Evaluation of the neuroprotective effect of antipsychotics by serum quantification of protein S100B.

IF 1 Q4 PHARMACOLOGY & PHARMACY
José D Santotoribio, Pilar Lozano, Consuelo Cañavate-Solano, Juan Corral-Pérez, Cristina O'Ferrall-González
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引用次数: 0

Abstract

Objective: This research delves into the intricate interplay between antipsychotic medications and neuroprotection focusing on the S100B protein-a central player in the regulation of neuroapoptotic activity.

Method: Blood samples were collected to assess serum S100B protein levels using an immunoassay of immunoelectrochemiluminescence. The first two samples were collected with a 3-month interval between each, and the third sample was obtained 6 months after the previous one. Changes in S100B protein levels throughout the study were assessed using Friedman's ANOVA test. This was followed by the Wilcoxon signed-rank test with Bonferroni correction to account for multiple comparisons.

Results: This study involved 40 patients diagnosed with severe mental disorders (34 schizophrenia, 4 schizoaffective disorder, 1 bipolar disorder, and 1 borderline personality disorder). These patients had been receiving antipsychotic treatment for an average duration of 17 years. The results revealed that the S100B protein remained within physiological levels (median values 39.0 ng/L for the first sample, median values 41.0 ng/L for the second sample, and median values 40.5 ng/L for the third sample) with no significant changes (p = 0.287), with all anti-psychotic medicaments values consistently below 50 ng/L, a lower value compared to maximum range of 105 ng/L. Importantly, there were no significant differences in S100B protein levels between patients on monotherapy and those on combination antipsychotic therapy (p = 0.873), suggesting that combination therapy did not increase neuroapoptotic activity.

Conclusions: These findings provide compelling evidence for the potential neuroprotective effects of long-term antipsychotic treatment in individuals with severe mental disorders. By maintaining physiological levels of the S100B protein, antipsychotic medications may help protect against neuronal damage and dysfunction. This research contributes valuable insights into the neuroprotective mechanisms of antipsychotic drugs, enhancing our understanding of their potential benefits in the treatment of severe mental disorders.

通过血清 S100B 蛋白定量评估抗精神病药物的神经保护作用。
研究目的本研究深入探讨抗精神病药物与神经保护之间错综复杂的相互作用,重点研究 S100B 蛋白--神经凋亡活动调控的核心参与者:方法:采集血液样本,使用免疫电化学发光法评估血清 S100B 蛋白水平。前两次采血间隔 3 个月,第三次采血间隔 6 个月。在整个研究过程中,S100B 蛋白水平的变化采用弗里德曼方差分析进行评估。然后进行Wilcoxon符号秩检验,并进行Bonferroni校正以考虑多重比较:这项研究涉及 40 名被诊断患有严重精神障碍的患者(34 名精神分裂症患者、4 名情感分裂症患者、1 名双相情感障碍患者和 1 名边缘型人格障碍患者)。这些患者接受抗精神病治疗的平均时间为 17 年。结果显示,S100B 蛋白保持在生理水平内(第一个样本的中位值为 39.0 纳克/升,第二个样本的中位值为 41.0 纳克/升,第三个样本的中位值为 40.5 纳克/升),没有发生显著变化(p = 0.287),所有抗精神病药物的数值始终低于 50 纳克/升,与最大值 105 纳克/升相比,数值较低。重要的是,接受单一疗法和联合抗精神病药物疗法的患者之间的S100B蛋白水平没有明显差异(p = 0.873),这表明联合疗法不会增加神经凋亡活性:这些发现为长期抗精神病治疗对严重精神障碍患者的潜在神经保护作用提供了令人信服的证据。通过维持 S100B 蛋白的生理水平,抗精神病药物可能有助于防止神经元损伤和功能障碍。这项研究为了解抗精神病药物的神经保护机制提供了有价值的见解,从而加深了我们对这些药物在治疗严重精神障碍方面的潜在益处的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
FARMACIA HOSPITALARIA
FARMACIA HOSPITALARIA PHARMACOLOGY & PHARMACY-
CiteScore
1.90
自引率
21.40%
发文量
46
审稿时长
37 days
期刊介绍: Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.
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