Grenhoff J, Svensson T H
Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Eur J Pharmacol. 1993 Mar 16;233(1):79-84. doi: 10.1016/0014-2999(93)90351-h.
Previous studies have indicated a noradrenergic modulation of midbrain dopamine cell activity. The effects of systemic administration of the alpha 1-adrenoceptor antagonist prazosin and the alpha 2-antagonist idazoxan on midbrain dopamine cell firing were now studied with extracellular recording from single dopamine neurons in the ventral tegmental area of chloral hydrate-anaesthetized male rats. Prazosin (0.15-0.6 mg/kg i.v.) dose dependently decreased burst firing and regularized the firing pattern of dopamine neurons, while the firing rate was unaffected. The prazosin-induced effects were abolished by pretreatment with reserpine. Idazoxan (0.5-2.0 mg/kg i.v.) increased firing rate and burst firing and made the firing pattern less regular, probably by increasing adrenergic transmission via blockade of presynaptic alpha 2-adrenoceptors. The effects of idazoxan were blocked by prazosin. The present results indicate that noradrenergic neurons modulate the dopamine cell firing pattern via excitatory postsynaptic alpha 1-adrenoceptors. This mechanism might be involved in the pathogenesis and pharmacological treatment of schizophrenia.
先前的研究表明中脑多巴胺细胞活动存在去甲肾上腺素能调节。现在,利用水合氯醛麻醉的雄性大鼠腹侧被盖区单个多巴胺神经元的细胞外记录,研究了全身给予α1肾上腺素能受体拮抗剂哌唑嗪和α2拮抗剂咪唑克生对中脑多巴胺细胞放电的影响。哌唑嗪(0.15 - 0.6毫克/千克静脉注射)剂量依赖性地减少爆发性放电并使多巴胺神经元的放电模式正常化,而放电频率不受影响。利血平预处理可消除哌唑嗪诱导的效应。咪唑克生(0.5 - 2.0毫克/千克静脉注射)增加放电频率和爆发性放电,并使放电模式变得不那么规则,这可能是通过阻断突触前α2肾上腺素能受体增加肾上腺素能传递所致。哌唑嗪可阻断咪唑克生的效应。目前的结果表明,去甲肾上腺素能神经元通过兴奋性突触后α1肾上腺素能受体调节多巴胺细胞的放电模式。该机制可能参与精神分裂症的发病机制和药物治疗。