Effects of molindone on central dopaminergic neuronal activity and metabolism: similarity to other neuroleptics.

Psychopharmacology communications Pub Date : 1975-01-01
B S Bunney, R H Roth, G K Aghajanian
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Abstract

The effect of molindone on the activity of dopaminergic (DA) neurons in the rat midbrain and on DA metabolism in the striatum and olfactory tubercles was studied using extracellular single unit recording and biochemical techniques respectively. Molindone in low intravenous doses (0.4-0.8 mg/kg) was found to reverse d-amphetamine and apomorphine induced depression of DA neurons and to block apomorphine induced depression of these cells. Molindone was also found to increase dopamine synthesis and dihydroxyphenylactic acid levels in the striatum and olfacotry tubercles. In all of these respects molindone behaves identically to most classical neuroleptics. However, unlike most antipsychotic drugs previously tested, molindone failed to increase the baseline firing rate of DA cells and blocked haloperidol induced increases in DA neuron activity. In this regard molindone most closely resembles thioridazine and clozapine. Possible mechanisms of action of molindone are discussed based on these findings.

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莫茚酮对中枢多巴胺能神经元活性和代谢的影响:与其他抗精神病药相似。
采用细胞外单单位记录和生化技术分别研究了莫茚酮对大鼠中脑多巴胺能神经元活性和纹状体及嗅结节多巴胺能代谢的影响。低剂量静脉注射(0.4 ~ 0.8 mg/kg)莫茚酮可逆转d-安非他明和阿波啡对DA神经元的抑制作用,并阻断阿波啡对DA神经元的抑制作用。莫林酮还被发现增加纹状体和嗅觉结节中的多巴胺合成和二羟基苯乳酸水平。在所有这些方面,莫茚酮的行为与大多数经典的抗精神病药相同。然而,与之前测试的大多数抗精神病药物不同,莫茚酮未能提高DA细胞的基线放电率,并阻断氟哌啶醇诱导的DA神经元活动的增加。在这方面,莫林酮最类似于噻嗪和氯氮平。在此基础上讨论了莫茚酮可能的作用机理。
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