Effect of protriptyline on ventilatory responses to hypercapnia and asphyxia in normal subjects

Eur Respir J. 1989 Sep;2(8):758-62.

Abstract

A double-blind crossover study was undertaken to assess the effect of protriptyline on ventilatory responses in normal subjects. Seven subjects received in random order placebo, 10 mg and 20 mg protriptyline daily for 2 weeks. Measurements of hypercapnic ventilatory response (HCVR) and asphyxial hypoxic ventilatory response (HVR) were made before treatment, 6-8 h after the first dose, and after 2 weeks treatment. Mean HCVR and HVR following 10 mg and 20 mg protriptyline did not differ significantly from measurements on placebo, neither for the single dose study or after 2 weeks.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Dibenzocycloheptenes / pharmacology*
  • Double-Blind Method
  • Female
  • Humans
  • Hypercapnia / drug therapy*
  • Hypoxia / drug therapy*
  • Male
  • Protriptyline / pharmacology*
  • Pulmonary Gas Exchange / drug effects
  • Randomized Controlled Trials as Topic

Substances

  • Dibenzocycloheptenes
  • Protriptyline