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地塞米松对培养的胎鼠肝细胞γ-谷氨酰转移酶的诱导作用。

Induction of gamma-glutamyl transferase by dexamethasone in cultured fetal rat hepatocytes.

作者信息

Cotariu D, Barr-Nea L, Papo N, Zaidman J L

机构信息

Institute of Biochemical Pathology, Assaf Harofeh Medical Center, Tel Aviv, Israel.

出版信息

Enzyme. 1988;40(4):212-6. doi: 10.1159/000469165.

Abstract

Hepatocytes isolated as a relatively pure population from normal fetal rats were maintained in primary monolayer culture for 4-10 days. Hepatocytes exhibited a small increase in basal gamma-glutamyl transferase (GGT) activity over time. Exposure to dexamethasone (10(-6) mol/l) elicited a rise in GGT activity after a lag of 24 h. The presence of the steroid was necessary to maintain induction, and its removal resulted in reversal of induction. The maximal response was 2- to 3-fold, 72 h after exposure to the steroid. After this maximal response, a gradual decay in enzyme activity occurred, despite the continuous presence of the hormone. Actinomycin D or cycloheximide given prior to/or simultaneously with the steroid prevented the induction, thus suggesting that both RNA and protein biosynthesis are necessary for induction to occur.

摘要

从正常胎鼠中分离出相对纯净的肝细胞群体,将其在原代单层培养中维持4至10天。随着时间的推移,肝细胞的基础γ-谷氨酰转移酶(GGT)活性略有增加。暴露于地塞米松(10⁻⁶ mol/l)24小时后,GGT活性开始上升。类固醇的存在对于维持诱导是必要的,去除类固醇会导致诱导作用逆转。暴露于类固醇72小时后,最大反应为2至3倍。在达到最大反应后,尽管激素持续存在,酶活性仍会逐渐下降。在给予类固醇之前或同时给予放线菌素D或环己酰亚胺可阻止诱导,因此表明RNA和蛋白质生物合成对于诱导的发生都是必要的。

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