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Phenolic, Flavonoids Content, Antioxidant Potential of Murraya koenigii L. (Curry Leave): in vitro and in vivo Protective Effects
Corresponding Author(s) : Abhishek Chauhan
Asian Journal of Chemistry,
Vol. 35 No. 1 (2023): Vol 35 Issue 1
Abstract
In the current investigation, the proximate value, total phenolic content, toal flavonoid content, antioxidant potential and in vitro and in vivo protective effects of Murraya koenigii L. (curry leave) extracts were carried out. Flavonoids, phenols and alkaloids were recorded in ethanol, methanol, ethyl acetate, petroleum ether, benzene and acetone extracts. A higher level of total phenolic content was recorded in ethanolic fraction followed by benzene, ethyl acetate, methanol, petroleum ether and acetone fractions. The total flavonoids content was recorded in the range of 5.12 mg RE g−1 to 9.24 mg RE g−1. 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity was estimated in all the solvent fractions at the concentration ranging from 312.5 μg mL-1 to 5000 μg mL−1. Percentage inhibition was recorded in the range of 39.40 to 72.32. To study the antimutagenic property, the plate incorporation method was used to see the effects of the MKLE fraction on S. typhimurium trains TA 1537, TA 1535, TA 98, TA 100 and TA 102 both in the absence and presence of S9 mix (5% v/v). Higher antimutagenic property at a concentration of 5000 μg/plate with 2-nitrofluorene 7.5 μg/plate was observed against TA 98. In vivo study indicates the protective effects of the extract of the MKLE against chlorpyrifos-induced toxicity in brain and lungs of the experimental rats. Four animal groups 5 male and 5 females were selected, group I serve as a control, group II was given a single dose of MKLE as such for 28 consecutive days while group III was treated with chlorpyrifos at the dose level of 60 mg/kg B.wt and group IV was dosed with chlorpyrifos at the dose level of 60 mg/kg B.wt simultaneously treated with the MKLE as such twice in a day (B.D.). Chlorpyrifos administration (group III) to the rats resulted in reduced body weight. decrease Ache level increases, SGOT, SGPT, ALP were observed while no significant alterations were noticed in any parameter in the II group animals, Histopathology of brain and lung of the chlorpyrifos treated animals shows the cellular deficit in the brain tissue and mild congestion in the lung tissue. The present study concluded that curry leaves are a rich source of phenolic, alkaloids, flavonoids and exhibit antioxidant and antimutagenic activity and appeared to be beneficial to rats to a great extent in attenuating and resulting in the damage sustained by chlorpyrifos exposure.
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M.P. Rajendran, B.B. Pallaiyan and N. Selvaraj, Avicenna J. Phytomed., 4, 200 (2014).
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U.K. Ganga, C. Hemalatha and B. Kishori, Int. J. Green Pharm., 12(Suppl. 1), S113 (2018).
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A.A. Hassan, K. Bel Hadj Salah, E.M. Fahmy, D.A. Mansour, S.A. Mohamed, A.A. Abdallah, M.F. Ashkan, K.A. Majrashi, S.J. Melebary, E.-S.A. El-Sheikh and N. El-Shaer, Life, 12, 1500 (2022); https://doi.org/10.3390/life12101500
P. Kaushik, P. Goyal, A. Chauhan and G. Chauhan, Iran. J. Pharm. Res., 9, 287 (2010).
B. Jacob, N. Rt, M.S.A.M. Nadar and P. Itsaranuwat, Chem. Data Coll., 39, 100874 (2022); https://doi.org/10.1016/j.cdc.2022.100874
A.J. Harborne, Phytochemical Methods A Guide To Modern Techniques of Plant Analysis, Springer Science & Business Media (1998).
H.X. Phong, N.T. Viet, N.T.N. Quyen, P. Van Thinh, N.M. Trung and T.T.K. Ngan, Mater. Today Proc., 56, A1 (2022); https://doi.org/10.1016/j.matpr.2021.12.142
B.N. Ames, J. McCann and E. Yamasaki, Mutat. Res., 31, 374 (1975); https://doi.org/10.1016/0165-1161(75)90046-1
OECD Guideline No.: 471 (Bacterial Reverse Mutation Test, Adopted: 21-July-1997, Corrected: 26 June 2020).
J.A. Turner, A World Compendium, The Pesticide Manual, British Crop Production Council, Omega Park, Alton, Hampshire United Kingdom; Edn. 18 (2018).
OECD Guideline for Testing of Chemicals and Acute Oral ToxicityAcute Toxic Class Method No. 423, Section 4: Health Effects (2001).
H. Lal, R. Dhupper, A. Chauhan, Y. Singh, R. Kant and M.L. Aggarwal, J. Pharm. Negat. Results, 13(Suppl. 8), 925 (2022); https://doi.org/10.47750/pnr.2022.13.S08.115
C.E. Igara, D.A. Omoboyowa, A.A. Ahuchaogu, N.U. Orji and M.K. Ndukwe, J. Pharmacogn. Phytochem., 5, 7 (2016).
D.T. Abeysinghe, K.A.H. Kumara, K.A.D. Kaushalya, U.G. Chandrika and D.D.D.H. Alwis, Heliyon, 7, e07449 (2021); https://doi.org/10.1016/j.heliyon.2021.e07449
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