妊娠前吗啡暴露是否会改变雄性Wistar大鼠吗啡依赖期间的焦虑样行为?

Saba Sabzevari, Kiyana Rohbani, Mahsa Sadeghi-Adl, Solmaz Khalifeh, Mitra-Sadat Sadat-Shirazi, Mohammad-Reza Zarrindast
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摘要

背景:焦虑是阿片类药物成瘾的合并症之一,它导致阿片类药物滥用或说服人们从事阿片类药物滥用。有证据表明,怀孕前接触吗啡会改变后代的表型。本研究旨在探讨吗啡依赖和戒断对吗啡暴露和drug-naïve后代焦虑样行为的影响。方法:雄性、雌性成年大鼠分别给予吗啡或载药治疗21 d。然后,所有大鼠不给药10天。一只暴露于吗啡的雌性大鼠与一只暴露于交通工具或吗啡戒断的雄性大鼠交配。根据父母吗啡暴露程度,将后代分为4个不同的组:(1)对照组(父母均为drug-naïve),(2)父亲吗啡暴露,(3)母亲吗啡暴露,(4)双亲吗啡暴露。采用吗啡暴露前(naïve)、吗啡暴露后21天(依赖)和最后一次吗啡暴露后10天(戒断)的开放场和升高的加迷宫测试来测量成年雄性后代的焦虑样行为。结果表明,吗啡暴露前,母代和双亲吗啡暴露子代的焦虑样行为增加(P<0.05)。然而,在吗啡暴露后,各组之间的焦虑水平没有变化。最后一次吗啡暴露后10天,只有双亲吗啡暴露子代的焦虑样行为增加(P<0.05)。结论:吗啡戒断父母的后代表现出焦虑表型。在母体和双亲吗啡暴露大鼠的后代中可见下丘脑轴的破坏。事实上,吗啡暴露21天并没有改变这些后代的焦虑样行为,这可能与它们的下丘脑轴断裂有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does Morphine Exposure Before Gestation Change Anxiety-Like Behavior During Morphine Dependence in Male Wistar Rats?
Background: Anxiety is one of the comorbid disorders of opioid addiction, which leads to opioid abuse or persuades people to engage in opioid abuse. Evidence revealed that morphine exposure before conception changes the offspring’s phenotype. The current study aimed to investigate the influence of morphine dependence and abstinence on anxiety-like behavior in morphine-exposed and drug-naïve offspring. Methods: Adult male and female rats were treated with morphine or vehicle for 21 days. Then, all rats were left without drug treatment for 10 days. A morphine-exposed female rat was mated with either a vehicle-exposed or morphine-abstinent male. According to parental morphine exposure, the offspring were categorized into four distinct groups: (1) control (both drug-naïve parents), (2) paternal morphine-exposed, (3) maternal morphine-exposed, and (4) biparental morphine-exposed. The anxiety-like behavior was measured in adult male offspring using open field and elevated plus-maze tests before morphine exposure (naïve), 21 days after morphine exposure (dependence), and ten days after the last morphine exposure (abstinence). Findings: The results indicated that anxiety-like behavior increased before morphine exposure in maternal and biparental morphine-exposed offspring (P<0.05). However, after morphine exposure, the anxiety level did not change among the groups. Ten days after the last morphine exposure, anxiety-like behavior increased only in biparental morphine-exposed offspring (P<0.05). Conclusion: The offspring of morphine-abstinent parents exhibited an anxious phenotype. Disruption of the HPA axis was seen in the progeny of maternal and biparental morphine-exposed rats. Indeed, morphine exposure for 21 days did not change anxiety-like behavior in these offspring which might be correlated to disruption of HPA axis in them.
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