Differential behavioral functioning in the offspring of rats with high vs. low self-administration of the opioid agonist remifentanil.
dc.contributor.author | Rezvani, Amir H | |
dc.contributor.author | Wells, Corinne | |
dc.contributor.author | Hawkey, Andrew | |
dc.contributor.author | Blair, Graham | |
dc.contributor.author | Koburov, Reese | |
dc.contributor.author | Ko, Ashley | |
dc.contributor.author | Schwartz, Andrea | |
dc.contributor.author | Kim, Veronica J | |
dc.contributor.author | Levin, Edward D | |
dc.date.accessioned | 2023-12-06T15:09:08Z | |
dc.date.available | 2023-12-06T15:09:08Z | |
dc.date.issued | 2021-10 | |
dc.date.updated | 2023-12-06T15:09:07Z | |
dc.description.abstract | Opioid use disorder (OUD) has a variety of adverse effects on both the users and their offspring. In the current study, a random group of Sprague-Dawley rats (25 females and 15 males) were tested for intravenous self-administration of the opioid agonist remifentanil to determine the range of acquisition for opioid. One-month after the end of self-administration of remifentanil, rats with the highest intake were mated together and rats with lowest intake were mated together. Then, the offspring of the two groups were tested for anxiety-like behavior, locomotor activity, nociception and intravenous remifentanil self-administration. The parents showed a range of remifentanil self-administration, especially in the female rats. The offspring of the parents with low and high remifentanil self-administration showed significant differences in specific behavioral functions. On the hotplate test of nociception, the female offspring parents with high remifentanil self-administration had significantly longer hotplate latencies, indicating reduced nociception, than the female offspring of parents with low remifentanil-self-administration, whereas there was no difference in the male offspring of low and high responding parents. In the elevated plus maze test of anxiety-like behavior, the offspring of the parents with high remifentanil intake showed more anxiety-like behavior than the offspring of the parents with low remifentanil intake regardless of sex. Locomotor activity was not significantly different. Interestingly, no significant differences in remifentanil self-administration in the offspring of parents with low and high remifentanil self-administration were detected. Overall, our data suggest a considerable range in remifentanil self-administration in rats and the offspring of rats with high opioid self-administration exhibit different behaviors vs offspring of rats with low opioid self-administration. | |
dc.identifier | S0014-2999(21)00560-4 | |
dc.identifier.issn | 0014-2999 | |
dc.identifier.issn | 1879-0712 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | European journal of pharmacology | |
dc.relation.isversionof | 10.1016/j.ejphar.2021.174407 | |
dc.subject | Animals | |
dc.subject | Humans | |
dc.subject | Rats | |
dc.subject | Opioid-Related Disorders | |
dc.subject | Disease Models, Animal | |
dc.subject | Analgesics, Opioid | |
dc.subject | Self Administration | |
dc.subject | Behavior, Animal | |
dc.subject | Maternal Exposure | |
dc.subject | Paternal Exposure | |
dc.subject | Dose-Response Relationship, Drug | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Remifentanil | |
dc.title | Differential behavioral functioning in the offspring of rats with high vs. low self-administration of the opioid agonist remifentanil. | |
dc.type | Journal article | |
duke.contributor.orcid | Levin, Edward D|0000-0001-7292-8084|0000-0002-5060-9602 | |
pubs.begin-page | 174407 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Nicholas School of the Environment | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Trinity College of Arts & Sciences | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Pharmacology & Cancer Biology | |
pubs.organisational-group | Psychiatry & Behavioral Sciences | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Psychology & Neuroscience | |
pubs.organisational-group | Environmental Sciences and Policy | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | University Institutes and Centers | |
pubs.organisational-group | Duke Institute for Brain Sciences | |
pubs.organisational-group | Initiatives | |
pubs.organisational-group | Duke Science & Society | |
pubs.organisational-group | Psychiatry & Behavioral Sciences, Behavioral Medicine & Neurosciences | |
pubs.publication-status | Published | |
pubs.volume | 909 |
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