The Secure Therapeutic Effects of Recently Developed Antipsychotic Drugs and Updated Neural Networks in Schizophrenia

F. Werner, R. Coveñas
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Abstract

Schizophrenia and schizoaffective disorder are treated in most cases with antipsychotic drugs of the second generation. These drugs block dopaminergic and serotonergic receptors, i.e., D2 and 5-HT2A receptors, and cause different adverse effects, for example, movement disturbances of the extrapyramidal system and adverse effects of vital parameters and of the heart. These drugs treat positive symptoms in schizophrenia and, to a lesser extent, negative symptoms. This review presents the development of newer antipsychotic drugs. References were taken from PubMed after using the following keywords: schizophrenia, schizoaffective disorder, antipsychotic drug, neurotransmitter and neuropeptide. Among these newer antipsychotic drugs are cariprazine, brexipiprazole and lumateperone, which exert a partial agonistic effect at D2 and 5-HT2A receptors, pimavanserin, a 5-HT2A receptor antagonist which treats negative symptoms in schizophrenia as add-on therapy, olanzapine combined with samidorphan, which reduces weight gain, and M4 or M1 receptor agonists, for example, xanomeline with an antipsychotic effect combined with trospium, an anticholinergic drug. Neural networks were updated in order to deduce the antipsychotic mechanism of action of newer antipsychotic drugs, especially xanomeline. The newer antipsychotic drugs cariprazine, brexipiprazole and lumateperone show antipsychotic, antimanic and anti-depressive effects, however, the efficacy on psychotic symptoms in long-term treatment has not yet been examined. Pimavanserin reduces negative symptoms in schizophrenia as an additional pharmacotherapy to treat this disorder. Olanzapine combined with samidorphan exerts good antipsychotic effects and reduces weight gain. The new antipsychotic drug xanomeline, the antipsychotic effect of which is quite different from the antidopaminergic effect, treats positive and negative symptoms in schizophrenia. Its mechanism of action was deduced from the neural networks presented. The long-term efficacy should still be examined. This review is focused on newer antipsychotic drugs. The long-term efficacy of cariprazine, brexipiprazole and lumateperone in the treatment of schizophrenia should be examined further. Neural networks in the brain areas involved in schizophrenia should be examined and updated furthermore. Newer antipsychotic drugs ,for example, xanomeline, an M4 or M1 receptor agonist, which has been combined with trospium, an anticholinergic drug, the mechanism of action of which can be derived from the neural network suggested in this review.
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最近开发的抗精神病药物和更新的神经网络在精神分裂症中的安全治疗效果
大多数情况下,精神分裂症和情感分裂症都使用第二代抗精神病药物进行治疗。这些药物阻断多巴胺能和血清素能受体,即 D2 和 5-HT2A 受体,并导致不同的不良反应,例如锥体外系运动障碍以及对生命参数和心脏的不良反应。这些药物可治疗精神分裂症的阳性症状,也可在较小程度上治疗阴性症状。本综述介绍了新型抗精神病药物的发展情况。参考文献来自 PubMed,并使用了以下关键词:精神分裂症、情感分裂症、抗精神病药物、神经递质和神经肽。在这些较新的抗精神病药物中,有对 D2 和 5-HT2A 受体有部分激动作用的卡立普嗪、布来西哌唑和鲁马特哌隆,有作为附加疗法治疗精神分裂症阴性症状的 5-HT2A 受体拮抗剂皮马伐林、奥氮平与可减少体重增加的萨米多啡(samidorphan)合用,以及 M4 或 M1 受体激动剂,如具有抗精神病作用的赛诺梅林与抗胆碱能药物曲司泮合用。为了推断较新的抗精神病药物,尤其是夏诺美林的抗精神病作用机制,对神经网络进行了更新。较新的抗精神病药物卡哌嗪、布来西哌唑和鲁拉哌酮显示出抗精神病、抗躁狂和抗抑郁的作用,但在长期治疗中对精神病症状的疗效尚未进行研究。Pimavanserin 可减轻精神分裂症的阴性症状,是治疗精神分裂症的辅助药物疗法。奥氮平与萨米多吗啡合用可发挥良好的抗精神病作用,并减少体重增加。新型抗精神病药物赛诺梅林(xanomeline)的抗精神病作用与抗多巴胺作用截然不同,可治疗精神分裂症的阳性和阴性症状。其作用机制是通过神经网络推断出来的。本综述侧重于较新的抗精神病药物。卡哌嗪、布来西哌唑和鲁米培酮治疗精神分裂症的长期疗效有待进一步研究。应进一步研究和更新精神分裂症相关脑区的神经网络。新型抗精神病药物,如M4或M1受体激动剂香诺美林(xanomeline),已与抗胆碱能药物曲司匹姆(trospium)联用,其作用机制可从本综述提出的神经网络中得出。
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来源期刊
Current Psychiatry Research and Reviews
Current Psychiatry Research and Reviews Medicine-Psychiatry and Mental Health
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0.60
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51
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