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普伐他汀对博来霉素诱导的急性肺损伤和肺纤维化的影响。

Effect of pravastatin on bleomycin-induced acute lung injury and pulmonary fibrosis.

机构信息

Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Catholic University of Korea, Seoul, Korea.

出版信息

Clin Exp Pharmacol Physiol. 2010 Nov;37(11):1055-63. doi: 10.1111/j.1440-1681.2010.05431.x.

Abstract
  1. Pravastatin is best known for its antilipidemic action. Recent studies have shown that statins have immunomodulatory and anti-inflammatory effects. The present study aimed to determine whether or not pravastatin can attenuate acute lung injury and fibrosis in a mouse model. 2. Bleomycin was given to C57BL6 mice through intratracheal instillation. Pravastatin was given through intraperitoneal injection. To study the effect of pravastatin on the early inflammatory phase and the late fibrotic phase, mice were killed on days 3, 7, 14 and 21. 3. Pravastatin attenuated the histopathological change of bleomycin-induced lung injury and fibrosis. The accumulation of neutrophils and increased production of tumor necrosis factor-α in bronchoalveolar lavage fluid were inhibited in the early inflammatory phase. Pravastatin effectively inhibited the increase of lung hydroxyproline content induced by bleomycin. Furthermore, pravastatin reduced the increased expression of transforming growth factor (TGF)-β1, connective tissue growth factor (CTGF), RhoA and cyclin D1. The increased levels of TGF-β1 and CTGF mRNA expression were also significantly inhibited by pravastatin. 4. Pravastatin effectively attenuated bleomycin-induced lung injury and pulmonary fibrosis in mice. Our results provide evidence for the therapeutic potential of pravastatin in the treatment of acute lung injury and pulmonary fibrosis.
摘要
  1. 普伐他汀以其抗脂作用而闻名。最近的研究表明,他汀类药物具有免疫调节和抗炎作用。本研究旨在确定普伐他汀是否可以减轻小鼠模型中的急性肺损伤和纤维化。

  2. 通过气管内滴注将博来霉素给予 C57BL6 小鼠。通过腹腔注射给予普伐他汀。为了研究普伐他汀对早期炎症期和晚期纤维化期的影响,在第 3、7、14 和 21 天处死小鼠。

  3. 普伐他汀减轻了博来霉素诱导的肺损伤和纤维化的组织病理学变化。在早期炎症期,抑制了中性粒细胞的积累和肿瘤坏死因子-α在支气管肺泡灌洗液中的产生增加。普伐他汀有效抑制了博来霉素引起的肺羟脯氨酸含量的增加。此外,普伐他汀降低了转化生长因子-β1(TGF-β1)、结缔组织生长因子(CTGF)、RhoA 和细胞周期蛋白 D1的表达增加。普伐他汀还显著抑制了 TGF-β1 和 CTGF mRNA 表达的增加。

  4. 普伐他汀可有效减轻博来霉素诱导的小鼠肺损伤和肺纤维化。我们的结果为普伐他汀在治疗急性肺损伤和肺纤维化方面的治疗潜力提供了证据。

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