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1.
J Food Sci ; 85(9): 2737-2744, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32844426

RESUMO

Olive fruits and leaves are recognized to have great potential as natural sources of antioxidants. The major phenolic antioxidant component in these plant tissues is oleuropein. The antioxidant activity of olive fruits and leaves was evaluated in this study using multiple free-radical scavenging (MULTIS) methods, wherein we determined the scavenging abilities of different extracts against five reactive oxygen species (ROS; HO·, O2 - ·, RO·, t-BuOO·, and 1 O2 ). Raw olive fruits taste bitter and are inedible without undergoing a debittering treatment. Following the NaOH-debittering process, the radical scavenging activity of olives decreased by 90%. The MULTIS measurements indicated that oleuropein and hydroxytyrosol are responsible for the radical scavenging activity of olive fruits. Furthermore, we evaluated the radical scavenging profiles of olive leaf extracts against five ROS and found significant seasonal variations in their antioxidant activities. Leaves picked in August possessed greater radical scavenging abilities (180% to 410% for different ROS) than those picked in the cold season (December and February). In roasted olive leaves, we found marked increases (230% to 300% and 180% to 220%) in the antioxidant activities of Maillard reaction products against RO· and t-BuOO·, respectively. This study presented a useful comparative analysis of the antioxidant capacities of food against various types of ROS. PRACTICAL APPLICATION: In this study, we evaluated the natural antioxidant activity of olive fruits and leaves against five reactive oxygen species (ROS). We found characteristic differences in the antioxidant profiles of different olive tissues, which varied after different treatments (debittering [fruit], drying [leaf], and roasting [leaf]). Comparative studies of the antioxidant capacities of foods against various ROS are useful to improve the functionality of food products.


Assuntos
Antioxidantes/química , Frutas/química , Olea/química , Extratos Vegetais/química , Folhas de Planta/química , Espécies Reativas de Oxigênio/química , Glucosídeos Iridoides , Iridoides/química , Fenóis/química
2.
Bioorg Med Chem Lett ; 29(16): 2145-2149, 2019 08 15.
Artigo em Inglês | MEDLINE | ID: mdl-31272792

RESUMO

Scavenging abilities of animal sera against six reactive species (OH, O2-, RO, t-BuOO, H3C, and 1O2) were determined with the use of multiple free-radical scavenging (MULTIS) method. Commercially available sera from pig, horse, rabbit, Guinea pig, hamster and chicken were subjected to MULTIS analysis and the results were compared with human specimen. In general, animal sera showed lower scavenging ability against OH and RO radicals than human serum. However, it is noteworthy that rabbit and chicken sera have higher scavenging ability against O2- than others. This is consistent with the known data that superoxide dismutase levels in these sera are high. In addition, we determined the uric acid level in animal sera using the uricase-TOOS method. In chicken serum, uric acid was found to be the major effective component in RO scavenging. This paper is first to quantitatively evaluate antioxidant capacities in animal sera.


Assuntos
Antioxidantes/química , Sequestradores de Radicais Livres/sangue , Soro/citologia , Animais , Humanos
3.
Bioorg Med Chem Lett ; 28(18): 3031-3033, 2018 10 01.
Artigo em Inglês | MEDLINE | ID: mdl-30098868

RESUMO

Monoterpenes are major active components of lavender, thyme, and mint. The X-ray radioprotective activity of pure monoterpenes is attributed to their scavenging ability against active species, but so far no firm evidence has been demonstrated. The objective of this study is to quantitatively determine antioxidant abilities of monoterpenes and collate it with radioprotective activity. Using multiple free-radical scavenging (MULTIS) method, we have determined the scavenging abilities of monoterpenes (linalool, thymol, and menthol) against six active species. A previous study has shown that the monoterpene linalool is a radioprotector for cellular systems, therefore, its scavenging ability was compared with known radioprotective agents such as cysteamine and amifostine. Results indicated that the monoterpene menthol but not linalool is a potent scavenger of reactive oxygen species and its scavenging magnitude is comparable to cysteamine and amifostine. This paper is first to show a correlation between ROS scavenging ability and radioprotective action.


Assuntos
Amifostina/farmacologia , Cisteamina/farmacologia , Sequestradores de Radicais Livres/farmacologia , Monoterpenos/farmacologia , Protetores contra Radiação/farmacologia , Espécies Reativas de Oxigênio/antagonistas & inibidores , Amifostina/química , Cisteamina/química , Relação Dose-Resposta a Droga , Sequestradores de Radicais Livres/química , Estrutura Molecular , Monoterpenos/química , Protetores contra Radiação/química , Espécies Reativas de Oxigênio/metabolismo , Relação Estrutura-Atividade
4.
Bioorg Med Chem Lett ; 27(23): 5203-5206, 2017 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-29110988

RESUMO

Resveratrol (RSV) analogues have attracted much attention because of the expected health functions including antioxidant activities. We have carried out a quantitative determination of the scavenging abilities of six trans-RSV analogues against various reactive oxygen species and methyl radical (hydroxyl radical, superoxide, alkoxyl radical, peroxyl radical, methyl radical, and singlet oxygen). RSV analogues are in general more potent scavenger than the parent RSV. Furthermore, piceatannol (PIC) having two OH groups in the ortho position of resveratrol was found to show 11 times higher scavenging ability against peroxyl radical than parent resveratrol. With the aid of previous theoretical studies, the enhanced antioxidant ability was interpreted based on the effects of substituent that modifies the original resveratrol structure and function.


Assuntos
Antioxidantes/farmacologia , Metano/análogos & derivados , Espécies Reativas de Oxigênio/antagonistas & inibidores , Estilbenos/farmacologia , Antioxidantes/síntese química , Antioxidantes/química , Relação Dose-Resposta a Droga , Humanos , Metano/antagonistas & inibidores , Metano/metabolismo , Estrutura Molecular , Espécies Reativas de Oxigênio/metabolismo , Resveratrol , Estilbenos/síntese química , Estilbenos/química , Relação Estrutura-Atividade
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