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产前暴露于抗抑郁药对大鼠脑内5-羟色胺刺激的磷酸肌醇水解及5-羟色胺2型受体的影响。

Effect of prenatal exposure to antidepressants on 5-HT-stimulated phosphoinositide hydrolysis and 5-HT2 receptors in rat brain.

作者信息

Romero G, Toscano E, Del Río J

机构信息

Department of Pharmacology, University of Navarra Medical School, Pamplona, Spain.

出版信息

Gen Pharmacol. 1994 Sep;25(5):851-6. doi: 10.1016/0306-3623(94)90086-8.

Abstract
  1. Female rats were given antidepressants, with different effects on 5-HT uptake, from day 6 of pregnancy until delivery. 2. 5-HT-stimulated inositol phosphate accumulation as well as 5-HT2 receptor density were measured at two different times in the pups. 3. Prenatal exposure to fluoxetine or iprindole reduced phosphoinositide hydrolysis in 25-day-old pups. However, chronic treatment of adult rats with fluoxetine or prenatal exposure to either desipramine or tianeptine did not modify inositol phosphate accumulation. 4. After prenatal exposure, only desipramine significantly decreased the density of [3H]ketanserin-labelled 5-HT2 receptors in the pups. 5. No correlation was found between changes in inositol phosphate formation and 5-HT2 receptor number.
摘要
  1. 从怀孕第6天到分娩,给雌性大鼠服用对5-羟色胺(5-HT)摄取有不同影响的抗抑郁药。2. 在幼崽的两个不同时间点测量5-HT刺激的肌醇磷酸积累以及5-HT2受体密度。3. 产前接触氟西汀或茚满二酮可降低25日龄幼崽的磷酸肌醇水解。然而,成年大鼠长期用氟西汀治疗或产前接触去甲丙咪嗪或噻奈普汀均未改变肌醇磷酸积累。4. 产前接触后,只有去甲丙咪嗪显著降低了幼崽中[3H]酮色林标记的5-HT2受体的密度。5. 未发现肌醇磷酸形成变化与5-HT2受体数量之间存在相关性。

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