Department of Biology, Texas Woman's University, Denton, TX 76204, USA.
Pharmacol Biochem Behav. 2011 Apr;98(2):311-5. doi: 10.1016/j.pbb.2011.01.014. Epub 2011 Jan 28.
Ovariectomized, Fischer rats were hormonally primed with 10 μg estradiol benzoate and 50 μg progesterone or were treated with the sesame seed oil vehicle. Food intake was measured 2 h and 24 h after treatment with 0.25 mg/kg of the 5-HT(1A) receptor agonist, (±)-8-hydroxy 2-(di-n-propylamino) tetralin (8-OH-DPAT), 5 mg/kg of the selective serotonin reuptake inhibitor, fluoxetine, or their combination. Consistent with prior studies, two hour food intake of rats given fluoxetine and 8-OH-DPAT did not differ from vehicle controls. 8-OH-DPAT-induced hyperphagia, evident at 2 h, was blocked by co-treatment with fluoxetine. However, in contrast to prior studies, 5 mg/kg fluoxetine, alone, had only modest effects on food intake. Differences in our experimental protocols and/or the strain of rat may account for the lower anorectic response to fluoxetine. Nevertheless, the absence of a significant response to fluoxetine, alone, coupled with the drug's attenuation of the hyperphagic effect of 8-OH-DPAT, leads to the suggestion that the behavioral response to the combined treatment is more complex than that of simple additivity. Consistent with this suggestion, 24 h food intake of rats given 8-OH-DPAT and fluoxetine was lower than that of vehicle or 8-OH-DPAT-treated rats.
去卵巢的 Fischer 大鼠接受 10μg苯甲酸雌二醇和 50μg孕酮的激素预刺激,或用芝麻籽油处理。在以 0.25mg/kg 的 5-HT(1A)受体激动剂(±)-8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)、5mg/kg 的选择性 5-羟色胺再摄取抑制剂氟西汀或其组合处理后 2 小时和 24 小时测量食物摄入量。与之前的研究一致,给予氟西汀和 8-OH-DPAT 的大鼠的 2 小时食物摄入量与载体对照没有差异。8-OH-DPAT 诱导的食欲亢进在 2 小时时明显,并被氟西汀共同治疗所阻断。然而,与之前的研究相反,单独给予 5mg/kg 的氟西汀仅对食物摄入量有适度的影响。我们的实验方案和/或大鼠品系的差异可能解释了对氟西汀的厌食反应较低。尽管如此,单独使用氟西汀没有明显的反应,加上药物对 8-OH-DPAT 的致食欲亢进作用的衰减,表明联合治疗的行为反应比简单的相加作用更为复杂。与这一建议一致,给予 8-OH-DPAT 和氟西汀的大鼠的 24 小时食物摄入量低于载体或 8-OH-DPAT 处理的大鼠。