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大鼠干扰素可抑制大鼠神经胶质瘤C6细胞中儿茶酚胺诱导的乳酸脱氢酶合成。

Rat interferon inhibits catecholamine-inducible synthesis of lactic dehydrogenase in rat glial tumoral C6 cells.

作者信息

Passaquin A C, Coupin G, Poindron P

出版信息

J Interferon Res. 1986 Apr;6(2):71-7. doi: 10.1089/jir.1986.6.71.

Abstract

The synthesis of lactic dehydrogenase (LDH) by rat glial tumoral C6 cells may be induced by catecholamines (i.e., isoproterenol, 3 X 10(-5) M). Three hours after beta-adrenergic agonist addition, there is a rapid increase in intracellular LDH activity that reaches a plateau within about 18-20 h. It has been shown elsewhere that this synthesis requires de novo RNA and protein synthesis. We observed here that pretreatment of C6 cells with rat interferon (IFN) for 18 h, prior to isoproterenol or noradrenaline addition, inhibits the induced synthesis of LDH. This suggests that IFN might act at the translational level. The inhibition observed is dependent on the dose of IFN used. There is an approximate correlation between the kinetics of development of the antiviral state and the kinetics of development of the inhibitory effect of IFN on the LDH-inducible synthesis. Both effects are maximal within approximately the same time.

摘要

大鼠神经胶质瘤C6细胞合成乳酸脱氢酶(LDH)可被儿茶酚胺(即异丙肾上腺素,3×10⁻⁵M)诱导。添加β-肾上腺素能激动剂3小时后,细胞内LDH活性迅速增加,约18 - 20小时内达到稳定水平。其他研究表明,这种合成需要从头进行RNA和蛋白质合成。我们在此观察到,在添加异丙肾上腺素或去甲肾上腺素之前,用大鼠干扰素(IFN)预处理C6细胞18小时,可抑制LDH的诱导合成。这表明IFN可能在翻译水平起作用。观察到的抑制作用取决于所用IFN的剂量。抗病毒状态的发展动力学与IFN对LDH诱导合成的抑制作用的发展动力学之间存在近似相关性。两种作用在大致相同的时间内达到最大值。

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