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纸质出版日期:2018
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路宇仁, 陈昳冰, 崔元璐, 等. 淫羊藿苷药理作用研究进展[J]. 中国实验方剂学杂志, 2018,24(17):209-220.
LU Yu-ren, CHEN Yi-bing, CUI Yuan-lu, et al. Progress of Pharmacological Research on Icariin[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(17): 209-220.
路宇仁, 陈昳冰, 崔元璐, 等. 淫羊藿苷药理作用研究进展[J]. 中国实验方剂学杂志, 2018,24(17):209-220. DOI: 10.13422/j.cnki.syfjx.20181734.
LU Yu-ren, CHEN Yi-bing, CUI Yuan-lu, et al. Progress of Pharmacological Research on Icariin[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(17): 209-220. DOI: 10.13422/j.cnki.syfjx.20181734.
淫羊藿作为我国传统中药,具有补肝肾、强筋骨、祛风湿的功效,是补肾壮阳、强阳起痿方剂的常用中药,主要用于肾阳不足,风湿痹痛和骨痿的治疗。现代研究表明,淫羊藿中的主要化学成分淫羊藿苷具有广泛的生物活性,如抗炎、抗氧化应激、抗抑郁和抗肿瘤等。分子药理学研究表明,淫羊藿苷可通过调控多个细胞信号转导通路中的靶点治疗神经系统疾病、骨质疏松症、心血管系统疾病、免疫性疾病和生殖系统疾病等。淫羊藿苷在骨保护方面的作用机制广泛,主要涉及雌激素受体α(ERα)-分泌型糖蛋白(Wnt)/β-链蛋白(β-catenin),核转录因子-κB(NF-κB),环磷酸腺苷(cAMP)依赖蛋白激酶(PKA)/cAMP/cAMP应答元件結合蛋白(CREB),细胞外信号调节激酶(ERK)和p38有丝分裂原活化蛋白激酶(MAPK),磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(protein kinase B,Akt)/内皮型一氧化氮合酶(eNOS)/NO/环磷鸟苷(cGMP)/cGMP依赖性蛋白激酶(PKG),RhoA-TAZ和PI3K/Akt/下调糖原合成激酶3β(GSK3β)/β-catenin等多个信号通路,显著地成骨作用使其成为治疗骨质疏松症的首选先导化合物。回顾文献,淫羊藿苷对于调节神经系统,保护心血管,调节免疫系统,改善性功能和抗肿瘤等机制研究方面缺乏详细的总结。为了加快淫羊藿苷药理作用分子机制的探索和发现,扩大其应用前景,本文综述近年来淫羊藿苷的药理作用及分子机制研究进展,为临床合理用药和新药研发提供参考依据。
Epimedii Folium is a type of traditional Chinese medicine with effects of nourishing liver and kidney
strengthening the bones and muscles and expelling wind-damp. It is the main component of formulation that could nourish the kidney
strengthen yang and treat impotency
and mainly used for treatment of kidney yang deficiency
rheumatism
osteoporosis and paralysis. Recent studies have shown that icariin is the most abundant flavonoid component in Epimedii and exerts extensive bioactivities of anti-inflammation
anti-oxidant stress
anti-depression and anti-tumor. The molecular pharmacology studies showed that icariin could be used to treat nervous system diseases
osteoporosis
cardiovascular diseases
immune disease and reproductive system diseases by regulating multiple targets and signaling pathways. The protective mechanisms of icariin on skeletal system were extensively studied
involving estrogen receptor α(ERα)-Wnt/beta-catenin
nuclear transcription factor-κB(NF-κB)
cyclic adenosine monophosphate(cAMP) dependent protein kinase(PKA)/cAMP/cAMP response element-binding protein(CREB)
extraeellular-signalregulatedki-nase(ERK)
p38 mitogen-activated protein kinase(MAPK)
RhoA-TAZ
phosphatidylinositol-3-kinases(PI3K)/protein kinase B(Akt)/glycogen synthase kinase 3β(GSK3β)/β-catenin
PI3K/Akt/endothelial nitric oxide synthase(eNOS)/NO/Cyclic guanosinc monophosphate(cGMP)/cGMP protein kinase G(PKG) and other signaling pathways. The significant osteogenesis effects made it a preferred compound in treatment of osteoporosis. However
there was only a few summaries on icariin's mechanisms in regulating the nervous system
protecting the cardiovascular system
regulating the immune system
improving the reproductive function and resisting tumor. In order to accelerate the exploration
discover other molecular mechanisms of icariin
and expand its application prospects
this study reviewed the progress of pharmacological studies on icariin in recent years
and elaborated the effect targets and pertinent pathways
so as to provide the reference for the rational clinical medication and drug research and development.
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