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Early postnatal effects of prenatal exposure to glucocorticoids on testosterone metabolism and biogenic monoamines in discrete neuroendocrine regions of the rat brain
We investigated the effects of hydrocortisone acetate and dexamethasone administered to pregnant rats during the last gestational week on sexual differentiation of testosterone metabolism and biogenic monoamine contents and turnover in the discrete brain regions in 10-day-old offspring. In the preop...
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Published in: | Comparative biochemistry and physiology. Toxicology & pharmacology 2004-06, Vol.138 (2), p.169-175 |
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container_title | Comparative biochemistry and physiology. Toxicology & pharmacology |
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creator | Reznikov, A.G. Nosenko, N.D. Tarasenko, L.V. |
description | We investigated the effects of hydrocortisone acetate and dexamethasone administered to pregnant rats during the last gestational week on sexual differentiation of testosterone metabolism and biogenic monoamine contents and turnover in the discrete brain regions in 10-day-old offspring. In the preoptic area, sex-dependent differences in aromatase activity were attenuated by prenatal glucocorticoids. Prenatal dexamethasone but not hydrocortisone acetate caused the inversion of sexual dimorphism of 5α-reductase activity in the preoptic area. In the brain preoptic area of the male pups prenatally exposed to hydrocortisone acetate, a decrease in noradrenaline turnover was found. Dopamine turnover in the preoptic area and 5-hydroxytryptamine metabolism in the preoptic area and medial basal hypothalamus increased in females as a result of hydrocortisone acetate treatment. Our results indicate that excess glucocorticoids in prenatal life modifies the basic neurochemical and neurophysiological mechanisms of sexual brain differentiation and might contribute to behavioral and reproductive disorders in adulthood. |
doi_str_mv | 10.1016/j.cca.2004.06.005 |
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In the preoptic area, sex-dependent differences in aromatase activity were attenuated by prenatal glucocorticoids. Prenatal dexamethasone but not hydrocortisone acetate caused the inversion of sexual dimorphism of 5α-reductase activity in the preoptic area. In the brain preoptic area of the male pups prenatally exposed to hydrocortisone acetate, a decrease in noradrenaline turnover was found. Dopamine turnover in the preoptic area and 5-hydroxytryptamine metabolism in the preoptic area and medial basal hypothalamus increased in females as a result of hydrocortisone acetate treatment. Our results indicate that excess glucocorticoids in prenatal life modifies the basic neurochemical and neurophysiological mechanisms of sexual brain differentiation and might contribute to behavioral and reproductive disorders in adulthood.</description><identifier>ISSN: 1532-0456</identifier><identifier>EISSN: 1878-1659</identifier><identifier>DOI: 10.1016/j.cca.2004.06.005</identifier><identifier>PMID: 15450864</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>5α-Reductase ; Animals ; Animals, Newborn ; Aromatase ; Biogenic Monoamines - metabolism ; Brain - drug effects ; Brain - metabolism ; Catecholamines ; Female ; Glucocorticoids ; Glucocorticoids - administration & dosage ; Male ; Neurosecretory Systems - drug effects ; Neurosecretory Systems - metabolism ; Pregnancy ; Prenatal exposure ; Prenatal Exposure Delayed Effects ; Rat ; Rats ; Rats, Wistar ; Serotonin ; Sex Differentiation - drug effects ; Sex Differentiation - physiology ; Sexual brain differentiation ; Testosterone - metabolism</subject><ispartof>Comparative biochemistry and physiology. 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Toxicology & pharmacology</title><addtitle>Comp Biochem Physiol C Toxicol Pharmacol</addtitle><description>We investigated the effects of hydrocortisone acetate and dexamethasone administered to pregnant rats during the last gestational week on sexual differentiation of testosterone metabolism and biogenic monoamine contents and turnover in the discrete brain regions in 10-day-old offspring. In the preoptic area, sex-dependent differences in aromatase activity were attenuated by prenatal glucocorticoids. Prenatal dexamethasone but not hydrocortisone acetate caused the inversion of sexual dimorphism of 5α-reductase activity in the preoptic area. In the brain preoptic area of the male pups prenatally exposed to hydrocortisone acetate, a decrease in noradrenaline turnover was found. Dopamine turnover in the preoptic area and 5-hydroxytryptamine metabolism in the preoptic area and medial basal hypothalamus increased in females as a result of hydrocortisone acetate treatment. Our results indicate that excess glucocorticoids in prenatal life modifies the basic neurochemical and neurophysiological mechanisms of sexual brain differentiation and might contribute to behavioral and reproductive disorders in adulthood.</description><subject>5α-Reductase</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Aromatase</subject><subject>Biogenic Monoamines - metabolism</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Catecholamines</subject><subject>Female</subject><subject>Glucocorticoids</subject><subject>Glucocorticoids - administration & dosage</subject><subject>Male</subject><subject>Neurosecretory Systems - drug effects</subject><subject>Neurosecretory Systems - metabolism</subject><subject>Pregnancy</subject><subject>Prenatal exposure</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Serotonin</subject><subject>Sex Differentiation - drug effects</subject><subject>Sex Differentiation - physiology</subject><subject>Sexual brain differentiation</subject><subject>Testosterone - metabolism</subject><issn>1532-0456</issn><issn>1878-1659</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkcuO1DAQRSMEYoaBD2CDvEJsEqoS20mLFRoND2kkNrC2HKfSuJXYje0g5of4TmroltgNKz_q1PXjVNVLhAYB9dtD45xtWgDZgG4A1KPqEod-qFGr3WOeq66tQSp9UT3L-QBMSNRPqwtUUsGg5WX1-8am5U4cYy7BFrsImmdyJYs4i2Oi894vrm-JRIliv2wuupiKd9FPzAVRKBfupxQDiZWKHePi8ypsmMTo456Cd2KNIdrVB8rCBzH57BIVEoG2FClM0SWuiUR7H8Pf08t3XtoixmR9eF49me2S6cV5vKq-fbj5ev2pvv3y8fP1-9vaSexKjVa3iC10s6a2tyBpBsWDHNQ8Shx3_bBrNVgcWmeVsx2g6xDdYCfoJzl2V9XrU-4xxR8bv8usfFNaFhsobtlovUMtQTP45kGQNahBauz1fzOZGRTLYBBPoEsx50SzOSa_2nRnEMy9cHMwLNzcCzegDevknlfn8G1cafrXcTbMwLsTQPxtPz0lk52n4GjyiUWbKfoH4v8AZBW-6A</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Reznikov, A.G.</creator><creator>Nosenko, N.D.</creator><creator>Tarasenko, L.V.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20040601</creationdate><title>Early postnatal effects of prenatal exposure to glucocorticoids on testosterone metabolism and biogenic monoamines in discrete neuroendocrine regions of the rat brain</title><author>Reznikov, A.G. ; Nosenko, N.D. ; Tarasenko, L.V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-1a6211203f6e27a04ef05a04485fb41b9789260a182ca5ca301c311c8ad07d4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>5α-Reductase</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Aromatase</topic><topic>Biogenic Monoamines - metabolism</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Catecholamines</topic><topic>Female</topic><topic>Glucocorticoids</topic><topic>Glucocorticoids - administration & dosage</topic><topic>Male</topic><topic>Neurosecretory Systems - drug effects</topic><topic>Neurosecretory Systems - metabolism</topic><topic>Pregnancy</topic><topic>Prenatal exposure</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Serotonin</topic><topic>Sex Differentiation - drug effects</topic><topic>Sex Differentiation - physiology</topic><topic>Sexual brain differentiation</topic><topic>Testosterone - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reznikov, A.G.</creatorcontrib><creatorcontrib>Nosenko, N.D.</creatorcontrib><creatorcontrib>Tarasenko, L.V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Comparative biochemistry and physiology. Toxicology & pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reznikov, A.G.</au><au>Nosenko, N.D.</au><au>Tarasenko, L.V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early postnatal effects of prenatal exposure to glucocorticoids on testosterone metabolism and biogenic monoamines in discrete neuroendocrine regions of the rat brain</atitle><jtitle>Comparative biochemistry and physiology. 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subjects | 5α-Reductase Animals Animals, Newborn Aromatase Biogenic Monoamines - metabolism Brain - drug effects Brain - metabolism Catecholamines Female Glucocorticoids Glucocorticoids - administration & dosage Male Neurosecretory Systems - drug effects Neurosecretory Systems - metabolism Pregnancy Prenatal exposure Prenatal Exposure Delayed Effects Rat Rats Rats, Wistar Serotonin Sex Differentiation - drug effects Sex Differentiation - physiology Sexual brain differentiation Testosterone - metabolism |
title | Early postnatal effects of prenatal exposure to glucocorticoids on testosterone metabolism and biogenic monoamines in discrete neuroendocrine regions of the rat brain |
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