Prenatal exposure to nicotine attenuates stress-induced hyperthermia in 7- to 8-week-old rats upon exposure to a novel environment

Physiol Behav. 2001 Nov-Dec;74(4-5):595-601. doi: 10.1016/s0031-9384(01)00609-6.

Abstract

Given that approximately 25% of women in the United States continue to smoke cigarettes during pregnancy, it is important to know if exposure to nicotine during development alters the physiological response of the adult to the "stressors" of everyday life. Our current experiments were carried out to determine if prenatal exposure to nicotine alters "stress-induced hyperthermia" in adult rats upon exposure to a novel environment such as a simulated open field. Forty-eight rats (23 males and 25 females) were exposed to a simulated open field or left in their home cage at 7 to 8 weeks of postnatal life (i.e., adulthood as defined by the ability to reproduce) following prenatal exposure to vehicle or nicotine (6 mg of nicotine tartrate per kilogram of maternal body weight per day) via a maternally implanted osmotic minipump from Day 6 or 7 of gestation. The simulated open field consisted of a 30(W)x60(L)x24(H)-in. white acrylic finish box illuminated by two hanging fluorescent lights and core temperature was measured by telemetry. Exposure to a simulated open field following prenatal exposure to vehicle elicited an increase in core temperature in male and female rats with a magnitude of approximately 1.2 degrees C and a duration of greater than 170 min. Prenatal exposure to nicotine significantly attenuated the thermogenic response of both genders; this was not only evident in the latency, magnitude and duration of the core temperature response but also in the core temperature index determined from the 3-h period following exposure to a simulated open field. Thus, our data provide evidence that prenatal exposure to nicotine attenuates stress-induced hyperthermia in male and female 7- to 8-week-old rats upon exposure to a "stressor" of everyday life (i.e., a novel environment).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arousal / drug effects*
  • Body Temperature Regulation / drug effects*
  • Female
  • Gestational Age
  • Homeostasis / drug effects
  • Male
  • Nicotine / pharmacology*
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • Rats
  • Social Environment*

Substances

  • Nicotine