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The disordering effect of SARMs on a biomembrane model.
Díaz-Salazar, Alma Jessica; Espinosa-Roa, Arián; Saldívar-Guerra, Enrique; Pérez-Isidoro, Rosendo.
Afiliação
  • Díaz-Salazar AJ; Laboratorio de Bio-fisicoquímica. Departamento de Fisicoquímica, Facultad de Química, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico. jessica.diaz@quimica.unam.mx.
  • Espinosa-Roa A; CONAHCyT-Centro de Investigación en Química Aplicada (CIQA), Unidad Monterrey. Alianza Sur no. 204, Parque de Investigación en Innovación Tecnológica (PIIT), km 10 autopista internacional Mariano Escobedo, C.P. 66628, Apodaca, Nuevo León, Mexico. arian.espinosa@ciqa.edu.mx.
  • Saldívar-Guerra E; Centro de Investigación en Química Aplicada (CIQA), Enrique Reyna, 140, 25294 Saltillo Coahuila, Mexico. enrique.saldivar@ciqa.edu.mx.
  • Pérez-Isidoro R; Centro de Investigación en Química Aplicada (CIQA), Enrique Reyna, 140, 25294 Saltillo Coahuila, Mexico. enrique.saldivar@ciqa.edu.mx.
Phys Chem Chem Phys ; 26(30): 20653-20662, 2024 Jul 31.
Article em En | MEDLINE | ID: mdl-39040033
ABSTRACT
From medicine to sport, selective androgen receptor modulators (SARMs) have represented promising applications. The ability of SARMs to selectively interact with the androgen receptor (AR) indicates that this kind of molecule can interfere with numerous physiological and pathological processes controlled by the AR regulatory mechanism. However, critical concerns in relation to safety and potential side effects of SARMs remain under discussion and investigation. SARMs, being hydrophobic/organic compounds, can be subjected to hydrophobic interactions. In this perspective, we hypothesize that SARMs interact with lipid membranes, producing significant physical and chemical changes that could be associated with several effects that SARMs represent in biological systems. In this context, the effect of SARMs on lipid membranes mediated by non-specific interactions is little explored. Here, we report significant information related to the changes that ostarine, ligandrol, andarine, and cardarine produce in the thermodynamic properties of a lipid biomembrane model. Physical changes and chemical interactions of the systems were investigated by differential scanning calorimetry (DSC), dynamic light scattering (DLS), attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), and theoretical calculations implementing density functional theory (DFT). We demonstrate that ostarine, ligandrol, andarine, and cardarine can strongly interact with a lipid biomembrane model composed of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), and accordingly, these molecules can be incorporated into the polar/hydrophobic regions of the lipid bilayer. By employing theoretical calculations, we gained insights into the possible electrostatic interactions between SARMs and phospholipid molecules, enhancing our understanding of the driving forces behind the interactions of SARMs with lipid membranes. Overall, this investigation provides relevant knowledge related to the biophysical-chemical effects that SARMs produce in biomembrane models and could be of practical reference for promising applications of SARMs in medicine and sport.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bicamadas Lipídicas Idioma: En Revista: Phys Chem Chem Phys Assunto da revista: BIOFISICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bicamadas Lipídicas Idioma: En Revista: Phys Chem Chem Phys Assunto da revista: BIOFISICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido