Role of cGMP signals in tetramethylpyrazine induced relaxation of the isolated rat aortic strip

Life Sci. 2005 Aug 12;77(13):1416-24. doi: 10.1016/j.lfs.2004.12.045.

Abstract

In the present study, role of guanosine-3',5'-cyclic monophosphate (cGMP) in the vasodilatation of tetramethylpyrazine (TMP), one of the active ingredients of the Chinese herb Chuang-xion, was investigated. We found that the TMP could decrease the vascular tone of isolated rat aorta precontracted with phenylephrine (10(-8) M) in a concentration-dependent manner from 10(-5) M to 10(-3) M. Also, the TMP-induced relaxation was reduced by 1H-(1,2,4)-oxadiazol-(4,3-a)-quinoxalin-1-one (ODQ) or methylene blue, the inhibitor of soluble guanylyl cyclase. Moreover, the vasodilative response to TMP was enhanced significantly in the presence of sildenafil, a well-known inhibitor of phosphodiestrase type 5 that is sensitive to cGMP. In addition, TMP could increase the cGMP level in the isolated aortic rings and TMP-induced vasodilatation was deleted by cGMP-dependent protein kinases (PKG) blockade. These results suggest that relaxation of rat aortic strip by TMP is induced in the cGMP-dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / drug effects*
  • Aorta / physiology
  • Cyclic GMP / physiology*
  • Cyclic GMP-Dependent Protein Kinases / antagonists & inhibitors
  • Guanylate Cyclase / antagonists & inhibitors
  • In Vitro Techniques
  • Male
  • Pyrazines / pharmacology*
  • Rats
  • Rats, Wistar
  • Vasodilation / drug effects*

Substances

  • Pyrazines
  • Cyclic GMP-Dependent Protein Kinases
  • Guanylate Cyclase
  • Cyclic GMP
  • tetramethylpyrazine