利多卡因无效提示新的精神药理学靶点。

Q3 Medicine
Psychopharmacology bulletin Pub Date : 2022-06-27
Mark Mintz, Victor Badner, Lynn K Feldman, Pnina Mintz, Mana Saraghi, Jonathan Diaz, Irina Mezhebovsky, Irene Axelrod, Joseph Gleeson, Chang Liu, Cathy Smith, Helen Chow, David Zurakowski, Michael M Segal
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引用次数: 0

摘要

目的:许多神经精神疾病的机制尚不清楚,但钠通道阻滞剂利多卡因的无效已被认为是注意缺陷多动障碍(ADHD)和严重形式的经前综合征(PMS)的生物标志物,被认为是精神病学。我们进行了单臂双盲临床试验,以测试利多卡因无效是否可以作为识别这些疾病患者的生物标志物,并为分子机制和潜在的精神药理学干预提供线索。实验设计:我们开发了一种非侵入性利多卡因无效的味觉测试,通过将12名受试者的利多卡因注射与疼痛测试进行比较,并对ADHD和经前综合症患者进行了评估。主要观察结果:在53名受试者和对照组中,利多卡因无效与ADHD +经前综合症的女性有很强的相关性(p < 0.001)。结论:这些结果提示了对ADHD和经前综合症合并的生物学理解的可能性,这是精神疾病经前烦躁不安障碍(PMDD)的特征。这些结果以及与具有重叠症状的神经肌肉通道病的家庭谱系的比较表明,经前不悦症的临床表型可能是由感觉过度刺激产生的,并且适合分子理解和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lidocaine Ineffectiveness Suggests New Psychopharmacology Drug Target.

Lidocaine Ineffectiveness Suggests New Psychopharmacology Drug Target.

Objectives: The mechanism of many neuropsychiatric disorders remains unknown, but the ineffectiveness of the sodium channel blocker lidocaine has been suggested to be a biomarker for Attention Deficit Hyperactivity Disorder (ADHD) and a severe form of Premenstrual Syndrome (PMS) that is considered psychiatric. We conducted single-arm double-blind clinical trials to test whether lidocaine ineffectiveness can be used as a biomarker to identify people with these conditions and provide a clue as to the molecular mechanism and potential psychopharmacological intervention.

Experimental design: We developed a noninvasive taste test for lidocaine ineffectiveness, validated by comparing lidocaine injections to pain testing in 12 subjects, and assessed it in individuals with ADHD and PMS.

Principal observations: Lidocaine ineffectiveness had a strong association in women with ADHD + PMS in a sample of 53 subjects and controls (p < 0.001).

Conclusions: These results suggest the possibility of the biological understanding of the combination of ADHD and PMS that is characteristic of the psychiatric disorder Premenstrual Dysphoric Disorder (PMDD). These results and comparison to family pedigrees of a neuromuscular channelopathy with overlapping symptoms suggest the possibility that the clinical phenotype in PMDD is produced by sensory overstimulation, and amenable to molecular understanding and treatment.

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来源期刊
Psychopharmacology bulletin
Psychopharmacology bulletin PHARMACOLOGY & PHARMACY-PSYCHIATRY
CiteScore
2.70
自引率
0.00%
发文量
32
期刊介绍: Information not localized
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