内毒素抑制腺苷酸环化酶作用的可能机制。

A Takáts, B Borsos, L Bertók
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引用次数: 0

摘要

探讨了内毒素对腺苷酸环化酶抑制作用的可能机制。分别从猪甲状腺和大鼠肝脏中分离出质膜。测定了内毒素对腺苷酸环化酶活性的影响。不同浓度的鸟苷-酰亚胺二磷酸(5 × 10(-8)-10(-6) M)和NaF (0.1 ~ 10 mM)存在时,腺苷酸环化酶活性均被内毒素显著抑制。此外,腺苷酸环化酶的基础活性也同样受到抑制。抑制作用呈浓度依赖性。当内毒素浓度为400微克/毫升时,在没有激活剂和存在激活剂的情况下,腺苷酸环化酶的抑制率均为60%。内毒素及其放射性解毒衍生物的抑制作用相似。两种内毒素制剂均不影响腺苷酸环化酶的3h -鸟苷-咪胺二磷酸结合活性(既不影响结合能力,也不影响Kd值)。福斯克林激活的腺苷酸环化酶也被内毒素和放射线解毒内毒素显著抑制。这些结果表明,除了其他膜作用外,内毒素可能对腺苷酸环化酶的催化亚基有直接抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A possible mechanism of the inhibitory effect of endotoxin on adenylate cyclase.

The possible mechanism of the inhibitory effect of endotoxin on adenylate cyclase was investigated. Plasma membranes were isolated from porcine thyroid gland and rat liver. The effects of endotoxin on adenylate cyclase activity was determined. The adenylate cyclase activity followed in the presence of various concentrations of guanosine-imidodiphosphate (5 x 10(-8)-10(-6) M) and NaF (0.1-10 mM) was markedly inhibited by endotoxin. Moreover, the basal activity of adenylate cyclase was inhibited similarly. The inhibition was concentration dependent. At 400 micrograms/ml of endotoxin a 60% inhibition of adenylate cyclase both without and in the presence of activators was detected. The inhibitory effects of endotoxin and its radiodetoxified derivative were similar. Neither of the two investigated endotoxin preparations tested had any effect on the 3H-guanosine-imidodiphosphate binding activity of adenylate cyclase (neither on the binding capacity, nor on the Kd value). Forskolin activated adenylate cyclase was also inhibited markedly by both endotoxin and radiodetoxified endotoxin. These results suggest that beyond the other membrane effects there is a probability of direct inhibitory effect of endotoxin on the catalytic subunit of adenylate cyclase.

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