Journals / Türk Biyokimya Dergisi / 2015 / Cilt: 40 - Sayı: 2

[Fare karaciğeri lipid peroksidayonuna karşı kültür zeytin'in Olive (Olea europaea) antioksidant ve inhibisyon etkileri]

Antioxidant activity and inhibitory effect of cultivars of Olive (Olea europaea) against lipid peroxidation in mice liver

Pages
188–196
Publication Date
2022-11-05
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

Principal component analysis showed that phenolics and flavonoids contributed to the antioxidant activity of olives.Conclusion: The oxidative stress in liver can be potentially managed/prevented by the dietary intake of olive fruit.

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Objective & Hypothesis:Objective: The aim of this study is to investigate the in vitro antioxidant activity, the total phenolic and flavonoid contents and the possible protective effects of seven cultivars of olive on lipid peroxidation induced by iron in mice liver.Methods: Antioxidant activity was evaluated by using different assays, including thiobarbituric acid reactive species (TBARS), total antioxidant, 2,2-diphenlyl-1-picrylhydrazyl (DPPH) radical and metal ion-chelating activities.Results: The aqueous extracts of fruit showed inhibition against thiobarbituric acid reactive species (TBARS) induced by pro-oxidant (10 µM FeSO4) in mice liver.
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Key Findings & Data:Moreover, the free radical scavenging activities of the extracts was evaluated by the scavenging of 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical (IC50, 85.9 µg/ml (Ascolano), 82.1 µg/ml (Mission), Pedolino and Carolea >200 µg/ml, 85.1 µg/ml (Picholine), 143.6 µg/ml (Maurino) and 150 µg/ml (Itrana).
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Conclusion & Impact:Principal component analysis showed that phenolics and flavonoids contributed to the antioxidant activity of olives.Conclusion: The oxidative stress in liver can be potentially managed/prevented by the dietary intake of olive fruit.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: The aim of this study is to investigate the in vitro antioxidant activity, the total phenolic and flavonoid contents and the possible protective effects of seven cultivars of olive on lipid peroxidation induced by iron in mice liver.Methods: Antioxidant activity was evaluated by using different assays, including thiobarbituric acid reactive species (TBARS), total antioxidant, 2,2-diphenlyl-1-picrylhydrazyl (DPPH) radical and metal ion-chelating activities.Results: The aqueous extracts of fruit showed inhibition against thiobarbituric acid reactive species (TBARS) induced by pro-oxidant (10 µM FeSO4) in mice liver. The order of the antioxidant activity among different cultivars on lipid peroxidation assay is Maurino>Mission>Picholine>Ascolano>Carolea>Itrana>Pedolina. Moreover, the free radical scavenging activities of the extracts was evaluated by the scavenging of 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical (IC50, 85.9 µg/ml (Ascolano), 82.1 µg/ml (Mission), Pedolino and Carolea >200 µg/ml, 85.1 µg/ml (Picholine), 143.6 µg/ml (Maurino) and 150 µg/ml (Itrana). Principal component analysis showed that phenolics and flavonoids contributed to the antioxidant activity of olives.Conclusion: The oxidative stress in liver can be potentially managed/prevented by the dietary intake of olive fruit.

Özet

Amaç: Bu çalışmanın amacı, fare karaciğerinde demir ile indüklenen lipit peroksidayonu üzerine, yedi farklı kültür zeytininin total fenolik ve flavanoidlerinin in vitro antioksidant aktivitelerini incelemektir.Metod: Antioksidant aktiviteler, tiyobarbitürik asit reaktif türler (TBARS), total antioksidant, 2,2-diphenlyl-1-picrylhydrazyl (DPPH) radikali ve metal iyon şelatlama aktiviteleri gibi farklı metotlarla incelenmiştir.Bulgular: Meyve ekstraktları fare karaciğerinde, pro-oksiidant (10 µM FeSO4) ile indüklenen TBARS üzerine inhibiyon etkisi göstermiştir. Lipit peroksidayonu üzerine farklı kültürlerin antioksidant aktiviteleri sırasıyla Maurino>Mission>Picholine>Ascolano>Carolea>Itrana> Pedolina'dır. Bunlardan başka, ekstraktların serbest radikal yakalama aktiviteleri 2,2-diphenyl1-picrylhydrazyl (DPPH) radikali ile ölçülmüştür. Buna gore türe gore IC50'ler 85.9 µg/ml (Ascolano), 82.1 µg/ml (Mission), Pedolino and Carolea >200 µg/ml, 85.1 µg/ml (Picholine), 143.6 µg/ml (Maurino) and 150 µg/ml (Itrana) olarak bulunmuştur. Zeytindeki fenoliklerin ve flavanoidlerin antioksidant aktivitesi gösterdiği bulunmuştur. Sonuç: Diyetsel zeytin alımıyla karaciğer oksidatif stressi potensiyal olarak önlendi.

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Cite This Article

SABİR, S. M., KHALİQ, A., AHMAD, S. D., KHAN, A. (2022). [Fare karaciğeri lipid peroksidayonuna karşı kültür zeytin'in Olive (Olea europaea) antioksidant ve inhibisyon etkileri]. Türk Biyokimya Dergisi, Cilt: 40 - Sayı: 2, 188–196. https://ajindex.com/articles/621156

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References (14)

  1. Halliwell B, Gutteridge JM, Cross CE. Free radicals, antioxidants, and human disease: where are we now? J Lab Clin Med 1992; 119(6):598-620. Halliwell B. Free radicals, antioxidants, and human disease: curi- osity, cause, or consequence? Lancet 1994; 344(8924):721-4.
  2. Hertog MGL, Hollman PCH, Van DPB. Content of potentially an- ticarcinogenic flavonoids of tea infusions, wines and fruit juice. J Agri Food Chem 1993; 41:1242-6.
  3. Soler-Rivas C, Epsin JC, Wichers HJ. Oleuropein and related com- pounds. J Sci Food Agric 2000; 80:1013-23.
  4. Ribarova F, Zanev R, Shishkov S, Rizov N. ?-Tocopherol, fatty ac- ids and their correlations in Bulgarian foodstuffs. J Food Compos Anal 2003; 16:659-67.
  5. Covas MI, Nyyssönen K, Poulsen HE, Kaikkonen J, Zunft HJ, et al. The effect of polyphenols in olive oil on heart disease risk fac- tors: a randomized trial. Ann Intern Med 2006; 145(5):333-41. Covas MI. Bioactive effects of olive oil phenolic compounds in humans: reduction of heart disease factors and oxidative damage. Inflammopharmacology 2008; 16(5):216-8.
  6. Somogyi A, Rosta K, Pusztai P, Tulassay Z, Nagy G. Antioxidant measurements. Physiol Meas 2007; 28(4):R41-55. Frei B. Nonezymatic defence system. In natural antioxidants in hu- man health and disease. Briviba K, Sies H, eds. Academic Press,
  7. London, UK. p. 107, 1994.
  8. Kumar A, Chattopadhyay S. DNA damage protecting activity and antioxidant potential of pudina extract. Food Chem 2007; 100:1377-84.
  9. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979; 95(2):351-8.
  10. Hatano T, Kagawa H, Yasuhara T, Okuda T. Two new flavonoids and other constituents in licorice root: their relative astringency and radical scavenging effects. Chem Pharm Bull (Tokyo) 1988; 36(6):2090-7.
  11. Prieto P, Pineda M, Aguilar M. Spectrophotometric quantitation of antioxidant capacity through the formation of a phosphomolybdenum complex: specific application to the determination of vitamin E. Anal Biochem 1999; 269(2):337-41.
  12. Puntel RL, Nogueira CW, Rocha JB. Krebs cycle intermediates modulate thiobarbituric acid reactive species (TBARS) production in rat brain in vitro. Neurochem Res 2005;30(2):225-35.
  13. Singleton VL, Orthofer R, Lamuela-Raventos RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Ciocalteu,s reagent. Methods Enzymol 1999; 299:152-78.
  14. Kosalec I, Bakmaz M, Pepeljnjak S, Vladimir-Knezevi? S. Quantitative analysis of the flavonoids in raw