Related Experiment Video
Updated: Jun 16, 2026

A Preterm Rat Model for Pain Studies
Published on: February 9, 2024
Gestational nicotine exposure exaggerates hyperthermic enhancement of laryngeal chemoreflex in rat pups
L Xia1, J C Leiter, D Bartlett
1Department of Physiology, Dartmouth Medical School, Lebanon, NH 03756, USA.
Laryngeal chemoreflex (LCR) apnea occurs in infant mammals in response to water or other liquids in the laryngeal lumen and is suspected to contribute to some cases of the sudden infant death syndrome. We have previously found that the LCR is prolonged in neonatal piglets and rats that are warmed 1-3 degrees C above their normal body temperatures and that this prolongation is exaggerated in rat pups whose mothers have been exposed to cigarette smoke during pregnancy. We have therefore examined the effects on the LCR of combined prenatal nicotine exposure and brief postnatal hyperthermia. Nicotine was infused in pregnant rats via implanted osmotic minipumps (6.5mg/kg per day) from gestational day 3 (G3) until G21, the day of delivery. Control animals received saline infusions. On postnatal days 4-12, LCR apnea and respiratory disruption, elicited by intralaryngeal water, were measured with and without hyperthermia in anesthetized pups. The results indicate that prenatal exposure to nicotine significantly exaggerates the hyperthermic prolongation of the LCR.
Laryngeal chemoreflex (LCR) apnea occurs in infant mammals in response to water or other liquids in the laryngeal lumen and is suspected to contribute to some cases of the sudden infant death syndrome. We have previously found that the LCR is prolonged in neonatal piglets and rats that are warmed 1-3 degrees C above their normal body temperatures and that this prolongation is exaggerated in rat pups whose mothers have been exposed to cigarette smoke during pregnancy. We have therefore examined the effects on the LCR of combined prenatal nicotine exposure and brief postnatal hyperthermia. Nicotine was infused in pregnant rats via implanted osmotic minipumps (6.5mg/kg per day) from gestational day 3 (G3) until G21, the day of delivery. Control animals received saline infusions. On postnatal days 4-12, LCR apnea and respiratory disruption, elicited by intralaryngeal water, were measured with and without hyperthermia in anesthetized pups. The results indicate that prenatal exposure to nicotine significantly exaggerates the hyperthermic prolongation of the LCR.
More Related Videos
15:27Construction of Vapor Chambers Used to Expose Mice to Alcohol During the Equivalent of all Three Trimesters of Human Development
Published on: July 13, 2014
05:13Preclinical Model of Prenatal Delta-9-Tetrahydrocannabinol Exposure to Assess Its Impact on Neurodevelopmental Outcomes
Published on: February 28, 2025