Joost H G, Göke R
FEBS Lett. 1984 Feb 13;167(1):5-9. doi: 10.1016/0014-5793(84)80821-2.
The effects of islet-activating protein (IAP), a Bordetella pertussis toxin, on insulin- and isoprenaline-stimulated glucose transport were studied in isolated rat adipocytes. Basal as well as insulin-stimulated glucose transport were not affected when cells were pretreated with IAP. In contrast, IAP pretreatment abolished the stimulatory effect of isoprenaline. When IAP-pretreated cells were exposed to a combination of insulin and isoprenaline, the catecholamine significantly reduced the stimulatory effect of insulin. Since IAP is supposed to specifically block the inhibitory component Ni of adenylate cyclase, the results suggest that: (a) the effect of insulin is unrelated to the regulation of adenylate cyclase; (b) isoprenaline may exert both stimulatory and inhibitory effects depending on activation of Ni. The inhibitory regulation of adenylate cyclase may thus be a pivotal link in the regulation of glucose transport.
研究了百日咳博德特氏菌毒素胰岛激活蛋白(IAP)对分离的大鼠脂肪细胞中胰岛素和异丙肾上腺素刺激的葡萄糖转运的影响。用IAP预处理细胞时,基础葡萄糖转运以及胰岛素刺激的葡萄糖转运均未受影响。相反,IAP预处理消除了异丙肾上腺素的刺激作用。当用IAP预处理的细胞暴露于胰岛素和异丙肾上腺素的组合时,儿茶酚胺显著降低了胰岛素的刺激作用。由于IAP被认为可特异性阻断腺苷酸环化酶的抑制成分Ni,结果表明:(a)胰岛素的作用与腺苷酸环化酶的调节无关;(b)异丙肾上腺素可能根据Ni的激活发挥刺激和抑制作用。因此,腺苷酸环化酶的抑制调节可能是葡萄糖转运调节中的关键环节。