Hormonal contraceptives alter amphetamine place preference and responsivity in the intact female rat.

IF 1.6 4区 医学 Q3 BEHAVIORAL SCIENCES
Emily N Hilz, Marcelle E Olvera, Dohyun Jun, Megha Chadha, Ross Gillette, Marie-H Monfils, Andrea C Gore, Hongjoo J Lee
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引用次数: 1

Abstract

Hormonal contraceptives (HCs) containing synthetic ovarian hormones are commonly used among reproductive aged women; HCs alter the physiological state of the user by interfering with endogenous hormone concentrations and their actions on the reproductive tract. As ovarian hormones modulate the incidence of substance abuse disorders in women, this experiment explores how modulating female rat ovarian hormonal states with an HC containing the synthetic progestin levonorgestrel influences measures of drug preference and responsivity. First, rats underwent food-light Pavlovian conditioning to measure conditioned orienting, a known predictor of amphetamine (AMP) place preference. Then, rats were conditioned and tested for AMP place preference with either an HC implant or during estrous cycle stages associated with opposing ovarian hormone levels, that is, proestrus (P) or metestrus/diestrus (M/D), while recording ultrasonic vocalizations (USVs) as an index of he donic drug responsivity. Because of dopamine's (DA's) role in reward learning and memory, DA cell number and activity were examined using tyrosine hydroxylase and FOS immunohistochemistry after a final AMP challenge. Conditioned orienting did not differ between cycling and HC-implanted rats. HC rats emitted fewer USVs in response to AMP, showed marginally less AMP place preference, and had lower DA cell activity in the substantia nigra after AMP compared to P rats. M/D rats showed a similar behavioral profile and neural response as HC rats. This experiment suggests ovarian hormones affect drug preference and responsivity, while providing novel insight into how hormone-altering contraceptives may reduce these measures. (PsycInfo Database Record (c) 2022 APA, all rights reserved).

激素避孕药改变安非他明在完整雌性大鼠的位置偏好和反应性。
含有合成卵巢激素的激素避孕药(HCs)通常用于育龄妇女;HCs通过干扰内源性激素浓度及其对生殖道的作用来改变使用者的生理状态。由于卵巢激素调节女性药物滥用障碍的发生率,本实验探讨了含有合成孕激素左炔诺孕酮的HC如何调节雌性大鼠卵巢激素状态影响药物偏好和反应性的测量。首先,大鼠接受了食物轻的巴甫洛夫条件反射来测量条件定向,这是一种已知的安非他明(AMP)位置偏好的预测因子。然后,用HC植入大鼠或在与卵巢激素水平相反的发情周期阶段(即发情前期(P)或初潮/初潮(M/D))对大鼠进行AMP位置偏好的条件反射和测试,同时记录超声发声(USVs)作为药物反应性的指标。由于多巴胺(DA)在奖励学习和记忆中的作用,在最后一次AMP刺激后,使用酪氨酸羟化酶和FOS免疫组织化学检测DA细胞的数量和活性。条件定向在循环大鼠和hc植入大鼠之间没有差异。与P大鼠相比,HC大鼠对AMP的反应释放出更少的usv, AMP的位置偏好略低,AMP后黑质DA细胞活性较低。M/D大鼠表现出与HC大鼠相似的行为特征和神经反应。该实验表明卵巢激素影响药物偏好和反应性,同时为改变激素的避孕药如何减少这些措施提供了新的见解。(PsycInfo Database Record (c) 2022 APA,版权所有)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Behavioral neuroscience
Behavioral neuroscience 医学-行为科学
CiteScore
3.40
自引率
0.00%
发文量
51
审稿时长
6-12 weeks
期刊介绍: Behavioral Neuroscience publishes original research articles as well as reviews in the broad field of the neural bases of behavior.
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