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Journal article
Hypocretin receptor 1 blockade early in abstinence prevents incubation of cocaine seeking and normalizes dopamine transmission
Neuropsychopharmacology, Forthcoming
04 Feb 2026
PMID: 41639572
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Abstract
Abstinence from cocaine use has been shown to elicit a progressive intensification or incubation of cocaine craving/seeking that is posited to increase the likelihood of relapse. While the mechanisms underlying incubation of cocaine seeking remain elusive, considerable evidence suggests that abstinence from cocaine promotes mesolimbic dopamine adaptations that contribute to exaggerated cocaine seeking. Consequently, preventing these dopamine adaptations may reduce incubation of cocaine seeking and thereby decrease the likelihood of relapse. In the present studies, we first examined the relationship between incubation of cocaine seeking and dopamine transmission in the nucleus accumbens following abstinence from intermittent access to cocaine. Given the extensive evidence that hypocretins/orexins regulate motivation for cocaine, we then examined to what extent an intraperitoneal injection of a hypocretin receptor 1 antagonist on the first day of abstinence would prevent incubation of cocaine seeking and dopamine adaptations later in abstinence. Results indicated that abstinence from intermittent access to cocaine engendered robust incubation of cocaine seeking in both female and male rats. We also observed aberrant dopamine transmission, but only in rats that displayed incubation of cocaine seeking. Further, we showed that a single injection of the hypocretin receptor 1 antagonist, RTIOX-276, on the first day of abstinence prevented incubation of cocaine seeking and aberrant dopamine transmission. These findings suggest that hypocretin receptor 1 antagonism may serve as a viable therapeutic for reducing cocaine craving/seeking early in abstinence, thus reducing the likelihood of relapse.
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Details
- Title
- Hypocretin receptor 1 blockade early in abstinence prevents incubation of cocaine seeking and normalizes dopamine transmission
- Creators
- Philip Joseph Clark - Drexel University, Neurobiology and AnatomyVolodar Michael Migovich - Drexel University, Neurobiology and AnatomySanjay Das - Drexel University, Microbiology and ImmunologyWei Xu - Drexel University, Microbiology and ImmunologyYanan Zhang - Research Triangle Park FoundationSandhya Kortagere - Drexel University, Microbiology and ImmunologyRodrigo A Espana (Corresponding Author) - Drexel University, Neurobiology and Anatomy
- Publication Details
- Neuropsychopharmacology, Forthcoming
- Publisher
- Springer Nature
- Number of pages
- 12
- Grant note
- U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA): AA030509 U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA): R01DA039100
This work was supported by the National Institute on Drug Abuse grant R01DA039100 (RAE) and the National Institute on Alcohol Abuse and Alcoholism R01AA030509 (YZ). The authors have nothing to disclose.
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Microbiology and Immunology; Neurobiology and Anatomy
- Web of Science ID
- WOS:001679744700001
- Other Identifier
- 991022157703904721