Volosin M, Cancela L M, Laino C, Massei M, Molina V A
Departamento de Farmacologia, Facultad de Ciencias Quimicas, Universidad Nacional de Córdoba, Argentina.
Neuropharmacology. 1991 Jul;30(7):719-25. doi: 10.1016/0028-3908(91)90179-f.
The influence of adrenocorticotropic hormone (ACTH) in the adaptive changes on central dopamine (DA) autoreceptors following chronic administration of desipramine (DMI) has been examined in rats. Dopamine had an inhibitory effect on basal and K(+)-induced release of [3H]DA from slices of striatum and n. accumbens of rats treated chronically (10 days) with ACTH (50 IU/kg, s.c.), DMI (10 mg/kg, i.p.) or the combination of ACTH and DMI. In slices of n. accumbens, but not in slices of striatum of rats exposed to the combined treatment of ACTH and DMI, a significant decrease in the inhibitory effect of exogenous DA on stimulated release of [3H]DA was observed. Chronic administration of ACTH or DMI alone had no effect. The effect of the combined treatment with both agents, on the reactivity of these DA receptors was evaluated by means of apomorphine-induced hypoactivity. The administration of ACTH and DMI (5 mg/kg, i.p.) reduced the hypoactivity induced by apomorphine, as compared to hypoactivity in rats treated with ACTH or DMI alone. Experiments with ACTH4-10 revealed that the peptide modified biochemical and behavioural parameters of dopaminergic function, which may implicate a direct action of the peptide on the brain, rather than on the release of adrenal hormones. These findings suggest that ACTH accelerates the onset of DMI-induced adaptive changes on dopamine in the mesolimbic area. However, because the effect of ACTH4-10 on release of adrenocortical hormone was not investigated, the possibility cannot be disregarded that the effect of the peptide was secondary to an enhancement of release of adrenal hormone.
在大鼠中研究了促肾上腺皮质激素(ACTH)对慢性给予地昔帕明(DMI)后中枢多巴胺(DA)自身受体适应性变化的影响。多巴胺对慢性(10天)接受ACTH(50 IU/kg,皮下注射)、DMI(10 mg/kg,腹腔注射)或ACTH与DMI联合治疗的大鼠纹状体和伏隔核切片中[3H]DA的基础释放和K⁺诱导释放具有抑制作用。在接受ACTH和DMI联合治疗的大鼠伏隔核切片中,但不是纹状体切片中,观察到外源性DA对[3H]DA刺激释放的抑制作用显著降低。单独慢性给予ACTH或DMI没有效果。通过阿扑吗啡诱导的活动减退评估两种药物联合治疗对这些DA受体反应性的影响。与单独接受ACTH或DMI治疗的大鼠相比,给予ACTH和DMI(5 mg/kg,腹腔注射)可减轻阿扑吗啡诱导的活动减退。ACTH4 - 10实验表明,该肽改变了多巴胺能功能的生化和行为参数,这可能意味着该肽对大脑有直接作用,而不是对肾上腺激素释放有作用。这些发现表明,ACTH加速了DMI诱导的中脑边缘区多巴胺适应性变化的发生。然而,由于未研究ACTH4 - 10对肾上腺皮质激素释放的影响,不能忽视该肽的作用可能继发于肾上腺激素释放增强的可能性。