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首页> 外文期刊>Psychopharmacology >Comparison of either norepinephrine-uptake inhibitors or phentermine combined with serotonergic agents on food intake in rats.
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Comparison of either norepinephrine-uptake inhibitors or phentermine combined with serotonergic agents on food intake in rats.

机译:去甲肾上腺素摄取抑制剂或芬特明联合血清素能药物对大鼠食物摄取的比较。

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摘要

RATIONALE: We have shown previously that the anorectic effects of the catecholamine-releasing agent phentermine (PHEN) and the serotonin (5-HT)-releasing agent dexfenfluramine (DFEN) are greater than additive in rats. In the present study, we examined whether the norepinephrine-uptake inhibitors desmethylimipramine (DMI) and thionisoxetine (TNIX) have additive effects with either DFEN or with the 5-HT-uptake inhibitor fluoxetine (FLX). We also examined whether PHEN interacts with a postsynaptically acting 5-HT agonist. METHODS: Undeprived rats were trained to eat a daily sweet-milk dessert and on test days were systemically administered single or combination drugs and the intakes recorded. RESULTS: Both DMI and TNIX produced dose-related suppressions of food intake. However, by isobolographic analysis, they did not enhance the anorectic actions of either DFEN or FLX. In contrast, confirming and extending our previous work, PHEN had a greater potentiating effect on the anorectic actions of DFEN and FLX than TNIX. Further, the anorectic action of the 5-HT2c receptor agonist TFMPP was enhanced by PHEN. CONCLUSIONS: These and other data are consistent with the idea that 5-HT agents may work "upstream" of critical catecholaminergic synapses in the production of anorexia, and explain the diminished efficacy of norepinephrine-uptake inhibitors relative to PHEN. The implications for clinically useful anorectic agents are discussed briefly.
机译:理由:我们以前已经证明,儿茶酚胺释放剂芬特明(PHEN)和5-羟色胺(5-HT)释放剂右芬氟拉明(DFEN)在大鼠中的厌食作用大于累加作用。在本研究中,我们检查了去甲肾上腺素摄取抑制剂desmethylimipramine(DMI)和硫代尼西汀(TNIX)是否与DFEN或5-HT摄取抑制剂氟西汀(FLX)具有加和作用。我们还检查了PHEN是否与突触后作用的5-HT激动剂相互作用。方法:训练未剥夺的大鼠每天吃甜牛奶甜点,并在测试日系统地给予单一或组合药物,并记录摄入量。结果:DMI和TNIX均产生与剂量有关的食物摄入抑制。但是,通过等效线描记法分析,它们没有增强DFEN或FLX的厌食作用。相反,与TNIX相比,PHEN对DFEN和FLX的厌食作用具有更大的增强作用,证实并扩展了我们之前的工作。此外,PHEN增强了5-HT2c受体激动剂TFMPP的厌食作用。结论:这些和其他数据与以下观点一致:5-HT药物可能在厌食症的产生中发挥关键儿茶酚胺突触的“上游”作用,并解释了去甲肾上腺素摄取抑制剂相对于PHEN的功效减弱。简要讨论了对临床有用的厌食药的影响。

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