Department of Pharmacology & Toxicology, National Institute of Pharmaceutical Education and Research (NIPER)-Guwahati, Changsari PIN-781101, Assam, India.
Department of Pharmacology & Toxicology, National Institute of Pharmaceutical Education and Research (NIPER)-Guwahati, Changsari PIN-781101, Assam, India.
Life Sci. 2021 Apr 15;271:119155. doi: 10.1016/j.lfs.2021.119155. Epub 2021 Feb 3.
Acute kidney injury (AKI) is a progressive renal complication which significantly affects the patient's life with huge economic burden. Untreated acute kidney injury eventually progresses to a chronic form and end-stage renal disease. Although significant breakthroughs have been made in recent years, there are still no effective pharmacological therapies for the treatment of acute kidney injury. Toll-like receptor 4 (TLR4) is a well-characterized pattern recognition receptor, and increasing evidence has shown that TLR4 mediated inflammatory response plays a pivotal role in the pathogenesis of acute kidney injury. The expression of TLR4 has been seen in resident renal cells, including podocytes, mesangial cells, tubular epithelial cells and endothelial cells. Activation of TLR4 signaling regulates the transcription of numerous pro-inflammatory cytokines and chemokines, resulting in renal inflammation. Therefore, targeting TLR4 and its downstream effectors could serve as an effective therapeutic intervention to prevent renal inflammation and subsequent kidney damage. For the first time, this review summarizes the literature on acute kidney injury from the perspective of TLR4 from year 2010 to 2020. In the current review, the role of TLR4 signaling pathway in AKI with preclinical evidence is discussed. Furthermore, we have highlighted several compounds of natural and synthetic origin, which have the potential to avert the renal TLR4 signaling in preclinical AKI models and have shown protection against AKI. This scientific review provides new ideas for targeting TLR4 in the treatment of AKI and provides strategies for the drug development against AKI.
急性肾损伤(AKI)是一种进行性的肾并发症,严重影响患者的生活,并带来巨大的经济负担。未经治疗的急性肾损伤最终会发展为慢性形式和终末期肾病。尽管近年来取得了重大突破,但目前仍然没有有效的药理学疗法来治疗急性肾损伤。Toll 样受体 4(TLR4)是一种特征明确的模式识别受体,越来越多的证据表明 TLR4 介导的炎症反应在急性肾损伤的发病机制中起着关键作用。TLR4 的表达已在固有肾细胞中观察到,包括足细胞、系膜细胞、肾小管上皮细胞和内皮细胞。TLR4 信号的激活调节了众多促炎细胞因子和趋化因子的转录,导致肾脏炎症。因此,靶向 TLR4 及其下游效应物可能成为预防肾脏炎症和随后的肾损伤的有效治疗干预措施。本文首次从 2010 年到 2020 年的 TLR4 角度综述了急性肾损伤的文献。在本综述中,讨论了 TLR4 信号通路在 AKI 中的作用及临床前证据。此外,我们还强调了几种天然和合成来源的化合物,这些化合物具有在临床前 AKI 模型中避免肾 TLR4 信号的潜力,并显示出对 AKI 的保护作用。本综述为靶向 TLR4 治疗 AKI 提供了新的思路,并为 AKI 的药物开发提供了策略。