학술논문

ENDOTHELIN IN THE CENTRAL CONTROL OF CARDIOVASCULAR AND RESPIRATORY FUNCTIONS.
Document Type
Article
Source
Clinical & Experimental Pharmacology & Physiology. Dec99, Vol. 26 Issue 12, p989-994. 6p. 1 Diagram, 4 Charts.
Subject
*ENDOTHELINS
*CENTRAL nervous system
*LABORATORY mice
Language
ISSN
0305-1870
Abstract
SUMMARY1. Exogenously administered endothelin (ET) modulates the activity of cardiovascular and respiratory neurons in the central nervous system (CNS) and, thus, affects arterial blood pressure (ABP) and ventilation. However, a physiological role(s) for endogenous ET in the CNS has not been elucidated. To address this question, we examined ABP and ventilation in mutant mice deficient in ET-1, ETA and ETB receptors and endothelin- converting enzyme-1, which were made by gene targeting. 2. Respiratory frequency and volume was measured in mice by whole body plethysmography when animals breathed normal room air and hypoxic and hypercapnic gas mixtures. A few days after respiratory measurements, a catheter was implanted into the femoral artery under halothane anaesthesia. On the following day, the ABP of awake mice was measured through the indwelling catheter and heart rate was calculated from the ABP signal. After 2 h ABP measurement, arterial blood was collected through the catheter and pH and the partial pressures of O2 and CO2 were measured by a blood gas analyser. 3. Compared with corresponding controls, the mean (±SEM) ABP in ET-1+/– and ETB-deficient mice was significantly higher (118±2 vs 106±3 mmHg for ET-1+/– (n = 22) and ET-1+/+ (n = 17) mice, respectively; 127±3 vs 109±4 mmHg for ETB–/s (n = 9) and ETB+/s (n = 9) mice, respectively; P < 0.05 for both). In ET-1+/– mice, PCO2 tended to be higher and PO2 was significantly lower than corresponding values in ET-1+/+ mice. Under resting conditions, there was no significant difference in respiratory parameters between mutants and their corresponding controls. However, reflex increases of ventilation to hypoxia and hypercapnia were significantly attenuated in ET-1+/–,... [ABSTRACT FROM AUTHOR]