Magnesium lithospermate B possesses inhibitory activity on Na+,K+-ATPase and neuroprotective effects against ischemic stroke

被引:73
作者
Tzen, Jason T. C. [1 ]
Jinn, Tzyy-rong
Chen, Yi-ching
Li, Feng-yin
Cheng, Fu-chou
Shi, Li-shian
She, Hank K. H.
Chen, Balance C. M.
Hsieh, Vic
Tu, Mu-lin
机构
[1] Natl Chung Hsing Univ, Grad Inst Biotechnol, Taichung 402, Taiwan
[2] Natl Chung Hsing Univ, Dept Chem, Taichung 402, Taiwan
[3] Taichung Vet Gen Hosp, Dept Med Res, Stem Cell Med Res Ctr, Taichung 407, Taiwan
[4] Natl Formosa Univ, Dept Biotechnol, Yunlin 632, Taiwan
[5] Herbal Source Biotechnol Co, Tainan 741, Taiwan
[6] Natl Chung Hsing Univ, Jason LIfe Tech Inc, Taichung 402, Taiwan
关键词
cardiac glycosides; magnesium lithospermate B; Na+; K+-ATPase; neuroprotection; ouabain; Salvia miltiorrhiza;
D O I
10.1111/j.1745-7254.2007.00544.x
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
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.
引用
收藏
页码:609 / 615
页数:7
相关论文
共 33 条
[1]
Three-dimensional structure-activity relationship modeling of digoxin inhibition and docking to Na+,K+-ATPase [J].
Ball, WJ ;
Farr, CD ;
Paula, S ;
Keenan, SM ;
Delisle, RK ;
Welsh, WJ .
NA,K-ATPASE AND RELATED CATION PUMPS: STRUCTURE, FUNCTION, AND REGULATORY MECHANISMS, 2003, 986 :296-297
[2]
EVALUATION OF 2, 3, 5-TRIPHENYLTETRAZOLIUM CHLORIDE AS A STAIN FOR DETECTION AND QUANTIFICATION OF EXPERIMENTAL CEREBRAL INFARCTION IN RATS [J].
BEDERSON, JB ;
PITTS, LH ;
GERMANO, SM ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, HM .
STROKE, 1986, 17 (06) :1304-1308
[3]
Acute treatment with MgSO4 attenuates long-term hippocampal tissue loss after brain trauma in the rat [J].
Browne, KD ;
Leoni, MJ ;
Iwata, A ;
Chen, XH ;
Smith, DH .
JOURNAL OF NEUROSCIENCE RESEARCH, 2004, 77 (06) :878-883
[4]
Synthesis and inotropic activity of 1-(O-aminoalkyloximes) of perhydroindene derivatives as simplified digitalis-like compounds acting on the Na+,K+-ATPase [J].
Cerri, A ;
Almirante, N ;
Barassi, P ;
Benicchio, A ;
De Munari, S ;
Marazzi, G ;
Molinari, I ;
Serra, F ;
Melloni, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (01) :189-207
[5]
17β-O-aminoalkyloximes of 5β-androstane-3β,14β-diol with digitalis-like activity:: Synthesis, cardiotonic activity, structure-activity relationships, and molecular modeling of the Na+,K+-ATPase receptor [J].
Cerri, A ;
Almirante, N ;
Barassi, P ;
Benicchio, A ;
Fedrizzi, G ;
Ferrari, P ;
Micheletti, R ;
Quadri, L ;
Ragg, E ;
Rossi, R ;
Santagostino, M ;
Schiavone, A ;
Serra, F ;
Zappavigna, MP ;
Melloni, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (12) :2332-2349
[6]
A new approach to the design of novel inhibitors of Na+,K+-ATPase:: 17α-substituted seco-D 5β-androstane as cassaine analogues [J].
De Munari, S ;
Barassi, P ;
Cerri, A ;
Fedrizzi, G ;
Gobbini, M ;
Mabilia, M ;
Melloni, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (16) :3033-3040
[7]
FUNG KP, 1993, LIFE SCI, V53, P189
[8]
17α-O-(aminoalkyl)oxime derivatives of 3β,14β-dihydroxy-5β-androstane and 3β-hydroxy-14-oxoseco-D-5β-androstane as inhibitors of Na+,K+-ATPase at the digitalis receptor [J].
Gobbini, M ;
Barassi, P ;
Cerri, A ;
De Munari, S ;
Fedrizzi, G ;
Santagostino, M ;
Schiavone, A ;
Torri, M ;
Melloni, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (23) :3821-3830
[9]
GOLDBERG H, 1996, CLIN CHEM, V12, P871
[10]
DEFENSE STRATEGIES AGAINST HYPOXIA AND HYPOTHERMIA [J].
HOCHACHKA, PW .
SCIENCE, 1986, 231 (4735) :234-241