Chlordiazepoxide-Induced Spatial Learning Deficits: Dose-Dependent Differences Following Prenatal Malnutrition

The sensitivity of prenatally protein-malnourished rats to the amnestic properties of the benzodiazepine (BZ) receptor agonist, chlordiazepoxide (CDP), was studied in the male offspring of rats provided with a protein-deficient diet (6% casein) for 5 weeks prior to mating and throughout pregnancy. R...

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Veröffentlicht in:Pharmacology, biochemistry and behavior biochemistry and behavior, 2000, Vol.65 (1), p.105-116
Hauptverfasser: Tonkiss, John, Shultz, Penny L, Shumsky, Jed S, Fiacco, Todd A, Vincitore, Michele, Rosene, Douglas L, Galler, Janina R
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container_issue 1
container_start_page 105
container_title Pharmacology, biochemistry and behavior
container_volume 65
creator Tonkiss, John
Shultz, Penny L
Shumsky, Jed S
Fiacco, Todd A
Vincitore, Michele
Rosene, Douglas L
Galler, Janina R
description The sensitivity of prenatally protein-malnourished rats to the amnestic properties of the benzodiazepine (BZ) receptor agonist, chlordiazepoxide (CDP), was studied in the male offspring of rats provided with a protein-deficient diet (6% casein) for 5 weeks prior to mating and throughout pregnancy. Rats were tested during acquisition of the submerged platform version of the Morris water maze task using three systemic doses of CDP (3.2, 5.6, and 7.5 mg/kg IP) at two ages (day 30 and day 90). At 30 days, prenatally malnourished rats showed less sensitivity to the amnestic effect of the 5.6-mg/kg dose when compared with well-nourished controls by displaying shorter swim paths during acquisition and a more selective search of the target quadrant upon removal of the platform (probe trial). At 90 days, prenatally malnourished rats again showed less sensitivity to CDP at a dose of 5.6 mg/kg, but more sensitivity to the 3.2-mg/kg dose (indicated on the probe trial). No obvious relationship was identified between the nutritional group differences in behavioral sensitivity to CDP at 90 days and their BZ receptor density in the hippocampus or medial septum. It can be concluded that prenatal malnutrition alters the amnestic response to CDP in a dose-dependent and developmentally specific manner, thus providing further support for functional changes within the GABAergic system subsequent to malnutrition.
doi_str_mv 10.1016/S0091-3057(99)00182-3
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Rats were tested during acquisition of the submerged platform version of the Morris water maze task using three systemic doses of CDP (3.2, 5.6, and 7.5 mg/kg IP) at two ages (day 30 and day 90). At 30 days, prenatally malnourished rats showed less sensitivity to the amnestic effect of the 5.6-mg/kg dose when compared with well-nourished controls by displaying shorter swim paths during acquisition and a more selective search of the target quadrant upon removal of the platform (probe trial). At 90 days, prenatally malnourished rats again showed less sensitivity to CDP at a dose of 5.6 mg/kg, but more sensitivity to the 3.2-mg/kg dose (indicated on the probe trial). No obvious relationship was identified between the nutritional group differences in behavioral sensitivity to CDP at 90 days and their BZ receptor density in the hippocampus or medial septum. 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subjects Animals
Anti-Anxiety Agents - pharmacology
Benzodiazepine receptor agonist
Biological and medical sciences
Body Weight - drug effects
CDP
Chlordiazepoxide
Chlordiazepoxide - pharmacology
Chlorides - metabolism
Dose-Response Relationship, Drug
Female
Flunitrazepam - metabolism
Gene Expression Regulation, Developmental
Learning Disorders - chemically induced
Medical sciences
Metabolic diseases
Morris maze
Motor Activity - drug effects
Other nutritional diseases (malnutrition, nutritional and vitamin deficiencies...)
Pregnancy
Pregnancy Complications
Prenatal protein malnutrition
Protein Deficiency - complications
Protein restriction
Rats
Rats, Sprague-Dawley
Receptors, GABA-A - genetics
Receptors, GABA-A - physiology
Water maze
title Chlordiazepoxide-Induced Spatial Learning Deficits: Dose-Dependent Differences Following Prenatal Malnutrition
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