María Cristina Márquez-Orozco, Irma Zarco de Coronado, Amalia Márquez-Orozco, Graciela de la Fuente-Juárez, María Verónica Gazca-Ramírez, Ignacio Méndez-Ramírez
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引用次数: 0
摘要
成年雌性小鼠对地西泮(DZ)的反应可以通过产前用药经历来塑造。实验是在子宫内暴露于DZ的ICR系(Harlan m xico)小鼠中进行的。在妊娠第6天至第17天,它们从注射2.7 mg/kg/bw DZ或仅注射生理盐水的母鼠中出生。它们被维持在12:12的暗/光循环,并随意提供食物和水。实验当天,将小鼠置于活动计(actometer)中5 min,以25 mm/min的速度进行记录。他们保持静止或明显困倦的时间以毫米为单位。之后,所有动物接受(s.c) 2.7 mg/kg/bw的DZ;15 min后再次进入测压仪5 min。DZ前,对照组妊娠期注射生理盐水为1.57 +/- 0.53 mm,实验组妊娠期注射生理盐水为3.69 +/- 1.72 mm (p =0.27)。DZ后,对照组小鼠静止时间为37.27 +/- 6.77 mm, DZ小鼠静止时间为59.95 +/- 7.10 mm (p=0.03)。这一结果表明,经预处理的动物对DZ的反应明显更大,表明发育中的胎儿暴露于DZ可能导致中枢神经系统几个区域的持续(14个月)形态学改变,对运动行为和学习产生生理影响,有时归因于脑回路改变或突触神经化学机制的发育脆弱性。
Motor response of 14-month-old female mice exposed to diazepam prenatally.
The response of adult female mice to diazepam (DZ) can be sculpted by the prenatal experience with the drug. Experiments were performed in ICR strain (Harlan México) mice exposed in utero to DZ. They were born from dams injected (s.c.) with 2.7 mg/kg/bw of DZ or just saline solution from day 6 to 17 of pregnancy. They were maintained at 12:12 dark/light cycles with food and water ad libitum. On the experimental day, mice were introduced in an activity meter (actometer) for 5 min. Recordings were run at 25 mm/min. The time they remained motionless or clearly sleepy was determined in millimeters. After that, all animals received (s.c.) 2.7 mg/kg/bw of DZ; 15 min later they were introduced into the actometer again for 5 min. Before DZ, control animals injected with saline during gestation showed 1.57 +/- 0.53 mm and the experimental (DZ) prenatally exposed to DZ, 3.69 +/- 1.72 mm (p =0.27). After DZ, control animals remained motionless for 37.27 +/- 6.77 mm and DZ mice, 59.95 +/- 7.10 mm (p=0.03). This result indicates a significantly larger response to DZ in the pretreated animals, suggesting that exposure of the developing fetus to the drug may lead to persistent (14 months) morphological alterations in several areas of the central nervous system with physiological repercussion on motor behavior and learning, sometimes attributed to brain circuitry modifications or to the developmental vulnerability of synaptic neurochemical mechanisms.