米氮平可减弱C57BL/6J和BALBA/cJ小鼠的运动致敏

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES Pharmacology Biochemistry and Behavior Pub Date : 2023-01-01 DOI:10.1016/j.pbb.2022.173507
Susana Barbosa Méndez, Alberto Salazar-Juárez
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引用次数: 0

摘要

背景临床研究已经描述了各种治疗方法的疗效。结果不一致,临床应用有限。临床试验表明,个体对药物治疗的反应和性别的差异会影响一些抗抑郁药物的疗效。小鼠菌株依赖性变异影响抗抑郁药物的反应。一些小鼠品系对抗抑郁药的反应比其他小鼠品系更快、更好。我们最近报道了一系列临床前研究,表明在雄性和雌性Wistar大鼠中给药米氮平(一种去甲肾上腺素能和5-羟色胺能抗抑郁药)降低了可卡因诱导的运动活性,并减弱了可卡因诱导运动增敏的诱导和表达。因此,本研究的目的是评估米氮平对C57BL/6J和BALB/cJ株雄性和雌性小鼠可卡因诱导的运动活性和可卡因诱导的活动致敏的影响,这两种小鼠对可卡因运动效应的敏感性和对抗抑郁药的反应不同。方法雄性和雌性BALB/cJ和C57BL/6J近交系小鼠(20-25g)在运动致敏的诱导和表达过程中每天给药10mg/kg可卡因。在停药期间,停药可卡因,两组每天接受米氮平(30 mg/kg,腹腔注射)或生理盐水。米氮平在可卡因前30分钟给药。每次给药后,在透明有机玻璃活动室中记录每只动物的运动活动30分钟。结果在运动致敏的诱导和表达阶段,C57BL/6J株小鼠的可卡因诱导的运动活性高于BALB/cJ株小鼠。两种品系的雌性小鼠都表现出比雄性更高的可卡因运动反应,米氮平显著降低了可卡因诱导的运动活性,以及运动致敏的诱导和表达,无论小鼠品系或性别如何。结论米氮平可能被认为是治疗具有不同遗传背景的男性和女性可卡因使用障碍的有效治疗选择。
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Mirtazapine attenuates the cocaine-induced locomotor sensitization in male and female C57BL/6J and BALBA/cJ mouse

Background

Clinical studies have described the efficacy of various therapeutic approaches. Results are inconsistent and clinical application is limited. Clinical trials have suggested that individual variability in the response to pharmacological therapies and sex affects the efficacy of some antidepressant drugs. Mouse strain-dependent variability influenced the response to antidepressant drugs. Some mouse strains respond faster and better to antidepressants than other mouse strains. We recently reported a series of preclinical studies that showed that dosing of mirtazapine, a noradrenergic and serotonergic antidepressant, in male and female Wistar rats decreased cocaine-induced locomotor activity and attenuated the induction and expression of cocaine-induced locomotor sensitization. Therefore, the aim of this study was to evaluate the mirtazapine effects, on cocaine-induced locomotor activity and cocaine-induced locomotor sensitization in male and female mice of the C57BL/6J and BALB/cJ strains, which differ in sensitivity to the cocaine motor effects and response to antidepressant drugs.

Methods

Male and female BALB/cJ and C57BL/6J inbred mice (20–25 g) were daily dosed with 10 mg/kg of cocaine during the induction and expression of locomotor sensitization. During drug withdrawal, cocaine was withdrawn, and the groups received daily mirtazapine (30 mg/kg, i.p.) or saline. Mirtazapine was administered 30 min before cocaine. After each administration, locomotor activity for each animal was recorded for 30 min in transparent Plexiglass activity chambers.

Results

Cocaine-induced locomotor activity were greater in C57BL/6J strain mice than BALB/cJ strain mice during the induction and expression phase of locomotor sensitization. The female mice of both strains showed a higher cocaine locomotor response than males and mirtazapine significantly decreased cocaine-induced locomotor activity, as well as the induction and expression of locomotor sensitization, regardless of mouse strain or sex.

Conclusion

The results suggest mirtazapine may be considered an effective therapeutic option to treat cocaine use disorder in men and women with very diverse genetic backgrounds.

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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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