ETHANOLIC EXTRACTS OF HEDYOTIS CORYMBOSA L. IMPROVES MONOSODIUM IODOACETATE-INDUCE OSTEOARTHRITIS IN RAT

Authors

  • Anton Bahtiar Universitas Indonesia
  • Fitri Arum Sari
  • Mega Audina
  • Natasha Linsie Corona Datunsolang
  • Ade Arsianti

DOI:

https://doi.org/10.22159/ajpcr.2017.v10i3.16558

Abstract

ABSTRACT
Objective: The objective of this study is to explore the effects of the 70% ethanolic extract of pearl grass on the immune system of the osteoarthritis
model rat, characterized by the number of leukocytes and lymphocytes, and the histology of the joint. Osteoarthritis is a degenerative disease
characterized by chronic inflammation in the joints. Based on the daily practice of herbal medicine in some community in Indonesia, pearl grass
usually used for anti-inflammation but not a lot of data to support it.
Methods: We used 36 male rats Sprague-Dawley strain divided into 6 groups. Normal group was given 0.5% of CMC, the negative control group was given
0.025 ml of sodium iodoacetate in 0.9% saline, the positive groups control group was given a suspension of glucosamine-chondroitin 135 mg/200 g bb,
three were given pearls grass extract in various dose 5.625 mg, 11.25 mg, and 22.5 mg, respectively. 28 days after sodium iodoacetate induction, the extracts
were given orally once daily for 21 days. Measurement of inflammation of knee joint and the number of leukocytes and lymphocytes were counted on day
14th, 28th, and 49th after sodium iodoacetate induction. After treatment, all rats were sacrified and all knee joints were collected to subject for histology.
Results: The results showed that the extract of pearl grass in all doses was able to decrease the number of leukocytes and lymphocytes significantly
and prevent proteoglycan degradation. The results showed that the extract of pearl grass with a given dose variations have antiinflammation effect
and been able to protect proteoglycan significantly.
Conclusion: Doses 3 (22.5 mg/200 g BW) is the best result. These results indicate that pearl grass can be further investigated as a treatment for osteoarthritis.
Keyword: Osteoarthritis, Sodium iodoacetate, Pearl grass, Hedyotis corymbosa L. Lamk., Immune system.

 

Downloads

Download data is not yet available.

References

REFERENCES

Haq I, Murphy E, Dacre J. Osteoarthritis. Postgrad Med J 2003;79(933):377-83.

Lad H, Dixit D, Joshi A, Bhatnagar D. Antioxidant and antiinflammatory effects of vitex negundo on freund’s complete adjuvant induced arthritis. Int J Pharm Sci 2015;7(1):81-5.

Paul S, Das A, Bhattacharjee S. Rheumatoid arthritis: Molecular basis and cures from nature. Int J Pharm Sci 2015;7(7):30-9.

Hochberg MC, Dougados M. Pharmacological therapy of osteoarthritis. Best Pract Res Clin Rheumatol 2001;15(4):583-93.

Matheu V, Gracia Bara MT, Pelta R, Vivas E, Rubio M. Immediate-hypersensitivity reaction to glucosamine sulfate. Allergy 1999;54(6):643.

Tallia AF, Cardone DA. Asthma exacerbation associated with glucosamine-chondroitin supplement. J Am Board Fam Pract 2002;15(6):481-4.

Danao-Camara T. Potential side effects of treatment with glucosamine and chondroitin. Arthritis Rheum 2000;43(12):2853.

Huskisson EC. Glucosamine and chondroitin for osteoarthritis. J Int Med Res 2008;36(6):1161-79.

Lu CM, Yang JJ, Wang PY, Lin CC. A new acylated flavonol glycoside and antioxidant effects of Hedyotis diffusa. Planta Med 2000;66(4):374-7.

Janusz MJ, Hookfin EB, Heitmeyer SA, Woessner JF, Freemont AJ, Hoyland JA, Brown KK, Hsieh LC, Almstead NG, De B, Natchus MG, Pikul S, Taiwo YO. Moderation of iodoacetate-induced experimental osteoarthritis in rats by matrix metalloproteinase inhibitors. Osteoarthritis Cartilage 2001;9(8):751-60.

Hoff J. Method of blood collection in the mouse. J Lab Anim 2000;29(10):47-53.

Pritzker MD, Gay MD, Jimenez SA. Osteoartritis cartilage histopathology: Grading and staging. J Osteoartritis Res Soc Int 2006;14(1)721-32.

Sathishkumar T, Baskar R, Shanmugam S, Rajasekaran P, Sadasivan S, Manikandan V. Optimization of flavonoids extraction from the leaves of Tabernaemontana heyneana Wall using L16 orthogonal design. Nat Sci 2008;6(3):10-21.

Bove SE, Calcaterra SL, Brooker RM, Huber CM, Guzman RE, Juneau PL, et al. Weight bearing as a measure of disease progression and efficacy of anti-inflammatory compounds in a model of monosodium iodoacetate-induced osteoarthritis. Osteoarthritis Cartilage 2003;11(11):821-30.

Woode E. Anti-arthritic and antioxidant properties of the ethanolic stem bark extract of Newbouldia laevis (P. Beauv.) Seaman ex Bereau (Bignoniaceae). J Med Plant Res 2008;2(8):180-8.

Kelly GS. The role of glucosamine sulfate and chondroitin sulfates in the treatment of degenerative joint disease. Altern Med Rev 1998;3(1):27-39.

Sherman AL, Ojeda-Correal G, Mena J. Use of glucosamine and chondroitin in persons with osteoarthritis. PM R 2012;4 5 Suppl: S110-6.

Mishra K, Dash AP, Swain BK, Dey N. Anti-malarial activities of Andrographis paniculata and Hedyotis corymbosa extracts and their combination with curcumin. Malar J 2009;8(26):26.

Published

01-03-2017

How to Cite

Bahtiar, A., F. A. Sari, Mega Audina, N. L. C. Datunsolang, and A. Arsianti. “ETHANOLIC EXTRACTS OF HEDYOTIS CORYMBOSA L. IMPROVES MONOSODIUM IODOACETATE-INDUCE OSTEOARTHRITIS IN RAT”. Asian Journal of Pharmaceutical and Clinical Research, vol. 10, no. 3, Mar. 2017, pp. 473-6, doi:10.22159/ajpcr.2017.v10i3.16558.

Issue

Section

Original Article(s)

Most read articles by the same author(s)

1 2 > >>