Journals / Harran Üniversitesi Tıp Fakültesi Dergisi / 2020 / Cilt: 17 - Sayı: 1

In Vitro Effect of Some Plant Extracts on Serum Catalase, Myeloperoxidase and Paraoxonase 1

Serum Katalaz, Miyeloperoksidaz ve Paraoksonaz 1 Üzerine Bazı Bitki Ekstraktlarının In Vitro Etkisi

Pages
127–132
Publication Date
2020-04-29
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

If the in vivo efficacy of these plants can be demonstrated, it can be said that in diseases such as atherosclerosis, it can inhibit plaque formation caused by intravascular lipid peroxidation and improve vascular functions.Key words: Medicinal Plant, Lipid peroxidation, Paraoxonase 1, Myeloperoxidase

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Objective & Hypothesis:Background: It is emphasized that natural plants rich in phenolic content can be used in traditional and complementary medicine for therapeutic purposes.
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Key Findings & Data:For this purpose, effects of the water extracts of Artemisia absinthium, Ferula communis, Achillea millefolium, Equisetum arvense and Hypericum perforatum on the serum total anti-oxidant (TAS) level and total oxidant level (TAS) and paraoxanase 1 (PON1), myeloperoxidase (MPO) and catalase (CAT) enzyme activities has been investigated.Material and method: The water extract of each plant was prepared, and these extracts were added to the serum samples in a certain amount and the final concentration was applied as 60 µg/mL.
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Conclusion & Impact:If the in vivo efficacy of these plants can be demonstrated, it can be said that in diseases such as atherosclerosis, it can inhibit plaque formation caused by intravascular lipid peroxidation and improve vascular functions.Key words: Medicinal Plant, Lipid peroxidation, Paraoxonase 1, Myeloperoxidase
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Çakşır otu · Tarla atkuyruğu · Paraoksanaz 1

Abstract

Background: It is emphasized that natural plants rich in phenolic content can be used in traditional and complementary medicine for therapeutic purposes. For this purpose, effects of the water extracts of Artemisia absinthium, Ferula communis, Achillea millefolium, Equisetum arvense and Hypericum perforatum on the serum total anti-oxidant (TAS) level and total oxidant level (TAS) and paraoxanase 1 (PON1), myeloperoxidase (MPO) and catalase (CAT) enzyme activities has been investigated.Material and method: The water extract of each plant was prepared, and these extracts were added to the serum samples in a certain amount and the final concentration was applied as 60 µg/mL. TAS and TOS parameters were measured by Erel, MPO activity Bradley, PON1 activity Eckerson, CAT activity Goth method to investigate the effects of these prepared extracts on serum parameters. The reagents were prepared in Harran University Medical Faculty Medical Biochemistry Department Laboratory and analyzes were performed spectrophotometrically in the routine Biochemistry Laboratory autoanalyst (Architect C16000, Abbott).Results: Control values CAT (23,233 ± 1,665 kU/L), MPO (103,483 ± 4,048 U/L), PON1 (24,833 ± 1,404 U/L), TAS (1,223 ± 0.080 mmol Trolox Eqv/L) and TOS (6.350 ± 0,481 µmol H2O2 Eqv/L) was detected quantitatively. Artemisia absinthium, Ferula communis, Achillea millefolium and Hypericum perforatum inhibited CAT, MPO and PON1 enzymes (p <0.05, p <0.01). Equisetum arvense only showed an inhibition effect on MPO (p <0.01). Achillea millefolium and Hypericum perforatum decreased the TOS level, while increasing the TAS level (p <0.05, p <0.01).Conclusion: Ferula communis and Equisetum arvense plant extracts showed an inhibition effect on MPO activity in vitro, while a weak inhibition effect on PON1 activity. If the in vivo efficacy of these plants can be demonstrated, it can be said that in diseases such as atherosclerosis, it can inhibit plaque formation caused by intravascular lipid peroxidation and improve vascular functions.Key words: Medicinal Plant, Lipid peroxidation, Paraoxonase 1, Myeloperoxidase

Özet

Amaç: Fenolik içerik bakımından zengin olan doğal bitkilerin geleneksel ve tamamlayıcı tıpta tedavi amaçlı kullanılabileceği vurgusu yapılmaktadır. Bu amaçla Artemisia absinthium (pelin otu), Ferula communis (çakşır otu), Achillea millefolium (civanperçemi), Equisetum arvense (tarla atkuyruğu) ve Hypericum perforatum (sarı kantaron) su ektraklarının paraoksanaz 1 (PON1), miyeloperoksidaz (MPO) ve katalaz (CAT) enzim aktiviteleri ile serum total anti-oksidan seviye (TAS) ve total oksidan seviye (TOS) üzerine etkileri araştırılmıştır.Materyal ve metod: Her bir bitkinin su ekstraktı hazırlanmış olup, bu ekstraktlar serum numunelerine belli oranda eklenerek nihai konsantrasyon 60 µg/mL olarak uygulanmıştır. Hazırlanan bu ekstraktların serum parametreleri üzerine etkilerini araştırmak için TAS ve TOS parametreleri Erel, MPO aktivitesi Bradley, PON1 aktivitesi Eckerson, CAT aktivitesi Goth yöntemiyle ölçülmüştür. Reaktifler, Harran Üniversitesi Tıp Fakültesi Tıbbi Biyokimya Anabilim Dalı Laboratuvarında hazırlanmış ve analizler rutin Biyokimya Laboratuvarı otoanalizöründe (Architect C16000, Abbott) spekrofotometrik olarak çalışılmıştır.Bulgular: Kontrol değerleri CAT (23,233± 1,665 kU/L), MPO (103,483± 4,048 U/L), PON1 (24,833± 1,404 U/L), TAS (1,223± 0,080 mmol Troloks Eqv/L) ve TOS (6,350± 0,481 µmol H2O2 Eqv/L) kantitatif olarak saptanmıştır. Pelin otu, çakşır otu, civanperçemi ve sarı kantaron CAT, MPO ve PON1 enzimlerini inhibe etmiştir (p <0.05, p <0.01). Tarla atkuyruğu ise sadece MPO üzerine inhibisyon etkisi göstermiştir (p <0.01). Civanperçemi ve sarı kantaron TOS düzeyini düşürürken TAS düzeyini artırmıştır (p <0.05, p <0.01).Sonuç: Çakşır otu ve tarla atkuyruğu bitki ekstraktları in vitro olarak MPO üzerine inhibisyon etkisi gösterirken PON1 üzerine ise zayıf inhibisyon etkisi göstermiştir. Bu bitkilerin in vivo etkinliği ortaya konulabilirse ateroskleroz gibi hastalıklarda intravasküler lipit peroksidasyonu sonucu meydana gelen plak oluşumunu inhibe edebileceği ve vasküler fonksiyonları iyileştirebileceği söylenebilir. Anahtar Kelimeler: Tıbbi Bitki, Lipit peroksidasyonu, Paraoksanaz 1, Miyeloperoksidaz

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Cite This Article

KİRMİT, A., IŞIK, M. (2020). In Vitro Effect of Some Plant Extracts on Serum Catalase, Myeloperoxidase and Paraoxonase 1. Harran Üniversitesi Tıp Fakültesi Dergisi, Cilt: 17 - Sayı: 1, 127–132. https://ajindex.com/articles/22311

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References (13)

  1. Devasagayam TP, Tilak JC, Boloor KK, Sane KS, Ghaskadbi SS, Lele RD. Free radicals and antioxidants in human health: current status and future prospects. J Assoc Physicians India. 2004;52:794-804
  2. Stocker R, Keaney JF, Jr. Role of oxidative modifications in atherosclerosis. Physiol Rev. 2004;84(4):1381-478
  3. Schwenke DC. Antioxidants, dietary fat saturation, lipoprotein oxidation and atherogenesis. Nutrition. 1996;12(5):377-9
  4. Serdar Z, Aslan K, Dirican M, Sarandol E, Yesilbursa D, Serdar A. Lipid and protein oxidation and antioxidant status in patients with angiographically proven coronary artery disease. Clin Biochem. 2006;39(8):794-803
  5. Mates JM, Perez-Gomez C, Nunez de Castro I. Antioxidant enzymes and human diseases. Clin Biochem. 1999;32(8):595-603
  6. Variji A, Shokri Y, Fallahpour S, Zargari M, Bagheri B, Abediankenari S, et al. The combined utility of myeloperoxidase (MPO) and paraoxonase 1 (PON1) as two important HDL-associated enzymes in coronary artery disease: Which has a stronger predictive role? Atherosclerosis. 2019;280:7-13
  7. Khine HW, Teiber JF, Haley RW, Khera A, Ayers CR, Rohatgi A. Association of the serum myeloperoxidase/high-density lipoprotein particle ratio and incident cardiovascular events in a multi-ethnic population: Observations from the Dallas Heart Study. Atherosclerosis. 2017;263:156-62
  8. Jornayvaz FR, Brulhart-Meynet MC, James RW. Myeloperoxidase and paraoxonase-1 in type 2 diabetic patients. Nutr Metab Cardiovasc Dis. 2009;19(9):613-9
  9. Sun H, Shen J, Liu T, Tan Y, Tian D, Luo T, et al. Heat shock protein 65 promotes atherosclerosis through impairing the properties of high density lipoprotein. Atherosclerosis. 2014;237(2):853-61
  10. Nussbaum C, Klinke A, Adam M, Baldus S, Sperandio M. Myeloperoxidase: a leukocyte-derived protagonist of inflammation and cardiovascular disease. Antioxid Redox Signal. 2013;18(6):692-713
  11. Palinkas Z, Furtmuller PG, Nagy A, Jakopitsch C, Pirker KF, Magierowski M, et al. Interactions of hydrogen sulfide with myeloperoxidase. Br J Pharmacol. 2015;172(6):1516-32. 12. van Dalen CJ, Whitehouse MW, Winterbourn CC, Kettle AJ. Thiocyanate and chloride as competing substrates for myeloperoxidase. Biochem J. 1997;327 ( Pt 2):487-92
  12. Gerber M, Boutron-Ruault MC, Hercberg S, Riboli E, Scalbert A, Siess MH. [Food and cancer: state of the art about the protective effect of fruits and vegetables]. Bulletin du cancer. 2002;89(3):293-312
  13. Krishnaiah D, Sarbatly R, Nithyanandam