亨宾0.6微摩尔抵消。总之,我们的结果表明,肾上腺素能对胰岛素分泌的抑制仅由α2-受体介导,而两种类型的肾上腺素能受体均参与血管收缩效应。肾上腺素能受体激动剂对胰岛素的抑制作用与血管收缩无关。