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[三七调控PI3K/Akt/mTORC1-线粒体能量代谢治疗血瘀证慢性肾衰竭大鼠的机制]

[Mechanism of Notoginseng Radix et Rhizoma in regulating PI3K/Akt/mTORC1-mitochondrial energy metabolism to treat chronic renal failure in rats with blood stasis syndrome].

作者信息

Liu Xiao-Yu, Huang Zhi-Min, Qiu Shao-Bin, Qiu Fei, Huang Xiao-Ying, Jiang Yi-Ni, Lin Ai-Tao, Zhang Zhi-Ying, Tang Yu, Wu Jin-Yu

机构信息

the First Clinical Faculty, Guangxi University of Chinese Medicine Nanning 530200, China.

Department of Rheumatology, the First Affiliated Hospital of Guangxi University of Chinese Medicine Nanning 530023, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2024 Apr;49(7):1888-1895. doi: 10.19540/j.cnki.cjcmm.20231009.403.

Abstract

This study observed the effects of Notoginseng Radix et Rhizoma on the phosphatidylinositol 3-kinase(PI3K)/protein kinase B(Akt)/mammalian target of rapamycin complex 1(mTORC1) signaling pathway and mitochondrial energy metabolism in the rat model of adriamycin-induced renal fibrosis with blood stasis syndrome to explore the mechanism of Notoginseng Radix et Rhizoma in protecting the kidney. Thirty male rats with adriamycin-induced renal fibrosis were randomized into model, low-, medium-, and high-dose Notoginseng Radix et Rhizoma, and positive control groups(n=6). Six clean SD male rats were selected into the normal group. The normal group and model group were administrated with normal saline, and other groups with corresponding drugs. After 8 weeks of treatment, the renal function, renal pathology, adenosine triphosphate(ATP) levels, Na+-K+-ATPase and Ca(2+)-Mg(2+)-ATPase activities, and the protein levels of ATP5B, mTORC1, 70 kDa ribosomal protein S6 kinase(P70S6K), P85, Akt, p-Akt, and SH2-containing inositol phosphatase(SHIP2) in the renal tissue were determined. Compared with the normal group, the model group showed elevated levels of blood urea nitrogen(BUN) and serum creatinine(SCr)(P<0.01). Compared with the model group, Notoginseng Radix et Rhizoma and the positive control lowered the levels of BUN and SCr, which were significant in the medium-and high-dose Noto-ginseng Radix et Rhizoma groups and the positive control group(P<0.05). Compared with the model group, Notoginseng Radix et Rhizoma and the positive control alleviated the pathological changes in the renal tissue, such as vacuolar and fibroid changes, glomerulus atrophy, cystic expansion of renal tubules, and massive infiltration of inflammatory cells. Compared with the normal group, the model group showed decreased mitochondrial ATP content and Na+-K+-ATPase and Ca(2+)-Mg(2+)-ATPase activities in the renal tissue(P<0.05), and medium-and high-dose Notoginseng Radix et Rhizoma and positive control mitigated such decreases(P<0.05). Compared with the model group, medium-and high-dose Notoginseng Radix et Rhizoma and the positive control up-regulated the protein levels of ATP5B and SHIP2 and down-regulated the protein levels of mTORC1, P70S6K, P85, Akt, and p-Akt(P<0.05 or P<0.01 or P<0.001). Notoginseng Radix et Rhizoma may exert an anti-fibrosis effect by inhibiting the activation of the PI3K/Akt/mTORC1 pathway to restore mitochondrial energy metabolism, thus protecting the kidney.

摘要

本研究观察了三七对阿霉素诱导的血瘀证肾纤维化大鼠模型中磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(Akt)/哺乳动物雷帕霉素靶蛋白复合物1(mTORC1)信号通路及线粒体能量代谢的影响,以探讨三七保护肾脏的作用机制。将30只阿霉素诱导的肾纤维化雄性大鼠随机分为模型组、三七低、中、高剂量组及阳性对照组(n = 6)。选取6只清洁级SD雄性大鼠作为正常组。正常组和模型组给予生理盐水,其他组给予相应药物。治疗8周后,检测大鼠肾功能、肾脏病理、三磷酸腺苷(ATP)水平、钠钾ATP酶和钙镁ATP酶活性,以及肾组织中ATP5B、mTORC1、70 kDa核糖体蛋白S6激酶(P70S6K)、P85、Akt、磷酸化Akt(p-Akt)和含SH2结构域的肌醇磷酸酶(SHIP2)的蛋白水平。与正常组相比,模型组血尿素氮(BUN)和血清肌酐(SCr)水平升高(P<0.01)。与模型组相比,三七及阳性对照组降低了BUN和SCr水平,其中三七中、高剂量组及阳性对照组差异有统计学意义(P<0.05)。与模型组相比,三七及阳性对照组减轻了肾组织的病理改变,如空泡样和纤维化改变肾小球萎缩、肾小管囊性扩张及炎性细胞大量浸润。与正常组相比,模型组肾组织线粒体ATP含量、钠钾ATP酶和钙镁ATP酶活性降低(P<0.05),三七中、高剂量组及阳性对照组减轻了这种降低(P<0.05)。与模型组相比,三七中、高剂量组及阳性对照组上调了ATP5B和SHIP2的蛋白水平,下调了mTORC1、P70S6K、P85、Akt和p-Akt的蛋白水平(P<0.05或P<0.01或P<0.001)。三七可能通过抑制PI3K/Akt/mTORC1通路的激活来恢复线粒体能量代谢,从而发挥抗纤维化作用,保护肾脏。

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