SYZYGIUM CUMINI (L.) SKEELS LEAF EXTRACT FRACTIONS AS ARGINASE INHIBITORS AND THE EFFECTS OF TANNINS ON THEIR ACTIVITY

Authors

  • ARI ARIEFAH HIDAYATI Graduate Program, Faculty of Pharmacy, Universitas Indonesia
  • BERNA ELYA Departement of Pharmacognosy-Pythochemistry, Faculty of Pharmacy, Universitas Indonesia, Depok, Jawa Barat 16424, Indonesia
  • RANI SAURIASARI 3Departement of Clinical Pharmacy, Faculty of Pharmacy, Universitas Indonesia, Depok, Jawa Barat 16424, Indonesia

DOI:

https://doi.org/10.22159/ijap.2020.v12s1.FF059

Keywords:

Arginase inhibitor, Ethyl acetate fraction, Methanol fraction, Syzygium cumini, Tannins

Abstract

Objective: Arginase inhibition could be a potential therapeutic approach for endothelial dysfunction. Syzygium cumini (L.) Skeels leaves contain
phenolic acids and flavonoids, which have been predicted to exhibit arginase inhibitory activity. Moreover, these leaves contain tannins, which can
form complexes with enzymes and lead to false-positive results during biological testing. Therefore, this study was conducted to evaluate the arginase
inhibitory activity of S. cumini leaf extract and fractions as well as to elucidate the effects of tannins on this activity.
Methods: S. cumini leaves were fractionated using n-hexane, ethyl acetate, and methanol. A colorimetric method was employed to evaluate arginase
inhibitory activity. Tannin elimination was performed through the gelatin precipitation method. Total phenolic and flavonoid contents of the fractions
were calculated using the Folin–Ciocalteu and aluminum chloride methods, respectively.
Results: Ethyl acetate and methanol fractions showed arginase inhibitory activity with half-maximal inhibitory concentrations (IC50) of 46.96 and
15.35 μg/mL, respectively. The methanol fraction was positive for tannins. After tannin elimination, this fraction exhibited less potent arginase
inhibitory activity, with an IC50 value of 53.03 μg/mL. The ethyl acetate fraction showed higher total phenolic and flavonoid contents than the methanol
fraction.
Conclusion: Tannins affected the arginase inhibitory activity of the methanol fraction of S. cumini leaves; however, the ethyl acetate fraction did not
contain tannins and could inhibit arginase activity.

Downloads

Download data is not yet available.

References

1. Steppan J, Nyhan D, Berkowitz DE. Development of novel arginase
inhibitors for therapy of endothelial dysfunction. Front Immunol
2013;4:278.
2. Kietadisorn R, Juni RP, Moens AL. Tackling endothelial dysfunction
by modulating NOS uncoupling: New insights into its pathogenesis
and therapeutic possibilities. Am J Physiol Endocrinol Metab
2012;302:E481-95.
3. Pudlo M, Demougeot C, Girard-Thernier C. Arginase inhibitors:
A rational approach over one century. Med Res Rev 2017;37:475-513.
4. Lundberg JO, Gladwin MT, Weitzberg E. Strategies to increase nitric
oxide signalling in cardiovascular disease. Nat Rev Drug Discov
2015;14:623-41.
5. Schnorr O, Brossette T, Momma TY, Kleinbongard P, Keen CL,
Schroeter H, et al. Cocoa flavanols lower vascular arginase activity
in human endothelial cells in vitro and in erythrocytes in vivo. Arch
Biochem Biophys 2008;476:211-5.
6. Shin W, Cuong TD, Lee JH, Min B, Jeon BH, Lim HK, et al. Arginase
inhibition by ethylacetate extract of Caesalpinia sappan lignum
contributes to activation of endothelial nitric oxide synthase. Korean J
Physiol Pharmacol 2011;15:123-8.
7. Shin W, Yoon J, Oh GT, Ryoo S. Korean red ginseng inhibits arginase and
contributes to endotheliumdependent vasorelaxation through endothelial
nitric oxide synthase coupling. J Ginseng Res 2013;37:64-73.
8. Kim SW, Cuong TD, Hung TM, Ryoo S, Lee JH, Min BS. Arginase
II inhibitory activity of flavonoid compounds from Scutellaria indica.
Arch Pharm Res 2013;36:922-6.
9. Sembiring EN, Elya B, Sauriasari R. Inhibitory effect on arginase and
total phenolic content determination of extracts from different parts of
Melastoma malabathricum L. J Young Pharm 2018;10:s114-7.
10. Bordage S, Pham TN, Zedet A, Gugglielmetti AS, Nappey M,
Demougeot C, et al. Investigation of mammal arginase inhibitory
properties of natural ubiquitous polyphenols by using an optimized
colorimetric microplate assay. Planta Med 2017;83:647-53.
11. Ribeiro RM, Pinheiro Neto VF, Ribeiro KS, Vieira DA, Abreu IC,
Silva Sdo N, et al. Antihypertensive effect of Syzygium cumini in
spontaneously hypertensive Rats. Evid Based Complement Alternat
Med 2014;2014:605452.
12. Sanches JR, França LM, Chagas VT, Gaspar RS, Dos Santos KA,
Gonçalves LM, et al. Polyphenol-rich extract of Syzygium cumini
leaf dually improves peripheral insulin sensitivity and pancreatic
islet function in monosodium L-glutamate-induced obese rats. Front
Pharmacol 2016;7:48.
13. Mahmoud II, Marzouk MS, Moharram FA, El-Gindi MR, Hassan AM.
Acylated flavonol glycosides from Eugenia jambolana leaves.
Phytochemistry 2001;58:1239-44.
14. Ruan ZP, Zhang LL, Lin YM. Evaluation of the antioxidant activity of
Syzygium cumini leaves. Molecules 2008;13:2545-56.
15. De Bona KS, Bellé LP, Sari MH, Schetinger MR, Morsch VM,
Boligon A, et al. Syzygium cumini extract decrease adenosine
deaminase, 5’ nucleotidase activities and oxidative damage in platelets
of diabetic patients. Cell Physiol Biochem 2010;26:729-38.
16. Chagas VT, França LM, Malik S, Paes AM. Syzygium cumini (L.) skeels:
A prominent source of bioactive molecules against cardiometabolic
diseases. Front Pharmacol 2015;6:259.
17. Adamczyk B, Simon J, Kitunen V, Adamczyk S, Smolander A.
Tannins and their complex interaction with different organic nitrogen
compounds and enzymes: Old paradigms versus recent advances.
ChemistryOpen 2017;6:610-4.
18. Mustarichie R, Runadi D, Ramdhani D. The Antioxidant activity and
phytochemical screening of ethanol extract, fractions of water, ethyl
acetate, and n-hexane from mistletoe tea (Scurrula atropurpurea Bl.
Dans). Asian J Pharm Clin Res 2017;10:343-7.
19. Prommajak T, Leksawasdi N, Rattanapanone N. Optimizing tannin
precipitation in cashew apple juice. CMU J Nat Sci 2018;17:14-23.
20. Nithya A, Jayanthi J, Ragunathan MG. Antioxidant activity, total phenol,
flavonoid, alkaloid, tannin, and saponin contents of leaf extracts of
Salvinia molesta D. S. Mitchell. Asian J Pharm Clin Res 2016;9:200-3.
21. Timbola AK, Szpoganicz B, Branco A, Monache FD, Pizzolatti MG.
A new flavonol from leaves of Eugenia jambolana. Fitoterapia
2002;73:174-6.
22. Ecker A, Araujo Vieira F, de Souza Prestes A, Mulling Dos Santos M,
Ramos A, Dias Ferreira R, et al. Effect of Syzygium cumini and
Bauhinia forficata aqueous-leaf extracts on oxidative and mitochondrial
parameters in vitro. EXCLI J 2015;14:1219-31.
23. dos Reis MB, Manjolin LC, Maquiaveli Cdo C, Santos-Filho OA, da
Silva ER. Inhibition of Leishmania (Leishmania) amazonensis and
rat arginases by green tea EGCG, (+)-catechin and (-)-epicatechin:
A comparative structural analysis of enzyme-inhibitor interactions.
PLoS One 2013;8:e78387.

Published

23-03-2020

How to Cite

HIDAYATI, A. A., ELYA, B., & SAURIASARI, R. (2020). SYZYGIUM CUMINI (L.) SKEELS LEAF EXTRACT FRACTIONS AS ARGINASE INHIBITORS AND THE EFFECTS OF TANNINS ON THEIR ACTIVITY. International Journal of Applied Pharmaceutics, 12(1), 268–270. https://doi.org/10.22159/ijap.2020.v12s1.FF059

Issue

Section

Original Article(s)

Most read articles by the same author(s)

1 2 3 4 > >>