Published ahead of print on February 28, 2008, doi:10.1164/rccm.200711-1739OC
© 2008 American Thoracic Society doi: 10.1164/rccm.200711-1739OC
Respiratory Control in Neonatal Rats Exposed to Prenatal Cigarette Smoke1 Department of Pediatrics and 2 Department of Physiology and Biophysics, Institute of Maternal and Child Health, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada Correspondence and requests for reprints should be addressed to Shabih U. Hasan, M.D., Health Sciences Center, 3330 Hospital Drive NW, Calgary, AB, T2N 4N1, Canada. E-mail: hasans{at}ucalgary.ca Rationale: Prenatal cigarette smoke (CS) exposure, increased environmental temperature, and hypoxic episodes have been postulated as major risk factors for sudden infant death syndrome. Objectives: To test the hypothesis that maternal CS exposure disrupts eupneic breathing and depresses breathing responses of neonatal rats to thermal and hypoxic challenges. Methods: Experiments were performed on 1-week-old rat pups exposed prenatally to CS (n = 39) or room air (sham; n = 30). Breathing patterns were recorded by whole-body plethysmography during thermoneutral or hyperthermic states under normoxic and hypoxic conditions. Measurements and Main Results: Mean pup weight, breaths per minute, and gasping respiratory patterns were measured for both smoke- and sham-exposed groups during thermoneutral and hyperthermic states under normoxic and hypoxic conditions. Under thermoneutral conditions, hypoxia caused gasping in CS-exposed animals but not in sham-exposed animals. Furthermore, under hyperthermic conditions, whereas hypoxia induced gasping in both groups, only CS-exposed animals exhibited a pronounced and longer lasting respiratory depression after the termination of hypoxia. Conclusions: We show that prenatal CS exposure increases the likelihood of gasplike respiration and provide the first experimental evidence that the combined effects of prenatal CS exposure and hyperthermia dramatically prolong the time required for neonates to return to eupneic breathing after hypoxia. These observations provide important evidence of how prenatal CS exposure, hypoxic episodes, and hyperthermia might place infants at higher risk for sudden infant death syndrome.
Key Words: apnea hyperthermia hypoxia nicotine sudden infant death syndrome
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