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A Comprehensive Study of the Radical Scavenging Activity of Rosmarinic Acid.
Vo, Quan V; Hoa, Nguyen Thi; Flavel, Matthew; Thong, Nguyen Minh; Boulebd, Houssem; Nam, Pham Cam; Quang, Duong Tuan; Mechler, Adam.
Afiliación
  • Vo QV; The University of Danang - University of Technology and Education, Danang550000, Vietnam.
  • Hoa NT; The University of Danang - University of Technology and Education, Danang550000, Vietnam.
  • Flavel M; TPM Bioactives Division, The Product Makers Pty. Ltd., Melbourne 3173, Australia.
  • Thong NM; School of Life Sciences, La Trobe University, Bundoora, Victoria 3086, Australia.
  • Boulebd H; The University of Danang-University of Science and Education, Danang 550000, Vietnam.
  • Nam PC; Laboratory of Synthesis of Molecules with Biological Interest, University of Frères Mentouri Constantine 1, Constantine 25017, Algeria.
  • Quang DT; Department of Chemical Engineering, The University of Danang - University of Science and Technology, Danang 550000, Vietnam.
  • Mechler A; University of Education, Hue University, Hue City 530000, Vietnam.
J Org Chem ; 88(24): 17237-17248, 2023 12 15.
Article en En | MEDLINE | ID: mdl-38011833
Rosmarinic acid (RA) is reported in separate studies to be either an inducer or reliever of oxidative stress, and this contradiction has not been resolved. In this study, we present a comprehensive examination of the radical scavenging activity of RA using density functional theory calculations in comparison with experimental data. In model physiological media, RA exhibited strong HO• radical scavenging activity with overall rate constant values of 2.89 × 1010 and 3.86 × 109 M-1 s-1. RA is anticipated to exhibit excellent scavenging properties for HOO• in an aqueous environment (koverall = 3.18 × 108 M-1 s-1, ≈2446 times of Trolox) following the hydrogen transfer and single electron transfer pathways of the dianion state. The neutral form of the activity is equally noteworthy in a lipid environment (koverall = 3.16 × 104 M-1 s-1) by the formal hydrogen transfer mechanism of the O6(7,15,16)-H bonds. Chelation with RA may prevent Cu(II) from reduction by the ascorbic acid anion (AA-), hence blocking the OIL-1 pathway, suggesting that RA in an aqueous environment also serves as an OIL-1 antioxidant. The computational findings exhibit strong concurrence with the experimental observations, indicating that RA possesses a significant efficacy as a radical scavenger in physiological environments.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antioxidantes Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article País de afiliación: Vietnam Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antioxidantes Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article País de afiliación: Vietnam Pais de publicación: Estados Unidos