San-Huang-Xie-Xin-Tang reduces lipopolysaccharides-induced hypotension and inflammatory mediators
San-Huang-Xie-Xin-Tang (SHXT) is a traditional Chinese medicinal formula containing Coptidis rhizoma, Scutellariae radix and Rhei rhizoma. The present study aimed to determine the preventive effects of standardized SHXT on lipopolysaccharides (LPS)-induced arterial hypotension, protein expression of...
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Veröffentlicht in: | Journal of ethnopharmacology 2005-01, Vol.96 (1), p.99-106 |
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Sprache: | eng |
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Zusammenfassung: | San-Huang-Xie-Xin-Tang (SHXT) is a traditional Chinese medicinal formula containing
Coptidis rhizoma,
Scutellariae radix and
Rhei rhizoma. The present study aimed to determine the preventive effects of standardized SHXT on lipopolysaccharides (LPS)-induced arterial hypotension, protein expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), cytokines formation and prostaglandin E
2 (PGE
2) production. LPS-induced activation of iNOS has been recognized to increase cytokines and nitric oxide, some of them play predominant roles in sepsis. Intravenous injection of LPS (10
mg/kg) caused a marked decrease of the mean arterial pressure in normotensive rats. However, the LPS-induced arterial hypotension was inhibited by SHXT (0.01 and 0.03
g/kg), when it was given 30
min before LPS. Moreover, plasma level of cytokines and PGE
2 were lowered by SHXT. In RAW 264.7 cells, SHXT (20–200
μg/ml) dose-dependently inhibited LPS (1
μg/ml)-induced iNOS and COX-2 expression, and it also significantly decreased LPS-induced cytokines in a dose-dependent manner. In conclusion, our data suggest that SHXT prevented LPS-induced arterial hypotension, which might be mediated through its inhibition activities on the expression of iNOS and COX-2, cytokines formation and PGE
2 production. Therefore, its protection activity against LPS-induced arterial hypotension and inflammatory mediators release might be beneficial in the treatment of endotoxin shock and/or associated inflammation. |
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ISSN: | 0378-8741 1872-7573 |
DOI: | 10.1016/j.jep.2004.09.023 |