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Histological and Histochemical Alternations in the Fetal Heart Tissue of Maternal Prozac Exposure

机译:母体百忧解暴露胎儿心脏组织中的组织学和组织化学变化

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Background and Objective: Depression during gestation destructively affects fetal development. Fluoxetine (Prozac) as a selective serotonin reuptake inhibitor (SSRIs) is used for handling of maternal despair. Anti-depressants cross the placenta and are transported to the fetus. This study aimed to determine the effects of fluoxetine on histopathological and histochemical changes in fetal heart tissue maternally treated with Fluoxetine. Materials and Methods: Forty pregnant rats were categorized into the following groups: Control group, group of 10 pregnant rats treated daily with 0.72 mg kgsup?/supsup1/sup b.wt. Fluoxetine (treatment started one month before pregnancy and continued till end of gestation), group of 10 pregnant rats treated daily with 1.44 mg kgsup?/supsup1/sup b.wt. Fluoxetine (treatment started from day zero till day 20 of pregnancy), group of 10 pregnant rats treated daily with 2.88 mg kgsup?/supsup1/sup b.wt. Fluoxetine (treatment started from day zero till day 20 of pregnancy). Pregnant mothers were sacrificed on day 19 of gestation and small samples of fetal heart were taken for the histological and histochemical studies. Results: Many histological and histochemical alternations were observed in fetal heart of all the treated groups compared with control group. The harshness of these changes increased with increasing the doses of Fluoxetine. Conclusion: Maternal fluoxetine exposure caused harmful changes in the fetal heart, therefore the use of this drug during gestation should be under strict precautions and further studies are recommended that it is essential to survey the roles of anti-depressant drugs on fatal development during pregnancy.
机译:背景与目的:妊娠期抑郁症对胎儿发育具有破坏性影响。氟西汀(Prozac)作为选择性5-羟色胺再摄取抑制剂(SSRIs)用于治疗孕妇的绝望感。抗抑郁药穿过胎盘并被运送至胎儿。本研究旨在确定氟西汀对经氟西汀治疗的胎儿心脏组织的组织病理学和组织化学变化的影响。材料与方法:40只怀胎大鼠分为以下几组:对照组,每天用0.72 mg kg ? 1 b.wt治疗的10只怀胎组。氟西汀(治疗从妊娠前一个月开始,一直持续到妊娠结束),每组10只,每天用1.44 mg kg ? 1 b.wt治疗的妊娠大鼠。氟西汀(治疗从怀孕的第0天开始到第20天开始),每组10只,每天用2.88 mg kg ? 1 b.wt治疗的妊娠大鼠。氟西汀(治疗从怀孕的第0天开始到第20天)。在妊娠的第19天,将怀孕的母亲处死,并取少量胎儿心脏进行组织学和组织化学研究。结果:与对照组相比,所有治疗组的胎心均观察到许多组织学和组织化学变化。这些变化的严酷性随着氟西汀剂量的增加而增加。结论:孕妇服用氟西汀会引起胎儿心脏的有害变化,因此在妊娠期间应严格预防使用这种药物,建议进行进一步研究,以调查抗抑郁药在妊娠期间致命发展中的作用。

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