EVALUATION OF THE ANTIDEPRESSANT EFFECTS OF ALCOHOLIC EXTRACTS OF PILEA MICROPHYLLA IN MICE

Authors

  • DARAH IBRAHIM Industrial Biotechnology Research Laboratory, School of Biological sciences, Universiti Sains Malaysia, 11800 Minden, Penang, Malaysia
  • AMIR MODARRESI CHAHARDEHI Industrial Biotechnology Research Laboratory, School of Biological sciences, Universiti Sains Malaysia, 11800 Minden, Penang, Malaysia
  • FARID ABOLHASSANI Department of Anatomy, Medical School, Tehran University of Medical Sciences, Iran

DOI:

https://doi.org/10.11113/jt.v57.1537

Keywords:

Pilea microphylla, antidepressant activity, forced swimming test (FST), tail suspension test (TST)

Abstract

To date, the search for novel pharmacotherapy from medicinal plants for psychiatric illnesses has significantly progressed. This study investigated the effect of selected crude extracts from Pilea microphylla in the mouse forced test (FST) and in the tail suspension test (TST), two models predictive of antidepressant activity. Selected crude extracts from Pilea microphylla produced an antidepressant–like effect, since the acute treatment of mice with extracts by intraperitoneal (i.p.) route significantly reduced the immobility time in the FST (50 and 100 mg/kg) and TST (50 and 100 mg/kg), as compared to positive controls (haloperidol and fluoxetine) at 1 and 10 mg/kg, respectively. The antidepressant–like effect of extracts was found to be significant at high doses, followed by an increase in the immobility time at dose of 100 mg/kg. A significant decreased of immobility was also found on the third day at the concentration of 100 mg/kg of chloroform extract of Pilea microphylla from extraction method II (CEPM II) and ethyl acetate extract of Pilea microphyllafrom extraction method II (EAEPM II); (except methanol extract ofPilea microphylla from extraction method I (MEPM I) at 100 mg/kg) with respect to the first day. Ethyl acetate and chloroform extract from extraction method II when administered at an acute dose of 100 mg/kg of body weight (P < 0.05) reduced the immobility time. Among all the three selected extracts with two doses administered there were differences compared to the control, EAEPM II led to reduction of immobility time, in the FST method by 38.50% for 50 mg/kg to as much as 75.97% for 100 mg/kg. Similar results of increased antidepressant effect, that was, of immobility time depending on the concentration administered, were obtained with the TST method. These results suggested the anti–depression activity of the plant extract. Therefore, P. microphylla may be served as a potential resource for natural psychotherapeutic agent against depression. However, further studies are still required.

References

B. Lerer, and F. Macciardi. 2002. Pharmacogenetics of Antidepressant and Moodstabilizing Drugs: A Review of Candidate-Gene Studies and Future Research Directions. International Journal of Neuropsychopharmacology. 5: 255-275.

G. Bondolfi, C. B. Eap, G. Bertschy, D. Zullino, A. Vermeulen, and P. Baumann. 2002. The Effect of Fluoxetine on the Pharmacokinetics and Safety of Riseperidone in Psychiatric Patients. Pharmacopsychiatry. 35: 50- 56.

L. T. Yi, J. M. Li, Y. C. Li, Y. Pan, Qun. Xu, and L. D. Kong. 2008. Antidepressant-like Behav- Ioral and Neurochemical Effects of the Citrus-Associated Chemical Apigenin. Life Sci. 82: 741-751.

Q. Xu, L. T. Yi, Y. Pan, X. Wang, Y. C. Li, J. M. Li, C. P. Wang, and L. D. Kong. 2008. Antidepressant-like Effects of mixture of Honokio Land Magnolol from the Barks of Magnolia Officinalis In Stressedrodents. Prog. Neuropsychopharmacol. Biol. Psychiatry. 32: 715 -725.

N. Farah Idayu, M. Taufik Hidayat, M. A. M. Moklas, F. Sharida, A. R. Nurul Raudzah, A. R. Shamima, and E. Apryani. 2010. Antidepressant-Like Effect of Mitragynine Isolated from Mitragyna Speciosa Korth in Mice Model of Depression. Phytomedicine. IN PRESS,

Z. Zhang. 2004. Therapeutic Effects of Herbal Extracts and Constituents in Animal Models of Psychiatric Disorders. Life Sci. 75: 1659-99.

S. Kwon, B. Lee, M. Kim, H. Lee, H. J. Park, and D. H. Hahm. 2010. Antidepressant-like Effect of the Methanolic Extract from Bupleurum falcatum in the Tail Suspension Test. Psychiatry. 34: 265-270.

R. D. Porsolt, A. Bertin, and M. Jalfre. 1977. Behavioral Despair in Mice: A Primary Screening Test for Antidepressants. Archives Internationales de Pharmacodynamie et de Therapie. 229: 327-336.

L. Steru, R. Chemat, B. Thierry, and P. Simon. 1985. The Tail Suspension Test: A New Method for Screening Antidepressants in Mice. Psychopharmacology. 85: 367-370.

D. G. Machado, L. E. B. Bettio, M. P. Cunha, J. C. Capra, J. B. Dalmarco, M. G. Pizzolai, and A. L. S. Rodrigues. 2009. Antidepressant-like Effect of the Extract of Rosmarinus Officinalis in Mice: Involvement of the Monoaminergic System. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 33: 642-650.

A. Modarresi Chahardehi, D. Ibrahim, and S. F. Sulaiman. 2009. Antioxidant activity and total phenolic content of some medicinal plants in Urticaceae family. Journal of Applied Biological Sciences. 2(3): 01-05.

A. Modarresi Chahardehi, D. Ibrahim, and S. F. Sulaiman. 2009. Antioxidant, antimicrobial activity and toxicity test of Pilea microphylla. International Journal of Microbiology. doi:10.1155/2010/826830.

A. S. Mellidis, V. P. Papageorgiou. 1993. Phenolic constituents from Onosma heterophylla. J. Nat. Prod. 56(6): 949-952.

A. L. Eckeli, F. Dach, and A. L. S. Rodrigues. 2000. Acute Treatment with GMP Produces Antidepressant-Like Effects in Mice. Neuro Rep. 11: 1839-1843.

A. D. E. Zomkowsi, A. O. Rosa, J. Lin, A. R. S. Santos, J. B. Calixto, and A. L. S. Rodrigues. 2004. Evidence for Serotonin Receptor Subtypes Involvement in Agmatine Antide- Pressant Like-Effect in the Mouse Forced Swimming Test. Brain Res. 1023: 256- 263.

M. P. Kaster, I. Raupp, R. W. Binfaré, R. Andreatini, S. A. C. Rodrigues. 2007. Antidepressant-like Effect of Lamotrigine in the Mouse Forced Swimming Test: Evidence for the Involvement of Noradrenergic System. Euro. J. Pharmacol. 565: 119- 124.

T. Deak, C. Bellamy, G. L. D`Agostino, M. Rosanoff, N. K. McElderry, and K. A. Bordner. 2005. Behavioral Responses During the Forced Swim Test are Not Affected by Anti-Inflammatory Agents or Acute Illness Induced by Lipopolysaccharide. Behavioural Brain Research.160: 125-134.

J. F. Cryan, C. Mombereau, and A. Vassout. 2005. The Tail Suspension Test As A Model To Assessing Antidepressant Activity: Review of Pharmacological and Genetic Studies in Mice. Neurosci. Biobehav. Rev. 29: 571-625.

B. Karolewicz, and I. A. Paul. 2001. Group Housing of Mice Increases Immobility and Antidepressant Sensitivity in the Forced Swim and Tail Suspension Tests. European Journal of Pharmacology. 415: 197-201.

J. B. Harborne. 1998. Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis. Third Edition. Chapman and Hall, UK. 292 – 293.

J. Avalos, and H. I. Maibach. 2000. Dermatologic Botany. Library of Congress Cataloging-in- Publication Data. CRC Press LLC,

V. K. Sharma, N. S. Chauhan, S. Lodhi, and A. K. Singhai. 2009. Anti-depressant Activity of Zizyphus xylopyrus. International Journal of Phytomedicine. 1: 12-17.

A. Paulke, M. Schubert-Zsilavecz, and M. Wurglics. 2006. Determination of St. John's Wort Flavonoid-Metabolites in Rat Brain Through High Performance Liquid Chromatography Coupled with Fluorescence Detection. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 832: 109-113.

P. Willner. 1984. The Validity of Animal Models of Depression. Psychopharmacology. 83: 1-16.

L. Bach-Rojecky, Z. Kalodera, and I. Samaržija. 2004. The Antidepressant Activity of Hypericum Perforatum L. Measured by Two Experimental Methods on Mice. Acta Pharm. 54: 157-162.

M. D. Shalam, S. M. Shantakumar, and M. L. 2007. Narasu. Pharmacological And Biochemical Evidence for the Antidepressant Effect of the Herbal Preparation Trans-01. Indian J. Pharmacol. 39: 231-234.

J. F. Cryan, A. Markou, and I. Lucki. 2002. Assessing Antidepressant Activity in Rodents: Recent Developments and Future Needs. Trends Pharmacol Sci. 23: 238-245.

B. Eisensamer, G. Rammes, G. Gimpl, M. Shapa, U. Ferrari, and G. Hapfelmeier. 2003. Antidepressants are Functional Antagonists at the Serotonin Type 3 (5-HT3) Receptor. Mol. Psychiatry. 12: 994-1007.

P. C. Shah, N. A. Trivedi, J. D. Bhatt and K. G. Hemavathi. 2006. Effect of Withania somniferona Forced Swimming Test Induced Immobility in Mice and its Interaction with Various Drugs. Indian J. Pharmacol. 50(4): 409-415.

A. Carlsson, and M. Lindqvist. 1963. Effect of Chlorpromazine or Haloperidol on Formation of 3-Mehoxytyramine and Normetanephrine in Mouse Brain. Acta Pharmacol et toxicol. 20: 140-144.

W. F. Pirl, and A. J. Roth. 1999. Diagnosis and Treatment of Depression in Cancer Patients. In: Licino, J. and Wang, M. L., Biology of Depression, From Novel Insights to Therapeutic Strategies. 1: 378.

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Published

2012-02-15

How to Cite

EVALUATION OF THE ANTIDEPRESSANT EFFECTS OF ALCOHOLIC EXTRACTS OF PILEA MICROPHYLLA IN MICE. (2012). Jurnal Teknologi (Sciences & Engineering), 57(1). https://doi.org/10.11113/jt.v57.1537