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血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)诱导的进食特征。

Characteristics of feeding induced by the serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT).

作者信息

Dourish C T, Hutson P H, Curzon G

出版信息

Brain Res Bull. 1985 Oct;15(4):377-84. doi: 10.1016/0361-9230(85)90005-x.

Abstract

The effects of the putative serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) on food intake in freely-feeding and food deprived rats were examined. In freely-feeding rats, low doses of 8-OH-DPAT (15-60 micrograms/kg) significantly increased food intake without affecting drinking, grooming, rearing or locomotion. Higher drug doses (125-4000 micrograms/kg) also produced feeding and caused locomotor stimulation and serotonin-related stereotyped behaviour (i.e., forepaw padding, headweaving, wet dog shakes, flat body posture). When feeding and stereotypy were observed concurrently, response competition was evident and feeding behaviour was fragmented into numerous short eating bouts. As drug-induced stereotypy declined with time, this fragmented pattern of eating was succeeded by long bouts of eating which were similar to those observed at doses of 15-60 micrograms/kg 8-OH-DPAT. In 24 hr food deprived rats, low doses of 8-OH-DPAT had no effect on food intake. However, high doses of 8-OH-DPAT (250-4000 micrograms/kg) decreased feeding in food deprived animals, an effect which was probably secondary to the induction of stereotypy. It is proposed that the behavioural effects of 8-OH-DPAT may be explained by a dual effect on brain serotonergic mechanisms, which is dose dependent. Thus, low doses of the drug may preferentially activate inhibitory presynaptic serotonin receptors (autoreceptors), decrease serotonin metabolism and thereby increase feeding. In contrast, high doses of 8-OH-DPAT appear to stimulate postsynaptic serotonin receptors and thus produce stereotypy. Alternatively, it is possible that 8-OH-DPAT may elicit feeding by postsynaptic serotonin receptor blockade.

摘要

研究了假定的血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)对自由进食和食物剥夺大鼠食物摄入量的影响。在自由进食的大鼠中,低剂量的8-OH-DPAT(15-60微克/千克)显著增加食物摄入量,而不影响饮水、梳理毛发、直立或运动。更高的药物剂量(125-4000微克/千克)也会引发进食,并导致运动刺激和与血清素相关的刻板行为(即前爪拍打、头部摆动、湿狗样抖动、身体扁平姿势)。当同时观察到进食和刻板行为时,反应竞争明显,进食行为被分解为许多短暂的进食回合。随着药物诱导的刻板行为随时间下降,这种碎片化的进食模式被长时间的进食回合所取代,这与在15-60微克/千克8-OH-DPAT剂量下观察到的情况相似。在24小时食物剥夺的大鼠中,低剂量的8-OH-DPAT对食物摄入量没有影响。然而,高剂量的8-OH-DPAT(250-4000微克/千克)会减少食物剥夺动物的进食,这种影响可能是刻板行为诱导的继发效应。有人提出,8-OH-DPAT的行为效应可能是由对脑血清素能机制的双重作用来解释的,这是剂量依赖性的。因此,低剂量的药物可能优先激活抑制性突触前血清素受体(自身受体),减少血清素代谢,从而增加进食。相反,高剂量的8-OH-DPAT似乎刺激突触后血清素受体,从而产生刻板行为。或者,8-OH-DPAT可能通过突触后血清素受体阻断引发进食。

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