首页> 美国卫生研究院文献>International Journal of Molecular Medicine >Incremental load training improves renal fibrosis by regulating the TGF-β1/TAK1/MKK3/p38MAPK signaling pathway and inducing the activation of autophagy in aged mice
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Incremental load training improves renal fibrosis by regulating the TGF-β1/TAK1/MKK3/p38MAPK signaling pathway and inducing the activation of autophagy in aged mice

机译:增量负荷训练通过调节TGF-β1/ TAK1 / MKK3 / p38MAPK信号通路并诱导衰老小鼠自噬激活来改善肾纤维化

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摘要

Recent studies have confirmed that kidney tissue fibrosis is closely linked to the natural aging of organs. One of its major characteristics is the reduction of autophagic activity. However, to date, few studies have assessed whether incremental load training is able to improve the occurrence of renal fibrosis caused by natural aging and the underlying mechanisms. In the present study involving male C57/BL mice, an elderly exercise group (OY group) was subjected to progressive load-increasing rotary-bar training (5 days/week, lasting for 6 weeks), with an elderly control group (OC group) and a young control group (YC group) used as controls. Renal fibrosis and autophagy-associated indicators were assessed by Masson's staining, reverse transcription-quantitative PCR analysis, western blotting, immunofluorescence and transmission electron microscopy. The results suggested that collagen deposition in the basal part of the renal tubular epithelium and glomeruli in the OY group was significantly lower than that in the OC group. In the OC group, the protein expression levels of E-cadherin, Beclin 1 and light chain 3 were significantly decreased, and increases in α-smooth muscle actin-positive signals were observed in the glomerular matrix and renal capsule wall. Furthermore, the expression of transforming growth factor (TGF)-β1 and its downstream signaling molecules TGF-β-activated kinase 1 (TAK1), mitogen-activated protein kinase (MAPK) kinase (MKK3) and p38MAPK were downregulated following training. The present study confirmed that incremental load training may improve renal fibrosis in aged mice by regulating the TGF-β1/TAK1/MMK3/p38MAPK signaling pathway and inducing the activation of autophagy to reduce the synthesis of extracellular matrix and delay the epithelial-mesenchymal transition. The present study provides a novel experimental basis for the intervention of incremental load training to prevent senile renal fibrosis.
机译:最近的研究证实,肾组织纤维化与器官的自然衰老紧密相关。其主要特征之一是自噬活性的降低。但是,迄今为止,很少有研究评估增量负荷训练是否能够改善由自然衰老和潜在机制引起的肾纤维化的发生。在本项涉及雄性C57 / BL小鼠的研究中,老年运动组(OY组)接受了渐进式增加的力量训练(5天/周,持续6周),而老年对照组(OC组) )和年轻对照组(YC组)作为对照。肾纤维化和自噬相关指标通过Masson染色,逆转录定量PCR分析,western印迹,免疫荧光和透射电镜进行评估。结果表明,OY组的肾小管上皮和肾小球基底胶原沉积明显低于OC组。在OC组中,在肾小球基质和肾囊壁中,E-钙黏着蛋白,Beclin 1和轻链3的蛋白表达水平显着降低,并且α-平滑肌肌动蛋白阳性信号增加。此外,训练后下调了转化生长因子(TGF)-β1及其下游信号分子TGF-β激活激酶1(TAK1),促分裂原激活蛋白激酶(MAPK)激酶(MKK3)和p38MAPK的表达。本研究证实,增量负荷训练可通过调节TGF-β1/ TAK1 / MMK3 / p38MAPK信号通路并诱导自噬激活来减少细胞外基质的合成并延缓上皮-间质转化,从而改善老年小鼠的肾纤维化。本研究为增加负荷训练预防老年性肾纤维化提供了新的实验基础。

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