National Institute of Pharmacy, Hungary.
Brain Res Bull. 2011 Jan 15;84(1):53-60. doi: 10.1016/j.brainresbull.2010.10.001. Epub 2010 Oct 8.
The aim of the present work was to further analyse the features of opioid dependence following chronic morphine treatment during pregnancy and lactation. Dams from the day of mating were treated either with saline or with morphine (10mg/kg) subcutaneously once daily. Physical and behavioural signs of morphine withdrawal were investigated both in the early postpartum period (maternal behaviour) and after weaning (physical signals, locomotion, anxiety-like behaviour). Maternal behaviour was evaluated after acute challenge with naloxone (3 mg/kgs.c.) or morphine (10 mg/kgs.c.) and morphine plus naloxone (10 mg/kgs.c. and 3 mg/kgs.c., respectively). After weaning sensitivity to the rewarding effect of morphine was measured by conditioned place preference and to the aversive effect of naloxone by conditioned place aversion tests. The intensity of physical and behavioural indices of dependence was also investigated by precipitation of withdrawal with naloxone (10 mg/kgs.c) after weaning. Naloxone impaired the maternal behaviour in morphine-treated dams but not in saline-ones. Acute challenge with morphine impaired maternal responsiveness both in saline and in morphine-treated dams, this effect of morphine, however could be completely antagonised by naloxone only in the saline-treated but not in the morphine-treated ones. Significantly increased sensitivity to the rewarding stimulus of morphine and more pronounced aversion to naloxone were observed in morphine-treated dams. Naloxone precipitated only moderate physical withdrawal signals in morphine-treated dams, while anxiety and locomotor activity after administration of naloxone (behavioural withdrawal) were not changed in them. In summary chronic, moderate dose morphine treatment during pregnancy and lactation resulted in only mild dependence, but it affected opioid-receptor sensitivity and presumably disrupted the functioning of endogenous opioid system.
本研究旨在进一步分析慢性吗啡治疗对妊娠和哺乳期后阿片类药物依赖的影响。从交配日起,每天给母体皮下注射生理盐水或吗啡(10mg/kg)。在产后早期(母性行为)和断奶后(身体信号、运动、焦虑样行为)研究吗啡戒断的身体和行为迹象。用纳洛酮(3mg/kg)或吗啡(10mg/kg)急性刺激后评估母性行为,以及吗啡加纳洛酮(分别为 10mg/kg 和 3mg/kg)。断奶后,通过条件位置偏好测量吗啡的奖赏效应敏感性,通过条件位置厌恶测试测量纳洛酮的厌恶效应敏感性。通过断奶后用纳洛酮(10mg/kg)诱发戒断来研究依赖的身体和行为指标的强度。纳洛酮损害了吗啡处理的母鼠的母性行为,但对生理盐水处理的母鼠没有影响。急性吗啡刺激损害了生理盐水和吗啡处理的母鼠的母性行为反应,然而,这种吗啡的作用只能在生理盐水处理的母鼠中被纳洛酮完全拮抗,而不能在吗啡处理的母鼠中被拮抗。在吗啡处理的母鼠中观察到对吗啡奖赏刺激的敏感性显著增加,对纳洛酮的厌恶反应更明显。纳洛酮仅在吗啡处理的母鼠中诱发中度身体戒断信号,而纳洛酮给药后的焦虑和运动活动(行为戒断)在它们中没有改变。总之,妊娠和哺乳期慢性、中等剂量吗啡治疗仅导致轻度依赖,但它影响阿片受体敏感性,并可能破坏内源性阿片系统的功能。