Effect of emodin on NO-cGMP signal pathway in rat vascular endothelium in vitro / 中国中西医结合杂志
Chinese Journal of Integrated Traditional and Western Medicine
;
(12): 636-639, 2006.
Article
in Chinese
| WPRIM
| ID: wpr-230141
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the vasorelaxation effect of emodin and its relationship with NO-cGMP signal pathway.</p><p><b>METHODS</b>Changes of tension of rat thoracic aortic rings were measured by MedLab biologic signal collection system, and the activity of total nitric oxide synthase (tNOS), constitutive NOS (cNOS) and inducible NOS (iNOS) in endothelium after being treated with emodin was determined with nitric acid reductase method.</p><p><b>RESULTS</b>Emodin relaxed the phenylephrine and potasium chlorate induced contraction of aortic rings, either with or without intact endothelium, in a concentration-dependent manner. Pretreatment of no-specific potassium channel blocker strontium chloride (CsCL) could attenuate the vasorelaxation effect of emodin on aortic rings without intact endothelium, but it could not inhibit vasorelaxation of emodin on aortic rings with intact endothelium. This vasorelaxation action of emodin (40 micromol/L) could be partial blocked by NOS inhibitor L-NAME and guanylate cyclase inhibitor ODQ, with the vasorelaxation range dropped to 64.76 +/- 13.73% and 6.28 +/- 4.79% respectively. Moreover, emodin (40 micromol/L) increased iNOS activity significantly.</p><p><b>CONCLUSION</b>The concentration-dependent vasorelaxation effect of emodin might act by activating the NO-cGMP pathway in vascular endothelium.</p>
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Aorta, Thoracic
/
Pharmacology
/
Vasodilator Agents
/
Endothelium, Vascular
/
Signal Transduction
/
Emodin
/
Rats, Sprague-Dawley
/
Cyclic GMP
/
Cell Biology
/
Metabolism
Limits:
Animals
Language:
Chinese
Journal:
Chinese Journal of Integrated Traditional and Western Medicine
Year:
2006
Type:
Article
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