Antioxidant and hepatoprotective activities of Pongamia pinnata (PP) Linn. leaves on anti-tubercular medicines (isoniazid & rifampin) induced hepatotoxicity in Wistar rats

https://doi.org/10.53730/ijhs.v6nS1.4940

Authors

  • Samba Siva Raju Derangula Ph.D. Scholar, Bharath Institute of Higher Education & Research, Selaiyur, Chennai, Tamilnadu, India
  • N. S. Muthiah Professor, Department of Pharmacology, Sree Balaji Medical College & Hospital, Chrompet, Chennai, Tamilnadu, India
  • Byna Jayachandra Babu Assistant Professor, Department of Pharmacology, Ananta Institute of Medical Sciences & Research Centre, Rajasamand, Rajasthan, India
  • H. S. Somashekar Professor & Head, Department of Pharmacology, Viswabharathi Medical College & Hospital, Kurnool, Andhra Pradesh, India
  • E. Sukumar Ex- Dean of Research, Saveetha Institute of Medical & Technical Sciences, Chennai, Tamilnadu, India
  • K. Prabhu Associate Professor, Department of Anatomy, Sree Balaji Medical College & Hospital, Chrompet, Chennai, Tamilnadu, India

Keywords:

antioxidant parameters, anti-TB medicines, hepatoprotective activity, liver biomarkers, Pongamia pinnata

Abstract

Objectives: -The goal of this study was to see if an aqueous extract of Pongamia Pinnata Linn. (APP) leaves could protect against the hepatotoxicity caused by anti-TB medications (ATM). Methods: -In order to cause hepatotoxicity in rats, anti-tubercular medications were utilised. Silymarin (100 mg/kg p.o.) be present utilised by means of the control medication. For 21 days, an aqueous extract of Pongamia Pinnata Linn. leaves (200 & 400 mg/kg p.o.) was given with anti-TB medicines given one hour before to the aqueous extract. Results: -Biomarker enzymes found in the liver are SGPT, SGOT, ALP, Total Bilirubin & total cholesterol remained raised on anti-TB medicines management. The management of aqueous extract of Pongamia Pinnata Linn.leaves200 mg/kg & 400 mg/kg with anti - TB medicines were considerably decreased biomarker enzymes found in the liver. Antioxidant factors like Super Oxide Dismutase (SOD), Glutathione(GSH), Catalase(CAT), Glutathione Peroxidase (GPx)& Glutathione Reductase(GRx) were inhibited and improved ThioBarbituric Acid Reactive Substances (TBARs)points in anti-TB medicines administration then returned these antioxidant points in the management of aqueous extract of Pongamia Pinnata Linn. Leavesatadosageof 200mg/kg& 400mg/kg. Conclusion: - According to the findings of this research, Pongamia Pinnata Linn. leaves have a protective consequence against hepatotoxicity caused through anti-TB medicines.

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References

Robbins J, Fleurentin C, Hefler A. Hepatoprotective properties ofcrepisrueAPPelliandanisotesTrisules.Journalofethanopharmacology.,76;2003:105-111.

AriasPS,BesseyAA,LoweryDMandBrockM.Lipidperoxidation Biochemistry measurement and significance in livercellinjury.Indian.J.Exp.Biol.,45;1989:87-89.

MichealeP,CynthiyaJu.MechanismofDruginducedliverinjury. TheAAPSJournal.,1;2006:48-54.

SrivastavaA.,MaggsJ.L.,AntoineD.J.,WilliamsD.P.,SmithD.A.,Park B.K. Role of reactive metabolites in drug-induced hepatotoxicity. Handb. Exp.Pharmacol. 2010;196:165-194.

Prince M.I., Burt A.D., Jones D.E.J. Hepatitis and liver dysfunction withrifampicin therapy for pruritus in primary biliary cirrhosis. Gut 2002; 50:436–439.

Cancado E.L.R., Leitao R.M.C., Carrilho F.J., Laudanna A.A. Unexpectedclinicalremissionofcholestasisafterrifampicintherapyinpatientswithnormal or slightly increased levels of gamma-glutamyltranspeptidase. Am. J.Gastroenterol. 1998;93:1510–1517.

Sharma S.K. Antituberculosis drugs and hepatotoxicity. Infect. Genet. Evol.2004;4:167-170.

DhimanRKandChawlaYK.Digestive DiseasesandSciences2005;10:1807–1812.

CalixtoJB.BrazJ MedBiolRes2000;33(2):179-189.

Kamboj VP.CurrSci2000;78:35-39.

DeSmetPAGM. Drugs1997;54:801-840.

Krishnamurthi A. 1969. The Wealth of India, vol. VIII. Publication and Information Directorate CSIR, New Delhi, India

Meera B., Kumar S., Kalidhar S.B., 2003. A review of the chemistryand biological activity of Pongamia pinnata. J. Med. Arom. Plant Sci. 25, 441 65.

Punitha R., Manohar, S., 2006. Antihyperglycemic and antilipidperoxidative effects of Pongamia pinnata (Linn.) Pierre flowers in alloxan induced diabetic rats. J. Ethnopharmacol. 105, 39 46.

Brijesh, S., Daswani, P.G., Tetali, P., 2006. Studies on Pongamia pinnata (L.) Pierre leaves: understanding the mechanism(s) of action in infectious diarrhea. J Zhejiang Univ. Sci. B. 7(8), 665 674

Shoba G.F. and Thomas M., 2001. Study of antidiarrhoeal activity of four medicinal plants in castor-oil induced diarrhoea. J. Ethnopharmacol. 76(1), 73 76.

ChopdeVV, TankarAN,PandeVV, TekadeAR,GowekarNM, BhandariSR,andKhandake,InternationalJournalofGreenPharmacy2008; 72-75.

OECD guidelines for the testing of chemicals revised draft guideline 423:acuteoraltoxicity: Paris:OECD:2000.

KakkarP,DasBandViswanathanPN.AmodifiedspectrophotometricassayofSOD.IndianJournalofBiochemistryBiophysics1984; 2:130-132.

Aebi H. Catalase in vitro. Methods in Enzymology 1984: 105:121-126.

Sener G, Sehirli AO, Gedik N and Dulger GA. Rosiglitazone, aPPAR-?ligand,protectsagainstburn-inducedoxidativeinjuryofremote organs.Burns2007; 33:587-593.

Paglia DE and Valentine WN. Studies on the quantitative and qualitative characterization of erythrocytesglutathioneperoxidase.J.Lab.Clin. Med1986;40:158-69.

Racker E. Glutathione reductase from bakers’ yeast and beefliver.TheJournalofBiologicalChemistry 1955;217:855-866.

RukkumaniR,ArunaK,VarmaPS,RajasekaranKNandMenon VP. Comparative effects of curcumin and an analog ofcurcuminonalcoholandPUFAinducedoxidativestress.Journal of Pharmacy & Pharmaceutical Sciences 2004; 7: 274-283.

VijayaPadmaV,SujaRandShyamalaDeviCS.HepatoprotetiveeffectofLiv.52onAntitubercularDruginduced Hepatotoxicity in rats, Fitoterapia(LXIX) 1998; 6:520.

Saraswathy SD, Suja V, Gurumurthy and Shyamaladevi C S.Effect of Liv.100 against anti-tuberculosis drugs (isoniazid,rifampicin and pyrazinamide) induced hepatotoxicity in rats.IndianJ Pharmacol,1998,30:233.

Man-Fung Y, Takanobu K, Masashi M et al. Clinical outcomeand virologic profiles of severe hepatitis B exacerbation dueto YMDDmutations.JHepatol2003;39:850-855.

Kissler H J, Hauffen J, Hennig R, Gepp H and Schwille PO.Glucose and lipid metabolism after liver transplantation in inbred rats: Consequencesofhepaticdenervation,Metabolism2005;54:881-890.

ViswanathaSwamyAHM, RuchaV.Kulakarni, A.H.M.Thippeswamy,B.C.KotiandAparnaGore.EvaluationofhepatoprotectiveactivityofCissusquadrangularisstemextract against isoniazid induced liver damage in rats. Indianjournalofpharmacology 2010,Dec,Vol42,Issue6:397-400.

Attri S, Rana SV, Vaiphei K, Sodhi CP, Katyai R, Goel RC et al.Isoniazid andrifampicin induced oxidative hepatic injuryprotection by N-acetylcysteine. Hum ExpToxicol2000; 19:517-24.

Published

22-03-2022

How to Cite

Derangula, S. S. R., Muthiah, N. S., Babu, B. J., Somashekar, H. S., Sukumar, E., & Prabhu, K. (2022). Antioxidant and hepatoprotective activities of Pongamia pinnata (PP) Linn. leaves on anti-tubercular medicines (isoniazid & rifampin) induced hepatotoxicity in Wistar rats. International Journal of Health Sciences, 6(S1), 1785–1795. https://doi.org/10.53730/ijhs.v6nS1.4940

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