Systemic administration of fractions from Nyctanthes arbor‑tristis attenuates chronic inflammatory response in Freund’s‑complete‑adjuvant‑induced arthritis in rats

Authors

  • Swapnil Goyal
  • Navin R. Sheth
  • D. N. Srivastava

DOI:

https://doi.org/10.22377/ijgp.v8i3.376

Abstract

Object: The present study was aimed to assess the anti‑arthritic activity of chloroform and n‑butanolic fraction of Nyctanthes
arbor‑tristis leaf extract against Freund’s‑complete‑adjuvant (FCA)‑induced arthritis in rats. Material and Method: Ethanolic extract of Nyctanthes arbor‑tristis leaves were fractionated in various organic solvents and on the basis of results of anti‑inflammatory activity, chloroform and n‑butanolic fractions were selected for anti‑arthritic activity. The active chloroform and n‑butanolic fraction were administered at the dose of 50 and 75 mg/kg body weight. The effects of both fractions on liver alkaline phosphatase (ALP),acid phosphatase (ACP) and lactate dehydrogenase (LDH) levels and malonaldehyde (MDA), glutathione (GSH) and superoxide dismutase (SOD) from articular cartilages in arthritic animals were studied. Prednisolone (10 mg/kg) was used as standard.

Results: In FCA‑induced arthritis, the chloroform and n‑butanolic fraction showed a highly significant reduction in paw volume
(75 mg/kg–76.49%; 70.94%). The levels of various membrane marker enzymes and oxidative free radicals were significantly decreased in the both fraction treated groups and GSH and SOD activities were significantly increased compared with the arthritic control. The chloroform fraction showed most prominent activity as compared to n‑butanolic fraction. Conclusion: The possible mechanism of action of the chloroform fraction of Nyctanthes arbor‑tristis leaf extract may be due to either stabilizing action of membrane marker enzymes or inhibition of oxidative free radicals and thereby preventing the spread of inflammation. Future studies will provide new insights into the anti‑arthritic activity of Nyctanthes arbor‑tristis and isolation of compound and its possible mechanism of action.
Key words: Arthritis, chloroform and n‑butanolic fraction, Nyctanthes arbor‑tristis, membrane marker enzymes, oxidative free radicals

Downloads

Download data is not yet available.

References

Lefkowitz DL, Gelderman MP, Fuhrmann SR, Graham S,

Starnes JD 3rd, Lefkowitz SS, et al. Neutrophil lysozyme macrophage

interactions perpetuate chronic inflammation associated with

experimental arthritis. Clin Immunol 1999;91:145‑55.

Pagella PG, Bellavite O, Agozzino S, Donà GC, Cremonesi P,

De Santis F. Pharmacological studies of imidazole-2-

hydroxybenzoate ITF 182, an anti‑ inflammatory compound with

an action on thromboxane A2 production. Arzneimittelforschung

;5:716‑26.

Yang GM, Wang D, Tang W, Chen X, Fan LQ, Zhang FF, et al.

Anti‑inflammatory and antioxidant activities of Oxytropis falcata

fractions and its possible anti inflammatory mechanism. Chin J

Nat Med 2010;4:285‑92.

Nadkarni AK. Nadkarni’s Indian materia medica. Bombay: Popular

Prakashan; 1976. p. 857‑8.

Puri A, Saxena R, Saxena RP, Saxena KC, Srivastava V,

Tandon JS. Immunostimulant activity of Nyctanthes arbor‑tristis L.

J Ethnopharmacol 1994;42:31‑7.

Saxena RS, Gupta B, Lata S. Tranquilizing, antihistaminic

and purgative activity of Nyctanthes arbor‑tristis leaf extract.

J Ethnopharmacol 2002;81:321‑5.

Khatune NA, Mosaddik MA, Haque ME. Antibacterial activity

and cytotoxicity of Nyctanthes arbor‑tristis flowers. Fitoterapia

;72:412‑4.

Tandon, JS, Srivastava V, Guru PY. Iridoids: A new class of

leishmanicidal agents from Nyctanthes arbo‑rtristis. J Nat Prod

;54:1102‑4.

Goyal S, Sheth NR, Srivastava DN. Evaluation of anti‑inflammatory

activity of various fractions from ethanolic extract of Nyctanthes

arbor‑tristis leaves and characterization of its bioactive fraction by

thin layer chromatography. Inventi Impact: Ethanopharmacology

;2013:1-4.

Harborne JB. Phytochemical methods. London: Thomson Science;

p. 44‑6.

OECD Guidelines –“Guidance document on acute oral toxicity

testing†Series on testing and assessment No. 23, organization

for economic cooperation and development, OECD Environment,

health and safety publications, Paris Available from: http://www.

Oecd.org/ehs. [Last accessed on 2013 Oct 15].

Goyal S, Sheth NR, Srivastava DN. Comparative evaluation of

Nyctanthes arbor‑tristis and Alstonia scholaris leaves extracts in

Freund’s complete adjuvant induced arthritis in rats. Int J Pharma

Biol Arch 2013;4:903‑8.

Campo GM, Avenoso A, Campo S, Ferlazzo AM, Altavilla D,

Calatroni A. Efficacy of treatment with glycosaminoglycans on

experimental collagen induced arthritis in rats. Arthritis Res Ther

;5:R122‑31.

Walter K, Schutt C. Acid and alkaline phosphatase in serum (two

point method). In: Bergmeyer HU, editor. Methods in Enzymatic

Analysis. London: Academic Press; 1974. p. 856-60.

King J. The transferase – alanine and aspartate transaminase. In:

Van D, editor. Practical Clinical Enzymology. London: Norstand

Company Limited; 1965a. p. 121‑38.

Sinnathambi A, Papiya MM, Lohidasan S, Purnima A. Anti‑arthritic

and antioxidant activity of leaves of Alstonia scholaris Linn. R. Br.

Eur J Integr Med 2011;e83‑90.

Nam JH, Jung HJ, Choi J, Lee KT, Park HJ. The anti‑gastropathic and

anti‑rheumatic effect of Nigaichigoside F1 and 23‑hydroxytormentic

acid isolated from the unripe fruits of Rubus coreanus in a rat

model. Biol Pharm Bull 2006;29:967‑70.

Verhoeven AC, Boers M, te Koppele JM, van der Laan WH,

Markusse HM, Geusens P, et al. Bone turnover, joint damage

and bone mineral density in early rheumatoid arthritis treated

with combination therapy including high‑dose prednisolone.

Rheumatol 2001;40:1231‑7.

Vanderburgh A, Geusens P, Raus J, Stinissen P. The autoimmune

pathogenesis of rheumatoid arthritis: Role of auto reactive T cells

and new immunotherapy. Semin Arthritis Rheum 2001;31:160‑75.

Aghdassi E, Allard JP. Breath alkanes as a marker of oxidative stress

in different clinical conditions. Free Radic Biol Med 2000;28:880‑6.

Li G, Liu Y, Tzeng N, Cui G, Block ML, Wilson B, et al. Protective

effect of dextromethorphan against endotoxic shock in mice.

Biochem Pharmacol 2005;69:233‑40.

Lau DC, Dhillon B, Yan H, Szmitko PE, Verma S. Adipokines:

Molecular links between obesity and atherosclerosis. Am J Physiol

Heart Cric Physiol 2005;288:2031‑41.

Wills ED. Evaluation of lipid peroxidation in lipid and biological

membranes. In: Snell K, Mullock B, editors. Biochemical toxicology:

A practical approach. Oxford: IRL Press; 1987. p. 127‑52.

Jira W, Spiteller G, Richter A. Increased levels of lipid oxidation

products in low density lipoproteins in patients suffering from

rheumatoid arthritis. Chem Phys Lipids 1997;87:81‑9.

Kizilntuc A, Cogalgil S, Cerrahoglu L. Carnitine and antioxidants

levels in patients with rheumatoid arthritis. Scand J Rheumatol

;27:441‑5.

Hassan MQ, Hadi RA, Al‑Rawi ZS, Padron VA, Stohs SJ. The

glutathione defense system in the pathogenesis of rheumatoid

arthritis. J Appl Toxicol 2001;21:69‑73.

Yasuda M, Okabe T, Itoth J, Takekoshi S, Hasegawa H, Nagata H,

et al. Differentiation of necrotic cell death with or without

lysosomal activation: Application of acute liver injury models

induced by CCl4 and dimethylnitrosamine (DMN). J Histochem

Cytochem 2000;48:1331‑9.

Geetha R. Effect of alpha‑tocopherol on doxorubicin‑induced

changes in rat heart lysosomal enzymes. Indian J Exp Biol

;31:288‑90.

De S, Ravishankar B, Bhausar GC. Investigation of the

anti‑inflammatory effects of Paederia foetida. J Ethnopharmacol

;43:31‑8.

Downloads

Issue

Section

Articles