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The effects of tetramethylpyrazine on the incidence of arrhythmias and the release of PGI2 and TXA2 in the ischemic rat heart.

Abstract
Pretreatment with tetramethylpyrazine (TMP, 12 mg/kg/day), a drug originally derived from the rhizomes of Ligusticum wallichii, significantly reduced the incidence of ischemia-induced ventricular tachycardia (VT) and fibrillation (VF) from 100% and 50% of control hearts to 41% (p < 0.05) and 0% (p < 0.05), respectively, in the ischemic rat heart. TMP also diminished the incidence of reperfusion-induced VT and VF from 100% and 100% of control hearts to 33% (p < 0.05) and 41% (p < 0.05), respectively. Pretreatment with TMP produced a slight, but significant increase of 6-keto-PGF1 alpha and a decrease of TXB2 production during aerobic perfusion. Ischemia and reperfusion markedly increased the release of 6-keto-PGF1 alpha and TXB2. Pretreatment with TMP significantly enhanced the release of 6-keto-PGF1 alpha and diminished TXB2 outflow following left coronary artery occlusion and reperfusion.
AuthorsJ Feng, G Wu, S Tang
JournalPlanta medica (Planta Med) Vol. 65 Issue 3 Pg. 268-70 (Apr 1999) ISSN: 0032-0943 [Print] GERMANY
PMID10232078 (Publication Type: Letter)
Chemical References
  • Pyrazines
  • Thromboxane A2
  • Epoprostenol
  • tetramethylpyrazine
Topics
  • Animals
  • Arrhythmias, Cardiac (prevention & control)
  • Epoprostenol (metabolism)
  • Heart (drug effects)
  • Male
  • Myocardial Ischemia (metabolism)
  • Pyrazines (pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • Thromboxane A2 (metabolism)

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