Lidocaine Ineffectiveness Suggests New Psychopharmacology Drug Target.
attention deficit hyperactivity disorder (ADHD)
channelopathies
hypokalemic periodic paralysis
lidocaine
premenstrual dysphoric disorder (PMDD)
Journal
Psychopharmacology bulletin
ISSN: 2472-2448
Titre abrégé: Psychopharmacol Bull
Pays: United States
ID NLM: 0101123
Informations de publication
Date de publication:
27 Jun 2022
27 Jun 2022
Historique:
pmc-release:
27
06
2023
pubmed:
12
7
2022
medline:
14
7
2022
entrez:
11
7
2022
Statut:
ppublish
Résumé
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. 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. Lidocaine ineffectiveness had a strong association in women with ADHD + PMS in a sample of 53 subjects and controls (p < 0.001). 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.
Substances chimiques
Lidocaine
98PI200987
Types de publication
Clinical Trial
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
20-30Subventions
Organisme : NICHD NIH HHS
ID : R43 HD094628
Pays : United States
Informations de copyright
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