American Journal of Food and Nutrition
ISSN (Print): 2374-1155 ISSN (Online): 2374-1163 Website: https://www.sciepub.com/journal/ajfn Editor-in-chief: Mihalis Panagiotidis
Open Access
Journal Browser
Go
American Journal of Food and Nutrition. 2015, 3(3), 64-68
DOI: 10.12691/ajfn-3-3-1
Open AccessArticle

Study of Antinociceptive Activity of Kaempferia galanga from Bangladesh in Swiss albino Mice

Pritesh Ranjan Dash1, Mahmuda Nasrin2, Mahmud Tareq Ibn Morshed1 and Mohammad Shawkat Ali1,

1Department of Pharmacy, BRAC University, Dhaka, Bangladesh

2Department of Pharmacy, Jahangirnagar University, Savar, Dhaka, Bangladesh

Pub. Date: May 05, 2015

Cite this paper:
Pritesh Ranjan Dash, Mahmuda Nasrin, Mahmud Tareq Ibn Morshed and Mohammad Shawkat Ali. Study of Antinociceptive Activity of Kaempferia galanga from Bangladesh in Swiss albino Mice. American Journal of Food and Nutrition. 2015; 3(3):64-68. doi: 10.12691/ajfn-3-3-1

Abstract

Kaempferia galanga (K. galanga) (Family: Zingiberaceae) has been used in the folk medicine for the treatment of inflammation, chest pain, cholera, headache, toothache, hypertension, and abdominal pain. Previous investigations on this plant suggested that the methanol extract of rhizome showed the analgesic activity. Therefore, the present study investigated the antinociceptive activity of different extracts of rhizome and leaves of K. galanga. The antinociceptive activity was evaluated by using acetic acid-induced writhing, hot plate and tail immersion tests in Swiss albino mice at the doses of 100 and 200 mg/kg body weight p.o. The acetone extract of rhizome (ACR), as well as petroether fraction (PEF), chloroform fraction (CHF), methanol fraction (MEF) and acetone extract of leaves (ACL) were examined for antinociceptive activity. In this study, all the extracts displayed significant (p<0.05 and p<0.001) antinociceptive action in a dose dependent manner. In acetic acid induced writhing method, chloroform and methanol extract of rhizome (200 mg/kg) showed 81.22% and 70.12% writhing inhibition, respectively whereas the standard drug Diclofenac-sodium (25 mg/kg) and Aspirin (100 mg/kg) exhibited 80.72% and 61.94% inhibition. In hot plate and tail immersion tests, the petroether extract of rhizome and acetone extract of leaves (200 mg/kg) produced maximum 69.41% and 81.69% nociception inhibition of thermal stimulus respectively. In this study Morphine (5 mg/kg) was used as standard. The present study revealed that the acetone extracts and fractions of rhizome and leaves of K. galanga possess an antinociceptive property which supports its use in traditional medicine and suggesting that the plant may be further investigated to discover its pharmacologically active natural products.

Keywords:
Kaempferia galanga Zingiberaceae writhing test hot plate test tail immersion test

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References:

[1]  Perry, M., and Metzger J., “Medical Plants of East and Southeast Asia. Attributed Properties and Uses”, Cambridge, MIT Press, p. 442, 1980.
 
[2]  Sirirugsa, P., “Thai Zingiberaceae: Species diversity and their uses”, Pure & Appl Chemistry, 70(11): 4-5, 1997.
 
[3]  Umar, M.I., Asmawi, M.Z.B., Sadikun, A., Altaf, R., an Iqbal M.A., “ Phytochemistry and medicinal properties of Kaempferia galanga L. (Zingiberaceae) extracts”, Afr. J. Pharm. Pharmacol, 5(14): 1638-1647, 2011.
 
[4]  Dash, P.R., Nasrin, M., Raihan, S.Z., and Ali, M.S., “Study of antidiarrhoeal activity of two medicinal plants of Bangladesh in castor-oil induced diarrhoea. Int J Pharm Sci Res, 5(9): 3864-3868, 2014.
 
[5]  Dash, P.R., Nasrin, M., and Ali, M.S., “In Vivo Cytotoxic and In Vitro Antibacterial activities of Kaempferia galanga”, Phyto Journal, 3 (1): 172-177, 2014.
 
[6]  Umar, M.I., Asmawi, M.Z., Sadikun, A., Atangwho, I.J., Yam, M.F., Altaf, R., and Ahmed, A., “Bioactivity-Guided Isolation of Ethyl-p-methoxycinnamate, an Anti-inflammatory Constituent, from Kaempferia galanga L. Extracts”, Molecules, 17: 8720-8734, 2012.
 
[7]  Ridtitid, W., Sae-wong, C., Reanmongkol, W., and Wongnawa, M., “Antinociceptive activity of the methanolic extract of Kaempferia galanga Linn. In experimental animals”,J Ethnoharmacol, 118(2): 225-230, 2008.
 
[8]  Ali, M.S., Nasrin, M., and Dash, P.R., “Evaluation of Analgesic and CNS Depressant Activities of Grewia Paniculata in Swiss albino Mice.” AJFN, 3( 1) : 21-27, 2015.
 
[9]  Walker, C.I., Trevisan, G., Rossato, M.F., Franciscato, C., Pereira, M.E., and Ferreira, J., “Antinociceptive activity of Mirabilis jalapa in mice”, J Ethnopharmacol, 120: 169-175, 2008.
 
[10]  Dash, P.R., Nasrin, M., and Saha, M.R, “Evaluation of Analgesic and Neuropharmacological Activities of Methanolic Rhizome Extract of Hedychium coronarium”, Int J Pharm Sci Res, 2(4): 979-984, 2011.
 
[11]  Eddy, N.B., and Leimbach, D., “Synthetic analgesics. II. Dithienylbutenyl- and dithienylbutylamines” J Pharmacol Exp Ther, 107: 385-393, 1953.
 
[12]  Toma, W., Gracioso, J.S., Hiruma-Lima, C.A., Andrade, F.D., Vilegas, W., and Souza Brito, A.R., “Evaluation of the analgesic and antiedematogenic activities of Quassia amara bark extract”, J Ethnopharmacol, 85: 19-23, 2003.
 
[13]  Deraedt, R., Jouquey, S., Delevallée, F., and Flahaut, M., “Release of prostaglandins E and F in an algogenic reaction and its inhibition”, Eur J Pharmacol, 61: 17-24, 1980.
 
[14]  Bentley, G.A., Newton, S.H., and Starr, J., “Studies on the antinociceptive action of alpha-agonist drugs and their interactions with opioid mechanisms”, Br J Pharmacol, 79: 125-134, 1983.
 
[15]  Adzu, B., Amos, S., Kapu, S.D., and Gamaniel, K.S., “Anti-inflammatory and anti-nociceptive effects of Sphaeranthus senegalensis”, J Ethnopharmacol , 84: 169-173, 2003.
 
[16]  Sánchez-Mateo, C.C., Bonkanka, C.X., Hernández-Pérez, M., and Rabanal, R.M., “Evaluation of the analgesic and topical anti-inflammatory effects of Hypericum reflexum L. fil”, J Ethnopharmacol, 107: 1-6, 2006.
 
[17]  Wong, C.H., Dey, P., Yarmush, J., Wu, W.H., and Zbuzek, V.K., “Nifedipineinduced analgesia after epidural injection in rats”, Anesth Analg, 79: 303-306, 1994.
 
[18]  Chapman, C.R., Casey, K.L., Dubner, R., Foley, K.M., Gracely, R.H., and Reading AE. “Pain measurement: An overview”,Pain 22: 1-31, 1985.
 
[19]  Srinivasan, K., Muruganandan, S., Lal, J., Chandra, S., Tandan, S.K., Raviprakash, V., and Kumar, D., “Antinociceptive and antipyretic activities of Pongamia pinnata leaves”, Phytother Res, 17: 259-264, 2003.
 
[20]  Yaksh, T.L., “Spinal systems and pain processing: development of novel analgesic drugs with mechanistically defined models” Trends Pharmacol Pharmacol Sci, 20: 329-337, 1999.