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聚肌苷酸:聚胞苷酸对大鼠肺和肝细胞色素P - 450及b5的影响

Effects of poly I: poly C on rat pulmonary and hepatic cytochromes P-450 and b5.

作者信息

Mettler N R, Yano S, Kikkawa Y

机构信息

Department of Pathology, New York Medical College, Valhalla 10595.

出版信息

Biochem Pharmacol. 1987 Nov 15;36(22):3873-8. doi: 10.1016/0006-2952(87)90452-7.

Abstract

Interferon inducing agents such as poly I:poly C have been shown to reduce the hepatic hemoproteins cytochromes P-450 and b5 along with the associated monooxygenase activities [el Azhary and Mannering, Molec. Pharmac. 15, 698 (1979)]. In a previous study [Kikkawa et al., Lab. Invest. 50, 62 (1984)], we demonstrated that the interferon inducing agent poly I:poly C reduces pulmonary microsomal hemoprotein by 50% when administered to rats. The current investigation was conducted to characterize these changes in more detail and compare them to analogous changes in the liver. Compared to controls, cytochrome P-450 in both the lungs and livers of poly I:poly C treated rats declined by 40% at 24 hr and 55% at 48 hr (P less than 0.01). By 72 hr the decline was only 25%. In contrast, cytochrome b5 levels declined by less than 30% of control values during the first 48 hr following poly I:poly C injection (P less than 0.01) and returned to control levels by 72 hr. These changes in both cytochrome P-450 and b5 were reflected in decreases in pulmonary microsomal hemoprotein. Benzphetamine-N-demethylase activity declined by 45% in lung microsomes at 48 hr (P less than 0.01) after injection of poly I:poly C, while 7-ethoxycoumarin-O-deethylase (P less than 0.05) and 7-ethoxyresorufin-O-deethylase activities declined by approximately 41%. In the liver from these same poly I:poly C treated groups, benzphetamine-N-demethylase declined by 66% (P less than 0.05), while 7-ethoxycoumarin-O-deethylase and 7-ethoxyresorufin-O-deethylase activities declined by 60% (P less than 0.02 and P less than 0.05 respectively).

摘要

诸如聚肌苷酸

聚胞苷酸(poly I:poly C)之类的干扰素诱导剂已被证明可降低肝脏血红素蛋白细胞色素P - 450和b5以及相关的单加氧酶活性[el Azhary和Mannering,《分子药理学》15, 698 (1979)]。在先前的一项研究中[Kikkawa等人,《实验研究》50, 62 (1984)],我们证明,给大鼠注射干扰素诱导剂聚肌苷酸:聚胞苷酸(poly I:poly C)后,肺微粒体血红素蛋白减少了50%。当前的研究旨在更详细地描述这些变化,并将它们与肝脏中的类似变化进行比较。与对照组相比,聚肌苷酸:聚胞苷酸(poly I:poly C)处理的大鼠在24小时时肺和肝脏中的细胞色素P - 450均下降了40%,在48小时时下降了55%(P < 0.01)。到72小时时,下降仅为25%。相比之下,在注射聚肌苷酸:聚胞苷酸(poly I:poly C)后的前48小时内,细胞色素b5水平下降不到对照值的30%(P < 0.01),并在72小时时恢复到对照水平。细胞色素P - 450和b5的这些变化反映在肺微粒体血红素蛋白的减少上。注射聚肌苷酸:聚胞苷酸(poly I:poly C)后48小时,肺微粒体中的苄非他明 - N - 脱甲基酶活性下降了45%(P < 0.01),而7 - 乙氧基香豆素 - O - 脱乙基酶(P < 0.05)和7 - 乙氧基试卤灵 - O - 脱乙基酶活性下降了约41%。在这些相同的聚肌苷酸:聚胞苷酸(poly I:poly C)处理组的肝脏中,苄非他明 - N - 脱甲基酶下降了66%(P < 0.05),而7 - 乙氧基香豆素 - O - 脱乙基酶和7 - 乙氧基试卤灵 - O - 脱乙基酶活性下降了60%(分别为P < 0.02和P < 0.05)。

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