Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring

<p>Abstract</p> <p>Co-administration of dextromethorphan (DM) with morphine during pregnancy and throughout lactation has been found to reduce morphine physical dependence and tolerance in rat offspring. No evidence was presented, however, for the effect of DM co-administered with...

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Main Authors: Tao Pao-Luh, Chen Jain-Fang, Wu Ling-Yi, Huang Eagle
Format: Article
Language:English
Published: BMC 2009-11-01
Series:Journal of Biomedical Science
Online Access:http://www.jbiomedsci.com/content/16/1/106
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spelling doaj-eb1ced3d9d9141b79a658e8848b10fe62020-11-24T23:39:29ZengBMCJournal of Biomedical Science1021-77701423-01272009-11-0116110610.1186/1423-0127-16-106Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspringTao Pao-LuhChen Jain-FangWu Ling-YiHuang Eagle<p>Abstract</p> <p>Co-administration of dextromethorphan (DM) with morphine during pregnancy and throughout lactation has been found to reduce morphine physical dependence and tolerance in rat offspring. No evidence was presented, however, for the effect of DM co-administered with morphine during pregnancy on morphine-induced reward and behavioral sensitization (possibly related to the potential to induce morphine addiction) in morphine-exposed offspring. Conditioned place preference and locomotor activity tests revealed that the p60 male offspring of chronic morphine-treated female rats were more vulnerable to morphine-induced reward and behavioral sensitization. The administration of a low dose of morphine (1 mg/kg, i.p.) in these male offspring also increased the dopamine and serotonin turnover rates in the nucleus accumbens, which implied that they were more sensitive to morphine. Co-administration of DM with morphine in the dams prevented this adverse effect of morphine in the offspring rats. Thus, DM may possibly have a great potential in the prevention of higher vulnerability to psychological dependence of morphine in the offspring of morphine-addicted mothers.</p> http://www.jbiomedsci.com/content/16/1/106
collection DOAJ
language English
format Article
sources DOAJ
author Tao Pao-Luh
Chen Jain-Fang
Wu Ling-Yi
Huang Eagle
spellingShingle Tao Pao-Luh
Chen Jain-Fang
Wu Ling-Yi
Huang Eagle
Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
Journal of Biomedical Science
author_facet Tao Pao-Luh
Chen Jain-Fang
Wu Ling-Yi
Huang Eagle
author_sort Tao Pao-Luh
title Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
title_short Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
title_full Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
title_fullStr Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
title_full_unstemmed Attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
title_sort attenuation by dextromethorphan on the higher liability to morphine-induced reward, caused by prenatal exposure of morphine in rat offspring
publisher BMC
series Journal of Biomedical Science
issn 1021-7770
1423-0127
publishDate 2009-11-01
description <p>Abstract</p> <p>Co-administration of dextromethorphan (DM) with morphine during pregnancy and throughout lactation has been found to reduce morphine physical dependence and tolerance in rat offspring. No evidence was presented, however, for the effect of DM co-administered with morphine during pregnancy on morphine-induced reward and behavioral sensitization (possibly related to the potential to induce morphine addiction) in morphine-exposed offspring. Conditioned place preference and locomotor activity tests revealed that the p60 male offspring of chronic morphine-treated female rats were more vulnerable to morphine-induced reward and behavioral sensitization. The administration of a low dose of morphine (1 mg/kg, i.p.) in these male offspring also increased the dopamine and serotonin turnover rates in the nucleus accumbens, which implied that they were more sensitive to morphine. Co-administration of DM with morphine in the dams prevented this adverse effect of morphine in the offspring rats. Thus, DM may possibly have a great potential in the prevention of higher vulnerability to psychological dependence of morphine in the offspring of morphine-addicted mothers.</p>
url http://www.jbiomedsci.com/content/16/1/106
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