黄芪及其成分在骨质疏松症动物模型中的疗效和可能机制:临床前综述与元分析》。

IF 3 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ning Cao, Zhangxuan Shou, Yi Xiao, Puqing Liu
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引用次数: 0

摘要

背景:黄芪(AR)作为抗骨质疏松症(OP)的传统中药已有悠久的历史。本研究旨在探讨黄芪及其主要成分(IAR)在骨质疏松症治疗中的效果和最佳治疗方案:方法:在 7 个数据库(PubMed、Web of Science、MEDLINE、SciELO 引文索引、Cochrane 图书馆、中国国家知识基础设施和万方数据库)中检索了符合条件的动物研究。主要结果是骨代谢指数。结果:本研究共纳入 21 项研究。本文的主要研究结果表明,IAR能显著增加骨矿物质密度(BMD)、骨总量、骨小梁数、骨小梁厚度、骨最大负荷和血清钙,而骨小梁分离度和血清1型胶原蛋白C端端肽显著降低(P<0.05)。在亚组分析中,长疗程组(≥ 10 周)的 BMD 效果优于短疗程组(< 10 周)(P < 0.05)。建模方法和动物性别是影响血清碱性磷酸酶和骨钙素水平的因素:研究结果表明,有可能将IAR开发为治疗OP的药物。无论动物品系和年龄如何,治疗时间更长的IAR可能会取得更好的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and Possible Mechanisms of Astragali Radix and its Ingredients in Animal Models of Osteoporosis: A Preclinical Review and Metaanalysis.

Background: Astragali Radix (AR) has a long history as a traditional Chinese medicine for anti-osteoporosis (OP) treatment. The aim of the study was to explore the effect and optimal regimens of AR and its main ingredients (IAR) in OP treatment.

Methods: Eligible animal studies were searched in seven databases (PubMed, Web of Science, MEDLINE, SciELO Citation Index, Cochrane Library, China National Knowledge Infrastructure and Wanfang). The primary outcomes were bone metabolic indices. The secondary outcome measure was the anti-OP mechanism of IAR.

Results: 21 studies were enrolled in the study. The primary findings of the present article illustrated that IAR could significantly increase the bone mineral density (BMD), bone volume over the total volume, trabecular number, trabecular thickness, bone maximum load and serum calcium, while trabecular separation and serum C-terminal telopeptide of type 1 collagen were remarkably decreased (P < 0.05). In subgroup analysis, the BMD in the long treatment group (≥ 10 weeks) showed better effect size than the short treatment group (< 10 weeks) (P < 0.05). Modeling methods and animal sex were factors affecting serum alkaline phosphatase and osteocalcin levels.

Conclusion: The findings suggest the possibility of developing IAR as a drug for the treatment of OP. IAR with longer treatment time may achieve better effects regardless of animal strain and age.

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来源期刊
Current drug targets
Current drug targets 医学-药学
CiteScore
6.20
自引率
0.00%
发文量
127
审稿时长
3-8 weeks
期刊介绍: Current Drug Targets aims to cover the latest and most outstanding developments on the medicinal chemistry and pharmacology of molecular drug targets e.g. disease specific proteins, receptors, enzymes, genes. Current Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of drug targets. The journal also accepts for publication mini- & full-length review articles and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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