Penehyclidine hydrochloride ameliorates renal ischemia reperfusion-stimulated lung injury in mice by activating Nrf2 signaling

Qiang Yang, Lei Li, Zhaohui Liu, Chunlei Li, Lili Yu, Yulin Chang
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Abstract

Introduction: Penehyclidine hydrochloride (PHC) is an anticholinergic with anti-inflammatory and anti-oxidation activities. PHC displayed protectivity against renal ischemia reperfusion (RIR) injury. Nevertheless, the precise protectivity of PHC on RIR-induced lung injury remains unknown. Methods: We examined the effects of PHC on RIR-induced lung injury and investigated the underlying mechanism. We induced RIR in mice and administrated PHC to RIR mice. Kidney function was monitored by measuring the blood urea nitrogen (BUN) and creatinine level in serum. We evaluated the lung injury, myeloperoxidase (MPO) activity in lung, pro-inflammatory cytokine level, and oxidative markers in serum and lung tissues. We tested the expression level of nuclear factor erythroid 2-related factor 2 (Nrf-2) and heme oxygenase 1 (HO-1) in lung of RIR mice after PHC treatment. Finally, we evaluated the effects of PHC in RIR Nrf2-/- mice. Results: PHC greatly downregulated the serum levels of BUN, creatinine, IL-6, NO, malondialdehyde (MDA), and matrix metalloproteinase-2. PHC also ameliorated the lung injury, decreased the MPO activity, and suppressed production of IL-6, TNF-α, IFN-γ, MDA, and O2-, while it promoted production of superoxide dismutase (SOD) and catalase (CAT) in lung. PHC improved the production of Nrf2 and HO-1. Conclusion: The protectivity of PHC was absent in Nrf2-/- mice. PHC ameliorated RIR-induced lung injury through Nrf2 pathway.
盐酸戊乙奎醚通过激活Nrf2信号通路改善小鼠肾缺血再灌注刺激肺损伤
简介:盐酸戊乙基醚(PHC)是一种具有抗炎、抗氧化作用的抗胆碱能药物。PHC对肾缺血再灌注(RIR)损伤具有保护作用。然而,PHC对核糖核酸诱导的肺损伤的确切保护作用尚不清楚。方法:观察PHC对rna诱导的肺损伤的影响,并探讨其机制。我们在小鼠体内诱导RIR,并给药PHC。通过测定血清尿素氮(BUN)和肌酐水平监测肾功能。我们评估了肺损伤、肺髓过氧化物酶(MPO)活性、促炎细胞因子水平以及血清和肺组织中的氧化标志物。我们检测了PHC治疗后RIR小鼠肺中核因子-红细胞2相关因子2 (Nrf-2)和血红素加氧酶1 (HO-1)的表达水平。最后,我们评估了PHC对RIR Nrf2-/-小鼠的影响。结果:PHC显著下调血清BUN、肌酐、IL-6、NO、丙二醛(MDA)、基质金属蛋白酶-2水平。PHC还能改善肺损伤,降低MPO活性,抑制IL-6、TNF-α、IFN-γ、MDA和O2-的产生,促进肺组织超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的产生。PHC提高了Nrf2和HO-1的生成。结论:PHC对Nrf2-/-小鼠无保护作用。PHC通过Nrf2通路改善rir诱导的肺损伤。
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