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J Appl Physiol 102: 2201-2206, 2007. First published March 15, 2007; doi:10.1152/japplphysiol.01436.2006
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Respiratory syncytial virus infection in anesthetized weanling rather than adult rats prolongs the apneic responses to right atrial injection of capsaicin

Wenhong Peng, Jianguo Zhuang, Kevin S. Harrod, and Fadi Xu

Pathophysiology Program, Lovelace Respiratory Research Institute, Albuquerque, New Mexico

Submitted 18 December 2006 ; accepted in final form 14 March 2007

Apnea is a common complication in infants infected by respiratory syncytial virus (RSV). A recent study has shown that intranasal inoculation of RSV in conscious weanling rats strengthens the apneic responses to right atrial injection of capsaicin (CAP), leading to 66% mortality. The objectives of the present study were to determine 1) whether RSV infection changes baseline minute ventilation (VE) and arterial blood gases in anesthetized rats; 2) what the effects of RSV infection are on the respiratory responses to CAP; and 3) whether the RSV-strengthened apneic responses are age dependent. Our experiments were conducted in anesthetized and spontaneously breathing rats divided into four groups of weanling and adult rats that received either intranasal inoculation of RSV or virus-free medium. Two days after RSV infection (0.7 ml/kg), animal blood gases, baseline VE, and VE responses to right atrial injection of three doses of CAP (4, 16, and 64 µg/kg) were measured and compared among the four groups. Our results showed that RSV infection increased respiratory frequency (~25%, P < 0.05) in weanling but not adult rats, with little effect on arterial blood gases. RSV infection amplified the apneic responses to CAP in weanling but not adult rats, characterized by increases in the initial (40%) and the longest apneic duration (650%), the number of apneic episodes (139%), and the total duration of apneas (60%). These amplifications led to 50% mortality (P < 0.05). We conclude that RSV infection increases respiratory frequency and strengthens the apneic responses to CAP only in anesthetized weanling but not adult rats.

age; hypoxia; upper airway infection; bronchopulmonary C fibers



Address for reprint requests and other correspondence: F. Xu, Lovelace Respiratory Research Institute, Pathophysiology Program, 2425 Ridgecrest Dr. SE, Albuquerque, NM 87108 (e-mail: fxu{at}lrri.org)







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