Characterisation and Anti-diabetic Activity of Phenylquinoline, and Narceine Isolated from Ficus polita Leaf
Annual Research & Review in Biology,
Page 102-114
DOI:
10.9734/arrb/2020/v35i730251
Abstract
The present study was conducted to evaluate anti-diabetic potentials of column chromatography fractions (F1-F6) of chloroform leaf extract of Ficus polita and to detect the probable bioactive compounds present in the most active fraction using spectroscopic techniques. Antidiabetic potential of the fractions (F1-F6) were tested at a dose of 50 mg/kg on wistar rats. Fraction 3 and metformin treated diabetic groups showed significant decreases in fasting blood glucose (FBS) level, ameliorate hepatic and renal damages by decreasing the levels of serum total bilirubin, direct bilirubin AST, ALT, creatinine, urea, potassium and chloride, but increasing the levels of serum total protein, albumin, sodium, and bicarbonate compared to untreated diabetic rats. Fraction 3 also stimulates insulin secretion by β cells. After alloxan administration, the levels of hepatic and renal tissues antioxidant markers such as GSH, SOD and catalase were decreased whereas the level of hepatic and renal tissues MDA was elevated. The levels of these antioxidant markers were brought to normalcy by fraction 3 (F3). Histological studies of the pancreas supported the biochemical findings, and treatment with fraction 3 (F3) was found to be effective in restoring alloxan-induced pancreatic toxicity in rats. FTIR and GCMS and analyses were conducted for the detection of bioactive compound(s) in fraction 3 (F3) and the result revealed the presence of "8-methoxy-4-phenylquinoline and narceine The study concludes that; the anti-diabetic property of the leaf of Ficus polita is mediated by the bioactive compounds " 8-methoxy-4-phenylquinoline, and narceine." through their antioxidant properties and stimulation of damaged pancreas to produce more insulin.
Keywords:
- Anti-diabetic activity
- column chromatography
- characterisation
- isolation
- Ficus polita.
How to Cite
References
Ghazanfar K, Ganai BA, Akbar S, Mubashir K, Dar SA, Dar MY, Tantry MA. Antidiabetic activity of Artemisia amygdalina Decne in streptozotocin induced diabetic rats. BioMed research international; 2014. Ghazanfar K, Ganai BA, Akbar S, Mubashir K, Dar SA, Dar MY, Tantry MA. Antidiabetic activity of Artemisia amygdalina Decne in streptozotocin induced diabetic rats. BioMed Research International; 2014.
Nostro A, Germano MP, D'Angelo V, Marino A, Cannatelli MA. Extraction methods and bioautography for evaluation of medicinal plant antimicrobial activity. Letters in Appl. Microbiol. 2000;30:37-384.
Ajayi FT, Omotoso SO, Odejide JO. Evaluation of fodder plants (Ficus polita, Azadirachta indica and Vernonia amygdalina) for their phytochemical and antibacterial properties, Cogent Food & Agriculture. 2016;2:1211466.
Egharevba HO, Ibrahim JA, Okhale SE, Wudil MI, Kunle OF. Phytochemistry, Pharmacognostic and HPLC profiling of methanolic extract of fruits of Ficus polita Vahl. International Journal of Basic and Applied Sciences. 2015;4(4):225-228.
Deepa P, Sowndhararajan K, Kim S, Park SJ. A role of Ficus species in the management of diabetes mellitus: A review. Journal of Ethnopharmacology. 2018;215:210-232.
Alhassan AJ, Muhammad IU, Sule MS, Wudil AM, Imam AA, Idi A, Muhammad A, Mohammed A, Alexander I, Nasir AA. Characterization and anti-diabetic activity of dihydrophenantherene isolated from Khaya senegalensis stem bark. Annual Research & Review in Biology. 2017;17(2):1-17.
Muhammad IU, Alhassan AJ, Sule MS, Idi A, Mohammed A, El- Ta’alu AB, Dangambo MA, Abdulmumin Y. Anti-hyperglycemic activity of solvents extract of Khaya senegalensis stem bark in alloxan induced diabetic rats. Journal of Advances in Biology and Biotechnology. 2016;6(2):1-8.
Yakubu MT, Ogunro OB. Effects of aqueous extract of Fadogia agrestis stem in alloxan induced diabetic rats. Bangladesh J Pharmacol. 2014;9:356-363.
Ananda PK, Kumarappan CT, Sunil C, Kalaichelvan VK. Effect of Biophytum sensitivum on streptozotocin and nicotinamide induced diabetic rats. Asian Pac J Tropical Biomed. 2012;11: 31-35.
Tierney LM, Mcphee SJ, Papadakis MA. Current medical diagnosis and treatment, international edition. In New York: Lange Medical Books? McGraw-Hill: New York, NY, USA. 2002;1203–1215.
Prakasam A, Sethupathy S, Pugalendi KV. Influence of Caseariaesculenta root extract on protein metabolism and marker enzymes in streptozotocin-induced diabetic rats. Pol. Journal of Pharmacology. 2004;56:587-593.
Okoduwa SIR, Umar IA, James DB, Inuwa HM. Anti-diabetic potential of Ocimum gratissimum leaf fractions in fortified diet-fed streptozotocin treated rat model of type-2 diabetes. Medicines. 2017;4(73):1-21.
Esterbauer H. Estimation of peroxidative damage: A critical review. Pathology Biology Paris. 1996;44:25–28.
Available:http://www.ncbi.nlm.nih.gov/pubmed/8734296
PMID: 8734296
Elekofehinti OO, Kamdem JP, Kade IJ, Rocha JBT, Adanlawo IG. Hypoglycemic, antiperoxidative and antihyperlipidemic effects of saponins from Solanum anguivi Lam. fruits in alloxan-induced diabetic rats. South African Journal of Botany. 2013;88:56–61.
Edziri H, Ammar S, Souad L, Mahjoub MA, Mastori M, Aouni M, Mighri Z, Verschaeve L. In vitro evaluation of antimicrobial and antioxidant activities of some Tunisian vegetables. South African Journal of Botany. 2012;78:252–256.
Sharma N, Garg V. Antidiabetic and antioxidant potential of ethanolic extract of Butea monosperma leaves in alloxan-induced diabetic mice. Indian Journal of Biochemistry and Biophysics. 2009;46:99–105.
Liu LZ, Zhao HL, Zuo J, Ho SK, Chan JC, Meng Y. Protein kinase C mediates insulin - induced glucose transport through actin remodeling in L6 muscle cells. Mol Biol Cell. 2006;17:2322–2330.
Holt LJ, Siddle K. Grb10 and Grb14: Enigmatic regulators of insulin action – and more. Biochem J. 2005;388:393–406.
Pavia DL, Lampman GM, Kriz GS, Vyvyan JR. Introduction to spectroscopy. Fourth Edition, Brooks/Cole, Belmont CA, USA. 2009;16(43):63,473,675.
[ISBN 10:0-495-11476-2]
Adams M, Wube AA, Bucar F, Bauer R, Kunert O, Haslinger E. Quinolone alkaloids from Evodia rutaecarpa: A potent new group of antimycobacterial compounds. Int J Antimicrob Agents. 2005;26:262–264.
Nam KW, Je KH, Shin YJ, Kang SS, Mar W. Inhibitory effects of furoquinoline alkaloids from Melicope confusa and Dictamnus albus against human phosphodiesterase 5 (hPDE5A) in vitro. Arch Pharm Res. 2005;28:675–679.
Lee HS, Oh WK, Choi HC. Inhibition of angiotensin II receptor binding by quinolone alkaloids from Evodia rutaecarpa. Phytother Res. 1998;12:212–214282.
Loya S, Rudi A, Tal R, Kashman Y, Loya Y, Hizi A. 3,5,8-Trihydroxy-4-quinolone, a novel natural inhibitor of the reverse transcriptases of human immunodeficiency viruses type 1 and type 2. Arch Biochem Biophys. 1994;309:315–322.
Ohtsu Y, Sasamura H, Shibata T, Nakajima H, Hino M, Fujii T. The novel gluconeogenesis inhibitors FR225659 and related compounds that originate from Helicomyces sp. No. 19353. II. Biological profiles. J Antibiot. 2003;56: 689–693.
Zenkoh T, Hatori H, Tanaka H. Design and synthesis of a solid-supported FR225659 derivative for its receptor screening. Org Lett. 2004;6:2477–248.
-
Abstract View: 450 times
PDF Download: 244 times