Dickinson S L, Curzon G
Neuropharmacology. 1983 Jul;22(7):805-12. doi: 10.1016/0028-3908(83)90124-7.
The roles of dopamine (DA) and 5-hydroxytryptamine (5-HT) in stereotyped and non-stereotyped components of the classical behavioural syndromes induced by 5-HT and DA were investigated by studying (a) behavioural interactions between the DA agonist apomorphine and the 5-HT agonist 5-methoxy-N,N-dimethyltryptamine (5-MeODMT) and (b) the effects of depletion of 5-HT on the behavioural responses to amphetamine and p-chloroamphetamine. In agreement with evidence [Andrews, Fernando and Curzon (1982) Neuropharmacology 21:63-68] that non-stereotyped (i.e. body shakes and hind limb abduction) and stereotyped (i.e. head weaving and reciprocal forepaw treading) behaviour induced by d-amphetamine (25 mg/kg, i.p.) were inhibited and enhanced respectively by DA, apomorphine inhibited two non-stereotyped behavioural responses induced by 5-MeODMT (hind limb abduction and Straub tail) but enhanced reciprocal forepaw treading. However, head weaving was inhibited. Evidence indicated that behaviour induced by DA (whether stereotyped or not) was inhibited by 5-HT. Thus, the induction by apomorphine of sniffing and mouth movements was enhanced when the synthesis of 5-HT was inhibited. Also, p-chloroamphetamine caused sniffing and mouth movements only when 5-HT synthesis was inhibited. Under the latter conditions, while most classical behavioural responses associated with 5-HT did not occur, hind limb abduction persisted. Similarly, amphetamine (25 mg/kg) caused hind limb abduction and forepaw treading even when 5-HT was almost completely depleted. These results may indicate that the amine releasers have some direct 5-HT agonist properties. Results in general indicate the multiplicity of behavioural interactions between DA and 5-HT.
通过研究以下内容,探究了多巴胺(DA)和5-羟色胺(5-HT)在由5-HT和DA诱导的经典行为综合征的刻板和非刻板成分中的作用:(a)DA激动剂阿扑吗啡与5-HT激动剂5-甲氧基-N,N-二甲基色胺(5-MeODMT)之间的行为相互作用;(b)5-HT耗竭对苯丙胺和对氯苯丙胺行为反应的影响。与证据[安德鲁斯、费尔南多和柯尔赞(1982年),《神经药理学》21:63 - 68]一致,即右旋苯丙胺(25毫克/千克,腹腔注射)诱导的非刻板行为(即身体颤抖和后肢外展)和刻板行为(即头部摆动和前爪交替踏地)分别被DA抑制和增强,阿扑吗啡抑制了5-MeODMT诱导的两种非刻板行为反应(后肢外展和施特劳布尾),但增强了前爪交替踏地。然而,头部摆动受到抑制。有证据表明,DA诱导的行为(无论是否刻板)被5-HT抑制。因此,当5-HT的合成被抑制时,阿扑吗啡诱导的嗅探和口部运动增强。此外,对氯苯丙胺仅在5-HT合成被抑制时才引起嗅探和口部运动。在后一种情况下,虽然大多数与5-HT相关的经典行为反应未出现,但后肢外展持续存在。同样,即使5-HT几乎完全耗竭,苯丙胺(25毫克/千克)仍会引起后肢外展和前爪踏地。这些结果可能表明胺释放剂具有一些直接的5-HT激动剂特性。总体结果表明DA和5-HT之间行为相互作用的多样性。