Exploring the potential anti-thyroid activity of Acetyl-L-carnitine: Lactoperoxidase inhibition profile, iodine complexation and scavenging power against H

Acetyl-L-carnitine Anti-thyroid activity Lactoperoxidase inhibition Lactoperoxidase structural Raman studies. Fluorescence studies. Molecular modeling

Journal

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
ISSN: 1873-3557
Titre abrégé: Spectrochim Acta A Mol Biomol Spectrosc
Pays: England
ID NLM: 9602533

Informations de publication

Date de publication:
29 Feb 2024
Historique:
received: 28 09 2023
revised: 07 02 2024
accepted: 27 02 2024
medline: 10 3 2024
pubmed: 10 3 2024
entrez: 9 3 2024
Statut: aheadofprint

Résumé

L-Acetylcarnitine (ALC), a versatile compound, has demonstrated beneficial effects in depression, Alzheimer's disease, cognitive impairment, and other conditions. This study focuses on its antithyroid activity. The precursor molecule, L-carnitine, inhibited the uptake of triiodothyronine (T3) and thyroxine (T4), and it is possible that ALC may reduce the iodination process of T3 and T4. Currently, antithyroid drugs are used to control the excessive production of thyroid hormones (TH) through various mechanisms: (i) forming electron donor-acceptor complexes with molecular iodine, (ii) eliminating hydrogen peroxide, and (iii) inhibiting the enzyme thyroid peroxidase. To understand the pharmacological properties of ALC, we investigated its plausible mechanisms of action. ALC demonstrated the ability to capture iodine (K

Identifiants

pubmed: 38460232
pii: S1386-1425(24)00264-6
doi: 10.1016/j.saa.2024.124098
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

124098

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Janetsi Y Caro-Ramírez (JY)

Centro de Química Inorgánica (CEQUINOR-CONICET-UNLP- Asoc CICPBA)-Departamento de Química-Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Boulevard 120 entre 60 y 64, C.C.962- (B1900AVV) -1900 La Plata, Argentina.

Carlos A Franca (CA)

Centro de Química Inorgánica (CEQUINOR-CONICET-UNLP- Asoc CICPBA)-Departamento de Química-Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Boulevard 120 entre 60 y 64, C.C.962- (B1900AVV) -1900 La Plata, Argentina.

Martín Lavecchia (M)

Centro de Química Inorgánica (CEQUINOR-CONICET-UNLP- Asoc CICPBA)-Departamento de Química-Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Boulevard 120 entre 60 y 64, C.C.962- (B1900AVV) -1900 La Plata, Argentina.

Luciana G Naso (LG)

Centro de Química Inorgánica (CEQUINOR-CONICET-UNLP- Asoc CICPBA)-Departamento de Química-Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Boulevard 120 entre 60 y 64, C.C.962- (B1900AVV) -1900 La Plata, Argentina.

Patricia A M Williams (PAM)

Centro de Química Inorgánica (CEQUINOR-CONICET-UNLP- Asoc CICPBA)-Departamento de Química-Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Boulevard 120 entre 60 y 64, C.C.962- (B1900AVV) -1900 La Plata, Argentina.

Evelina G Ferrer (EG)

Centro de Química Inorgánica (CEQUINOR-CONICET-UNLP- Asoc CICPBA)-Departamento de Química-Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Boulevard 120 entre 60 y 64, C.C.962- (B1900AVV) -1900 La Plata, Argentina. Electronic address: evelina@quimica.unlp.edu.ar.

Classifications MeSH