Increased cocaine reward in offspring of females exposed to morphine during adolescence
Rationale A growing body of evidence demonstrates that environmental exposures can impact the physiology and behavior of subsequent generations. We have previously demonstrated reduced morphine self-administration in the F1 and F2 offspring of female rats exposed to morphine during adolescence. Obje...
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description | Rationale
A growing body of evidence demonstrates that environmental exposures can impact the physiology and behavior of subsequent generations. We have previously demonstrated reduced morphine self-administration in the F1 and F2 offspring of female rats exposed to morphine during adolescence.
Objectives
The current study was designed to determine whether attenuated self-administration for a substance not in the opioid class is also observed in the F1 progeny of adolescent morphine exposed females.
Methods
Female adolescent rats were administered morphine at increasing doses for 10 days (P30–39). Females then remained drug free for at least 3 weeks prior to mating with drug-naïve males. As adults, male and female offspring (F1 animals) were tested for cocaine self-administration acquisition, progressive ratio, extinction, and reinstatement. In addition, β-endorphin peptide levels were measured in the nucleus accumbens (NAc) of behaviorally experienced animals following reinstatement and in behaviorally naïve littermates after acute cocaine (0 or 10 mg/kg, i.p.). Proopiomelanocortin, the polypeptide that is cleaved to produce β-endorphin, as well as β-endorphin, was examined in the arcuate nucleus of the hypothalamus and the nucleus accumbens, respectively. Finally, corticosterone was measured following acute cocaine.
Results
While no differences were observed during the cocaine acquisition phase (FR-1 and FR-5 schedules), under a PR schedule, Mor-F1 animals (both males and females) had increased motivated responding for cocaine. In addition, Mor-F1 males demonstrated enhanced reinstatement compared to Sal-F1 males. In Mor-F1 males, an acute injection of cocaine (10 mg/kg, i.p.) decreased β-endorphin levels in the NAc compared to a saline injection while acute cocaine increased β-endorphin in the NAc in Sal-F1 males compared to saline injection. Following acute cocaine, Mor-F1 males had significantly lower levels of β-endorphin in the Nac compared to Sal-F1 males. Additionally, β-endorphin levels in the nucleus accumbens were negatively correlated with reinstatement behavior only in Mor-F1 males. Levels of POMC in the arcuate nucleus were elevated in Mor-F1 males compared to Sal-F1 males, a main effect driven primarily by POMC levels in the acute cocaine condition. These changes were not observed in Mor-F1 females. Finally, plasma corticosterone was increased in Mor-F1 males regardless of acute injection while Mor-F1 females displayed increased corticoster |
doi_str_mv | 10.1007/s00213-018-5132-0 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2149027450</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A590722051</galeid><sourcerecordid>A590722051</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-526cea486bc11f4db6dab4ddf73fa3c649f2a53b690f8b3544ce49624582994c3</originalsourceid><addsrcrecordid>eNp1kU1v1DAQhi0EotstP4ALisSll5Tx58bHqoK2UiUuII6WY49Lqo29tTei_Hsc0g-1AvvgkfW8o3fmJeQ9hRMKsPlUABjlLdCulZSzFl6RFRW1YLBhr8kKgPOWU9kdkMNSbqAe0Ym35ICDBMW4WpEfl9FltAV945KzQ8Qm4y-bfTPEJoVQdnmI17VqAo52i6XBu12a8X1qxpR3P2eJn_5S1qdKOIwOj8ibYLcF392_a_L9y-dvZxft1dfzy7PTq9YJrvetZMqhFZ3qHaVB-F552wvvw4YHy50SOjArea80hK7nUgiHQismZMe0Fo6vyfHSd5fT7YRlb8ahOthubcQ0FcOo0MA2QkJFP75Ab9KUY3VXKa47phSVT9R1ndYMMaR9tm5uak6lrntlUHe9Jif_oOr1OA4uRQxD_X8moIvA5VRKxmDqYkebfxsKZg7TLGGaGqaZwzSz4Q_3hqd-RP-oeEivAmwBlpQwP030_65_AJkfp38</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2139826615</pqid></control><display><type>article</type><title>Increased cocaine reward in offspring of females exposed to morphine during adolescence</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Vassoler, Fair M. ; Toorie, Anika M. ; Byrnes, Elizabeth M.</creator><creatorcontrib>Vassoler, Fair M. ; Toorie, Anika M. ; Byrnes, Elizabeth M.</creatorcontrib><description>Rationale
A growing body of evidence demonstrates that environmental exposures can impact the physiology and behavior of subsequent generations. We have previously demonstrated reduced morphine self-administration in the F1 and F2 offspring of female rats exposed to morphine during adolescence.
Objectives
The current study was designed to determine whether attenuated self-administration for a substance not in the opioid class is also observed in the F1 progeny of adolescent morphine exposed females.
Methods
Female adolescent rats were administered morphine at increasing doses for 10 days (P30–39). Females then remained drug free for at least 3 weeks prior to mating with drug-naïve males. As adults, male and female offspring (F1 animals) were tested for cocaine self-administration acquisition, progressive ratio, extinction, and reinstatement. In addition, β-endorphin peptide levels were measured in the nucleus accumbens (NAc) of behaviorally experienced animals following reinstatement and in behaviorally naïve littermates after acute cocaine (0 or 10 mg/kg, i.p.). Proopiomelanocortin, the polypeptide that is cleaved to produce β-endorphin, as well as β-endorphin, was examined in the arcuate nucleus of the hypothalamus and the nucleus accumbens, respectively. Finally, corticosterone was measured following acute cocaine.
Results
While no differences were observed during the cocaine acquisition phase (FR-1 and FR-5 schedules), under a PR schedule, Mor-F1 animals (both males and females) had increased motivated responding for cocaine. In addition, Mor-F1 males demonstrated enhanced reinstatement compared to Sal-F1 males. In Mor-F1 males, an acute injection of cocaine (10 mg/kg, i.p.) decreased β-endorphin levels in the NAc compared to a saline injection while acute cocaine increased β-endorphin in the NAc in Sal-F1 males compared to saline injection. Following acute cocaine, Mor-F1 males had significantly lower levels of β-endorphin in the Nac compared to Sal-F1 males. Additionally, β-endorphin levels in the nucleus accumbens were negatively correlated with reinstatement behavior only in Mor-F1 males. Levels of POMC in the arcuate nucleus were elevated in Mor-F1 males compared to Sal-F1 males, a main effect driven primarily by POMC levels in the acute cocaine condition. These changes were not observed in Mor-F1 females. Finally, plasma corticosterone was increased in Mor-F1 males regardless of acute injection while Mor-F1 females displayed increased corticosterone in response to acute cocaine.
Conclusions
These data indicate that morphine prior to conception increases the rewarding effects of cocaine in male and female offspring. In addition, sex-specific alterations in endogenous opioids and hypothalamic physiology were observed.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s00213-018-5132-0</identifier><identifier>PMID: 30506236</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescence ; Adolescents ; Age Factors ; Analgesics, Opioid - pharmacology ; Animals ; Arcuate nucleus ; Behavior, Animal - drug effects ; Behavior, Animal - physiology ; Beta endorphin ; beta-Endorphin - blood ; Biomedical and Life Sciences ; Biomedicine ; Brain ; Child development ; Cocaine ; Cocaine - pharmacology ; Corticosterone ; Corticosterone - blood ; Dopamine Uptake Inhibitors - pharmacology ; Drug self-administration ; Endogenous opioids ; Endorphins ; Environmental toxicology ; Exposure ; Extinction behavior ; Female ; Females ; Hypothalamus ; Injection ; Male ; Males ; Melanocyte stimulating hormone ; Morphine ; Morphine - pharmacology ; Narcotics ; Neuropeptides ; Neurosciences ; Nucleus accumbens ; Nucleus Accumbens - drug effects ; Nucleus Accumbens - metabolism ; Offspring ; Opioids ; Original Investigation ; Peptides ; Pharmacology/Toxicology ; Physiological aspects ; Physiology ; Pro-Opiomelanocortin - blood ; Proopiomelanocortin ; Psychiatry ; Public relations ; Rats ; Rats, Sprague-Dawley ; Receptors, Opioid, mu - metabolism ; Reinforcement ; Reinstatement ; Reward ; Rodents ; Schedules ; Self Administration ; Sex Characteristics ; Steroids (Organic compounds) ; Teenagers ; Women</subject><ispartof>Psychopharmacology, 2019-04, Vol.236 (4), p.1261-1272</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Psychopharmacology is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-526cea486bc11f4db6dab4ddf73fa3c649f2a53b690f8b3544ce49624582994c3</citedby><cites>FETCH-LOGICAL-c439t-526cea486bc11f4db6dab4ddf73fa3c649f2a53b690f8b3544ce49624582994c3</cites><orcidid>0000-0001-5317-7174</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00213-018-5132-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00213-018-5132-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30506236$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vassoler, Fair M.</creatorcontrib><creatorcontrib>Toorie, Anika M.</creatorcontrib><creatorcontrib>Byrnes, Elizabeth M.</creatorcontrib><title>Increased cocaine reward in offspring of females exposed to morphine during adolescence</title><title>Psychopharmacology</title><addtitle>Psychopharmacology</addtitle><addtitle>Psychopharmacology (Berl)</addtitle><description>Rationale
A growing body of evidence demonstrates that environmental exposures can impact the physiology and behavior of subsequent generations. We have previously demonstrated reduced morphine self-administration in the F1 and F2 offspring of female rats exposed to morphine during adolescence.
Objectives
The current study was designed to determine whether attenuated self-administration for a substance not in the opioid class is also observed in the F1 progeny of adolescent morphine exposed females.
Methods
Female adolescent rats were administered morphine at increasing doses for 10 days (P30–39). Females then remained drug free for at least 3 weeks prior to mating with drug-naïve males. As adults, male and female offspring (F1 animals) were tested for cocaine self-administration acquisition, progressive ratio, extinction, and reinstatement. In addition, β-endorphin peptide levels were measured in the nucleus accumbens (NAc) of behaviorally experienced animals following reinstatement and in behaviorally naïve littermates after acute cocaine (0 or 10 mg/kg, i.p.). Proopiomelanocortin, the polypeptide that is cleaved to produce β-endorphin, as well as β-endorphin, was examined in the arcuate nucleus of the hypothalamus and the nucleus accumbens, respectively. Finally, corticosterone was measured following acute cocaine.
Results
While no differences were observed during the cocaine acquisition phase (FR-1 and FR-5 schedules), under a PR schedule, Mor-F1 animals (both males and females) had increased motivated responding for cocaine. In addition, Mor-F1 males demonstrated enhanced reinstatement compared to Sal-F1 males. In Mor-F1 males, an acute injection of cocaine (10 mg/kg, i.p.) decreased β-endorphin levels in the NAc compared to a saline injection while acute cocaine increased β-endorphin in the NAc in Sal-F1 males compared to saline injection. Following acute cocaine, Mor-F1 males had significantly lower levels of β-endorphin in the Nac compared to Sal-F1 males. Additionally, β-endorphin levels in the nucleus accumbens were negatively correlated with reinstatement behavior only in Mor-F1 males. Levels of POMC in the arcuate nucleus were elevated in Mor-F1 males compared to Sal-F1 males, a main effect driven primarily by POMC levels in the acute cocaine condition. These changes were not observed in Mor-F1 females. Finally, plasma corticosterone was increased in Mor-F1 males regardless of acute injection while Mor-F1 females displayed increased corticosterone in response to acute cocaine.
Conclusions
These data indicate that morphine prior to conception increases the rewarding effects of cocaine in male and female offspring. In addition, sex-specific alterations in endogenous opioids and hypothalamic physiology were observed.</description><subject>Adolescence</subject><subject>Adolescents</subject><subject>Age Factors</subject><subject>Analgesics, Opioid - pharmacology</subject><subject>Animals</subject><subject>Arcuate nucleus</subject><subject>Behavior, Animal - drug effects</subject><subject>Behavior, Animal - physiology</subject><subject>Beta endorphin</subject><subject>beta-Endorphin - blood</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Child development</subject><subject>Cocaine</subject><subject>Cocaine - pharmacology</subject><subject>Corticosterone</subject><subject>Corticosterone - blood</subject><subject>Dopamine Uptake Inhibitors - pharmacology</subject><subject>Drug self-administration</subject><subject>Endogenous opioids</subject><subject>Endorphins</subject><subject>Environmental toxicology</subject><subject>Exposure</subject><subject>Extinction behavior</subject><subject>Female</subject><subject>Females</subject><subject>Hypothalamus</subject><subject>Injection</subject><subject>Male</subject><subject>Males</subject><subject>Melanocyte stimulating hormone</subject><subject>Morphine</subject><subject>Morphine - pharmacology</subject><subject>Narcotics</subject><subject>Neuropeptides</subject><subject>Neurosciences</subject><subject>Nucleus accumbens</subject><subject>Nucleus Accumbens - drug effects</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Offspring</subject><subject>Opioids</subject><subject>Original Investigation</subject><subject>Peptides</subject><subject>Pharmacology/Toxicology</subject><subject>Physiological aspects</subject><subject>Physiology</subject><subject>Pro-Opiomelanocortin - blood</subject><subject>Proopiomelanocortin</subject><subject>Psychiatry</subject><subject>Public relations</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Opioid, mu - metabolism</subject><subject>Reinforcement</subject><subject>Reinstatement</subject><subject>Reward</subject><subject>Rodents</subject><subject>Schedules</subject><subject>Self Administration</subject><subject>Sex Characteristics</subject><subject>Steroids (Organic compounds)</subject><subject>Teenagers</subject><subject>Women</subject><issn>0033-3158</issn><issn>1432-2072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kU1v1DAQhi0EotstP4ALisSll5Tx58bHqoK2UiUuII6WY49Lqo29tTei_Hsc0g-1AvvgkfW8o3fmJeQ9hRMKsPlUABjlLdCulZSzFl6RFRW1YLBhr8kKgPOWU9kdkMNSbqAe0Ym35ICDBMW4WpEfl9FltAV945KzQ8Qm4y-bfTPEJoVQdnmI17VqAo52i6XBu12a8X1qxpR3P2eJn_5S1qdKOIwOj8ibYLcF392_a_L9y-dvZxft1dfzy7PTq9YJrvetZMqhFZ3qHaVB-F552wvvw4YHy50SOjArea80hK7nUgiHQismZMe0Fo6vyfHSd5fT7YRlb8ahOthubcQ0FcOo0MA2QkJFP75Ab9KUY3VXKa47phSVT9R1ndYMMaR9tm5uak6lrntlUHe9Jif_oOr1OA4uRQxD_X8moIvA5VRKxmDqYkebfxsKZg7TLGGaGqaZwzSz4Q_3hqd-RP-oeEivAmwBlpQwP030_65_AJkfp38</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Vassoler, Fair M.</creator><creator>Toorie, Anika M.</creator><creator>Byrnes, Elizabeth M.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature 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>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5317-7174</orcidid></search><sort><creationdate>20190401</creationdate><title>Increased cocaine reward in offspring of females exposed to morphine during adolescence</title><author>Vassoler, Fair M. ; Toorie, Anika M. ; Byrnes, Elizabeth M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-526cea486bc11f4db6dab4ddf73fa3c649f2a53b690f8b3544ce49624582994c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescence</topic><topic>Adolescents</topic><topic>Age Factors</topic><topic>Analgesics, Opioid - pharmacology</topic><topic>Animals</topic><topic>Arcuate nucleus</topic><topic>Behavior, Animal - drug effects</topic><topic>Behavior, Animal - physiology</topic><topic>Beta endorphin</topic><topic>beta-Endorphin - blood</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain</topic><topic>Child development</topic><topic>Cocaine</topic><topic>Cocaine - pharmacology</topic><topic>Corticosterone</topic><topic>Corticosterone - blood</topic><topic>Dopamine Uptake Inhibitors - pharmacology</topic><topic>Drug self-administration</topic><topic>Endogenous opioids</topic><topic>Endorphins</topic><topic>Environmental toxicology</topic><topic>Exposure</topic><topic>Extinction behavior</topic><topic>Female</topic><topic>Females</topic><topic>Hypothalamus</topic><topic>Injection</topic><topic>Male</topic><topic>Males</topic><topic>Melanocyte stimulating hormone</topic><topic>Morphine</topic><topic>Morphine - pharmacology</topic><topic>Narcotics</topic><topic>Neuropeptides</topic><topic>Neurosciences</topic><topic>Nucleus accumbens</topic><topic>Nucleus Accumbens - drug effects</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Offspring</topic><topic>Opioids</topic><topic>Original Investigation</topic><topic>Peptides</topic><topic>Pharmacology/Toxicology</topic><topic>Physiological aspects</topic><topic>Physiology</topic><topic>Pro-Opiomelanocortin - blood</topic><topic>Proopiomelanocortin</topic><topic>Psychiatry</topic><topic>Public relations</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Opioid, mu - metabolism</topic><topic>Reinforcement</topic><topic>Reinstatement</topic><topic>Reward</topic><topic>Rodents</topic><topic>Schedules</topic><topic>Self Administration</topic><topic>Sex Characteristics</topic><topic>Steroids (Organic compounds)</topic><topic>Teenagers</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vassoler, Fair M.</creatorcontrib><creatorcontrib>Toorie, Anika M.</creatorcontrib><creatorcontrib>Byrnes, Elizabeth M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vassoler, Fair M.</au><au>Toorie, Anika M.</au><au>Byrnes, Elizabeth M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased cocaine reward in offspring of females exposed to morphine during adolescence</atitle><jtitle>Psychopharmacology</jtitle><stitle>Psychopharmacology</stitle><addtitle>Psychopharmacology (Berl)</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>236</volume><issue>4</issue><spage>1261</spage><epage>1272</epage><pages>1261-1272</pages><issn>0033-3158</issn><eissn>1432-2072</eissn><abstract>Rationale
A growing body of evidence demonstrates that environmental exposures can impact the physiology and behavior of subsequent generations. We have previously demonstrated reduced morphine self-administration in the F1 and F2 offspring of female rats exposed to morphine during adolescence.
Objectives
The current study was designed to determine whether attenuated self-administration for a substance not in the opioid class is also observed in the F1 progeny of adolescent morphine exposed females.
Methods
Female adolescent rats were administered morphine at increasing doses for 10 days (P30–39). Females then remained drug free for at least 3 weeks prior to mating with drug-naïve males. As adults, male and female offspring (F1 animals) were tested for cocaine self-administration acquisition, progressive ratio, extinction, and reinstatement. In addition, β-endorphin peptide levels were measured in the nucleus accumbens (NAc) of behaviorally experienced animals following reinstatement and in behaviorally naïve littermates after acute cocaine (0 or 10 mg/kg, i.p.). Proopiomelanocortin, the polypeptide that is cleaved to produce β-endorphin, as well as β-endorphin, was examined in the arcuate nucleus of the hypothalamus and the nucleus accumbens, respectively. Finally, corticosterone was measured following acute cocaine.
Results
While no differences were observed during the cocaine acquisition phase (FR-1 and FR-5 schedules), under a PR schedule, Mor-F1 animals (both males and females) had increased motivated responding for cocaine. In addition, Mor-F1 males demonstrated enhanced reinstatement compared to Sal-F1 males. In Mor-F1 males, an acute injection of cocaine (10 mg/kg, i.p.) decreased β-endorphin levels in the NAc compared to a saline injection while acute cocaine increased β-endorphin in the NAc in Sal-F1 males compared to saline injection. Following acute cocaine, Mor-F1 males had significantly lower levels of β-endorphin in the Nac compared to Sal-F1 males. Additionally, β-endorphin levels in the nucleus accumbens were negatively correlated with reinstatement behavior only in Mor-F1 males. Levels of POMC in the arcuate nucleus were elevated in Mor-F1 males compared to Sal-F1 males, a main effect driven primarily by POMC levels in the acute cocaine condition. These changes were not observed in Mor-F1 females. Finally, plasma corticosterone was increased in Mor-F1 males regardless of acute injection while Mor-F1 females displayed increased corticosterone in response to acute cocaine.
Conclusions
These data indicate that morphine prior to conception increases the rewarding effects of cocaine in male and female offspring. In addition, sex-specific alterations in endogenous opioids and hypothalamic physiology were observed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30506236</pmid><doi>10.1007/s00213-018-5132-0</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5317-7174</orcidid></addata></record> |
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subjects | Adolescence Adolescents Age Factors Analgesics, Opioid - pharmacology Animals Arcuate nucleus Behavior, Animal - drug effects Behavior, Animal - physiology Beta endorphin beta-Endorphin - blood Biomedical and Life Sciences Biomedicine Brain Child development Cocaine Cocaine - pharmacology Corticosterone Corticosterone - blood Dopamine Uptake Inhibitors - pharmacology Drug self-administration Endogenous opioids Endorphins Environmental toxicology Exposure Extinction behavior Female Females Hypothalamus Injection Male Males Melanocyte stimulating hormone Morphine Morphine - pharmacology Narcotics Neuropeptides Neurosciences Nucleus accumbens Nucleus Accumbens - drug effects Nucleus Accumbens - metabolism Offspring Opioids Original Investigation Peptides Pharmacology/Toxicology Physiological aspects Physiology Pro-Opiomelanocortin - blood Proopiomelanocortin Psychiatry Public relations Rats Rats, Sprague-Dawley Receptors, Opioid, mu - metabolism Reinforcement Reinstatement Reward Rodents Schedules Self Administration Sex Characteristics Steroids (Organic compounds) Teenagers Women |
title | Increased cocaine reward in offspring of females exposed to morphine during adolescence |
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