MICT ameliorates hypertensive nephropathy by inhibiting TLR4/NF-κB pathway and down-regulating NLRC4 inflammasome

被引:2
|
作者
Dong, Wenyu [1 ]
Luo, Minghao [2 ]
Li, Yun [1 ]
Chen, Xinhua [1 ]
Li, Lingang [1 ]
Chang, Qing [3 ]
机构
[1] Chongqing Med Univ, Affiliated Rehabil Hosp, Chongqing, Peoples R China
[2] Chongqing Med Univ, Affiliated Hosp 1, Dept Cardiol, Chongqing, Peoples R China
[3] Chongqing Med Univ, Coll Exercise Med, Chongqing, Peoples R China
来源
PLOS ONE | 2024年 / 19卷 / 07期
关键词
CHRONIC KIDNEY-DISEASE; BLOOD-PRESSURE; FIBROSIS; MECHANISMS; EXERCISE; ASSOCIATION; DYSFUNCTION; ACTIVATION; ADULTS; DRUG;
D O I
10.1371/journal.pone.0306137
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Hypertensive nephropathy (HN) is one of the main causes of end-stage renal disease (ESRD), leading to serious morbidity and mortality in hypertensive patients. However, existing treatment for hypertensive nephropathy are still very limited. It has been demonstrated that aerobic exercise has beneficial effects on the treatment of hypertension. However, the underlying mechanisms of exercise in HN remain unclear.Methods The spontaneously hypertensive rats (SHR) were trained for 8 weeks on a treadmill with different exercise prescriptions. We detected the effects of moderate intensity continuous training (MICT) and high intensity interval training (HIIT) on inflammatory response, renal function, and renal fibrosis in SHR. We further investigated the relationship between TLR4 and the NLRC4 inflammasome in vitro HN model.Results MICT improved renal fibrosis and renal injury, attenuating the inflammatory response by inhibiting TLR4/NF-kappa B pathway and the activation of NLRC4 inflammasome. However, these changes were not observed in the HIIT group. Additionally, repression of TLR4/NF-kappa B pathway by TAK-242 inhibited activation of NLRC4 inflammasome and alleviated the fibrosis in Ang II-induced HK-2 cells.Conclusion MICT ameliorated renal damage, inflammatory response, and renal fibrosis via repressing TLR4/NF-kappa B pathway and the activation of NLRC4 inflammasome. This study might provide new references for exercise prescriptions of hypertension.
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页数:16
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