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Effect of prenatal stress on opioid component of exploration in different experimental situations.

机译:在不同的实验情况下,产前应激对阿片样物质成分的影响。

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Prenatal stress interferes with the expression of opioid systems in rats. The present study determined the effect of prenatal stress on the opioid-influenced component of exploratory behavior, defined as the difference between the behavior of vehicle-treated and naloxone-treated rats, in three novel situations previously shown to cause different degrees of arousal. Pregnant rats were stressed three times weekly on a random basis by noise and flashing lights. Experiments were performed on 60-70-day-old offspring (male and female) of control and stressed dams. Fifteen minutes after injection of vehicle or naloxone (1 mg/kg), the proportion of time spent in eight different behavioral parameters, including locomotion, rearing, sniffing, hole poking, pivoting, and grooming, was assessed during 4 min of exposure to an open field, either with or without prior exposure to a hole box. The magnitude of the depressant effect of naloxone on exploration depended on the nature of the environment, previous experienceof the animal in another situation, and the parameter of exploration assessed. The opioid-influenced component of locomotion and rearing was significantly reduced by prenatal stress, particularly in female rats. Further studies using a cross-fostering design are needed to assess the relative contributions of pre- and postnatal factors to the reduction of opioid activity in prenatally stressed rats. More specific opioid antagonists could be used to determine the nature of the opioid receptors involved.
机译:产前压力会干扰大鼠阿片样物质系统的表达。本研究确定了产前应激对阿片类药物影响的探索行为的影响,该行为定义为在先前证明会引起不同程度唤醒的三种新情况下,用媒介物治疗和纳洛酮治疗的大鼠之间的行为差​​异。怀孕的老鼠每周随机受到噪音和闪光灯的压力3次。实验是在60-70天大的对照和应激大坝后代(雄性和雌性)中进行的。注射媒介物或纳洛酮(1 mg / kg)后十五分钟,在暴露于人体的4分钟内,评估了在八个不同的行为参数中所花费的时间比例,包括运动,饲养,嗅探,戳孔,枢转和修饰等八个行为参数露天场,无论是否暴露在孔盒中。纳洛酮对探索的抑制作用的大小取决于环境的性质,动物在其他情况下的过往经历以及评估的评估参数。阿片类药物影响的运动和饲养成分通过产前应激得到明显降低,尤其是在雌性大鼠中。需要使用交叉培养设计进行进一步研究,以评估产前和产后因素对降低产前应激大鼠阿片类药物活性的相对贡献。可以使用更特异性的阿片拮抗剂来确定所涉及的阿片受体的性质。

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