Ventilatory effects of 8 h of isocapnic hypoxia with and without b-blockade in humans

نویسندگان

  • CHRISTINE CLAR
  • KEITH L. DORRINGTON
  • PETER A. ROBBINS
چکیده

Clar, Christine, Keith L. Dorrington, and Peter A. Robbins. Ventilatory effects of 8 h of isocapnic hypoxia with and without b-blockade in humans. J. Appl. Physiol. 86(6): 1897–1904, 1999.—This study investigated whether changing sympathetic activity, acting via b-receptors, might induce the progressive ventilatory changes observed in response to prolonged hypoxia. The responses of 10 human subjects to four 8-h protocols were compared: 1) isocapnic hypoxia (endtidal PO2 5 50 Torr) plus 80-mg doses of oral propranolol; 2) isocapnic hypoxia, as in protocol 1, with oral placebo; 3) air breathing with propranolol; and 4) air breathing with placebo. Exposures were conducted in a chamber designed to maintain end-tidal gases constant by computer control. Ventilation (V̇E) was measured at regular intervals throughout. Additionally, the subjects’ ventilatory hypoxic sensitivity and their residual V̇E during hyperoxia (5 min) were assessed at 0, 4, and 8 h by using a dynamic end-tidal forcing technique. b-Blockade did not significantly alter either the rise in V̇E seen during 8 h of isocapnic hypoxia or the changes observed in the acute hypoxic ventilatory response and residual V̇E in hyperoxia over that period. The results do not provide evidence that changes in sympathetic activity acting via b-receptors play a role in the mediation of ventilatory changes observed during 8 h of isocapnic hypoxia.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ventilatory effects of 8 h of isocapnic hypoxia with and without beta-blockade in humans.

This study investigated whether changing sympathetic activity, acting via beta-receptors, might induce the progressive ventilatory changes observed in response to prolonged hypoxia. The responses of 10 human subjects to four 8-h protocols were compared: 1) isocapnic hypoxia (end-tidal PO2 = 50 Torr) plus 80-mg doses of oral propranolol; 2) isocapnic hypoxia, as in protocol 1, with oral placebo;...

متن کامل

Modulation of ventilatory sensitivity to hypoxia by dopamine and domperidone before and after prolonged exposure to hypoxia in humans.

Effect of 8 Hours of Isocapnic/Poikilocapnic Hypoxia on the Ventilatory Response to CO[subscript 2] p. 17 Ventilatory Responses to Hypoxia after 6 Hours Passive Hyperventilation in Humans p. 21 Ventilatory Effects of 8 Hours of Isocapnic Hypoxia with and without [beta]-Blockade p. 25 Modulation of Ventilatory Sensitivity to Hypoxia by Dopamine and Domperidone before and after Prolonged Exposure...

متن کامل

Respiratory control in humans after 8 h of lowered arterial PO2, hemodilution, or carboxyhemoglobinemia.

In humans exposed to 8 h of isocapnic hypoxia, there is a progressive increase in ventilation that is associated with an increase in the ventilatory sensitivity to acute hypoxia. To determine the relative roles of lowered arterial PO2 and oxygen content in generating these changes, the acute hypoxic ventilatory response was determined in 11 subjects after four 8-h exposures: 1) protocol IH (iso...

متن کامل

Effects of haloperidol on ventilation during isocapnic hypoxia in humans.

Exposure to isocapnic hypoxia produces an abrupt increase in ventilation [acute hypoxic ventilatory response (AHVR)], which is followed by a subsequent decline [hypoxic ventilatory depression or decline (HVD)]. In cats, both anesthetized and awake, haloperidol has been reported to increase AHVR and almost entirely abolish HVD. To investigate whether this occurs in humans, the ventilatory respon...

متن کامل

Selected contribution: chemoreflex responses to CO2 before and after an 8-h exposure to hypoxia in humans.

The ventilatory sensitivity to CO2, in hyperoxia, is increased after an 8-h exposure to hypoxia. The purpose of the present study was to determine whether this increase arises through an increase in peripheral or central chemosensitivity. Ten healthy volunteers each underwent 8-h exposures to 1) isocapnic hypoxia, with end-tidal PO2 (PET(O2)) = 55 Torr and end-tidal PCO2 (PET(CO2)) = eucapnia; ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 1999