Kee Choi Yong, Tarazi Frank I
Department of Psychiatry and Neuroscience Program, Harvard Medical School and McLean Hospital, Belmont, MA, 02478, USA.
Synapse. 2018 Jun 23:e22039. doi: 10.1002/syn.22039.
The atypical antipsychotic drug iloperidone has high affinity for a wide range of neurotransmitter receptors, including dopaminergic (DA), serotonergic, and adrenergic receptors. We examined the long-term effects of multiple doses of iloperidone on DA D , D , D , and D receptor subtypes. Sprague-Dawley adult rats (n = 8/group) received daily intraperitoneal injections of iloperiodone (0.5, 1, or 5 mg/kg) or vehicle for 4 weeks. Receptor autoradiography quantified the levels of DA receptors in medial prefrontal cortex (MPC), dorsolateral frontal cortex (DFC), caudate putamen (CPu), nucleus accumbens (NAc), and hippocampus (HIP). Four weeks of iloperidone treatment at 5 mg/kg significantly increased D receptors in NAc (36%) and CPu (38%). Iloperidone (1.5 and 5 mg/kg) dose-dependently increased D receptors in MPC (37 and 47%) and HIP (32 and 40%). Only the high dose of iloperidone (5 mg/kg) increased D receptors in NAc (39%) and CPu (38%). Repeated treatment with iloperidone (1.5 and 5 mg/kg) increased D receptors in the NAc (39 and 78%), CPu (42 and 83%) and HIP (54 and 72%). The three doses of iloperidone failed to alter D receptors in the brain regions examined in this study. These results suggest that iloperidone exerts region- and dose-specific effects on forebrain DA receptor subtypes, which may contribute to its therapeutic benefits in improving the positive and negative symptoms of schizophrenia with minimal extrapyramidal side effects.
非典型抗精神病药物伊潘立酮对多种神经递质受体具有高亲和力,包括多巴胺能(DA)、5-羟色胺能和肾上腺素能受体。我们研究了多剂量伊潘立酮对DA D 、D 、D 和D 受体亚型的长期影响。成年Sprague-Dawley大鼠(每组n = 8)每天腹腔注射伊潘立酮(0.5、1或5 mg/kg)或赋形剂,持续4周。受体放射自显影法定量检测内侧前额叶皮质(MPC)、背外侧额叶皮质(DFC)、尾状壳核(CPu)、伏隔核(NAc)和海马体(HIP)中DA受体的水平。5 mg/kg的伊潘立酮治疗4周显著增加了NAc(36%)和CPu(38%)中的D 受体。伊潘立酮(1.5和5 mg/kg)剂量依赖性地增加了MPC(37%和47%)和HIP(32%和40%)中的D 受体。只有高剂量的伊潘立酮(5 mg/kg)增加了NAc(39%)和CPu(38%)中的D 受体。重复给予伊潘立酮(1.5和5 mg/kg)增加了NAc(39%和78%)、CPu(42%和83%)和HIP(54%和72%)中的D 受体。本研究中使用的三个剂量的伊潘立酮均未改变所检测脑区中的D 受体。这些结果表明,伊潘立酮对前脑DA受体亚型具有区域和剂量特异性作用,这可能有助于其在改善精神分裂症的阳性和阴性症状方面发挥治疗作用,同时将锥体外系副作用降至最低。