Iversen J
J Clin Invest. 1973 Sep;52(9):2102-16. doi: 10.1172/JCI107395.
During perfusion with a glucose concentration of 150 mg/100 ml, infusions of l-epinephrine, l-norepinephrine, and d-l-isoproterenol at physiological concentrations of 2 ng/ml for 9 min stimulated secretion of glucagon in a monophasic response pattern, in contrast to the biphasic response normally encountered after glucagon releasing stimuli as previously reported from our laboratory (1971. J. Clin. Invest.50: 2123). Glucagon was stimulated in spite of a glucose concentration which in itself effectively inhibits glucagon release. Release of insulin was strongly inhibited after epinephrine and norepinephrine, and strongly stimulated after isoproterenol. During perfusion with a glucose concentration of 25 mg/100 ml, secretion of glucagon was greatly accentuated by the catechols investigated. Secretion of insulin remained unchanged after epinephrine and norepinephrine, but was stimulated by isoproterenol. The catechol induced glucagon release was suppressed or abolished when the beta-blocking agent propanolol was simultaneously infused at a concentration of 1 muM, while the inhibition of insulin became further accentuated. The catechol induced glucagon release remained unchanged when alpha blockade was performed using either phentolamine (1 muM) or dibenzyline (10 mug/ml), while the inhibition of insulin was converted to a stimulation. Evidence is thus presented that both the alpha cells and the bet cells are under the influence of adrenergic substances, the stimulation of glucagon release being mediated through a beta receptor and the inhibition of insulin release being mediated through an alpha receptor.
在葡萄糖浓度为150毫克/100毫升的灌注过程中,以2纳克/毫升的生理浓度输注左旋肾上腺素、左旋去甲肾上腺素和消旋异丙肾上腺素9分钟,刺激胰高血糖素分泌呈现单相反应模式,这与我们实验室先前报道的(1971年。《临床研究杂志》50: 2123)胰高血糖素释放刺激后通常遇到的双相反应形成对比。尽管葡萄糖浓度本身有效抑制胰高血糖素释放,但胰高血糖素仍受到刺激。肾上腺素和去甲肾上腺素后胰岛素释放受到强烈抑制,而异丙肾上腺素后则受到强烈刺激。在葡萄糖浓度为25毫克/100毫升的灌注过程中,所研究的儿茶酚胺大大增强了胰高血糖素的分泌。肾上腺素和去甲肾上腺素后胰岛素分泌保持不变,但异丙肾上腺素刺激胰岛素分泌。当以1微摩尔的浓度同时输注β受体阻滞剂普萘洛尔时,儿茶酚胺诱导的胰高血糖素释放受到抑制或消除,而胰岛素的抑制作用则进一步增强。当使用酚妥拉明(1微摩尔)或双苄胺(10微克/毫升)进行α受体阻滞时,儿茶酚胺诱导的胰高血糖素释放保持不变,而胰岛素的抑制作用则转变为刺激作用。因此有证据表明,α细胞和β细胞都受到肾上腺素能物质的影响,胰高血糖素释放的刺激是通过β受体介导的,而胰岛素释放的抑制是通过α受体介导的。