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六味地黄丸通过上调类心肌营养素1表达经Janus激酶/信号转导子和转录激活子信号通路治疗肾阴虚型绝经后骨质疏松症

Liuwei Dihuang Pill () Treats Postmenopausal Osteoporosis with Shen (Kidney) Yin Deficiency via Janus Kinase/Signal Transducer and Activator of Transcription Signal Pathway by Up-regulating Cardiotrophin-Like Cytokine Factor 1 Expression.

作者信息

Ge Ji-Rong, Xie Li-Hua, Chen Juan, Li Sheng-Qiang, Xu Hui-Juan, Lai Yu-Lian, Qiu Long-Long, Ni Chen-Bo

机构信息

Key Research Laboratory of Osteoporosis Syndrome Genomics, Fujian Academy of Traditional Chinese Medicine, Fuzhou, 350003, China.

出版信息

Chin J Integr Med. 2018 Jun;24(6):415-422. doi: 10.1007/s11655-016-2744-2. Epub 2016 Dec 27.

Abstract

OBJECTIVES

To investigate the mechanism of Liuwei Dihuang Pill (, LDP) in treating postmenopausal osteoporosis (PMOP) with Shen (Kidney) yin deficiency.

METHODS

In this study, 205 cases of PMOP were divided into the PMOP Shen-yin deficiency group (Group A), PMOP Shen-yang deficiency group (Group B), PMOP without Shen deficiency group (Group C), and control group (Group N). Real-time polymerase chain reaction (RT-PCR) and Western blot techniques were used to observe the effects of LDP treatment on the cardiotrophin-like cytokine factor 1 (CLCF1), ankyrin repeat and SOCS box containing 1 (ASB1), and prokineticin 2 (PROK2) genes and the Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling pathway.

RESULTS

The mRNA (P<0.05) and protein (P<0.01) expression levels of the CLCF1 gene in Group A were significantly lower than the corresponding levels in Group N. After LDP treatment for 3 months, the mRNA expression levels of the CLCF1 gene were obviously up-regulated (P<0.01). After 6-month treatment, the expression levels of CLCF1 mRNA and protein were significantly up-regulated (both P<0.01), and the average bone density of the top femur had significantly increased (P<0.05). In vitro, CLCF1 overexpression resulted in a significant increase in the total protein and phosphorylated protein levels of JAK2 and STAT3.

CONCLUSIONS

The CLCF1 gene is an important gene associated with PMOP Shen-yin deficiency and the therapeutic effects of LDP may be mediated by up-regulation of CLCF1 gene expression and activation of the JAK/STAT signaling pathway.

摘要

目的

探讨六味地黄丸治疗肾阴虚型绝经后骨质疏松症(PMOP)的机制。

方法

本研究将205例PMOP患者分为肾阴虚型PMOP组(A组)、肾阳虚型PMOP组(B组)、非肾虚型PMOP组(C组)和对照组(N组)。采用实时聚合酶链反应(RT-PCR)和蛋白质印迹技术观察六味地黄丸治疗对心肌营养素样细胞因子1(CLCF1)、含锚蛋白重复序列和SOCS盒蛋白1(ASB1)、促动力蛋白2(PROK2)基因及Janus激酶/信号转导子和转录激活子(JAK/STAT)信号通路的影响。

结果

A组CLCF1基因的mRNA表达水平(P<0.05)和蛋白表达水平(P<0.01)显著低于N组。六味地黄丸治疗3个月后,CLCF1基因的mRNA表达水平明显上调(P<0.01)。治疗6个月后,CLCF1 mRNA和蛋白表达水平均显著上调(均P<0.01),股骨近端平均骨密度显著增加(P<0.05)。体外实验中,CLCF1过表达导致JAK2和STAT3的总蛋白及磷酸化蛋白水平显著增加。

结论

CLCF1基因是与肾阴虚型PMOP相关的重要基因,六味地黄丸的治疗作用可能通过上调CLCF1基因表达及激活JAK/STAT信号通路介导。

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