Demirel Mustafa Enes, Ekici Abdurrahman, Yunusoğlu Oruç
Department of Emergency Medicine, Bolu Abant Izzet Baysal University, Faculty of Medicine, Bolu, Türkiye.
Department of Parasitology, Yuzuncu Yıl University, Faculty of Medicine, Van, Türkiye.
Biomol Biomed. 2025 Sep 26;26(3):490-498. doi: 10.17305/bb.2025.13026.
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 nicotine-induced 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.
尼古丁成瘾对公众健康构成重大威胁,尤其是在急诊医学领域,它与包括心血管事件和呼吸窘迫在内的严重并发症相关。当前针对尼古丁依赖的药物治疗效果有限,这凸显了对创新且有效治疗方法的迫切需求。最近的研究表明,抗寄生虫药物伊维菌素可调节参与成瘾病理生理学的γ-氨基丁酸能、谷氨酸能和嘌呤能系统。本研究旨在利用条件性位置偏爱(CPP)试验(药物成瘾研究中一种广泛认可的方法),研究伊维菌素对小鼠尼古丁依赖的获得、消退和复吸的影响。在尼古丁依赖的获得阶段,连续三天将伊维菌素(1和5毫克/千克,腹腔注射)与尼古丁(0.5毫克/千克,腹腔注射)联合给药。在另一项实验中,在消退期后,使用单次尼古丁激发注射(0.1毫克/千克)评估伊维菌素对尼古丁诱导的CPP复吸的影响。结果表明,伊维菌素(1和5毫克/千克)显著降低了尼古丁依赖的形成(p<0.05)。此外,伊维菌素(5毫克/千克)促进了尼古丁诱导的CPP的消退(p<0.01),并减弱了由尼古丁激发剂量引发的尼古丁诱导的CPP的复吸(p<0.01)。相比之下,较低剂量的伊维菌素(1毫克/千克)给药对消退期或复吸期均未产生统计学上的显著影响(p>0.05)。此外,单独给予尼古丁或与测试剂量的伊维菌素联合给药,对运动协调性或运动活性均未产生显著变化。这些发现表明,伊维菌素可能会减弱尼古丁诱导的CPP的获得和复吸,同时促进尼古丁依赖的消退。总体而言,结果表明伊维菌素在治疗尼古丁成瘾方面具有作为治疗剂的潜力。