Journals / IUFS Journal of Biology / 2014 / Cilt: 73 - Sayı: 2

Bazı Bitki Ekstreleri ve Kimyasal Bileşiklerin Lipoksijenaz İnhibitör Aktiviteleri

Lipoxygenase Inhibitory Activities of Some Plant Extracts and Chemical Compounds

Pages
47–52
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The results obtained in the present study indicate that plant extracts and chemical compounds examined can be a potential source of novel antiinflammatory therapeutics.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Lipoxygenases (LOXs, linoleate: oxygen reductase, E.C. 1.13.11.12) are a family of non-heme ironcontaining dioxygenases.
📊
Key Findings & Data:In this study, the inhibitory effects of ethanolic extracts prepared from 12 different plants and 12 different chemical compounds were investigated on the activity of LOX which has an important value in the health area.
💡
Conclusion & Impact:The results obtained in the present study indicate that plant extracts and chemical compounds examined can be a potential source of novel antiinflammatory therapeutics.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Lipoxygenases (LOXs, linoleate: oxygen reductase, E.C. 1.13.11.12) are a family of non-heme ironcontaining dioxygenases. LOXs are associated with several inflammation-related diseases such as arthritis, asthma, cardiovascular, kidney, skin and allergic diseases, neurodegenerative disorders, cancer and metabolic syndrome. In this study, the inhibitory effects of ethanolic extracts prepared from 12 different plants and 12 different chemical compounds were investigated on the activity of LOX which has an important value in the health area. All the plant extracts and chemical substances used in our study showed LOX inhibitory effect. The enzyme inhibitory activities of the extracts and chemical compounds were increasing in a dose-dependent manner. The results obtained in the present study indicate that plant extracts and chemical compounds examined can be a potential source of novel antiinflammatory therapeutics.

Özet

Lipoksijenazlar (LOXs, linoleat: oksijen redüktaz, E.C.1.13.11.12) hem içermeyen, demir içeren dioksijenaz ailesidir. Lipoksijenazlar, artrit, astım, kalp damar, böbrek, deri ve alerjik hastalıklar, nörodejeneratif hastalıklar, kanser ve metabolik sendrom gibi çeşitli inflamasyon ile ilişkili hastalıklar ile ilgilidir. Bu çalışmada, farklı bitkilerden hazırlanan etanollü ekstrelerin ve bazı kimyasal bileşiklerin sağlık alanında önemli bir alana sahip olan LOX aktivitesi üzerine inhibe edici etkileri incelenmiştir. Çalışmada kullanılan tüm bitki ekstreleri ve kimyasal maddelerin LOX inhibitör etkisine sahip olduğu belirlenmiştir. Bitki ekstreleri ve kimyasal bileşiklerin enzim inhibitör aktiviteleri, doza bağlı olarak artmaktadır. Bu çalışmadan elde edilen sonuçlara göre, incelenen bitki ekstreleri ve bazı kimyasal bileşikler antiinflamatuar tedavide yeni bir potansiyel kaynak olabilirler.

🔖

Cite This Article

TURHAN, E. Y., SAÇAN, Ö. (2022). Bazı Bitki Ekstreleri ve Kimyasal Bileşiklerin Lipoksijenaz İnhibitör Aktiviteleri. IUFS Journal of Biology, Cilt: 73 - Sayı: 2, 47–52. https://ajindex.com/articles/543999

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (12)

  1. Aparoy P., Reddy R. N., L. Gurupsarad, M. R. Reddy and P. Reddanna. (2008) Homology modeling of 5-lipoxygenase and hints for better inhibitor design. Journal of Computer-Aided Molecular Design, 22: 611–619. Arts I. C. W. and Hollman P. C. H. (2005) Polyphenols and disease risk in epidemiologic studies1-4. The American Journal of Clinical Nutrition, 81:317S- 325. Atac A. I., Peksel A., Yanardag R., Sokmen B. B., Doger M. M. and Bilen G. Z. (2006) The effect of combined treatment with niacin and chromium (III) chloride on the different tissues of hyperlipemic rats. Drug and Chemical Toxicology, 29:363-377.
  2. Blake R. A. (2015) Target validation in drug discovery. Methods in Molecular and Cellular Biology, 356: 367-377.
  3. Bolkent S., Yanardag R., Bolkent S. and Döger M. M. (2004) Beneficial effects of combined treatment with niacin and chromium on the liver of hyperlipemic rats. Biological Trace Element Research, 101:219-229.
  4. Brash A. R. (1999) Catalysis, and acquisition of substrate lipoxygenases: occurrence, functions. Journal of Biological Chemistry, 274:23679-23682.
  5. Celik Onar H., Yusufoglu A., Turker G. and Yanardag R. (2012) Elastase, tyrosinase and lipoxygenase inhibition and antioxidant activity an aqueous extract from Epilobium angustifolium L. leaves. Journal of Medicinal Plant Research, 6: 716-726.
  6. Charlier C. and Michaux C. (2003) Dual inhibition of cyclooxygenase-2 (COX- 2) and 5-lipoxygenase (5-LOX) as a new strategy to provide safer non-steroidal antiinflammatory drugs. European Journal of Medicinal Chemistry, 38: 645-659.
  7. Chen M. T., Sheu J. Y. and Lin T. H. (2000). Protective effects of manganese against lipid peroxidation. Journal of Toxicology and Environmental Health, PartA:, 61:569-577.
  8. Dobrian A. D., Lieb D. C., Cole B. K. and Taylor-Fishwick D. A. (2011) Functional and pathological roles of the 12- and 15-lipoxygenases. Progress in Lipid Research, 50: 115-131.
  9. Funk C. D. (1996) The molecular biology of mammalian lipoxygenases and the quest for eicosanoid functions using lipoxygenase-deficient mice. Biochimica et Biophysica Acta, 1304: 65-84.
  10. Iversen L. and Kragbella K. (2000) Arachidonic acid metabolism in skin health and disease. Prostaglandins Other Lipid Mediators, 63: 25-42.
  11. Jiang Q. (2014) Natural forms of vitamin E: metabolism, antioxidant, and antiinflammatory activities and their role in disease prevention and therapy. Free Radical Biology and Medicine, 72:76-90.
  12. Juntachote T. and Berghofer E. (2005) Antioxidant properties and stabi