首页> 美国卫生研究院文献>International Journal of Medical Sciences >Tanshinone IIA Attenuates Bleomycin-Induced Pulmonary Fibrosis via Modulating Angiotensin-Converting Enzyme 2/ Angiotensin-(1-7) Axis in Rats
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Tanshinone IIA Attenuates Bleomycin-Induced Pulmonary Fibrosis via Modulating Angiotensin-Converting Enzyme 2/ Angiotensin-(1-7) Axis in Rats

机译:丹参酮IIA通过调节大鼠血管紧张素转换酶2 /血管紧张素-(1-7)轴减轻博莱霉素诱导的肺纤维化。

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摘要

Pulmonary fibrosis (PF) is a common complication in those interstitial lung diseases patients, which will result in poor prognosis and short survival. Traditional therapeutic methods such as glucocorticoid and cytotoxic drugs are insufficient for treating PF and may cause severe side effects. Recent studies showed that traditional Chinese herbal abstraction such as Tanshinone IIA (TIIA) was displayed significant anti-PF effects in animal models. However, the exact mechanisms underlying the protective effects of TIIA were not fully understood. Here we further investigated the protective effects of TIIA and its mechanisms underlying. PF models of rat were induced by bleomycin (BLM); TIIA was administered subsequently. The PF changes were identified by histopathological analyses. The results showed that BLM resulted in severe PF and alveolar inflammation; together with significant elevation of transforming growth factor-β 1 (TGF-β1). Angiotensin-converting enzyme 2 (ACE-2) together with angiotensin-(1-7) [ANG-(1-7)] were both greatly reduced after BLM administration. TIIA treatment notably attenuated BLM induced PF and inflammation, decreased expression of TGF-β1 and reversed ACE-2 and ANG-(1-7) production in rat lungs. Thus we may draw the conclusion that TIIA may exert protective effects on BLM induced PF in rats, and the ACE-2/ANG-(1-7) axis may ascribe to those protective effects.
机译:肺纤维化(PF)是那些间质性肺疾病患者的常见并发症,将导致预后不良和生存期短。传统的治疗方法(如糖皮质激素和细胞毒性药物)不足以治疗PF,并可能引起严重的副作用。最近的研究表明,诸如丹参酮IIA(TIIA)等传统中草药提取物在动物模型中显示出显着的抗PF效应。但是,尚未完全了解TIIA保护作用的确切机制。在这里,我们进一步研究了TIIA的保护作用及其潜在机制。博来霉素(BLM)诱导大鼠PF模型;随后对TIIA进行了管理。 PF变化通过组织病理学分析确定。结果显示,BLM导致严重的PF和肺泡发炎;以及转化生长因子-β1(TGF-β1)的显着升高。服用BLM后,血管紧张素转换酶2(ACE-2)与血管紧张素-(1-7)[ANG-(1-7)]均大大降低。 TIIA处理可明显减轻BLM诱导的PF和炎症,降低TGF-β1的表达,并逆转大鼠肺中ACE-2和ANG-(1-7)的产生。因此我们可以得出结论,TIIA可能对BLM诱导的大鼠PF发挥保护作用,而ACE-2 / ANG-(1-7)轴可能归因于这些保护作用。

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