Prenatal inhibition of hypothalamic sex steroid uptake by cocaine: effects on neurobehavioral sexual differentiation in male rats
Several adrenergically active drugs have been shown to prevent the masculinizing and/or defeminizing effects of testosterone on brain sexual differentiation. We examined the ability of the neuronal norepinephrine uptake blocker, cocaine, to produce similar effects. The ability of cocaine to inhibit...
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Veröffentlicht in: | Brain research. Developmental brain research 1990-05, Vol.53 (2), p.230-236 |
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description | Several adrenergically active drugs have been shown to prevent the masculinizing and/or defeminizing effects of testosterone on brain sexual differentiation. We examined the ability of the neuronal norepinephrine uptake blocker, cocaine, to produce similar effects. The ability of cocaine to inhibit sex steroid incorporation into the hypothalamus during a critical period for sexual differentiation of the brain was examined in females treated at birth with testosterone. Sixty minutes after administration, cocaine was observed to inhibit both testosterone and estradiol incorporation into the hypothalamus by approximately 50%. Long-term consequences of prenatal cocaine exposure were studied by injecting Sprague-Dawley dams twice daily with 3, 10 or 30 mg/kg of cocaine hydrochloride on days 15 through 20 of gestation and examining the offspring. In adulthood, cocaine-exposed males, but not females were found to exhibit significantly less marking behavior than controls. Cocaine-exposed males in the 10 mg/kg group tested for sex behavior exhibited demasculinization in some aspects of the behaviors tested. Measurement of plasma hormone levels in this group revealed elevated levels of plasma LH, but normal levels of FSH and testosterone. No differences were observed in cocaine-exposed males with respect to sex organ or adrenal weights, but thymus was approximately 25% smaller compared to control males at 80 days of age. In a separate experiment, dams were treated with 3 mg/kg of cocaine twice daily from days 15 through 21 of gestation and half of the male pups received additional injections twice a day for the first 5 days postnatally. Compared to controls, scent marking behavior in adulthood was significantly less in animals exposed to cocaine either prenatally or prenatally and postnatally, but the cocaine-treated groups did not differ from each other. Overall, these findings indicate that prenatal cocaine exposure can demasculinize adult male sex related behaviors. This may occur through an ability of the drug to interfere with nuclear uptake of sex hormones in brain during the critical period for neurobehavioral sexual differentiation. |
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We examined the ability of the neuronal norepinephrine uptake blocker, cocaine, to produce similar effects. The ability of cocaine to inhibit sex steroid incorporation into the hypothalamus during a critical period for sexual differentiation of the brain was examined in females treated at birth with testosterone. Sixty minutes after administration, cocaine was observed to inhibit both testosterone and estradiol incorporation into the hypothalamus by approximately 50%. Long-term consequences of prenatal cocaine exposure were studied by injecting Sprague-Dawley dams twice daily with 3, 10 or 30 mg/kg of cocaine hydrochloride on days 15 through 20 of gestation and examining the offspring. In adulthood, cocaine-exposed males, but not females were found to exhibit significantly less marking behavior than controls. Cocaine-exposed males in the 10 mg/kg group tested for sex behavior exhibited demasculinization in some aspects of the behaviors tested. Measurement of plasma hormone levels in this group revealed elevated levels of plasma LH, but normal levels of FSH and testosterone. No differences were observed in cocaine-exposed males with respect to sex organ or adrenal weights, but thymus was approximately 25% smaller compared to control males at 80 days of age. In a separate experiment, dams were treated with 3 mg/kg of cocaine twice daily from days 15 through 21 of gestation and half of the male pups received additional injections twice a day for the first 5 days postnatally. Compared to controls, scent marking behavior in adulthood was significantly less in animals exposed to cocaine either prenatally or prenatally and postnatally, but the cocaine-treated groups did not differ from each other. Overall, these findings indicate that prenatal cocaine exposure can demasculinize adult male sex related behaviors. This may occur through an ability of the drug to interfere with nuclear uptake of sex hormones in brain during the critical period for neurobehavioral sexual differentiation.</description><identifier>ISSN: 0165-3806</identifier><identifier>DOI: 10.1016/0165-3806(90)90011-M</identifier><identifier>PMID: 2357796</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Behavior ; Body Weight - drug effects ; Brain development ; Cocaine ; Cocaine - toxicity ; Estradiol ; Estradiol - pharmacokinetics ; Estradiol - physiology ; Female ; Hypothalamus - drug effects ; Hypothalamus - growth & development ; Hypothalamus - metabolism ; Male ; Noradrenaline ; Organ Size - drug effects ; Pregnancy ; Prenatal Exposure Delayed Effects ; Rats ; Rats, Inbred Strains ; Sexual Behavior, Animal - drug effects ; Sexual differentiation ; Testosterone ; Testosterone - pharmacokinetics ; Testosterone - physiology</subject><ispartof>Brain research. Developmental brain research, 1990-05, Vol.53 (2), p.230-236</ispartof><rights>1990</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-749f05f7ca856273be2db60cde701a0369bd7a0130c9e4294e98ce2b26743a783</citedby><cites>FETCH-LOGICAL-c483t-749f05f7ca856273be2db60cde701a0369bd7a0130c9e4294e98ce2b26743a783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2357796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raum, William J.</creatorcontrib><creatorcontrib>McGivern, Robert F.</creatorcontrib><creatorcontrib>Peterson, Margaret A.</creatorcontrib><creatorcontrib>Shryne, James H.</creatorcontrib><creatorcontrib>Gorski, Roger A.</creatorcontrib><title>Prenatal inhibition of hypothalamic sex steroid uptake by cocaine: effects on neurobehavioral sexual differentiation in male rats</title><title>Brain research. Developmental brain research</title><addtitle>Brain Res Dev Brain Res</addtitle><description>Several adrenergically active drugs have been shown to prevent the masculinizing and/or defeminizing effects of testosterone on brain sexual differentiation. We examined the ability of the neuronal norepinephrine uptake blocker, cocaine, to produce similar effects. The ability of cocaine to inhibit sex steroid incorporation into the hypothalamus during a critical period for sexual differentiation of the brain was examined in females treated at birth with testosterone. Sixty minutes after administration, cocaine was observed to inhibit both testosterone and estradiol incorporation into the hypothalamus by approximately 50%. Long-term consequences of prenatal cocaine exposure were studied by injecting Sprague-Dawley dams twice daily with 3, 10 or 30 mg/kg of cocaine hydrochloride on days 15 through 20 of gestation and examining the offspring. In adulthood, cocaine-exposed males, but not females were found to exhibit significantly less marking behavior than controls. Cocaine-exposed males in the 10 mg/kg group tested for sex behavior exhibited demasculinization in some aspects of the behaviors tested. Measurement of plasma hormone levels in this group revealed elevated levels of plasma LH, but normal levels of FSH and testosterone. No differences were observed in cocaine-exposed males with respect to sex organ or adrenal weights, but thymus was approximately 25% smaller compared to control males at 80 days of age. In a separate experiment, dams were treated with 3 mg/kg of cocaine twice daily from days 15 through 21 of gestation and half of the male pups received additional injections twice a day for the first 5 days postnatally. Compared to controls, scent marking behavior in adulthood was significantly less in animals exposed to cocaine either prenatally or prenatally and postnatally, but the cocaine-treated groups did not differ from each other. Overall, these findings indicate that prenatal cocaine exposure can demasculinize adult male sex related behaviors. This may occur through an ability of the drug to interfere with nuclear uptake of sex hormones in brain during the critical period for neurobehavioral sexual differentiation.</description><subject>Animals</subject><subject>Behavior</subject><subject>Body Weight - drug effects</subject><subject>Brain development</subject><subject>Cocaine</subject><subject>Cocaine - toxicity</subject><subject>Estradiol</subject><subject>Estradiol - pharmacokinetics</subject><subject>Estradiol - physiology</subject><subject>Female</subject><subject>Hypothalamus - drug effects</subject><subject>Hypothalamus - growth & development</subject><subject>Hypothalamus - metabolism</subject><subject>Male</subject><subject>Noradrenaline</subject><subject>Organ Size - drug effects</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Sexual Behavior, Animal - drug effects</subject><subject>Sexual differentiation</subject><subject>Testosterone</subject><subject>Testosterone - pharmacokinetics</subject><subject>Testosterone - physiology</subject><issn>0165-3806</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P3DAQhn2gArr0H1DJp6ocUux8Oe6hEkIUkFjBoZytiTPRTpvEW9tZsUf-eb3simMP1kh-P0bzMHYuxTcpZH2ZXpUVjai_anGhhZAyWx6x0_fvE_YxhN8iCUUjj9lxXlRK6fqUvT55nCDCwGlaUUuR3MRdz1fbtYsrGGAkywO-8BDRO-r4vI7wB3m75dZZoAm_c-x7tDHwlJxw9q7FFWzI-VSaknMaHSVLWhQJ3hbQxEcYkHuI4Yx96GEI-OkwF-z5582v67vs4fH2_vrqIbNlU8RMlboXVa8sNFWdq6LFvGtrYTtUQoIoat12CtJ9wmosc12ibizmbV6rsgDVFAv2Zd-79u7vjCGakYLFYYAJ3RyMrJTUla6SsdwbrXcheOzN2tMIfmukMDvaZofV7LAaLcwbbbNMsc-H_rkdsXsPHVAn_cdex3TkhtCbYAknix35hM90jv6_4B8TCJNF</recordid><startdate>19900501</startdate><enddate>19900501</enddate><creator>Raum, William J.</creator><creator>McGivern, Robert F.</creator><creator>Peterson, Margaret A.</creator><creator>Shryne, James H.</creator><creator>Gorski, Roger A.</creator><general>Elsevier B.V</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>7QG</scope><scope>7TK</scope></search><sort><creationdate>19900501</creationdate><title>Prenatal inhibition of hypothalamic sex steroid uptake by cocaine: effects on neurobehavioral sexual differentiation in male rats</title><author>Raum, William J. ; McGivern, Robert F. ; Peterson, Margaret A. ; Shryne, James H. ; Gorski, Roger A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-749f05f7ca856273be2db60cde701a0369bd7a0130c9e4294e98ce2b26743a783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Behavior</topic><topic>Body Weight - drug effects</topic><topic>Brain development</topic><topic>Cocaine</topic><topic>Cocaine - toxicity</topic><topic>Estradiol</topic><topic>Estradiol - pharmacokinetics</topic><topic>Estradiol - physiology</topic><topic>Female</topic><topic>Hypothalamus - drug effects</topic><topic>Hypothalamus - growth & development</topic><topic>Hypothalamus - metabolism</topic><topic>Male</topic><topic>Noradrenaline</topic><topic>Organ Size - drug effects</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Sexual Behavior, Animal - drug effects</topic><topic>Sexual differentiation</topic><topic>Testosterone</topic><topic>Testosterone - pharmacokinetics</topic><topic>Testosterone - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raum, William J.</creatorcontrib><creatorcontrib>McGivern, Robert F.</creatorcontrib><creatorcontrib>Peterson, Margaret A.</creatorcontrib><creatorcontrib>Shryne, James H.</creatorcontrib><creatorcontrib>Gorski, Roger A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Brain research. Developmental brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raum, William J.</au><au>McGivern, Robert F.</au><au>Peterson, Margaret A.</au><au>Shryne, James H.</au><au>Gorski, Roger A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prenatal inhibition of hypothalamic sex steroid uptake by cocaine: effects on neurobehavioral sexual differentiation in male rats</atitle><jtitle>Brain research. Developmental brain research</jtitle><addtitle>Brain Res Dev Brain Res</addtitle><date>1990-05-01</date><risdate>1990</risdate><volume>53</volume><issue>2</issue><spage>230</spage><epage>236</epage><pages>230-236</pages><issn>0165-3806</issn><abstract>Several adrenergically active drugs have been shown to prevent the masculinizing and/or defeminizing effects of testosterone on brain sexual differentiation. We examined the ability of the neuronal norepinephrine uptake blocker, cocaine, to produce similar effects. The ability of cocaine to inhibit sex steroid incorporation into the hypothalamus during a critical period for sexual differentiation of the brain was examined in females treated at birth with testosterone. Sixty minutes after administration, cocaine was observed to inhibit both testosterone and estradiol incorporation into the hypothalamus by approximately 50%. Long-term consequences of prenatal cocaine exposure were studied by injecting Sprague-Dawley dams twice daily with 3, 10 or 30 mg/kg of cocaine hydrochloride on days 15 through 20 of gestation and examining the offspring. In adulthood, cocaine-exposed males, but not females were found to exhibit significantly less marking behavior than controls. Cocaine-exposed males in the 10 mg/kg group tested for sex behavior exhibited demasculinization in some aspects of the behaviors tested. Measurement of plasma hormone levels in this group revealed elevated levels of plasma LH, but normal levels of FSH and testosterone. No differences were observed in cocaine-exposed males with respect to sex organ or adrenal weights, but thymus was approximately 25% smaller compared to control males at 80 days of age. In a separate experiment, dams were treated with 3 mg/kg of cocaine twice daily from days 15 through 21 of gestation and half of the male pups received additional injections twice a day for the first 5 days postnatally. Compared to controls, scent marking behavior in adulthood was significantly less in animals exposed to cocaine either prenatally or prenatally and postnatally, but the cocaine-treated groups did not differ from each other. Overall, these findings indicate that prenatal cocaine exposure can demasculinize adult male sex related behaviors. This may occur through an ability of the drug to interfere with nuclear uptake of sex hormones in brain during the critical period for neurobehavioral sexual differentiation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>2357796</pmid><doi>10.1016/0165-3806(90)90011-M</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Behavior Body Weight - drug effects Brain development Cocaine Cocaine - toxicity Estradiol Estradiol - pharmacokinetics Estradiol - physiology Female Hypothalamus - drug effects Hypothalamus - growth & development Hypothalamus - metabolism Male Noradrenaline Organ Size - drug effects Pregnancy Prenatal Exposure Delayed Effects Rats Rats, Inbred Strains Sexual Behavior, Animal - drug effects Sexual differentiation Testosterone Testosterone - pharmacokinetics Testosterone - physiology |
title | Prenatal inhibition of hypothalamic sex steroid uptake by cocaine: effects on neurobehavioral sexual differentiation in male rats |
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