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α-肾上腺素能受体与正常及糖尿病大鼠胰岛的胰岛素释放

Alpha-adrenoceptors and insulin release from pancreatic islets of normal and diabetic rats.

作者信息

Ostenson C G, Cattaneo A G, Doxey J C, Efendic S

机构信息

Department of Endocrinology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Am J Physiol. 1989 Sep;257(3 Pt 1):E439-43. doi: 10.1152/ajpendo.1989.257.3.E439.

Abstract

The role of alpha-adrenoceptors in the regulation of glucose-induced insulin release (GIR) was investigated in islets of normal and neonatally streptozotocin-injected non-insulin-dependent diabetic rats (STZ). In normal islets GIR was suppressed to approximately 50% by 10(-8) M of the alpha 2-adrenergic agonist UK 14304, whereas 10(-9) M of the agonist induced a similar inhibition in STZ islets. In normal islets, suppression of GIR by UK 14304 (10(-8) M) was totally antagonized by 10(6) M idazoxan (alpha 2-antagonist) or 10(6) M phentolamine (alpha 1 + alpha 2-antagonist). In STZ islets, the inhibitory effect of UK 14304 (10(-9) M) was entirely reversed by 10(-5) M idazoxan or 10(-6) M phentolamine. The alpha 1-antagonist prazosin (10(-7)-10(-5) M) was without effect on insulin release suppressed by UK 14304 in normal and STZ islets. Insulin release at 3.3, 8.3, or 16.7 mM glucose was augmented by phentolamine but not by idazoxan. It is concluded that the inhibitory effect of catecholamines on insulin release is mediated by alpha 2-receptors in normal and STZ islets. Phentolamine augments basal and glucose-induced insulin release by a mechanism that does not involve alpha 2-adrenoceptors.

摘要

在正常大鼠及新生期注射链脲佐菌素的非胰岛素依赖型糖尿病大鼠(STZ)的胰岛中,研究了α-肾上腺素能受体在调节葡萄糖诱导的胰岛素释放(GIR)中的作用。在正常胰岛中,10^(-8) M的α2-肾上腺素能激动剂UK 14304可将GIR抑制至约50%,而10^(-9) M的该激动剂在STZ胰岛中可诱导类似的抑制作用。在正常胰岛中,UK 14304(10^(-8) M)对GIR的抑制作用被10^(-6) M的咪唑克生(α2-拮抗剂)或10^(-6) M的酚妥拉明(α1 + α2-拮抗剂)完全拮抗。在STZ胰岛中,UK 14304(10^(-9) M)的抑制作用被10^(-5) M的咪唑克生或10^(-6) M的酚妥拉明完全逆转。α1-拮抗剂哌唑嗪(10^(-7) - 10^(-5) M)对UK 14304在正常和STZ胰岛中抑制的胰岛素释放无影响。酚妥拉明可增强3.3、8.3或16.7 mM葡萄糖刺激下的胰岛素释放,但咪唑克生无此作用。结论是,儿茶酚胺对胰岛素释放的抑制作用在正常和STZ胰岛中均由α2-受体介导。酚妥拉明通过一种不涉及α2-肾上腺素能受体的机制增强基础和葡萄糖诱导的胰岛素释放。

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