Evaluation of Anti-Diabetic and Anti-Allergic Activities of Brownlowia tersa (L.) Kosterm Leaves Extract and Determination of its Phenolic Compounds by HPLCDAD
doi.org/10.26538/tjnpr/v4i8.1
Keywords:
Anti-allergy, anti-diabetes, Atreptozotocin, Brownlowia tersaAbstract
Brownlowia tersa (L.), family Malvaceae, a shrub from Sundarbans (the largest Mangrove Forest of the World) has been traditionally used by the surrounding peoples for different ailments like inflammation, pain, diarrhea, allergy, etc. In this study, we investigated the antidiabetic and anti-allergic activities of ethanol leaves extract of this plant. Oral glucose tolerance test (OGTT) was used to screen the anti-hyperglycemic activity. Streptozotocin (STZ)-induced diabetic mice were used to investigate the anti-diabetic activity. Anti-allergic activity was checked by using Toluene 2,4-diisocyanate (TDI)-induced allergic mice model by assessing allergic symptoms and WBC counts. HPLC-DAD analysis was used to detect the selected phenolic compounds. In OGTT, the extract showed a significant anti-yperglycemic activity at 300 and 500 mg/kg doses in glucose loaded mice. In STZ-induced diabetic mice, the extract at both doses significantly reduced the blood and urine glucose levels. In addition, biochemical parameters such as serum glutamic-pyruvic transaminase (SGPT), serum glutamic-oxaloacetic transaminase (SGOT), creatinine, bilirubin, urea, and triglycerides levels were also decreased. The extract at 300 and 500 mg/kg doses also significantly reduced the TDI induced allergic symptoms like sneezing (P < 0.05), scratching (P < 0.05) and nasal score (P < 0.05) and blood WBC counts. HPLC analysis revealed the presence of ten phenolic compounds which might be responsible for the reported activities in this study.
References
Hossain H, Jahan IA, Howlader SI, Shilpi JA, Dey SK, Hira A. Anti-inflammatory and antioxidant activities of ethanolic leaf extract of Brownlowia tersa (L.) Kosterm. OPEM. 2013; 13(3):181-189.
Sariful I, Jamil A, Shubhra K, Arpona H, Ferdoushi J, Hemayet H. Antinociceptive and antidiarrhoeal properties of the ethanolic extract of Brownlowia tersa leaves. Int J Pharm Phytopharmacol Res. 2012; 1(5):292-296.
Shvedova A, Castranova V, Kisin E, Schwegler-Berry D, Murray A, Gandelsman V. Exposure to carbon nanotube material: assessment of nanotube cytotoxicity using human keratinocyte cells. J Toxcol Env Heal A. 2003; 66(20):1909-1926.
Giugliano D, Ceriello A, Esposito K. Glucose metabolism and hyperglycemia. Am J Clin Nutr. 2008; 87(1):217-222.
Gracza R. Prevention of Type II Diabetes in Honduras: El Cacao as a Case Study. Retrieved from the University of Minnesota Digital Conservancy. 2016; http://hdl.handle.net/11299/195438.
Szkudelski T. The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiol Res. 2001; 50(6):537-546.
Ban M, Morel G, Langonné I, Huguet N, Pépin E, Binet S. TDI can induce respiratory allergy with Th2-dominated response in mice. Toxicol. 2006; 218(1):39-47.
Bernstein IL. Isocyanate-induced pulmonary diseases: a current perspective. J Allerg Clin Immun. 1982; 70(1):24- 31.
Rietschel RL. Occupational contact dermatitis. The Lancet. 1997; 349(9058):1093-1105.
Slater JW, Zechnich AD, Haxby DG. Second-generation antihistamines. Drugs 1999; 57(1):31-47.
Mohan Y, Jesuthankaraj GN, Ramasamy Thangavelu N. Antidiabetic and antioxidant properties of Triticum aestivum in streptozotocin-induced diabetic rats. Adv Pharmacol Sci. 2013; 2013:7160-7173.
Fischer UA, Carle R, Kammerer DR. Identification and quantification of phenolic compounds from pomegranate (Punica granatum L.) peel, mesocarp, aril and differently produced juices by HPLC-DAD–ESI/MSn. Food Chem 2011; 127(2):807-821.
Singh A, Holvoet S, Mercenier A. Dietary polyphenols in the prevention and treatment of allergic diseases. Clin Exp Allerg. 2011; 41(10):1346-1359.
Sofowora A. Research on medicinal plants and traditional medicine in Africa: J Altern Compl Med. 1996; 2(3):365- 372.
Chuanphongpanich S and Phanichphant S. Method development and determination of phenolic compounds in broccoli seeds samples. Chiang Mai J Sci. 2006; 33(1):103- 107.
Islam MK, Mahmud I, Saha S, Sarker AB, Mondal H, ASM M. Preliminary pharmacological evaluation of Alocasia indica Schott tuber. JIM. 2013; 11:343-351.
Joy K and Kuttan R. Anti-diabetic activity of Picrorrhiza kurroa extract. J Ethnopharmacol. 1999; 67(2):143-148.
King AJ. The use of animal models in diabetes research. Br J Pharmacol. 2012;166(3):877-894.
Singh AK and Singh J. Evaluation of anti-diabetic potential of leaves and stem of Flacourtia jangomas in streptozotocininduced diabetic rats. Ind J Pharmacol. 2010; 42(5):301- 305.
Parasuraman S, Raveendran R, Kesavan R. Blood sample collection in small laboratory animals. J Pharmacol Pharmacother. 2010; 1(2):87-93.
Li ZP, Xin RJ, Yang H, Jiang GJ, Deng YP, Li DJ, Shen FM. Diazoxide accelerates wound healing by improving EPC function. Front Biosci. 2016; 21(5):1039-1051.
Dev S, Mizuguchi H, Das AK, Maeyama K, Horinaga S, Kato S, et al. Kujin Suppresses Histamine Signaling at the Transcriptional Level in Toluene 2, 4-Diisocyanate– Sensitized Rats. J Pharmacol Sci. 2009; 109(4):606-617.
Sardar PK, Dev S, Al Bari MA, Paul S, Yeasmin MS, Das AK. Antiallergic, anthelmintic and cytotoxic potentials of dried aerial parts of Acanthus ilicifolius L. Clin Phytosci. 2018; 4(1):34.
Tanaka KI, Okamoto Y, Nagaya Y, Nishimura F, Takeoka A, Hanada S. A nasal allergy model developed in the guinea pig by intranasal application of 2, 4-toluene diisocyanate. Int Arch Allerg Immun. 1988; 85(4):392-407.
Mahajan SG, Mali RG, Mehta AA. Effect of Moringa oleifera Lam. seed extract on toluene diisocyanate-induced immune-mediated inflammatory responses in rats. J Immunotoxicol. 2007; 4(2):85-96.
Abo K, Fred-Jaiyesimi A, Jaiyesimi A. Ethnobotanical studies of medicinal plants used in the management of diabetes mellitus in South Western Nigeria. J Ethnopharmacol. 2008; 115(1):67-71.
Dawid-Pać R. Medicinal plants used in treatment of inflammatory skin diseases. Advan. Dermatol Allergol. 2013; 30(3):170-177.
Juríková T, Mlček J, Sochor J, Hegedűsová A. Polyphenols and their mechanism of action in allergic immune response. Glob J Allerg. 2015; 1(2):037-039.
Wojdyło A, Nowicka P, Grimalt M, Legua P, Almansa MS, Amorós A. Polyphenol compounds and biological activity of caper (Capparis spinosa L.) flowers buds. Plants 2019; 8(12):539.
Mlcek J, Jurikova T, Skrovankova S, Sochor J. Quercetin and its anti-allergic immune response. Molecules 2016; 21(5):623.
Kumari M and Jain S. Tannins: An antinutrient with positive effect to manage diabetes. Res J Rec Sci. 2012; 1(12):11-18.
Gaikwad SB, Mohan KG, Rani SM. Phytochemicals for diabetes management. Pharm Crops. 2014; 5:11-28.
Bellik Y, Hammoudi SM, Abdellah F, Iguer-Ouada M, Boukraâ L. Phytochemicals to prevent inflammation and allergy. Rec. Patent Inflam. Allerg Drug Discov. 2012; 6(2):147-158.
Zimmet P and Alberti G. The metabolic syndrome: perhaps an etiologic mystery but far from a myth where does the International Diabetes Federation stand. Diabet Endocrinol. 2006; 23(5):469-480.
Sreedhar B, Reddy PS, Krishna CV, Babu PV. An efficient synthesis of propargylamines using a silica gel anchored copper chloride catalyst in an aqueous medium. Tetrahedron Lett. 2007; 48(44):7882-7886.
Chen SCC, Tsai SP, Jhao JY, Jiang WK, Tsao CK, Chang LY. Liver fat, hepatic enzymes, alkaline phosphatase and the risk of incident type 2 diabetes: a prospective study of 132,377 adults. Sci Rep. 2017; 7(1):1-9.
Srinivasan K and Ramarao P. Animal model in type 2 diabetes research: An overview. Ind J Med Res. 2007; 125(3):451-472.
Ong KC and Khoo HE. Biological effects of myricetin. Vasc Pharmacol. 1997; 29(2):121-126.
Jadhav R and Puchchakayala G. Hypoglycemic and antidiabetic activity of flavonoids: boswellic acid, ellagic acid, quercetin, rutin on streptozotocin-nicotinamide induced type 2 diabetic rats. Int J Pharm Pharm Sci. 2012; 4(2):251-256.
Nauta AJ, Engels F, Knippels LM, Garssen J, Nijkamp FP, Redegeld FA. Mechanisms of allergy and asthma. Eur J Pharmacol. 2008; 585(2-3):354-360.
White MV. The role of histamine in allergic diseases. J Allerg Clin Immun. 1990; 86(4):599-605.
Kawai M, Hirano T, Higa S, Arimitsu J, Maruta M, Kuwahara Y, et al. Flavonoids and related compounds as anti-allergic substances. Allergol Int. 2007; 56(2):113-123.
Schleimer RP, Liechtenstein LM, Gillespie E. Inhibition of basophil histamine release by anti-inflammatory steroids. Nature 1981; 292(5822):454-455.
Horn BR, Robin ED, Theodore J, Van Kessel A. Total eosinophil counts in the management of bronchial asthma. N Engl J Med. 1975; 292(22):1152-1155.
Medeiros KC, Figueiredo CA, Figueredo TB, Freire KR, Santos FA, Alcântara-Neves NM, Silva TM, Piclvezam MR. Anti-allergic effect of bee pollen phenolic extract and myricetin in ovalbumin-sensitized mice. J Ethnopharmacol. 2008; 119(1):41-46.
Jeong HJ, Nam SY, Kim HY, Jin MH, Kim MH, Roh SS, Kim HM. Anti-allergic inflammatory effect of vanillic acid through regulating thymic stromal lymphopoietin secretion from activated mast cells. Nat Prod Res. 2018; 32(24):2945-2949.
Published
How to Cite
Issue
Section
License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.