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远程肝脏缺血预处理通过磷酸化细胞外信号调节激酶 1 和 2 保护小鼠免受肾缺血/再灌注损伤。

Remote liver ischemic preconditioning protects against renal ischemia/reperfusion injury via phosphorylation of extracellular signal-regulated kinases 1 and 2 in mice.

机构信息

Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Laboratory of Anesthesia and Critical Care Medicine, National-Local Joint Engineering Research Centre of Translational Medicine of Anesthesiology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

PLoS One. 2024 Aug 19;19(8):e0308977. doi: 10.1371/journal.pone.0308977. eCollection 2024.

Abstract

Perioperative acute kidney injury (AKI), which is mainly mediated by renal ischemia‒reperfusion (I/R) injury, is commonly observed in clinical practice. However, effective measures for preventing and treating this perioperative complication are still lacking in the clinic. Thus, we designed this study to examine whether remote liver ischemic preconditioning (RLIPC) has a protective effect on damage caused by renal I/R injury. In a rodent model, 30 mice were divided into five groups to assess the effects of RLIPC and ERK1/2 inhibition on AKI. The groups included the sham-operated (sham), kidney ischemia and reperfusion (CON), remote liver ischemic preconditioning (RLIPC), CON with the ERK1/2 inhibitor U0126 (CON+U0126), and RLIPC with U0126 (RLIPC+U0126). RLIPC consisted of 4 liver ischemia cycles before renal ischemia. Renal function and injury were assessed through biochemical assays, histology, cell apoptosis and protein phosphorylation analysis. RLIPC significantly mitigated renal dysfunction, tissue damage, inflammation, and apoptosis caused by I/R, which was associated with ERK1/2 phosphorylation. Furthermore, ERK1/2 inhibition with U0126 negated the protective effects of RLIPC and exacerbated renal injury. To summarize, we demonstrated that RLIPC has a strong renoprotective effect on kidneys post I/R injury and that this effect may be mediated by phosphorylation of ERK1/2.

摘要

围手术期急性肾损伤(AKI)主要由肾缺血再灌注(I/R)损伤介导,在临床实践中很常见。然而,临床上仍然缺乏预防和治疗这种围手术期并发症的有效措施。因此,我们设计了这项研究来检验远程肝缺血预处理(RLIPC)是否对肾 I/R 损伤引起的损伤具有保护作用。在啮齿动物模型中,将 30 只小鼠分为五组,以评估 RLIPC 和 ERK1/2 抑制对 AKI 的影响。这些组包括假手术(sham)、肾缺血再灌注(CON)、远程肝缺血预处理(RLIPC)、CON 与 ERK1/2 抑制剂 U0126(CON+U0126)和 RLIPC 与 U0126(RLIPC+U0126)。RLIPC 包括肾缺血前的 4 个肝缺血循环。通过生化测定、组织学、细胞凋亡和蛋白磷酸化分析来评估肾功能和损伤。RLIPC 显著减轻了 I/R 引起的肾功能障碍、组织损伤、炎症和细胞凋亡,这与 ERK1/2 磷酸化有关。此外,用 U0126 抑制 ERK1/2 消除了 RLIPC 的保护作用,并加重了肾损伤。总之,我们证明了 RLIPC 对 I/R 损伤后的肾脏具有很强的保护作用,这种作用可能是通过 ERK1/2 的磷酸化介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b88e/11332924/7e256609339d/pone.0308977.g001.jpg

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