Moraes A P, Schwarz A, Spinosa H S, Florio J C, Bernardi M M
Department of Pharmacology, Biomedical Science Institute, University of São Paulo, São Paulo, Brazil.
Neurotoxicol Teratol. 2004 Sep-Oct;26(5):681-92. doi: 10.1016/j.ntt.2004.04.008.
Previous research from our laboratory suggested that the administration of antihistaminics (H(1) receptor antagonists) to pregnant Wistar rats throughout pregnancy altered brain sexual differentiation and dopaminergic physiology of the offspring. In the present study, we assessed the effects of 20 mg/kg diphenhydramine (DPH) administration to pregnant rats during the fetal period of pregnancy [Gestation Days (GDs) 16-21], a critical period for brain sexual differentiation and central nervous system (CNS) maturation. Maternal body weight and water and food consumption were measured during pregnancy and offspring physical and behavioral development were evaluated during lactation. Offspring open-field behavior was assessed at 21 and 100 days of age. After the final open-field test, male and female sexual behavior, stereotypy following an apomorphine challenge, striatal content of dopamine (DA), the dopamine metabolites 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanilic acid (HVA), serotonin (5-HT) and the serotonin metabolite 5-hydroxyindolacetic acid (5-HIAA) were assessed. There were no significant treatment-related changes in maternal reproductive parameters, but DPH treatment decreased maternal body weight gain during the treatment period. Offspring physical parameters were not altered in the treated group, and no significant treatment-related changes were found in female open-field measures, sexual behavior or in striatal neurochemical measurements. However, delayed testis descent and altered patterns of sexual behavior occurred in male offspring accompanied by increased striatal DA, decreased striatal DOPAC as well as reduced DOPAC/DA, HVA/DA and 5-HIAA/5-HT ratios. Taken together, these data suggest that exposure to DPH during the fetal period of rat development altered postnatal CNS maturation and sexual development of male offspring via changes in striatal bioamine systems.
我们实验室之前的研究表明,在整个孕期给怀孕的Wistar大鼠施用抗组胺药(H(1)受体拮抗剂)会改变后代的脑性分化和多巴胺能生理。在本研究中,我们评估了在孕期的胎儿期[妊娠天数(GDs)16 - 21天]给怀孕大鼠施用20 mg/kg苯海拉明(DPH)的影响,这是脑性分化和中枢神经系统(CNS)成熟的关键时期。在孕期测量母鼠体重以及水和食物消耗量,并在哺乳期评估后代的身体和行为发育。在21日龄和100日龄时评估后代的旷场行为。在最后一次旷场试验后,评估雄性和雌性的性行为、阿扑吗啡激发后的刻板行为、纹状体多巴胺(DA)含量、多巴胺代谢物3,4 - 二羟基苯乙酸(DOPAC)和高香草酸(HVA)、血清素(5 - HT)以及血清素代谢物5 - 羟吲哚乙酸(5 - HIAA)。与治疗相关的母鼠生殖参数没有显著变化,但DPH治疗在治疗期间降低了母鼠体重增加。治疗组后代的身体参数没有改变,在雌性旷场测量、性行为或纹状体神经化学测量中未发现与治疗相关的显著变化。然而,雄性后代出现睾丸下降延迟和性行为模式改变,同时伴有纹状体DA增加、纹状体DOPAC减少以及DOPAC/DA、HVA/DA和5 - HIAA/5 - HT比值降低。综上所述,这些数据表明,在大鼠发育的胎儿期暴露于DPH会通过纹状体生物胺系统的变化改变雄性后代出生后的CNS成熟和性发育。