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糖皮质激素使肺中编码肾上腺素生成酶的mRNA水平升高。

Glucocorticoid elevation of mRNA encoding epinephrine-forming enzyme in lung.

作者信息

Kennedy B, Elayan H, Ziegler M G

机构信息

Department of Medicine, University of California, San Diego Medical Center 92103-8341.

出版信息

Am J Physiol. 1993 Aug;265(2 Pt 1):L117-20. doi: 10.1152/ajplung.1993.265.2.L117.

Abstract

The epinephrine-forming enzyme phenylethanolamine N-methyltransferase (PNMT) is present in lung and its activity is increased by the glucocorticoid dexamethasone. Chronic administration of dexamethasone (0.5 mg/kg twice daily) doubled levels of mRNA coding for PNMT in rat lung. Administration of the glucocorticoid antagonist RU 486 after 7 days of dexamethasone treated reduced PNMT mRNA by about two-thirds within 24 h. Lung epinephrine (E) levels correlated with lung PNMT activity in these dexamethasone-treated and control rats. In a separate experiment, lung PNMT mRNA levels were nearly tripled 6 h after dexamethasone (1 mg/kg sc). In a third experiment chronic administration of the PNMT inhibitor SKF 64139 (50 mg/kg twice daily) reduced in vitro lung PNMT activity in chronically dexamethasone-treated adrenalectomized rats by approximately 96% and reduced lung E levels by approximately 75%. We conclude that glucocorticoids increase lung PNMT activity by increasing levels of mRNA coding for this enzyme. The data also suggest that a substantial fraction of lung E is locally synthesized. We speculate that enhanced lung E synthesis may participate in glucocorticoid-induced dilation of the bronchioles.

摘要

生成肾上腺素的酶苯乙醇胺N - 甲基转移酶(PNMT)存在于肺中,其活性可被糖皮质激素地塞米松增强。对地塞米松(0.5毫克/千克,每日两次)进行慢性给药,可使大鼠肺中编码PNMT的mRNA水平翻倍。在接受地塞米松治疗7天后给予糖皮质激素拮抗剂RU 486,可在24小时内使PNMT mRNA水平降低约三分之二。在这些接受地塞米松治疗的大鼠和对照大鼠中,肺肾上腺素(E)水平与肺PNMT活性相关。在另一项实验中,地塞米松(1毫克/千克,皮下注射)6小时后肺PNMT mRNA水平几乎增加两倍。在第三个实验中,对慢性接受地塞米松治疗的肾上腺切除大鼠长期给予PNMT抑制剂SKF 64139(50毫克/千克,每日两次),可使体外肺PNMT活性降低约96%,并使肺E水平降低约75%。我们得出结论,糖皮质激素通过增加编码该酶的mRNA水平来提高肺PNMT活性。数据还表明,肺中相当一部分E是在局部合成的。我们推测,肺E合成增强可能参与了糖皮质激素诱导的细支气管扩张。

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