Amphetamine and stress responses in developmentally lead-exposed rats. 2004

Miriam B Virgolini, and M Volosin, and A S Fulginiti, and L M Cancela
Department of Pharmacology, Faculty of Chemical Sciences, National University of Cordoba, Cordoba, Argentina. virgolin@eohsi.rutgers.edu

In this study, pregnant Wistar dams were exposed to 220 ppm of lead (Pb) in drinking water during gestation and lactation. The response to the locomotor-stimulating effects of 0.5 mg/kg of amphetamine (AMPH) was evaluated in 35-day-old male offspring. The results demonstrated that developmental Pb exposure induced no differences in the response to the drug, although an increase in locomotor activity induced by a single saline (SAL) injection was observed selectively in the Pb-exposed group. Considering evidence that suggests a relationship between increased locomotor activity and stress response, a time course analysis of corticosterone (CS) secretion and locomotor performance was carried out. Higher basal levels of CS and elevated stress-induced secretion of this hormone in response to the injection were observed in Pb-exposed rats compared to controls, a pattern that showed a time-related increase in locomotor activity. Habituation to SAL injections prior to testing restored both CS secretion and locomotor response to SAL to levels comparable to controls and did not modify AMPH locomotor response measured in these new experimental conditions. Additionally, we demonstrated that these behavioral/hormonal disruptions were no longer detectable later in adulthood. Collectively, these data suggest that the stimulant-locomotor effect of AMPH in Pb-exposed rats is independent of the arousal of the animal at the time of its administration. They also support a unique profile of integrated behavioral and hormonal hyperresponsiveness in 35-day-old low-level Pb-exposed rats evidenced as hyperlocomotion and altered secretion of CS in response to an environmental manipulation, an effect that was no longer present later in life.

UI MeSH Term Description Entries
D007854 Lead A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
D008297 Male Males
D009043 Motor Activity Body movements of a human or an animal as a behavioral phenomenon. Activities, Motor,Activity, Motor,Motor Activities
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D011297 Prenatal Exposure Delayed Effects The consequences of exposing the FETUS in utero to certain factors, such as NUTRITION PHYSIOLOGICAL PHENOMENA; PHYSIOLOGICAL STRESS; DRUGS; RADIATION; and other physical or chemical factors. These consequences are observed later in the offspring after BIRTH. Delayed Effects, Prenatal Exposure,Late Effects, Prenatal Exposure
D003345 Corticosterone An adrenocortical steroid that has modest but significant activities as a mineralocorticoid and a glucocorticoid. (From Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p1437)
D004347 Drug Interactions The action of a drug that may affect the activity, metabolism, or toxicity of another drug. Drug Interaction,Interaction, Drug,Interactions, Drug
D005106 Exploratory Behavior The tendency to explore or investigate a novel environment. It is considered a motivation not clearly distinguishable from curiosity. Curiosity,Novelty-Seeking Behavior,Behavior, Exploratory,Behavior, Novelty-Seeking,Behaviors, Exploratory,Behaviors, Novelty-Seeking,Curiosities,Exploratory Behaviors,Novelty Seeking Behavior,Novelty-Seeking Behaviors
D005260 Female Females
D006185 Habituation, Psychophysiologic The disappearance of responsiveness to a repeated stimulation. It does not include drug habituation. Habituation (Psychophysiology),Habituation, Psychophysiological,Psychophysiologic Habituation,Psychophysiological Habituation,Habituations (Psychophysiology)

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