Home Ficus cunia Buch.-Ham. ex Roxb. (leaves): An experimental evaluation of the cytotoxicity, thrombolytic, analgesic and neuropharmacological activities of its methanol extract
Article
Licensed
Unlicensed Requires Authentication

Ficus cunia Buch.-Ham. ex Roxb. (leaves): An experimental evaluation of the cytotoxicity, thrombolytic, analgesic and neuropharmacological activities of its methanol extract

  • Abul Hasanat , Mohammad Shah Hafez Kabir , Md. Alam Ansari , Tanvir Ahmad Chowdhury , Mohammed Munawar Hossain , Mohammad Nazmul Islam , Shabbir Ahmed , Md. Nazim Uddin Chy ORCID logo , Md. Adnan and A.T.M. Mostafa Kamal EMAIL logo
Published/Copyright: July 8, 2019

Abstract

Background

The aim of this experiment was to evaluate the cytotoxic, thrombolytic, analgesic, sedative-hypnotic and anxiolytic activities of the methanolic extract of Ficus cunia leaves.

Methods

Primary phytochemical screening was accomplished by using established methods. Cytotoxicity was studied by brine shrimp lethality test, and the thrombolytic assay was conducted through clot lysis method with human blood. The in vivo action was done using mice of both sexes. The analgesic activity was evaluated by acetic acid-induced writhing test and formalin-induced paw licking test. Open field, hole cross and thiopental Na-induced sleeping time test were used to examine the sedative-hypnotic activity, and elevated plus maze (EPM) and hole board test were used to identify the anxiolytic activity.

Results

The results elicited that the extract contained several phytochemicals such as alkaloid, flavonoid, and tannin. The extract was found to have a median lethal concentration (LC50) value of 55.48 μg/mL in the brine shrimp lethality bioassay. It was also assessed for antithrombotic activity when compared with streptokinase; it has significant (p < 0.001) thrombolytic effect (34.72 ± 1.74%) contrasted with standard streptokinase (67 ± 1.56%). The extract at doses of 200 and 400 mg/kg produced inhibition of 32.58% and 46.63% in acetic acid-induced pain and 45.88 and 61.18% in formalin-induced pain. The sedative and hypnotic activities on the central nervous system of the methanol extract of F. cunia (MEFC) leaves were evaluated. The extract delivered critical sedative impact at the doses of 200 and 400 mg/kg (by oral route) treated with reference to the substance diazepam, and the hypnotic impact was also observed in the case of mice. MEFC at its maximum dose (400 mg/kg) significantly (p < 0.01) increased the time spent in the open arms of the EPM. In the hole board test, there was a dose-dependent (at 200 and 400 mg/kg) and a significant (p < 0.05 and p < 0.01) increase in the number of head pokes in comparison to control.

Conclusions

The results of the present study gave a helpful baseline in progression for the possible use of MEFC as a cytotoxic, thrombolytic, analgesic, sedative-hypnotic and anxiolytic drug.

Acknowledgments

The authors are thankful to the Department of Pharmacy, International Islamic University Chittagong (IIUC) for providing the facilities to carry out the experiment. The authors are also thankful to all the members of GUSTO A research group (http://gustoarg.org) for their kind help in the experiment.

  1. Competing interests: The authors declare that they have no competing interests.

  2. Authors’ contributions: AH, MAA, MNI, and MA collected and prepared the plant extract. AH, MSHK, TAC, MMH, and SA conducted the whole experiments. MSHK conceived and designed the study, did the literature review, collected and interpreted the data, performed statistical analysis and also wrote the manuscript. MNUC did the literature study and assisted in the preparation of the original draft and revision of the final version of the manuscript. ATMMMK supervised the study design and manuscript preparation.

References

[1] Birru EM, Asrie AB, Adinew GM, Tsegaw A. Antidiarrheal activity of crude methanolic root extract of Idigofera spicata Forssk.(Fabaceae). BMC Complement Altern Med 2016;16:272.10.1186/s12906-016-1252-4Search in Google Scholar

[2] Hossain MF, Talukder B, Rana MN, Tasnim R, Nipun TS, Uddin SM, et al. In vivo sedative activity of methanolic extract of Stericulia villosa Roxb. leaves. BMC Complement Altern Med 2016;16:398.10.1186/s12906-016-1374-8Search in Google Scholar

[3] Wagstaff DJ. Genesis to genesis: a historic perspective of plant toxicology. In: Tam G, Catherine AB eds. Toxic Plants Other Nat Toxic. Wallingford, London: CABI (1st edition); 1998, p. 9–10.Search in Google Scholar

[4] Farnsworth NR, Akerele O, Bingel AS, Soejarto DD, Guo Z. Medicinal plants in therapy. Bull World Health Organ 1985;63:965.10.1016/0378-8741(87)90016-XSearch in Google Scholar

[5] Shajib M, Akter S, Ahmed T, Imam MZ. Antinociceptive and neuropharmacological activities of methanol extract of Phoenix sylvestris fruit pulp. Front Pharmacol 2015;6:212.10.3389/fphar.2015.00212Search in Google Scholar

[6] Kundal J, Singh SV PM. Extraction of natural dye from Ficus cunia and dyeing of polyester cotton and wool fabric using different mordants, with evaluation of colour fastness properties. Nat Prod Chem Res 2016;4:214.10.4172/2329-6836.1000214Search in Google Scholar

[7] Lansky EP, Paavilainen HM. Figs: the genus Ficus. Boca Raton, FL: CRC Press, 2010:415.10.1201/9781420089677Search in Google Scholar

[8] Sheikh Y, Maibam BC, Biswas D, Laisharm S, Deb L, Talukdar NC, et al. Anti-diabetic potential of selected ethno-medicinal plants of north east India. J Ethnopharmacol 2015;171:37–41.10.1016/j.jep.2015.05.030Search in Google Scholar

[9] Al-douri NA. A survey of medicinal plants and their traditional uses in Iraq. Pharm Biol 2000;38:74–9.10.1076/1388-0209(200001)3811-BFT074Search in Google Scholar

[10] Singh HB, Prasad P, Rai LK. Folk medicinal plants in the Sikkim Himalayas of India. Asian Folkl Stud 2002;295–310.10.2307/1178975Search in Google Scholar

[11] Ray S, Ahmed H, Basu S, Chatterjee BP. Purification, characterisation, and carbohydrate specificity of the lectin of Ficus cunia. Carbohydr Res 1993;242:247–63.10.1016/0008-6215(93)80038-GSearch in Google Scholar

[12] Adhya M, Singha B, Chatterjee BP. Ficus cunia agglutinin for recognition of bacteria. Indian J Biochem Biophys 2006;43:94–7.Search in Google Scholar

[13] Sofowora A. Medicinal plants and traditional medicine in Africa. Somerset, NJ: John Wiley & Sons, 1982:256.Search in Google Scholar

[14] Meyer BN, Ferrigni NR, Putnam JE, Jacobsen LB, Nichols DE, McLaughlin JL. Brine shrimp: a convenient general bioassay for active plant constituents. Planta Med 1982;45:31–4.10.1055/s-2007-971236Search in Google Scholar

[15] Prasad S, Kashyap RS, Deopujari JY, Purohit HJ, Taori GM, Daginawala HF. Development of an in vitro model to study clot lysis activity of thrombolytic drugs. Thromb J 2006;4:14.10.1186/1477-9560-4-14Search in Google Scholar

[16] Walum E. Acute oral toxicity. Environ Heal Perspect 1998;106:497–503.10.1289/ehp.98106497Search in Google Scholar

[17] Korster R, Anderson M, de Veer EJ. Acetic acid for analgesic screening. Fed Pro 1959;18:412.Search in Google Scholar

[18] Kabir MS, Hossain MM, Rahman MM, Hossain MS. Antidepressant, anxiolytic and anti-nociceptive activities of ethanol extract of Steudnera colocasiifolia K. Koch leaves in mice model. J Coast Life Med 2015;3:890–4.10.12980/jclm.3.2015j5-60Search in Google Scholar

[19] Okokon JE, Nwafor PA. Antiinflammatory, analgesic and antipyretic activities of ethanolic root extract of Croton zambesicus. Pak J Pharm Sci 2010;23:385–92.Search in Google Scholar

[20] Kulkarni SK, Reddy DS. Animal behavioral models for testing antianxiety agents. Methods Find Exp Clin Pharmacol 1996;18:219–30.Search in Google Scholar

[21] Takagi K, Watanabe M, Saito H. Studies of the spontaneous movement of animals by the hole cross test; effect of 2-dimethyl-aminoethanol and its acyl esters on the central nervous system. Jpn J Pharmacol 1971;21:797–810.10.1016/S0021-5198(19)36179-7Search in Google Scholar

[22] Ferrini R, Miragoli G, Taccardi B. Neuro-pharmacological studies on SB 5833, a new psychotherapeutic agent of the benzodiazepine class. Arzneimittelforschung 1974;24:2029.Search in Google Scholar

[23] Pellow S, File SE. Anxiolytic and anxiogenic drug effects on exploratory activity in an elevated plus-maze: a novel test of anxiety in the rat. Pharmacol Biochem Behav 1986;24:525–9.10.1016/0091-3057(86)90552-6Search in Google Scholar

[24] Sonavane GS, Sarveiya VP, Kasture VS, Kasture SB. Anxiogenic activity of Myristica fragrans seeds. Pharmacol Biochem Behav 2002;71:239–44.10.1016/S0091-3057(01)00660-8Search in Google Scholar

[25] Apu AS, Muhit MA, Tareq SM, Pathan AH, Jamaluddin AT, Ahmed M. Antimicrobial activity and brine shrimp lethality bioassay of the leaves extract of Dillenia indica Linn. J Young Pharm 2010;2:50–3.10.4103/0975-1483.62213Search in Google Scholar

[26] Roncal C, Martinez de Lizarrondo S, Salicio A, Chevilley A, Rodriguez JA, Rosell A, et al. New thrombolytic strategy providing neuroprotection in experimental ischemic stroke: MMP10 alone or in combination with tissue-type plasminogen activator. Cardiovasc Res. 2017;113(10):1219–29.10.1093/cvr/cvx069Search in Google Scholar

[27] Mukhametova LI, Aisina RB, Zakharyan EM, Karakhanov EA, Gershkovich KB, Varfolomeyev SD. Thrombolytic and fibrinogenolytic properties of bioconjugate streptokinase-polyamidoamine dendrimers in vitro. Thromb Res 2017;154:50–2.10.1016/j.thromres.2017.04.008Search in Google Scholar

[28] Ali MS, Amin MR, Kamal CM, Hossain MA. In vitro antioxidant, cytotoxic, thrombolytic activities and phytochemical evaluation of methanol extract of the A. philippense L. leaves. Asian Pac J Trop Biomed 2013;3:464–9.10.1016/S2221-1691(13)60097-0Search in Google Scholar

[29] Riaz M, Zia-Ul-Haq M, Saad B. Anthocyanins and human health: biomolecular and therapeutic aspects. SpringerBriefs Food, Heal Nutr. 2016;125–138. DOI: 10.1007/978-3-319-26456-1.Search in Google Scholar

[30] Raj PP. Pain medicine: a comprehensive review. Maryland Heights, MO: Mosby, 1996:571.Search in Google Scholar

[31] Ikeda Y, Ueno A, Naraba H, Oh-ishi S. Involvement of vanilloid receptor VR1 and prostanoids in the acid-induced writhing responses of mice. Life Sci 2001;69:2911–9.10.1016/S0024-3205(01)01374-1Search in Google Scholar

[32] Islam S, Shajib S, Ahmed T. Antinociceptive effect of methanol extract of Celosia cristata Linn. in mice. BMC Complement Altern Med 2016;16:400.10.1186/s12906-016-1393-5Search in Google Scholar

[33] Middleton E, Kandaswami C, Theoharides TC. The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease, and cancer. Pharmacol Rev 2000;52:673–751.Search in Google Scholar

[34] Havsteen BH. The biochemistry and medical significance of the flavonoids. Pharmacol Ther 2002;96:67–202.10.1016/S0163-7258(02)00298-XSearch in Google Scholar

[35] Aquila S, Giner RM, Recio MC, Spegazzini ED, Ríos JL. Anti-inflammatory activity of flavonoids from Cayaponia tayuya roots. J Ethnopharmacol 2009;121:333–7.10.1016/j.jep.2008.11.002Search in Google Scholar

[36] Dubuisson D, Dennis SG. The formalin test: a quantitative study of the analgesic effects of morphine, meperidine, and brain stem stimulation in rats and cats. Pain 1977;4:161–74.10.1016/0304-3959(77)90130-0Search in Google Scholar

[37] Hunskaar S, Berge O-G, Hole K. Dissociation between antinociceptive and anti-inflammatory effects of acetylsalicylic acid and indomethacin in the formalin test. Pain 1986;25:125–32.10.1016/0304-3959(86)90014-XSearch in Google Scholar

[38] Chen Y-F, Tsai H-Y, Wu T-S. Anti-inflammatory and analgesic activities from roots of Angelica pubescens. Planta Med 1995;61:2–8.10.1055/s-2006-957987Search in Google Scholar PubMed

[39] Verma PR, Joharapurkar AA, Chatpalliwar VA, Asnani AJ. Antinociceptive activity of alcoholic extract of Hemidesmus indicus R. Br. in mice. J Ethnopharmacol 2005;102:298–301.10.1016/j.jep.2005.05.039Search in Google Scholar PubMed

[40] Huang F, Xiong Y, Xu L, Ma S, Dou C. Sedative and hypnotic activities of the ethanol fraction from Fructus Schisandrae in mice and rats. J Ethnopharmacol 2007;110:471–5.10.1016/j.jep.2006.10.008Search in Google Scholar PubMed

[41] Herrera-Ruiz M, Gutiérrez C, Jiménez-Ferrer JE, Tortoriello J, Mirón G, León I. Central nervous system depressant activity of an ethyl acetate extract from Ipomoea stans roots. J Ethnopharmacol 2007;112:243–7.10.1016/j.jep.2007.03.004Search in Google Scholar

[42] File SE, Wardill AG. Validity of head-dipping as a measure of exploration in a modified hole-board. Psychopharmacology (Berl) 1975;44:53–9.10.1007/BF00421184Search in Google Scholar

[43] Roy-Byrne PP. The GABA-benzodiazepine receptor complex: structure, function, and role in anxiety. J Clin Psychiatry 2004;66:14–20.Search in Google Scholar

[44] Zhou, Yun Danbolt N. GABA and glutamate transporters in brain. Front Endocrinol (Lausanne) 2013;4:165.10.3389/fendo.2013.00165Search in Google Scholar

[45] Steinbach JH, Akk G. Modulation of GABAA receptor channel gating by pentobarbital. J Physiol 2001;537:715–33.10.1113/jphysiol.2001.012818Search in Google Scholar

[46] Sivam SP, Nabeshima T, Ho IK. Acute and chronic effects of pentobarbital in relation to postsynaptic GABA receptors: a study with muscimol. J Neurosci Res 1982;7:37–47.10.1002/jnr.490070105Search in Google Scholar

[47] Takeda H, Tsuji M, Matsumiya T. Changes in head-dipping behavior in the hole-board test reflect the anxiogenic and/or anxiolytic state in mice. Eur J Pharmacol 1998;350:21–9.10.1016/S0014-2999(98)00223-4Search in Google Scholar

Received: 2016-09-11
Accepted: 2019-04-02
Published Online: 2019-07-08

© 2019 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Minireview
  2. Glial pathology in neuropsychiatric disorders: a brief review
  3. Original Articles
  4. Fenugreek seed extract ameliorates cognitive deficits in streptozotocin-induced diabetic rats
  5. The effect of silymarin supplementation on cognitive impairment induced by diabetes in rats
  6. Evaluation of the antianxiety and antidepressant activities of mosapride in Wistar albino rats
  7. Sexual stimulant effects of the mixture of Mondia whitei, Dracaena arborea, and Bridelia ferruginea in normal and prediabetic male Wistar rats
  8. Evaluating exercise challenge to validate cardiac autonomic dysfunction in lean PCOS phenotype
  9. Involvement of proinflammatory cytokines and metallothionein in the repairing of arsenic-mediated uterine tissue damage by curcumin
  10. Antioxidant potentials and effects on the hematology and osmotic fragility scores of a polyherbal formulation used in Southeast Nigeria
  11. Protective mechanisms of protocatechuic acid against doxorubicin-induced nephrotoxicity in rat model
  12. Phytochemicals and antidiabetic activity of the aqueous extract of the Punica granatum fruit in streptozotocin-induced diabetic mice
  13. Ficus cunia Buch.-Ham. ex Roxb. (leaves): An experimental evaluation of the cytotoxicity, thrombolytic, analgesic and neuropharmacological activities of its methanol extract
  14. Ameliorative effects of Annona muricata Linn. (Annonaceae) against potassium dichromate-induced hypertension in vivo: involvement of Kim-1/p38 MAPK/Nrf2 signaling
  15. Case Report
  16. A rare case of clomiphene-induced leukocytoclastic vasculitis
Downloaded on 10.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jbcpp-2016-0140/html
Scroll to top button