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Oxoberberine: a promising natural antioxidant in physiological environments

Oxoberberine (OB, 2,10-dihydroxy-3,9-dimethoxy-8-oxo-protoberberine, artathomsonine), which was isolated from Artabotrys thomsonii, was shown to exhibit potent antioxidant activity in vitro, however that is the only reported evidence of the radical scavenging activity of this compound thus far. In t...

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Autores principales: Nam, Pham Cam, Trung, Nguyen Quang, Hoa, Nguyen Thi, Bich, Huynh Ngoc, Manh, Tran Duc, Quang, Duong Tuan, Mechler, Adam, Vo, Quan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961270/
https://www.ncbi.nlm.nih.gov/pubmed/35424953
http://dx.doi.org/10.1039/d2ra01372j
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author Nam, Pham Cam
Trung, Nguyen Quang
Hoa, Nguyen Thi
Bich, Huynh Ngoc
Manh, Tran Duc
Quang, Duong Tuan
Mechler, Adam
Vo, Quan V.
author_facet Nam, Pham Cam
Trung, Nguyen Quang
Hoa, Nguyen Thi
Bich, Huynh Ngoc
Manh, Tran Duc
Quang, Duong Tuan
Mechler, Adam
Vo, Quan V.
author_sort Nam, Pham Cam
collection PubMed
description Oxoberberine (OB, 2,10-dihydroxy-3,9-dimethoxy-8-oxo-protoberberine, artathomsonine), which was isolated from Artabotrys thomsonii, was shown to exhibit potent antioxidant activity in vitro, however that is the only reported evidence of the radical scavenging activity of this compound thus far. In the present study, thermodynamic and kinetic calculations were used to determine the free radical scavenging activity of OB against a range of biologically important species, under physiological conditions. In the first part the activity is calculated against the HOO˙ radical that is both biologically important and a reference radical for comparison. It was found that OB has high antiradical capacity against HOO˙ in both lipid medium and water at physiological pH with k(overall) = 1.33 × 10(5) and 1.73 × 10(6) M(−1) s(−1), respectively. The formal hydrogen transfer mechanism defined the activity in nonpolar environments, whereas in the aqueous solution the single electron transfer competes with the hydrogen transfer pathway. The results showed that, in lipid medium, the HOO˙ trapping capability of OB is better than typical antioxidants such as Trolox, BHT, resveratrol and ascorbic acid. Similarly, the activity of OB in water at pH 7.4 is roughly 19 and 7 times faster than those of Trolox and BHT, respectively, but slightly lower than the activities of resveratrol or ascorbic acid. In the second part, it was found that OB also exhibits high activity against other typical free radicals such as CH(3)O˙, CH(3)OO˙, CCl(3)OO˙, NO(2), SO(4)˙(−), DPPH and ABTS˙(+) with k(f) ranging from 2.03 × 10(5) to 5.74 × 10(7) M(−1) s(−1). Hence, it is concluded that OB is a promising radical scavenger in the physiological environment.
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spelling pubmed-89612702022-04-13 Oxoberberine: a promising natural antioxidant in physiological environments Nam, Pham Cam Trung, Nguyen Quang Hoa, Nguyen Thi Bich, Huynh Ngoc Manh, Tran Duc Quang, Duong Tuan Mechler, Adam Vo, Quan V. RSC Adv Chemistry Oxoberberine (OB, 2,10-dihydroxy-3,9-dimethoxy-8-oxo-protoberberine, artathomsonine), which was isolated from Artabotrys thomsonii, was shown to exhibit potent antioxidant activity in vitro, however that is the only reported evidence of the radical scavenging activity of this compound thus far. In the present study, thermodynamic and kinetic calculations were used to determine the free radical scavenging activity of OB against a range of biologically important species, under physiological conditions. In the first part the activity is calculated against the HOO˙ radical that is both biologically important and a reference radical for comparison. It was found that OB has high antiradical capacity against HOO˙ in both lipid medium and water at physiological pH with k(overall) = 1.33 × 10(5) and 1.73 × 10(6) M(−1) s(−1), respectively. The formal hydrogen transfer mechanism defined the activity in nonpolar environments, whereas in the aqueous solution the single electron transfer competes with the hydrogen transfer pathway. The results showed that, in lipid medium, the HOO˙ trapping capability of OB is better than typical antioxidants such as Trolox, BHT, resveratrol and ascorbic acid. Similarly, the activity of OB in water at pH 7.4 is roughly 19 and 7 times faster than those of Trolox and BHT, respectively, but slightly lower than the activities of resveratrol or ascorbic acid. In the second part, it was found that OB also exhibits high activity against other typical free radicals such as CH(3)O˙, CH(3)OO˙, CCl(3)OO˙, NO(2), SO(4)˙(−), DPPH and ABTS˙(+) with k(f) ranging from 2.03 × 10(5) to 5.74 × 10(7) M(−1) s(−1). Hence, it is concluded that OB is a promising radical scavenger in the physiological environment. The Royal Society of Chemistry 2022-03-29 /pmc/articles/PMC8961270/ /pubmed/35424953 http://dx.doi.org/10.1039/d2ra01372j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Nam, Pham Cam
Trung, Nguyen Quang
Hoa, Nguyen Thi
Bich, Huynh Ngoc
Manh, Tran Duc
Quang, Duong Tuan
Mechler, Adam
Vo, Quan V.
Oxoberberine: a promising natural antioxidant in physiological environments
title Oxoberberine: a promising natural antioxidant in physiological environments
title_full Oxoberberine: a promising natural antioxidant in physiological environments
title_fullStr Oxoberberine: a promising natural antioxidant in physiological environments
title_full_unstemmed Oxoberberine: a promising natural antioxidant in physiological environments
title_short Oxoberberine: a promising natural antioxidant in physiological environments
title_sort oxoberberine: a promising natural antioxidant in physiological environments
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961270/
https://www.ncbi.nlm.nih.gov/pubmed/35424953
http://dx.doi.org/10.1039/d2ra01372j
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