Department of Critical Care Medicine, Wuxi 9th People's Hospital Affiliated to Soochow University, Wuxi, Jiangsu 214000, P.R. China.
Department of Science and Education, Wuxi 9th People's Hospital Affiliated to Soochow University, Wuxi, Jiangsu 214000, P.R. China.
Exp Anim. 2023 Aug 7;72(3):346-355. doi: 10.1538/expanim.22-0175. Epub 2023 Mar 2.
An increasing number of studies have suggested that oxidative stress and inflammation play momentous roles in acute pulmonary embolism (APE). Honokiol, a bioactive biphenolic phytochemical substance, is known for its strong anti-oxidative and anti-inflammatory effects, and it served as an activator of sirtuin3 (SIRT3) in the present study. The purposes of the study were to explore the effects of honokiol on APE rats and investigate whether the function of honokiol is mediated by SIRT3 activation. In the study, the rats received a right femoral vein injection of dextran gel G-50 particles (12 mg/kg) to establish the APE model and were subsequently administered honokiol and/or a selective SIRT3 inhibitor 3-(1H-1,2,3-triazol-4-yl)pyridine (3-TYP; 5 mg/kg) intraperitoneally. The results showed that SIRT3 activation by honokiol attenuated the loss in lung function, ameliorated the inflammatory response and oxidative damage, and inhibited apoptosis in lung tissues of the rats with APE but that this was reversed by 3-TYP. In addition, we found that the AMP-activated protein kinase (AMPK)/mammalian target of rapamycin (mTOR) pathway might be activated by honokiol but restrained by 3-TYP. These results indicated that honokiol was capable of suppressing the adverse effects of APE and that this was diminished by SIRT3 suppression, implying that activation of SIRT3 might serve as a therapeutic method for APE.
越来越多的研究表明,氧化应激和炎症在急性肺栓塞(APE)中起着重要作用。厚朴酚是一种生物活性的双酚类植物化学物质,以其强大的抗氧化和抗炎作用而闻名,在本研究中它被用作 SIRT3 的激活剂。本研究旨在探讨厚朴酚对 APE 大鼠的影响,并研究厚朴酚的功能是否通过 SIRT3 激活来介导。在研究中,大鼠接受右股静脉注射葡聚糖凝胶 G-50 颗粒(12mg/kg),以建立 APE 模型,随后腹腔内给予厚朴酚和/或选择性 SIRT3 抑制剂 3-(1H-1,2,3-三唑-4-基)吡啶(3-TYP;5mg/kg)。结果表明,厚朴酚通过激活 SIRT3 减轻了肺功能的丧失,改善了炎症反应和氧化损伤,并抑制了 APE 大鼠肺组织的细胞凋亡,但 3-TYP 逆转了这一作用。此外,我们发现厚朴酚可能激活了 AMP 激活的蛋白激酶(AMPK)/雷帕霉素靶蛋白(mTOR)通路,但被 3-TYP 抑制。这些结果表明,厚朴酚能够抑制 APE 的不良影响,而 SIRT3 的抑制则削弱了这一作用,这表明 SIRT3 的激活可能成为 APE 的一种治疗方法。