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体育锻炼通过免疫系统调节成为急性肾脏疾病的朋友而非敌人。

Physical exercise as a friend not a foe in acute kidney diseases through immune system modulation.

机构信息

Instituto Sírio-Libanês de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, Brazil.

Faculdade Israelita de Ciências da Saúde Albert Einstein, Hospital Israelita Albert Einstein, São Paulo, Brazil.

出版信息

Front Immunol. 2023 Oct 20;14:1212163. doi: 10.3389/fimmu.2023.1212163. eCollection 2023.

DOI:10.3389/fimmu.2023.1212163
PMID:37928533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10623152/
Abstract

Regular and moderate exercise is being used for therapeutic purposes in treating several diseases, including cancer, cardiovascular diseases, arthritis, and even chronic kidney diseases (CKDs). Conversely, extenuating physical exercise has long been pointed out as one of the sources of acute kidney injury (AKI) due to its severe impact on the body's physiology. AKI development is associated with increased tubular necrosis, which initiates a cascade of inflammatory responses. The latter involves cytokine production, immune cell (macrophages, lymphocytes, and neutrophils, among others) activation, and increased oxidative stress. AKI can induce prolonged fibrosis stimulation, leading to CKD development. The need for therapeutic alternative treatments for AKI is still a relevant issue. In this context arises the question as to whether moderate, not extenuating, exercise could, on some level, prevent AKI. Several studies have shown that moderate exercise can help reduce tissue damage and increase the functional recovery of the kidneys after an acute injury. In particular, the immune system can be modulated by exercise, leading to a better recovery from different pathologies. In this review, we aimed to explore the role of exercise not as a trigger of AKI, but as a modulator of the inflammatory/immune system in the prevention or recovery from AKI in different scenarios. In AKI induced by ischemia and reperfusion, sepsis, diabetes, antibiotics, or chemotherapy, regular and/or moderate exercise could modulate the immune system toward a more regulatory immune response, presenting, in general, an anti-inflammatory profile. Exercise was shown to diminish oxidative stress, inflammatory markers (caspase-3, lactate dehydrogenase, and nitric oxide), inflammatory cytokines (interleukin (IL)-1b, IL-6, IL-8, and tumor necrosis factor-α (TNF-α)), modulate lymphocytes to an immune suppressive phenotype, and decrease tumor necrosis factor-β (TGF-β), a cytokine associated with fibrosis development. Thus, it creates an AKI recovery environment with less tissue damage, hypoxia, apoptosis, or fibrosis. In conclusion, the practice of regular moderate physical exercise has an impact on the immune system, favoring a regulatory and anti-inflammatory profile that prevents the occurrence of AKI and/or assists in the recovery from AKI. Moderate exercise should be considered for patients with AKI as a complementary therapy.

摘要

定期和适度的运动被用于治疗多种疾病,包括癌症、心血管疾病、关节炎,甚至慢性肾脏病(CKD)。相反,剧烈的体力活动长期以来一直被指出是急性肾损伤(AKI)的来源之一,因为它对身体的生理机能有严重的影响。AKI 的发展与肾小管坏死的增加有关,这会引发一系列炎症反应。后者涉及细胞因子的产生、免疫细胞(巨噬细胞、淋巴细胞和中性粒细胞等)的激活以及氧化应激的增加。AKI 会引发长期的纤维化刺激,导致 CKD 的发生。因此,寻找 AKI 的治疗替代方法仍然是一个重要的问题。在这种情况下,人们开始质疑适度而非剧烈的运动是否在某种程度上可以预防 AKI。许多研究表明,适度运动可以帮助减轻组织损伤,并在急性损伤后增加肾脏的功能恢复。特别是,运动可以调节免疫系统,从而更好地从不同的病理中恢复。在这篇综述中,我们旨在探讨运动的作用不是作为 AKI 的触发因素,而是作为炎症/免疫系统的调节剂,在不同情况下预防或恢复 AKI。在缺血再灌注、脓毒症、糖尿病、抗生素或化疗引起的 AKI 中,有规律的和/或适度的运动可以调节免疫系统,使其产生更具调节性的免疫反应,总体上呈现抗炎表型。运动被证明可以减少氧化应激、炎症标志物(半胱天冬酶-3、乳酸脱氢酶和一氧化氮)、炎症细胞因子(白细胞介素(IL)-1b、IL-6、IL-8 和肿瘤坏死因子-α(TNF-α))、调节淋巴细胞向免疫抑制表型,并降低与纤维化发展相关的细胞因子肿瘤坏死因子-β(TGF-β)。因此,它创造了一个具有较少组织损伤、缺氧、细胞凋亡或纤维化的 AKI 恢复环境。总之,定期适度的体育锻炼对免疫系统有影响,有利于调节和抗炎表型,可预防 AKI 的发生和/或有助于 AKI 的恢复。适度运动应被视为 AKI 患者的一种补充治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6514/10623152/02aa4772bb9f/fimmu-14-1212163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6514/10623152/e1a442a1133d/fimmu-14-1212163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6514/10623152/02aa4772bb9f/fimmu-14-1212163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6514/10623152/e1a442a1133d/fimmu-14-1212163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6514/10623152/02aa4772bb9f/fimmu-14-1212163-g002.jpg

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