Is yohimbine-induced increase in salivary secretion a kinin-dependent mechanism?

Fundam Clin Pharmacol. 1992;6(1):17-20. doi: 10.1111/j.1472-8206.1992.tb00089.x.

Abstract

We have previously reported that the alpha 2-adrenoceptor antagonist yohimbine induced a significant increase in both salivary flow rate and kallikrein output. In order to assess the possible role of the kinin-kallikrein system in the increase in salivary secretion elicited by yohimbine, the effects of aprotinin, an inhibitor of kallikrein activity, were investigated in yohimbine-treated conscious dogs. Aprotinin (at a dose, 5000 IU/kg iv, which reduced both resting and yohimbine-induced increase in kininogenase and amidolytic activities of saliva) which remained inactive alone, failed to modify the increase in salivary volume elicited by yohimbine (0.5 mg/kg iv). These results show that the rise in salivary flow rate observed under alpha 2-adrenoceptor antagonist is not induced by the kinin-kallikrein system. The release of kallikrein into saliva observed after yohimbine is rather the consequence than the cause of the increase in salivary secretion.

MeSH terms

  • Animals
  • Aprotinin / pharmacology
  • Dogs
  • Female
  • Kallikreins / analysis
  • Kinins / physiology*
  • Male
  • Saliva / chemistry
  • Salivation / drug effects*
  • Yohimbine / pharmacology*

Substances

  • Kinins
  • Yohimbine
  • Aprotinin
  • Kallikreins