首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Chronic nicotine and dizocilpine effects on nicotinic and NMDA glutamatergic receptor regulation: interactions with clozapine actions and attentional performance in rats.
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Chronic nicotine and dizocilpine effects on nicotinic and NMDA glutamatergic receptor regulation: interactions with clozapine actions and attentional performance in rats.

机译:慢性尼古丁和地佐西平对烟碱和NMDA谷氨酸能受体的调节作用:与氯氮平作用的相互作用和大鼠的注意力表现。

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摘要

Blockade of NMDA glutamate receptors with dizocilpine (MK-801) has been shown to cause substantial cognitive deficits and has been used to model symptoms of schizophrenia. Nicotine or nicotinic agonists, in contrast, may enhance cognitive or attentional functions and be of therapeutic potential in schizophrenia. Nicotinic-glutamatergic interactions, therefore, may have important implications in cognitive functions and antipsychotic treatments. Clozapine, a widely used antipsychotic drug, has been shown in some studies to be effective in ameliorating the cognitive deficits associated with schizophrenia. However, there is some evidence to suggest that clozapine similar to haloperidol may impair sustained attention in rats. In this study, we sought to determine whether chronic nicotine or dizocilpine may modify the effects of acute clozapine on attentional parameters and whether the behavioral effects would correlate with nicotinic or NMDA receptor densities in discrete brain regions. Adult female rats trained on an operant visual signal detection task were given 4 weeks of nicotine (5 mg/kg/day), dizocilpine (0.15 mg/kg/day), the same doses of both nicotine and dizocilpine as a mixture, or saline by osmotic minipump. While on chronic treatment, rats received acute injections of various doses of clozapine (0, 0.625, 1.25, 2.5 mg/kg, sc) 10 min prior to tests on attentional tasks. The pumps were removed on day 28 and 24 h later the animals were sacrificed for measurements of receptor densities in specific brain regions. The percent correct hit as a measure of sustained attention was significantly impaired by clozapine in a dose-related manner. Neither chronic nicotine nor dizocilpine affected this measure on their own or modified the effects of clozapine. Both nicotine and dizocilpine affected the receptor bindings in a region specific manner and their combination further modified the effects of each other in selective regions. Attentional performance was inversely correlated with alpha-bungarotoxin binding in the frontal cortex only. In conclusion, the data suggest attentional impairments with clozapine alone and no modification of this effect with nicotine or dizocilpine. Moreover, cortical low affinity nicotinic receptors may have a role in attentional functions.
机译:已证明用地佐西平(MK-801)阻断NMDA谷氨酸受体会导致严重的认知缺陷,并已被用于模拟精神分裂症的症状。相反,尼古丁或烟碱激动剂可增强认知或注意力功能,在精神分裂症中具有治疗潜力。因此,烟碱味之间的相互作用可能对认知功能和抗精神病药物治疗具有重要意义。氯氮平是一种广泛使用的抗精神病药物,在一些研究中已显示可有效缓解与精神分裂症有关的认知缺陷。但是,有一些证据表明,类似于氟哌啶醇的氯氮平可能会损害大鼠的持续注意力。在这项研究中,我们试图确定慢性尼古丁或地佐西平是否可以改变急性氯氮平对注意力参数的影响,以及行为影响是否与离散脑区域的烟碱或NMDA受体密度相关。对成年雌性大鼠进行视觉视觉信号检测,给予其4周尼古丁(5 mg / kg /天),地佐西平(0.15 mg / kg /天),相同剂量的尼古丁和地佐西平的混合物或生理盐水通过渗透微型泵。在进行慢性治疗时,大鼠在进行注意力测试前10分钟接受了各种剂量的氯氮平(0、0.625、1.25、2.5 mg / kg,sc)的急性注射。在第28和24小时后移开泵,处死动物以测量特定脑区域中的受体密度。氯氮平以剂量相关的方式显着损害了正确击球百分比作为持续注意力的衡量指标。慢性尼古丁和地佐西平均未自行影响该措施或改变氯氮平的作用。尼古丁和地佐西平均以区域特异性方式影响受体结合,并且它们的组合进一步改变了彼此在选择性区域中的作用。注意表现与仅在额叶皮层中的α-邦加毒素结合成反比。总之,数据表明单独使用氯氮平可引起注意障碍,而尼古丁或地佐西平则无此作用改变。此外,皮质低亲和力烟碱样受体可能在注意功能中起作用。

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