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首页> 外文期刊>Japanese Journal of Pharmacology >Developmental Alterations in Maturing Rats Caused by Chronic Prenatal and Postnatal Diazepam Treatments
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Developmental Alterations in Maturing Rats Caused by Chronic Prenatal and Postnatal Diazepam Treatments

机译:慢性产前和产后地西ze治疗引起的成熟大鼠发育变化

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References(29) Cited-By(8) The post treatment effects of early prenatal, late prenatal, early postnatal or combined prenatal and neonatal treatment with diazepam on the development of pain sensitivity, acoustic startle responsiveness, and benzodiazepine receptors in the cerebral cortex were investigated in rats between 14 and 90 days of age. Tail-flick latency was significantly decreased by combined prenatal and neonatal and by early prenatal diazepam treatment, but not by diazepam during the last half of gestation or during the neonatal period alone. Acoustic startle response was decreased by either late prenatal or neonatal diazepam treatment, but not by early prenatal treatment alone. Density of benzodiazepine receptors in the cortex was increased from postnatal day 1 to 21 by either early or late prenatal diazepam treatment. Neonatal diazepam treatment suppressed cortical benzodiazepine receptor or development until postnatal day 21; thereafter, receptor density increased to significantly higher values than in controls at 90 days of age. The results demonstrate that diazepam can alter development of pain sensitivity by actions during early gestation, startle responsiveness by actions late in pregnancy, and cortical benzodiazepine receptors by actions throughout gestation and the early postnatal period.
机译:参考文献(29)被引用(8)产前,产前晚期,产后早期或产前和新生儿联合地西epa的治疗对大脑皮层疼痛敏感性,听觉惊吓反应和苯二氮卓受体发展的影响如下:在14至90天大的老鼠中进行了调查。通过合并产前和新生儿以及通过早期产前地西epa治疗,甩尾潜伏期显着减少,但在妊娠的后半段或仅在新生儿期,地西epa并没有减少甩尾潜伏期。产前后期或新生儿地西epa治疗可降低声音惊吓反应,但单独产前早期治疗并不能减少。通过产前地西epa的早期或晚期治疗,皮质中苯二氮卓类受体的密度从出生后的第1天增加到第21天。新生儿地西epa治疗可抑制皮质苯并二氮杂receptor受体或发育直至出生后第21天。此后,在90天龄时,受体密度增加到比对照组高得多的值。结果表明,地西epa可以通过早期妊娠的作用改变疼痛敏感性的发展,在妊娠后期的作用引起的惊吓反应,在整个妊娠和产后早期的作用都可以改变皮质苯并二氮杂receptor受体。

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