Reduced Progesterone Metabolites Are Not Critical for Plus-Maze Performance of Lactating Female Rats

Lactation has been associated with anxiolysis in several tests of anxiety. These observations, considered together with observations that progesterone and its 5α-reduced metabolites are anxiolytic in cycling, nonlactating females, raised the question of whether the changes in anxiety-related behavio...

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Veröffentlicht in:Pharmacology, biochemistry and behavior biochemistry and behavior, 1999-07, Vol.63 (3), p.441-448
Hauptverfasser: Kellogg, Carol K, Barrett, Kathy A
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Barrett, Kathy A
description Lactation has been associated with anxiolysis in several tests of anxiety. These observations, considered together with observations that progesterone and its 5α-reduced metabolites are anxiolytic in cycling, nonlactating females, raised the question of whether the changes in anxiety-related behaviors that accompany lactation are driven by reduced progesterone metabolites. Lactating female rats were tested on the plus-maze on postpartum days 2 or 7, and demonstrated enhanced open-arm performance relative to cycling, nonlactating females. Hormonal analysis indicated that while serum levels of both progesterone and its 3α,5α-reduced metabolite were increased in lactating females, the turnover of progesterone to the metabolite was markedly reduced during lactation. Furthermore, treatment with a 5α-reductase inhibitor for 3 days prior to testing potentiated the open-arm performance in lactating females, implying that enhanced open-arm performance was not mediated by the reduction of progesterone or other steroids. Additionally, analysis of GABA A receptor function indicated that parturition and lactation did not alter the sensitivity of the receptor to GABA or to modulation by reduced steroids. The mechanisms driving enhanced plus-maze behavior in lactating females appear to differ from mechanisms identified in nonlactating females.
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These observations, considered together with observations that progesterone and its 5α-reduced metabolites are anxiolytic in cycling, nonlactating females, raised the question of whether the changes in anxiety-related behaviors that accompany lactation are driven by reduced progesterone metabolites. Lactating female rats were tested on the plus-maze on postpartum days 2 or 7, and demonstrated enhanced open-arm performance relative to cycling, nonlactating females. Hormonal analysis indicated that while serum levels of both progesterone and its 3α,5α-reduced metabolite were increased in lactating females, the turnover of progesterone to the metabolite was markedly reduced during lactation. Furthermore, treatment with a 5α-reductase inhibitor for 3 days prior to testing potentiated the open-arm performance in lactating females, implying that enhanced open-arm performance was not mediated by the reduction of progesterone or other steroids. 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The mechanisms driving enhanced plus-maze behavior in lactating females appear to differ from mechanisms identified in nonlactating females.</description><subject>5-alpha Reductase Inhibitors</subject><subject>5α-Reductase</subject><subject>Adaptive behavior</subject><subject>Aminoacid receptors (glycine, glutamate, gaba)</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Behavioral psychophysiology</subject><subject>Biological and medical sciences</subject><subject>Cell receptors</subject><subject>Cell structures and functions</subject><subject>Cerebral Cortex - drug effects</subject><subject>Cerebral Cortex - enzymology</subject><subject>Cerebral Cortex - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Finasteride - analogs &amp; derivatives</subject><subject>Finasteride - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GABA A Receptors</subject><subject>Hormones and behavior</subject><subject>Lactation - drug effects</subject><subject>Lactation - physiology</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Maze Learning - physiology</subject><subject>Molecular and cellular biology</subject><subject>Progesterone - blood</subject><subject>Progesterone - metabolism</subject><subject>Progesterone - physiology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. 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Psychology</topic><topic>GABA A Receptors</topic><topic>Hormones and behavior</topic><topic>Lactation - drug effects</topic><topic>Lactation - physiology</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Maze Learning - physiology</topic><topic>Molecular and cellular biology</topic><topic>Progesterone - blood</topic><topic>Progesterone - metabolism</topic><topic>Progesterone - physiology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. 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subjects 5-alpha Reductase Inhibitors
5α-Reductase
Adaptive behavior
Aminoacid receptors (glycine, glutamate, gaba)
Animals
Anxiety
Behavioral psychophysiology
Biological and medical sciences
Cell receptors
Cell structures and functions
Cerebral Cortex - drug effects
Cerebral Cortex - enzymology
Cerebral Cortex - metabolism
Enzyme Inhibitors - pharmacology
Female
Finasteride - analogs & derivatives
Finasteride - pharmacology
Fundamental and applied biological sciences. Psychology
GABA A Receptors
Hormones and behavior
Lactation - drug effects
Lactation - physiology
Male
Maze Learning - drug effects
Maze Learning - physiology
Molecular and cellular biology
Progesterone - blood
Progesterone - metabolism
Progesterone - physiology
Psychology. Psychoanalysis. Psychiatry
Psychology. Psychophysiology
Rats
Rats, Long-Evans
Receptors, GABA-A - drug effects
Vigilance
title Reduced Progesterone Metabolites Are Not Critical for Plus-Maze Performance of Lactating Female Rats
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