首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Role of angiotensin-converting enzyme in Bacille Calmette-Guérin-induced granulomatous inflammation. Increased angiotensin-converting enzyme levels in lung lavage and suppression of inflammation with captopril.
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Role of angiotensin-converting enzyme in Bacille Calmette-Guérin-induced granulomatous inflammation. Increased angiotensin-converting enzyme levels in lung lavage and suppression of inflammation with captopril.

机译:血管紧张素转换酶在卡介苗诱导的肉芽肿性炎症中的作用。肺灌洗中血管紧张素转换酶水平升高卡托普利抑制炎症。

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摘要

Lung lavage levels of angiotensin-converting enzyme (ACE)-like activity were increased in C57BL/6 mice with Bacille Calmette-Guérin (BCG)-induced chronic granulomatous pulmonary inflammation and splenomegaly. Contrariwise, ACE activity was not increased in lung lavage fluids of CBA mice that developed only minimal pulmonary inflammation in response to BCG. ACE-like activity correlated with the intensity of inflammation and Captopril, a specific competitive inhibitor of ACE activity, markedly suppressed the induction and maintenance of the BCG-induced inflammatory response in both lungs and spleen. It was necessary, however, to provide sustained treatment with large doses of Captopril in order to reduce the inflammatory response. After a single intraperitoneal injection of Captopril, ACE levels in lung lavage of BCG-injected mice were reduced but returned to preinjection levels or greater within 24 h. The highest dose of Captopril was more effective in reducing the lung fluid level of ACE in BCG-inflamed lungs. This suggests that sustained daily injections of Captopril were necessary to maintain reduced ACE levels. In vitro studies indicated that high concentrations of Captopril did not affect macrophage mobility or chemotactic activity for macrophages. Thus, ACE may act as a molecular mediator of BCG-induced granulomatous inflammation in the lung.
机译:在带有BacilleCalmette-Guérin(BCG)诱导的慢性肉芽肿性肺部炎症和脾肿大的C57BL / 6小鼠中,肺灌洗的血管紧张素转换酶(ACE)样活性水平增加。相反,CBA小鼠的肺灌洗液中的ACE活性并未增加,CBA小鼠仅对BCG产生了最小的肺部炎症。 ACE样活性与炎症的强度有关,而Captopril是ACE活性的一种特殊竞争性抑制剂,在肺和脾脏中均显着抑制了BCG诱导的炎症反应的产生和维持。然而,有必要用大剂量的卡托普利提供持续治疗以减少炎症反应。腹膜内注射卡托普利后,注射BCG的小鼠肺灌洗液中的ACE水平降低,但在24小时内恢复到注射前水平或更高。卡托普利的最高剂量在降低BCG刺激的肺中ACE的肺液水平方面更有效。这表明持续每天注射卡托普利对于维持降低的ACE水平是必要的。体外研究表明,高浓度的卡托普利不会影响巨噬细胞的移动性或巨噬细胞的趋化活性。因此,ACE可以充当BCG诱导的肺肉芽肿性炎症的分子介质。

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