Goldstein R
Endocrinologie. 1985 Jan-Mar;23(1):23-7.
In order to investigate the effects of arginine vasotocin (AVT), (a pineal nonapeptide hormone) on the brain maturation, the sleep-wake cycle, the day of eyelids opening and the total brain lipids level were followed up in new-born rats receiving daily (between day 2 and 8 of life) 100 ng of synthetic AVT, arginine-vasopressin (AVP), oxytocin (OT) or 0.1 ml saline solution. While AVP and OT had no effect, AVT induced: 1) an increase in the amount of active sleep (AS); 2) a decrease in the brain weight and the total brain lipids, and 3) a delay in the eyelids opening. These findings demonstrate that chronic administration of AVT induces a delay in the brain maturation of the new-born rats. Association of low brain lipids with a high percentage of AS is a very useful index of brain maturation. It is suggested that the drop in the endogenous brain levels of AVT below a critical threshold might represent a hormonal signal for triggering the beginning of brain maturation in mammals.
为了研究精氨酸血管加压素(AVT,一种松果体九肽激素)对大脑成熟的影响,对新生大鼠进行了如下跟踪观察:在出生后第2天至第8天期间,每天给新生大鼠注射100纳克合成AVT、精氨酸加压素(AVP)、催产素(OT)或0.1毫升生理盐水,观察其睡眠 - 觉醒周期、睁眼日以及全脑脂质水平。结果发现,AVP和OT没有影响,而AVT导致:1)主动睡眠(AS)量增加;2)脑重量和全脑脂质减少;3)睁眼延迟。这些研究结果表明,长期给予AVT会导致新生大鼠大脑成熟延迟。低脑脂质与高比例的主动睡眠相关联是大脑成熟的一个非常有用的指标。有人提出,内源性大脑AVT水平降至临界阈值以下可能代表一种激素信号,触发哺乳动物大脑成熟的开始。