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Erratum: Investigation of antioxidant, enzyme inhibition and antiproliferative activities of blackthorn (Prunus spinosa L.) extracts

Year 2023, Volume: 6 Issue: 3, 360 - 380, 20.12.2023
The original article was published on December 15, 2021. https://dergipark.org.tr/en/pub/ijlsb/issue/62833/851220

Erratum Note

The text you provided seems to be a correction statement related to an article titled "Investigation of Antioxidant, Enzyme Inhibition and Antiproliferative Activities of Blackthorn (Prunus spinosa L.) Extracts," published in Volume 4, Issue 3 of the year 2021. The correction addresses an error in the project number mentioned in the article. The corrected project number is "FYL 2014/212" instead of the previously reported "FYL 2014/222." This correction is being made by the responsible author(s) to rectify the mistake and apologize to the readers for any confusion caused by the error. Reported number corrected version is: "This work was supported by Çanakkale Onsekiz Mart University, The Scientific Research Coordination Unit, Project number: FYL 2014/212 as MSc Thesis of MS."

Abstract

Natural products have a key role in drug discovery in pharmacology and medicine. Prunus spinosa L. (blackthorn) grown in Çanakkale province in western Turkey, is known as a medicinal plant, a rich source of biologically active compounds such as phenolics, flavonoids and anthocyanidins. The flower and fruit extracts of the plant are subjects of many studies, but they usually lack in details of its potential for bio-inhibition studies. Thus, this study aimed to investigate the antioxidant, enzyme inhibition and antiproliferative activity studies of the methanol, ethyl acetate, dichloromethane, and n-hexane extracts of the plant. The ethyl acetate and methanol extracts demonstrated more better antioxidant activity with DPPH, FRAP, CUPRAC, and TEAC assays. Enzyme inhibition studies of the extracts were performed using β-lactamase and various proteases. The methanol (FL) and ethyl acetate (FL and L) extracts at the concentration of 10 mg/mL, showed good inhibition against α-chymotrypsin, trypsin, and papain with values of 22.6%, 34.7% and 92.1%, respectively. Furthermore, the methanol and ethyl acetate extracts have displayed higher cytotoxic effect against cancer cells such as Hep3B and HT29 when compared to healthy cells (HUVEC) using MTT assay. The findings suggest that P. spinosa L. extracts and their components may be potential for further investigations of novel drug candidates.

Supporting Institution

Çanakkale Onsekiz Mart University, The Scientific Research Coordination Unit

Project Number

FYL 2014/212

Thanks

We thank Çanakkale Onsekiz Mart University for financial support. The authors also thank Ersin Karabacak for the identification of the plant.

References

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Erratum: Yaban Eriği (Prunus spinosa L.) Özütlerinin Antioksidan, Enzim İnhibisyonu ve Antiproliferatif Etkinliklerinin İncelenmesi

Year 2023, Volume: 6 Issue: 3, 360 - 380, 20.12.2023
The original article was published on December 15, 2021. https://dergipark.org.tr/en/pub/ijlsb/issue/62833/851220

Erratum Note

2021 yılı 4. Cilt 3. Sayıda yayınlanan; “Yaban Eriği (Prunus spinosa L.) Özütlerinin Antioksidan, Enzim İnhibisyonu ve Antiproliferatif Etkinliklerinin İncelenmesi”, “Investigation of Antioxidant, Enzyme Inhibition and Antiproliferative Activities of Blackthorn (Prunus spinosa L.) Extracts” başlıklı makalede yer alan; “This work was supported by Çanakkale Onsekiz Mart University, The Scientific Research Coordination Unit, Project number: FYL 2014/222 as MSc Thesis of MS.” ifadesinde proje numarası sehven yanlış yazılmıştır ve makalede sorumlu yazar tarafından hatalı olarak yazıldığı beyan edilmiştir. Yapılan bu hatadan dolayı yazarlar, okuyuculardan özür dilemektedir. Makalede yer alan hatanın giderilmesi amacıyla bu düzeltme metni sunulmuştur. Bildirilen Proje numarası düzeltilmiş hali: “This work was supported by Çanakkale Onsekiz Mart University, The Scientific Research Coordination Unit, Project number: FYL 2014/212 as MSc Thesis of MS.”

Abstract

Doğal ürünler, farmakoloji ve tıpta ilaç keşfinde anahtar bir role sahiptir. Türkiye'nin batısındaki Çanakkale ilinde yetişen Prunus spinosa L. (karaçalı), tıbbi bir bitki olarak bilinir ve fenolikler, flavonoidler ve antosiyanidinler gibi biyolojik olarak aktif bileşiklerin zengin bir kaynağıdır. Bitkinin çiçek ve meyve özleri birçok çalışmanın konusudur, ancak genellikle biyoinhibisyon çalışmaları için potansiyelinin ayrıntılarından yoksundurlar. Bu nedenle, bu çalışmada bitkinin metanol, etil asetat, diklorometan ve n-hekzan özütlerinin antioksidan, enzim inhibisyonu ve antiproliferatif etkinlik çalışmalarının incelenmesi amaçlanmıştır. Etil asetat ve metanol özütleri, DPPH, FRAP, CUPRAC ve TEAC analizlerinde daha iyi antioksidan etkinlik sergiledi. Özütlerin enzim inhibisyon çalışmaları, β-laktamaz ve çeşitli proteazlar kullanılarak yapıldı. 10 mg/mL derişimdeki metanol (FL) ve etil asetat (FL ve L) özütleri, sırasıyla % 22.6, % 34.7 ve % 92.1 değerleriyle a-kimotripsin, tripsin ve papine karşı iyi inhibisyon gösterdi. Ayrıca metanol ve etil asetat özütleri, MTT testi kullanılarak sağlıklı hücrelere (HUVEC) kıyasla Hep3B ve HT29 gibi kanser hücrelerine karşı daha yüksek sitotoksik etki göstermiştir. Bulgular, P. spinosa L. özütleri ve bileşenlerinin yeni ilaç adaylarının ileri incelemeleri için potansiyel olabileceğini gösterdi.

Supporting Institution

Çanakkale Onsekiz Mart University, The Scientific Research Coordination Unit

Project Number

FYL 2014/212

Thanks

We thank Çanakkale Onsekiz Mart University for financial support. The authors also thank Ersin Karabacak for the identification of the plant.

References

  • Albertini, M., Fraternale, D., Semprucci, F., Cecchini, S., Colomba, M. & Rocchi, M.B.L. 1983. Bioeffects of Prunus spinosa L. fruit ethanol extract on reproduction and phenotypic plasticity of Trichoplax adhaerens Schulze. PeerJ, https://doi.org/10.7717/peerj.6789.
  • Apak, R., Güçlü, K., Demirata, B., Ozyürek, M., Çelik, S.E., Bektaso̧glu, B., Berker, K.I. & Ozyurt, D. 2007. Comparative evaluation of various total antioxidant capacity assays applied to phenolic compounds with the CUPRAC assay. Molecules, 12: 1496−1547.
  • Aryal, S., Baniya, M.K., Danekhu, K., Kunwar, P., Gurung, R. & Koirala, N. 2019. Total phenolic content, flavonoid content and antioxidant potential of wild vegetables from Western Nepal. Plants (Basel), 8(4): 96.
  • Barros, L., Carvalho, A.M., Morais, JSá. & Ferreira, I.C.F.R. 2010. Strawberry-tree, blackthorn and rose fruits: Detailed characterisation in nutrients and phytochemicals with antioxidant properties. Food Chemistry, 120: 247–254. Benoit, C.Y.R. Plant extracts and compositions comprising extracellular protease inhibitors. WO/2002/069992.
  • Benzie, I.F.F. & Strain, J.J. 1996. The ferric reducing ability of plasma (FRAP) as a measure of ‘‘antioxidant power’’ the FRAP assay. Analytical Biochemistry, 239: 70−76.
  • Bonesi, M., Xiao, J., Tundis, R., Aiello, F., Sicari, V., Loizzo, M.R. 2019. Advances in the Tyrosinase Inhibitors from Plant Source. Current Medicinal Chemistry, 26(18): 3279-3299.
  • Cömert Önder, F., Ay, M. & Sarker, S.D. 2013. Comparative study of antioxidant properties and total phenolic content of the extracts of Humulus lupulus L. and quantification of bioactive components by LC−MS/MS and GC−MS. Journal of Agricultural and Food Chemistry, 61: 10498−10506.
  • Cömert Önder, F., Ay, M., Aydoğan Türkoğlu, S., Tura Köçkar, F. & Çelik, A. 2016. Antiproliferative activity of Humulus lupulus extracts on human hepatoma (Hep3B), colon (HT-29) cancer cells and proteases, tyrosinase, β-lactamase enzyme inhibition studies. Journal of Enzyme Inhibition and Medicinal Chemistry, 31(1): 90-98.
  • Divya, C., Sreejina Sreedharan, K., Parambath, B.P. & Meethal. K.V. 2014. Identification of plant extracts expressing trypsin inhibitor. Acta Biologica Indica, 3(1): 522-526.
  • Drawz, S.M., Papp-Wallace, K.M. & Bonomo, R.A. 2014. New β-lactamase inhibitors: a therapeutic renaissance in an MDR world. Antimicrobial Agents Chemotherapy, 58(4): 1835-1846.
  • Fais, A., Corda, M., Era, B., Fadda, M.B., Matos, M.J., Quezada, E., Santana, L., Picciau, C., Podda, G. & Delogu, G. 2009. Tyrosinase inhibitor activity of coumarin-resveratrol hybrids. Molecules. 14: 2514–20.
  • Gangoué-Piéboji, J., Baurin, S., Frère, J-M., Ngassam, P., Ngameni, B., Azebaze, A., Pegnyemb, D.E., Watchueng, J., Goffin, C. & Galleni, M. 2007. Screening of some medicinal plants from cameroon for lactamase inhibitory activity. Phytotherapy Research, 21: 284–287.
  • Ghorbanpour, M., Hadian, J., Nikabad, S. & Varma, A. 2017. Importance of medicinal and aromatic plants in human life. In: Ghorbanpour M., Varma A. (eds) Medicinal plants and environmental challenges. Springer, Cham. https://doi.org/10.1007/978-3-319-68717-9_1
  • Guimarães, R., Barros, L., Calhelha, R.C., Carvalho, A.M., Queiroz M.J. & Ferreira, I.C. 2014. Bioactivity of different enriched phenolic extracts of wild fruits from Northeastern Portugal: A comparative study. Plant Foods for Human Nutrition, 69: 37–42.
  • Hae, G.D., Jo, J.M., Kim, S.Y. & Kim, J.W. 2019. Tyrosinase inhibitors from natural source as skin-whitening agents and the application of edible insects: A Mini Review. International Journal of Clinical Nutrition, 5: 141.
  • Hou, N., Liu, N., Han, J., Yan, Y. & Li, J. 2017. Chlorogenic acid induces reactive oxygen species generation and inhibits the viability of human colon cancer cells. Anticancer Drugs, 28(1): 59–65.
  • Irizar, A.C. & Fernandez, M.F. 1992. Constituents of Prunus spinosa. Journal of Natural Products, 55(4): 450-454.
  • Kim, Y.J. & Uyama, H. 2005. Tyrosinase inhibitors from natural and synthetic sources: Structure, inhibition mechanism and perspective for the future. CMLS, Cellular and Molecular Life Sciences, 62: 1707–1723.
  • Kim, Y., Kang, K. & Yokozawa, T. 2008. The anti-melanogenic effect of pycnogenol by its anti-oxidative actions. Food Chemical Toxicology, 46: 2466–2471.
  • Kim, J.Y., Park, S.C., Hwang, I., Kim, J. Y., Park, S. C., Hwang, I., Cheong, H., Nah, J. W., Hahm, K. S., & Park, Y. 2009. Protease inhibitors from plants with antimicrobial activity. Internatinal Journal of Molecular Science, 10(6): 2860-2872.
  • Kim, M., Park, J., Song, K., Kim, H.G., Koh, J.S. & Boo, Y.C. 2012. Screening of plant extracts for human tyrosinase inhibiting effects. International Journal of Cosmetic Science, 34(2): 202-208.
  • Korkmaz, N., Sener, S.O., Akkaya, S., Badem, M., Aliyazicioglu, R., Abudayyak, M., Oztas, E. & Ozgen, U. 2019. Investigation of antioxidant, cytotoxic, tyrosinase inhibitory activities, and phenolic profiles of green, white, and black teas. Turk Journal of Biochemistry, 44(3): 278–288.
  • Kumarasamy, Y., Fergusson, M., Nahar, L. & Sarker, S.D. 2002. Biological activity of moschamindole from Centaurea moschata. Pharmaceutical Biology, 4: 307−310.
  • Kumarasamy, Y., Cox, P.J., Jaspars, M., Nahar, L. & Sarker, S.D. 2004. Comparative studies on biological activities of Prunus padus and P. Spinosa. Fitoterapia. 75: 77–80.
  • Liu, Y., Zhao, G., Li, X., Shen, Q., Wu, Q., Zhuang, J., Zhang, X., Xia, E., Zhang, Z., Qian, Y., Gao, L. & Xia, T. 2020. Comparative analysis of phenolic compound metabolism among tea plants in the section Thea of the genus Camellia. Food Research International, 135: 109276.
  • Lo ́pez-Otín, C. & Bond, J.S. 2008. Proteases: Multifunctional Enzymes in Life and Disease. Journal of Biological Chemistry, 283(4): 30433–30437.
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There are 55 citations in total.

Details

Primary Language English
Subjects Biochemistry and Cell Biology (Other)
Journal Section Research Articles
Authors

Merve Sönmez 0000-0002-6577-5363

Ferah Cömert Önder 0000-0002-4037-1979

Esra Tokay 0000-0001-9993-2753

Ayhan Celık 0000-0003-1355-9252

Feray Köçkar 0000-0003-2572-8391

Mehmet Ay 0000-0002-1095-1614

Project Number FYL 2014/212
Early Pub Date December 11, 2023
Publication Date December 20, 2023
Published in Issue Year 2023 Volume: 6 Issue: 3

Cite

EndNote Sönmez M, Cömert Önder F, Tokay E, Celık A, Köçkar F, Ay M (December 1, 2023) Investigation of antioxidant, enzyme inhibition and antiproliferative activities of blackthorn (Prunus spinosa L.) extracts. International Journal of Life Sciences and Biotechnology 6 3 360–380.



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