Dergiler / International Journal of Secondary Metabolite / 2019 / Cilt: 6 - Sayı: 4

In vitro and in silico Evaluation of Some Natural Molecules as Potent Glutathione Reductase Inhibitors

Sayfa
310–316
Yayın Tarihi
2022-10-19
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

In current study first time, β-sitosterol, stigmasterol, diosgenin and jervine were found to be much more glutathione reductase inhibitors.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Glutathione reductase inhibitors are very popular antimalarial and anticancer agents.
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Temel Bulgular & Veri:According to the results obtained, IC50 values of β-sitosterol, stigmasterol, diosgenin and jervine were found as 1.2580, 5.2116, 0.1916 and 0.7701 µM, respectively.
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Sonuç & Katkı:In current study first time, β-sitosterol, stigmasterol, diosgenin and jervine were found to be much more glutathione reductase inhibitors.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Secondary metabolites · Glutathione reductase · Inhibition

Özet

Glutathione reductase inhibitors are very popular antimalarial and anticancer agents. In this study, in vitro inhibition effects of β-sitosterol, stigmasterol, diosgenin and jervine which containing steroidal structure were determined against glutathione reductase enzyme. β-sitosterol, diosgenin and jervine were isolated from Veratrum album and stigmasterol was isolated from Artemisia dracunculus L. by chromatographic methods. According to the results obtained, IC50 values of β-sitosterol, stigmasterol, diosgenin and jervine were found as 1.2580, 5.2116, 0.1916 and 0.7701 µM, respectively. Among test compounds, diosgenin showed the strongest inhibitory effect against glutathione reductase with Swissdock docking figure. In current study first time, β-sitosterol, stigmasterol, diosgenin and jervine were found to be much more glutathione reductase inhibitors.

Abstract

Glutathione reductase inhibitors are very popular antimalarial and anticancer agents. In this study, in vitro inhibition effects of β-sitosterol, stigmasterol, diosgenin and jervine which containing steroidal structure were determined against glutathione reductase enzyme. β-sitosterol, diosgenin and jervine were isolated from Veratrum album and stigmasterol was isolated from Artemisia dracunculus L. by chromatographic methods. According to the results obtained, IC50 values of β-sitosterol, stigmasterol, diosgenin and jervine were found as 1.2580, 5.2116, 0.1916 and 0.7701 µM, respectively. Among test compounds, diosgenin showed the strongest inhibitory effect against glutathione reductase with Swissdock docking figure. In current study first time, β-sitosterol, stigmasterol, diosgenin and jervine were found to be much more glutathione reductase inhibitors.

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Bu Makaleye Atıf Yap

AYDIN, T. (2022). In vitro and in silico Evaluation of Some Natural Molecules as Potent Glutathione Reductase Inhibitors. International Journal of Secondary Metabolite, Cilt: 6 - Sayı: 4, 310–316. https://ajindex.com/articles/541681

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Kaynakça (3)

  1. . Shahi, Y. Samadi, F.M., Mukherjee, S. (2019). The influence of Tumor Necrosis Factor-alpha gene polymorphism on oxidative stress in patients with oral precancerous lesions and oral cancer, Gene Rep, 17, 1-8. doi: doi.org/10.1016/j.genrep.2019.100525 [2]. Tsai, Y.C., Hong, C.Y., Liu, L.F., Kao C.H. (2005). Expression of ascorbate peroxidase and glutathione reductase in roots of rice seedlings in response to NaCl and H2O2, J Plant Physiol, 162, 291-299. doi: 10.1016/j.jplph.2004.06.004 [3]. Meister A. Anderson M.E. (1983).
  2. Glutathione, Annu Rev Biochem., 52, 711-760. doi: 10.1146/annurev.bi.52.070183.003431 [4]. Schirmer, R.H., Muller, J.G., Krauthsiegel, R.L., (1995). Disulfide-reductase inhibitors as chemotherapeutic - agents - the design of drugs for trypanosomiasis and malaria, Angew Chem Int Edit., 34, 141-154. doi: doi.org/10.1002/anie.199501411 [5]. Bohme, C.C., Arscott, L.D., Becker, K., Schirmer, R.H. (2000).
  3. Jr. Williams, C.H. Kinetic characterization of glutathione reductase from the malarial parasite Plasmodium falciparum. Comparison with the human enzyme, J Biol Chem., 275, 37317-37323. doi: 10.1074/jbc.M007695200 [6]. Burkard, L., Scheuermann, A., Simithy, J., Calderon, A.I. (2016). Development of a functional assay to detect inhibitors of Plasmodium falciparum glutathione reductase utilizing liquid chromatography-mass spectrometry, Biomed Chromatogr., 30, 543-547. doi: doi.org/10.1002/bmc.3580 [7]. Talisuna, A.O., Okello, P.E., Erhart, A., Coosemans, M., D'Alessandro, U. (2007). Intensity of malaria transmission and the spread of Plasmodium falciparum-resistant malaria: A review of epidemiologic field evidence, Am J Trop Med Hyg., 77, 170 180. WOS:000252212600027 [8]. Hainley, C.A., Filer, C.N. (2017). Selective D ring side chain tritiation of steroidal natural products, J Radioanal Nucl Ch., 313, 467-472. doi:10.1007/s10967-017-5322-y [9]. Aydin, T., Cakir, A., Kazaz, C., Bayrak, N., Bayir, Y., Taskesenligil, Y. (2014). Insecticidal metabolites from the rhizomes of Veratrum album against adults of Colorado Potato Beetle, Leptinotarsa decemlineata, Chem Biodivers., 11, 1192-1204. doi:doi.org/10.1002/cbdv.201300407 [10]. Lee, S.T., Panter, K.E., Gaffield, W., Stegelmeier, B.L. (2003). Development of an enzyme-linked immunosorbent assay for the Veratrum plant teratogens: Cyclopamine and jervine, J Agr Food Chem., 51, 582-586. doi: doi.org/10.1021/jf020961s [11]. Khanfar, M.A., El Sayed, K.A. (2013). The Veratrum alkaloids jervine, veratrami