Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Hepatoprotective and Antioxidant Potential of Calotropis gigantea in Cyclosporine-An Induced Hepatotoxicity


Affiliations
1 Pad. Dr. D. Y. Patil Institute of Pharmaceutical sciences and research, Pimpari, Pune-411 018, India, India
2 AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India
3 Department of Pharmacology, K.L.E.S's College of Pharmacy, Bangalore-560010, India
     

   Subscribe/Renew Journal


The ethanolic fraction of Calotropis gigantea flowers (CGFE) was evaluated for its possible hepatoprotective potential in Wistar rats. The CGFE (250mg/kg and 500mg/kg, bw p.o.) showed a remarkable hepatoprotective activity against cyclosporine-A induced hepatotoxicity as judged from the level of serum markers for liver damage. Cyclosporine-A induced a significant rise in serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase (ALP) and lipid profile levels. The cotreatment of animals with CGFE (250mg/kg and 500mg/kg, p.o.) significantly decreased the elevated serum marker enzyme and lipid profile levels near to normal. The activity of the CGFE was comparable to the standard drug, silymarin (100mg/kg, p.o.). Further histopathological studies support the above finding.

Keywords

Antioxidant, Calotropis gigantea, Cyclosporine-A, Hepatotoxicity.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Braunwald E, Fauci AS, Casper DL, Hauser SL, Longo DL and Jameson JL. Harrison's Principles of Internal Medicine. The McGraw-Hill Companies, Inc., USA. 2001.
  • Bhanwra S, Singh J and Khosla P. Effect of Azadirachta indica leaf aqueous extract on paracetamol-induced liver damage in rats. J Physiol Pharmacol. 2000; 44: 64-8.
  • Dass EE and Shah KK. Paracetamol and conventional antimalarial drugs induced hepatotoxicity and its protection by methionine in rats. Indian J Exp Biol. 2000; 38: 1138-42.
  • Saraswathy SD, Suja V, Gurumurthy P and Shyamala devi CS. Effect of Liv.100 against antitubercular drugs (Isoniazid, Rifampicin and Pyrazinamide) induced hepatotoxicity in rats. Indian J Pharmacol. 1998; 30: 233-8.
  • Josephine A, Nithya K, Amudha G, Coothan KV, Sreenivasan PP and Palaninathan V. Role of sulphated polysaccharides from Sargassum Wightii in Cyclosporine A-induced oxidative liver injury in rats. BMC Pharmacol. 2008; 8: 40.
  • Herfindal ET and Gourley DR. Text Book of Therapeutics Drug and Disease Management. Williams and Wilkins, USA. 1996.
  • Borel JF, Baumann G, Chapman I, Donatsch P, Fahr A, Mueller EA and Vigouret JM. In vivo Pharmacological effects of cyclosporine and some analogues. Adv Pharmacol. 1996; 35: 115–246.
  • Deters M, Strubelt O and Younes M. Reevaluation of cyclosporine induced hepatotoxicity in the isolated perfused rat liver. Toxicol. 1997; 123: 197-206.
  • Mohamed BA and Khater MR. Evaluation of the protective potential of Ambrosia maritime extract on acetaminopheninduced liver damage. J. Ethnopharmacol. 2001; 75: 169–74.
  • Gulati RK, Agarwal S and Agrawal SS. Hepatoprotective studies on Phyllanthus emblica Linn. and Quercetin. Indian J. Exp. Biol. 1995; 33: 261-8.
  • Publications and Information Directorate, CSIR. The Wealth of India, Dictionary of Indian Raw Materials and Industrial Products, New Delhi.
  • Kshirsagar AD and Ashok P. Evaluation of Calotropis gigantea R. Br. flowers extract on alcohol induced hepatotoxicity. J. Cell Tissue Res. 2008; 8: 1551-6.
  • Kirtikar KR and Basu BD. Indian Medicinal Plants. Prabasi Press, Calcutta. 1980.
  • Pathak K and Argal A. Analgesic activity of Calotropis gigantea flower. Fitoterpia. 2007; 78: 40–2.
  • Kshirsagar AD, Patil PA, Ashok P and Hulkoti B. Antiinflammatory and anti-ulcer effects of Calotropis gigantea R. Br. flowers in rodents. J. Nat. remed. 2008; 8: 183-90.
  • Chitme HR, Chandra R and Kaushik S. Studies on antidiarrhoeal activity of Calotropis gigantea R. Br. in experimental animals. J. Pharm. Pharmaceut. Sci. 2004; 7: 70-5.
  • Argal A and Pathak AK. CNS activity of Calotropis gigantea ischolar_mains. J. Ethnopharmacol. 2006; 106: 142–5.
  • Srivastavaa SR, Keshria G, Bhargavana B, Singh C and Singha MM. Pregnancy interceptive activity of the ischolar_mains of Calotropis gigantea Linn. in rats. Contracep. 2007; 75: 318– 22.
  • Khandelwal KR. Practical Pharmacognosy, Techniques Experiments. Nirali prakashan, Pune. 2001.
  • Garrat DC. The quantitative analysis of drugs. Chapman and Hall, Japan. 1964.
  • Liu F, Ooi VEC and Chang ST. Free radical scavenging activity of mushroom polysaccharide extracts. Life Sci. 1997; 60: 763-71.
  • Wright PJ, Leathwood PD and Plummer DT. Enzymes in rats urine: Alkaline phosphatase. Enzymology. 1972; 42: 317-27.
  • Reitman S and Frankel S. Colorimetric method for the determination of serum glutamate oxalo-acetate and glutamae pyruvate transaminase. Am.J. Clin. Path. 1957; 28: 56- 63.
  • Francisco AO, Mariana HC, Fernanda RCA, Roberto CPL, Regilane MS, Juliana LM, Gerly ACB, Flavia AS and Vietla SR. Protective effect of alpha- and beta amyrin, a triterpene mixture from Protium heptaphyllum (Aubl.) March. trunk wood resin, against acetaminophen-induced liver injury in mice. J. Ethnopharmacol. 2005; 98: 103-8.
  • Sen S, Sahu PN and Mahato SB. Flavonol glycosides from Calotropis gigantea. Phytochem. 1992; 31: 2919-21.
  • Abdel-Rahman MK and Abd El-Megeid AA. Hepatoprotective Effect of Soapworts (Saponaria officinalis), Pomegranate Peel (Punica granatum L) and Cloves (Syzygium aromaticum linn) on Mice with CCl4 Hepatic Intoxication. World J. Chem. 2006, 1: 41-6.
  • Salducci MD, Chauvet-Monges AM, Berland Y, Dussol B, Elsen R and Crevat A. The restoration of ATP synthesis may explain the protective effect of calcium antagonist against cyclosporine A nephrotoxicity. Life Sciences. 1992; 50: 2053-8.
  • Recknagel RO. Carbon tetrachloride hepatotoxicity. Pharmacol. Rev. 1967: 19: 145-208.
  • Shaarawy SM, Tohamy AA, Elgendy SM, Abd Elmageed ZY, Bahnasy A, Mohamed MS, Kandil E and Matrougui K. Protective Effects of Garlic and Silymarin on NDEA-Induced Rats Hepatotoxicity. Int. J. Biol. Sci. 2009; 5: 549-57.
  • Schade RR, Guglielmi A, Van Thiel DH, Thompson ME, Warty V, Griffith B, Sanghvi A, Bahnson H and Hardesty R. Cholestasis in Heart Transplant Recipients Treated Cyclosporine. Transplant. Proc. 1983; 25: 2757–60.
  • Roman ID, Monte MJ, Gonzalez-buitrago JM, Esteller A and Jimenez R. Inhibition of hepatocytatory vesicular transport by cyclosporin A in the rat: Relationship with Cholestasis and Hyperbilirubinemia. Hepatology. 1990; 12: 83–91.
  • Mentha G and Houssin D. La Ciclosporine: Un Immunosuppresseur Selectif en Hepatogie, Gastroenterol. Clin. Biol. 1986; 10: 641–7.
  • Ames BN, Shigenaga MK and Hagen TM. Oxidants, antioxidants, and the degenerative diseases of aging. Proc. Natl. Acad. Sci. U.S.A. 1993: 90; 7915–22.
  • Kehrer JP. Free Radicals as Mediators of Tissue Injury and Disease. Crit. Rev. Toxicol. 1993; 23: 21–48.

Abstract Views: 247

PDF Views: 0




  • Hepatoprotective and Antioxidant Potential of Calotropis gigantea in Cyclosporine-An Induced Hepatotoxicity

Abstract Views: 247  |  PDF Views: 0

Authors

Ajay Kshirsagar
Pad. Dr. D. Y. Patil Institute of Pharmaceutical sciences and research, Pimpari, Pune-411 018, India, India
Deepa Ingawale
AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India
Purnima Ashok
Department of Pharmacology, K.L.E.S's College of Pharmacy, Bangalore-560010, India
Vrushali Thorve
AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India
Tanmay Dodal
AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India
Anurag Dodal
AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India
Mahesh Kahane
AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India
Bharat Zope
AISSMS College of Pharmacy, Near RTO, Kennedy road, Pune-411 001, India

Abstract


The ethanolic fraction of Calotropis gigantea flowers (CGFE) was evaluated for its possible hepatoprotective potential in Wistar rats. The CGFE (250mg/kg and 500mg/kg, bw p.o.) showed a remarkable hepatoprotective activity against cyclosporine-A induced hepatotoxicity as judged from the level of serum markers for liver damage. Cyclosporine-A induced a significant rise in serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase (ALP) and lipid profile levels. The cotreatment of animals with CGFE (250mg/kg and 500mg/kg, p.o.) significantly decreased the elevated serum marker enzyme and lipid profile levels near to normal. The activity of the CGFE was comparable to the standard drug, silymarin (100mg/kg, p.o.). Further histopathological studies support the above finding.

Keywords


Antioxidant, Calotropis gigantea, Cyclosporine-A, Hepatotoxicity.

References