Kinsley C H, Bridges R S
Harvard Medical School, Department of Anatomy and Cellular Biology, Boston, Massachusetts 02115.
Biol Reprod. 1988 Sep;39(2):270-8. doi: 10.1095/biolreprod39.2.270.
Behavioral and physiological responses differ between primiparous and multiparous female rodents. Specifically, multiparous females respond with the full repertoire of maternal behaviors much more rapidly and with greater intensity than their primiparous counterparts. Since opiates inhibit the expression of maternal behavior in postpartum rats and can be reversed by means of the opiate antagonist naloxone, we investigated whether multiparous females would be resistant to the inhibitory effects of opiates on maternal behavior, relative to primiparous females. In Experiment 1 we evaluated the effects of a range of doses of morphine sulfate (MS; 0.625, 1.25, 2.5, 5.0, and 10.0 mg/kg or saline) on maternal behavior in primiparous females on Days 5-6 of lactation. The 5.0 and 10.0 mg/kg doses effectively disrupted maternal behavior, whereas the lower doses were ineffective or only marginally disruptive. In Experiment 2, age-matched female rats were timed-mated and tested for maternal behavior from Day 5 to 13 of lactation, after daily injections of the 5.0 mg/kg dose of MS. On Day 5 of lactation, this morphine treatment eliminated full maternal behavior in 87% of the primiparous animals, but only 37% of the multiparous animals were affected. By Day 10 of lactation, 100% of the multiparous females displayed full maternal behavior after MS treatment, whereas only 69% of primiparous females were responsive. In Experiment 3, analgesic responses were measured both in rats experiencing their initial or second pregnancy, and in postpartum, lactating rats after MS (5.0 mg/kg) administration. Using a tail-flick apparatus to measure analgesia, we found multigravid females to be significantly less analgesic prepartum than primigravid females, suggesting less sensitivity to endogenous opioids.(ABSTRACT TRUNCATED AT 250 WORDS)
初产和经产雌性啮齿动物的行为和生理反应有所不同。具体而言,经产雌性比初产雌性更快且更强烈地展现出全套母性行为。由于阿片类药物会抑制产后大鼠的母性行为表达,且可通过阿片类拮抗剂纳洛酮逆转,我们研究了经产雌性相对于初产雌性是否对阿片类药物抑制母性行为的作用具有抗性。在实验1中,我们评估了一系列剂量的硫酸吗啡(MS;0.625、1.25、2.5、5.0和10.0毫克/千克或生理盐水)对初产雌性在哺乳期第5至6天的母性行为的影响。5.0和10.0毫克/千克的剂量有效干扰了母性行为,而较低剂量则无效或仅有轻微干扰。在实验2中,对年龄匹配的雌性大鼠进行定时交配,并在从哺乳期第5天至13天每天注射5.0毫克/千克剂量的MS后测试其母性行为。在哺乳期第5天,这种吗啡处理使87%的初产动物完全丧失母性行为,但只有37%的经产动物受到影响。到哺乳期第10天,经产雌性中有100%在接受MS处理后表现出完全的母性行为,而初产雌性中只有69%有反应。在实验3中,对经历首次或第二次怀孕的大鼠以及产后哺乳期大鼠在给予MS(5.0毫克/千克)后测量镇痛反应。使用甩尾装置测量镇痛效果,我们发现多胎妊娠雌性在产前的镇痛效果明显低于初孕雌性,这表明对内源性阿片类物质的敏感性较低。(摘要截选至250字)