Ivermectin Attenuates Nicotine-Induced Reward-Like Behaviors in Mice

dc.contributor.author Demirel, Mustafa Enes
dc.contributor.author Ekici, Abdurrahman
dc.contributor.author Yunusoglu, Oruc
dc.date.accessioned 2025-11-30T19:13:58Z
dc.date.available 2025-11-30T19:13:58Z
dc.date.issued 2026
dc.description.abstract Nicotine addiction poses a significant public health threat, particularly within the realm of emergency medicine, where it is associated with serious complications, including cardiovascular events and respiratory distress. The limited effectiveness of current pharmacological treatments for nicotine dependence underscores the urgent need for innovative and effective therapeutic approaches. Recent studies have shown that ivermectin, an antiparasitic agent, modulates the GABAergic, glutamatergic, and purinergic systems, which are implicated in the pathophysiology of addiction. This study aimed to examine the effects of ivermectin on the acquisition, extinction, and reinstatement of nicotine dependence in mice, utilizing the conditioned place preference (CPP) test, a widely recognized methodology in drug addiction research. Ivermectin (1 and 5 mg/kg, i.p.) was co-administered with nicotine (0.5 mg/kg, i.p.) over three consecutive days during the acquisition phase of nicotine dependence. In a separate experiment, the influence of ivermectin on the reinstatement of nicotineinduced CPP was assessed following an extinction period, using a single nicotine priming injection (0.1 mg/kg). Results indicated that ivermectin (1 and 5 mg/kg) significantly reduced the development of nicotine dependence (p < 0.05). Furthermore, ivermectin (5 mg/kg) facilitated the extinction of nicotine-induced CPP (p < 0.01) and attenuated the reinstatement of nicotine-induced CPP triggered by a priming dose of nicotine (p < 0.01). In contrast, administration of the lower dose of ivermectin (1 mg/kg) did not yield statistically significant effects on either the extinction or reinstatement phases (p > 0.05). Additionally, nicotine administration, alone or in combination with ivermectin at the tested doses, did not produce significant changes in motor coordination or locomotor activity. These findings suggest that ivermectin may attenuate both the acquisition and reinstatement of nicotine-induced CPP while facilitating the extinction of nicotine dependence. Collectively, the results indicate that ivermectin holds potential as a therapeutic agent in the treatment of nicotine addiction. en_US
dc.identifier.doi 10.17305/bb.2025.13026
dc.identifier.issn 2831-0896
dc.identifier.issn 2831-090X
dc.identifier.scopus 2-s2.0-105018619576
dc.identifier.uri https://doi.org/10.17305/bb.2025.13026
dc.identifier.uri https://hdl.handle.net/20.500.14720/28993
dc.language.iso en en_US
dc.publisher Assoc Basic Medical Sci Federation Bosnia & Herzegovina Sarajevo en_US
dc.relation.ispartof Biomolecules and Biomedicine en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Ivermectin en_US
dc.subject Nicotine en_US
dc.subject CPP en_US
dc.subject Emergency Medicine en_US
dc.subject Health Burden en_US
dc.subject Dependence en_US
dc.title Ivermectin Attenuates Nicotine-Induced Reward-Like Behaviors in Mice en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 57220870585
gdc.author.scopusid 55682206500
gdc.author.scopusid 57211217097
gdc.author.wosid Demirel, Mustafa Enes/Aba-2207-2021
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Demirel, Mustafa Enes] Abant Izzet Baysal Univ, Fac Med, Dept Emergency Med, Bolu, Turkiye; [Ekici, Abdurrahman] Yuzuncu Yil Univ, Fac Med, Dept Parasitol, Van, Turkiye; [Yunusoglu, Oruc] Bolu Abant Izzet Baysal Univ, Fac Med, Dept Pharmacol, Bolu, Turkiye en_US
gdc.description.endpage 498 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 490 en_US
gdc.description.volume 26 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q3
gdc.identifier.pmid 41001892
gdc.identifier.wos WOS:001583209700001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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