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Magnesium lithospermate B possesses inhibitory activity on Na^+,K^+-ATPase and neuroprotective effects against ischemic stroke
引用本文:Tzen JT,Jinn TR,Chen YC,Li FY,Cheng FC,Shi LS,She HKh,Chen BC,Hsieh V,Tu ML. Magnesium lithospermate B possesses inhibitory activity on Na^+,K^+-ATPase and neuroprotective effects against ischemic stroke[J]. Acta pharmacologica Sinica, 2007, 28(5): 609-615
作者姓名:Tzen JT  Jinn TR  Chen YC  Li FY  Cheng FC  Shi LS  She HKh  Chen BC  Hsieh V  Tu ML
摘    要:

关 键 词:紫草酸镁盐B  钠钾ATP酶  抑制活性  神经保护作用  缺血性中风  丹参酸

Magnesium lithospermate B possesses inhibitory activity on Na+,K+-ATPase and neuroprotective effects against ischemic stroke
Tzen Jason Tc,Jinn Tzyy-Rong,Chen Yi-Ching,Li Feng-Yin,Cheng Fu-Chou,Shi Li-Shian,She Hank Kh,Chen Balance Cm,Hsieh Vic,Tu Mu-Lin. Magnesium lithospermate B possesses inhibitory activity on Na+,K+-ATPase and neuroprotective effects against ischemic stroke[J]. Acta pharmacologica Sinica, 2007, 28(5): 609-615
Authors:Tzen Jason Tc  Jinn Tzyy-Rong  Chen Yi-Ching  Li Feng-Yin  Cheng Fu-Chou  Shi Li-Shian  She Hank Kh  Chen Balance Cm  Hsieh Vic  Tu Mu-Lin
Affiliation:[1]Graduate Institute of Biotechnology [2]Department of Chemistry, National Chung Hsing University, Taichung, Taiwan 402 China; [3]Stem Cell Medical Research Center, Department of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan 407 China; [4]Department of Biotechnology, National Formosa University, Yunlin, Taiwan 632 China [5]Herbal Source Biotechnology Co, Tainan County, Taiwan 741 China [6]Jason Life Tech lnc, National Chung Hsing University, Taichung, Taiwan 402 China
Abstract:AIM: To examine if magnesium lithospermate B (MLB) extracted from Danshen, the dried roots of Salvia miltiorrhiza, may act as an active component responsible for the cardiac therapeutic effect of this traditional Chinese herb via the same molecular mechanism triggered by cardiac glycosides, such as ouabain and digoxin. Moreover, we wanted to test if MLB may provide neuroprotection against ischemic stroke as observed for cardiac glycosides. METHODS: Similarity in the chemical structure and molecular configuration between MLB and ouabain was analyzed. The inhibition potency of MLB and ouabain on Na( +),K( +) -ATPase activity of a commercial product, as well as in purified membrane fractions from rat brain and heart tissues, was examined and compared. Neuroprotective effect of MLB against ischemic stroke was also evaluated using a cortical brain slice-based assay model. RESULTS: Dose-dependent inhibition on the commercial Na( +),K( +)-ATPase equivalent to that for ouabain was observed for MLB of approximately half dosage by weight. This relative potency of ouabain and MLB was also observed for their inhibition on Na( +),K( +)-ATPase activity of plasma membrane purified from rat tissues, although these 2 inhibitors exhibited somewhat lower competence in these crude extracts. In ischemic gerbil brains, post-treatment with MLB significantly reduced the infarct size, visualized by 2,3,5-triphenyltetrazolium chloride staining, by approximately 55% when compared with the control group. CONCLUSION: These results evidently suggest that the cardiac therapeutic effect of Danshen should be at least partly attributed to the effective inhibition of Na( +),K( +)-ATPase by MLB, and that MLB provides anti-ischemic neuroprotection in gerbils subjected to focal ischemia and reperfusion.
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