PROTECTIVE EFFECT OF ETHANOLIC EXTRACT OF PROPOLIS ON ISONIAZID INDUCED HEPATOTOXICITY IN MALE ALBINO MICE.
ABSTRACTBackground: Different herbal extracts and drugs had been tried to combat the isoniazid induced hepa- totoxicity; there is no study before using propolis for abating isoniazid induced liver toxicity.Objective: The purpose of this study was to assess protective effect of ethanolic extract of propolis (EEP)in isoniazid induced hepatotoxicity in male albino mice.Methods: Forty five male albino mice were divided into five groups i.e. group A served as control gro- ups B C D and E were experimental. Group B was treated with isoniazid 100 mg/kg for 30 days. Gro- ups C D and E were pretreated with EEP 150 mg/kg for 10 20 and 30 days respectively followed by treatment with isoniazid for another 30 days. Blood samples were obtained on 30th day in groups A and B and on 40th 50th and 60th days respectively in groups C D and E for assessing liver enzymes and total bilirubin. Serial sections of liver 4m thick were stained with H and E PAS and PASD for microscopic exa- mination.Results: Group B showed an increase in serum ALT AST ALP and total bilirubin levels; the general architecture of liver was deranged; necrosis apoptosis pyknosis vacuoles and periportal inflammation were also observed. A decrease in the level of liver enzymes was observed in mice of groups C D and E. Preparations from groups C and D showed some evidence of recovery whereas in group E significant recovery was observed.Conclusion: Pretreatment with EEP (150 mg/kg) showed time related hepatoprotection against INH in- duced hepatotoxicity in male albino mice.Key words: Isoniazid ALT AST ALP Bilirubin Propolis.
INTRODUCTIONMycobacterium tuberculosis (TB) is one of the major causes of morbidity and mortality among infectious diseases which primarily affects lungs and secondarily other organs of the body.1 Standard treatment of tube- rculosis consists of a six to nine months course of anti- biotics named isoniazid (INH) pyrazinamide (PZA) rifampicin (RIF) and ethambutol or streptomycin.2These antitubercular drugs are also hepatotoxic; the rate of their hepatotoxicity is much higher in develop- ing countries such as India and China (8 28%) com- pared to that in advanced countries (2 - 3%) even when the same dose schedule is used3. Other common side effects of anti-tubercular drugs are skin allergic reactions gastrointestinal and neurological disorders. Among these side effects hepatotoxicity is the one re- garded as serious and is the focus of the present study;2 3% cases of jaundice 7 8% of other side effects reported in hospitals and about 30% of sudden and severe liver failure are caused by drugs induced liver injury.4 Isoniazid is acetylated by the liver enzyme N- acetyltransferase 2 (NAT2) and then hydrolyzed resul- ting in formation of isonicotinic acid and acetylhydra- zine; the later compound is activated by cytochrome P-450.5 The metabolic oxidation of acetylhydrazine leads to reactive acetylating species diacetylhydrazine. Ace- tyl hydrazine and diacetylhydrazine bind with liver cell macromolecules causing liver damage.6 These toxic metabolites produce many histological changes such as hepatocyte vacuolar degeneration and necrosis.7 Dif- fuse micro vesicular fatty change with mild portal tri- aditis and necrosis was also reported.3 It was reported in another study that oxidative stress produced by antitubercular drugs caused hepatic injury7. Human genetic researches have revealed that cytochrome P450 2E1 (CYP2E1) is involved in isoniazid induced he- patotoxicity. An elevated CYP2E1 activity may lead to a higher production of hepatotoxins. Experimental stud- ies showed that isoniazid and hydrazine stimulate CY- P2E1 activity.1235Experimental studies on animals suggest that iso-niazid administration in toxic doses distress hepato- cellular membrane integrity producing an increase in alanine transaminase (ALT) aspartate transaminase (AST) alkaline phosphatase (ALP) and total bilirubin in serum values. The regression of isoniazid hepatoto- xicity generally takes weeks after discontinuation of isoniazid.The word pro-polis' is derivative of Greek wordspro'- for and polis'- the city i.e. protection of the hive. It consists of strongly adhesive sticky gum colle- cted converted and used by bees to close up cracks in their hives8. Bees (Apis mellifera L.) collect a sequence of gums resins and balms of viscous consistency from flower buds and tree barks.9Propolis consists of 50 70% resins and 10 15% essential oils mixed with 30 50% wax for proper uni- formity and 5 10% pollen.10 Propolis also containsvitamins folic acid nicotinic acid and many minerals including calcium magnesium manganese vanadium iron copper strontium aluminum and silicon.11 Pro- polis is antibacterial antiviral antiprotozoan and anti- fungal in its properties. Propolis possesses curative and preventive effects against inflammation cardiac disease diabetes mellitus12 and cancer. Hippocrates the well known Greek general practitioner prescri- bed propolis externally to treat sores wounds and for resolution of indurations and ulcers.10Although protective effect of different herbs anddrugs on hepatotoxicity had been studied further it has been reported that treatment with propolis showed a dose dependent protective effect on alcohol13 carbon tetrachloride (CCl4)14 and paracetamol15 induced hepa- totoxicity there is hardly any work to show the effect of EEP on isoniazid induced hepatotoxicity. Conseque- ntly the present study was undertaken to see the effect of propolis on isoniazid induced hepatotoxicity.
METHODSIt was a randomized control trial study. Simple ran- dom sampling technique using lottery method was used. Forty five healthy adult male albino mice 6-8 weeks old weighing 30g 5g were obtained from the colony raised at Veterinary Research Institute (VRI) Lahore; these were divided into five groups A B C D and E each having nine mice. Each group was housed in an individual stainless steel cage with wooden sha- vings at the floor in the experimental research labora- tory of University of Health Sciences Lahore. The ani- mals were kept at controlled room temperature (23 2C) humidity (50 5%) and light and dark cycle of12 hours each. The animals were fed on standard mou- se diet and water ad libitum. The body weight of ani- mals was recorded in the beginning regularly every week and at the end. The experiment started after a period of 1 week of acclimatization.Group A served as control; each mouse was given10 ml/kg of normal saline (0.9%) orally for 30 days; in Group B mice were given isoniazid 100 mg/kg daily dissolved in 10 ml distilled water orally for 30 days; the animals were sacrificed the next day after the ex- perimental period. Mice belonging to Groups C D and E were given ethanolic extract of propolis150 mg/kg daily dissolved in 10 ml normal saline orally for first10 20 and 30 days respectively and then isoniazid 100 mg/kg dissolved in 10 ml distilled water orally for next 30 days; these were sacrificed on 40 50 and 60 days respectively.Crude Propolis was obtained from the hive of Apis mellifera. L from the University of Agriculture Faisal- abad. Ethanolic extract of propolis was prepared at PC-SIR (Pakistan Council of Scientific and Industrial Re- search) laboratory12 Lahore was standardized by kee- ping it in ultraviolet light for 24 hours and stored in amber colored bottles at 4C. Ethanolic extract of pro- polis was given orally daily at a dose of 150 mg/kg bo- dy weight dissolved in 10 ml of 0.9% normal saline.9Isoniazid was obtained in powdered form from Sigma Chemicals Company (St. Louis MO USA). Dose of isoniazid was based on previous studies in which isoniazid was given at 100 mg/kg/day orally for 30 days716 dissolved in 10 ml distilled water17 using mou- se as experimental models respectively.The animals were sacrificed under anesthesia and2 3 ml of blood was taken using 3 ml disposable syri- nge by cardiac puncture on 30th day in groups A and B 40th 50th and 60th day in groups C D and E respe- ctively. It was collected in sterile vacuotainers with gel. The blood was allowed to stand for 1 hour centrifuged at a speed of 3000 rpm for 10 minutes using bench top centrifuge. The serum was collected with the help of sterilized dropper and stored in sterile appendorf tubes and kept at -20oC until used for the biochemical estimations.Kits for ALT (Alanine aminotransferase) AST (As- partate aminotransferase) and total bilirubin were obt- ained from Randox Laboratories Ltd. United Kingdom and kit for ALP (Alkaline phosphatase) was obtained from Human Company. Germany.The liver of the mouse was removed soon after sac- rificing the animal and 3 5 mm thick pieces were ex- cised after gross examinations fixed in formalin for 48 hours and processed to prepare paraffin blocks. Sect- ions 4m thick were obtained and stained with Hae- matoxylin and eosin (H and E) Periodic acid Schiff's (PAS) and Periodic acid Schiff's diastase (PASD) sta- ins.
Statistical AnalysisThe data of the groups was entered into and analyzed by computer software SPSS (Statistical Package for Social Sciences) version 18.0. Mean ( S.E) was given for quantitative variables like number of cells body weight ALT AST etc. One way ANOVA (Analysis of Variance) was applied to compare the mean body weight AST ALT etc. among study groups. Sphapiro Wilk test was applied to check normality. Post Hoc Tukey test was applied to observe mean difference
Table 1: Mean values of serum biochemical parameters of liver in U/L /mg/dl among groups.
###Biochemical###Group A###Group B###Group C###Group D###Group E
###parameters###Mean ( S.E)###Mean ( S.E)###Mean ( S.E)###Mean ( S.E)###Mean ( S.E)
Mean value of serum
###61.222 3.22###153.00 14.079###96.88 10.842###75.44 4.167###59.88 2.750###0.001
ALT in U/L
Mean value of serum
###71.33 4.99###190.22 14.61###82.66 8.42###67.44 5.177###58.22 3.90###0.001
AST in U/L
Mean value of serum
###97.55 6.664###187.77 19.73###96.22 7.15###95.44 7.02###89.00 3.24###0.001
ALP in U/L
Mean value of serum
###0.457 0.074###2.166 0.265###1.11 0.193###0.744 0.182###0.566 0.076###0.001
T. Bil. in mg/dl
among groups. Fisher's exact test was applied to obser- ve associations between qualitative variables. P value= 0.05 was considered as statistically significant.
RESULTSLiver functions were assessed biochemically using en- zymatic markers ALT AST ALP and total serum bili- rubin; their values were raised significantly (p value less than 0.001) in group B confirming isoniazid as hepatotoxic drug; the values of the test came down significantly by EEP in groups C D and E showing its hepatoprotec- tive effect (Table 1).In the present study all animals were active and healthy; however those of group B showed a slight degree of sluggishness. The difference in the body wei- ght of mice was statistically insignificant at the start of experiment (p value 0.207). The gain in body weights was less in animals of group B when compared to other groups at the end of the experimental period and the difference was statistically significant. A statistically significant reduction in weight and volume of liver was observed in isoniazid treated group B when compared to group A (p value less than 0.039 and 0.026 respectively). Upon administration of ethanolic extract of propolis there was a statistically significant increase in the liver weight and volume in groups C D and E when compa- red to group B. There was statistically insignificant dif- ference in liver weight and volume when groups C D and E were compared with group A (p value greater than 0.05) at the end of experimental period.
Group A showed normal liver histology i.e. dark brown color of liver having smooth surface. Microsco- pically each hepatic lobule had a vein in its centre and portal triads at its periphery. The hepatocytes were arranged in radiating cords proceeding to the peri- phery from the central vein having sinusoids in bet- ween lined by discontinuous endothelial cells with flattened nuclei; among them were kupffer cells withrounded prominent nuclei. The hepatic sinusoids were seen to be anastomosing with each other and opening into the lumen of central vein lined by flattened endo- thelial cells. Hepatocytes were polyhedral in form each with a vesicular nucleus and 1 2 nucleoli. Some nuclei were pyknotic and binucleated. Dilatation of sinusoids and central veins filled with RBCs was an evidence of vascular congestion. Portal area comprised a branch each of the portal vein hepatic artery and bile duct. Branch of portal vein had wide lumen lined by endothelial cells and contained erythrocytes; that of the hepatic artery had narrow lumen and thick wall as compared to the portal vein; the bile duct had how- ever a lining of low cuboidal epithelium. There was noevidence of periportal inflammation. In group B the histopathological studies of liver showed loss of gene- ral architecture of liver ballooning degeneration of he- patocytes focal areas of hepatocyte necrosis pyknosis apoptosis vacuolar degeneration vascular congestion with periportal inflammation (Fig. 2) all supported by biochemical analysis which showed rise in animals of groups C D and E which were pretreated with EEP for10 20 and 30 days respectively and were subsequently given INH for 30 days each histological examination of the liver and biochemical parameters gradually imp-roved and near normal values were obtained in group E (Fig. 3 4 and 5). Group C mice were given EEP (150 mg/kg) for 10 days and INH for next 30 days showed some evidence of recovery and regeneration in some hepatocytes with some pyknotic nuclei and lymphocy- tes (Fig. 3). Group D mice were given EEP (150 mg/kg) for 20 days and INH for next 30 days showed evidence of greater regeneration than in group C (Fig. 4). Group E mice were given EEP (150 mg/kg) for 30 days and INH for next 30 days showed marked evidence of re- generation Liver injury by isoniazid and its protection with propolis was assessed by examining liver histologi- cally. Statistical analysis of the findings by ANOVA and Post Hoc Tukey test showed increase in size of hepato- cytes their nuclei size of central vein and number of kupffer cells in group B and the difference when com- pared with group A was statistically significant (p val- ue less than 0.001); however size of hepatocytes in groups C D and size of their nuclei in C D and E decreased and was comparable to those of group A. Size of central vein and number of kupffer cells in groups C D and E decreased but were not comparable to group A. This means that in groups C D and E the toxic effects of INH were reduced progressively depending upon the length of treatment with EEP; the enzyme levels and the histological picture of the liver structure came to nearly normal level of the control in group E where EEP was given for 30 days before treating the animals with INH. Evidences of regeneration were observed in the form of multinucleated hepatocytes with promi- nent nucleoli and increased cytoplasmic eosinophilia of the cells. Statistical analysis by ANOVA and Fisher's exact test showed highly significant differences bet- ween values of the control group and EEP treated gro- ups when compared to isoniazid treated group (p val- ue less than 0.001). This is clearly indicative of protective eff- ect of ethanolic extract of propolis in isoniazid induced hepatotoxicity.
DISCUSSIONIn the current study we found that the ethanolic ex- tract of propolis prevented the reduction in body wei- ghts in groups C D and E upon treatment with isonia- zid. It had been reported earlier that propolis extract prevented experimentally induced diabetic nephropa- thy in rats; further oral administration of propolis ex- tract in doses of 100 200 and 300 mg/kg/day signifi- cantly increased the body weight of rats which was reduced on account of oxidative stress produced by diabetes. Propolis has a strong antioxidant and free radical scavenging effect.12In present investigations there was a statistically significant reduction in relative weight and volume of liver with isoniazid treatment in mice of group B as compared to the mice in group A Treatment with etha- nolic extract of propolis increased the liver weight and volume in groups C and D; the increase was statisti- cally significant when compared to group B (p valueless than 0.039 and 0.027). Our results were not in accord with previous studies in which supplementation of var- ious antioxidants i.e. garlic3 and carotenoids were re- ported to prevent the isoniazid induced hepatotoxicity and there was no effect on the liver weight of experi- mental animals.Hepatic injury is indicated by release of intracellu- lar enzymes into circulation such as AST ALT ALP and LDH.18 Their estimations are useful quantitative marker for measuring the extent of hepato-cellular damage by toxic substances. In the current investigat- ions it was observed that in group B the serum levels of diagnostic liver enzymes ALT AST ALP and total bilirubin were significantly increased as compared to group A (p less than 0.001); this was positively indicative of damage to the plasmalemma of hepatocytes by isonia- zid resulting in leakage of the enzymes. Our observat- ions are in accord with those reported earlier that CCl4 is hepatotoxic as was evident by increased levels of he- patic enzymes in rat model of the experimental work.14In the current study pretreatment with ethanolic ex- tract of propolis is considered to be responsible for keeping the enzymes near to normal values. Similar results were reported earlier where propolis pretreat- ment was reported to decrease the elevation of serum transaminases produced by paracetamol (acetamino- phen) CCl414 and abuse of alcohol.1513In the current study hepatocytes and their nuclei in group B were observed to increase in size and so wasthe case with hepatocytes. Similar observation was re- ported earlier in which isoniazid treatment in rodents produced fat vacuoles and inflammatory changes in liver further vascular dilatation was also seen in iso- niazid treated group.7In the current study pretreatment of groups C D and E with EEP maintained the size of hepatocytes and nuclei to near normal and comparable to the control group. Further the changes in vascular size seen upon isoniazid treatment were nearly comparable to the control group in EEP pretreated groups C D and E although the changes were statistically insignificant. Comparable results had been reported earlier when the central vein and portal triad congestion was reduced to normal on administering propolis in the experimental model of rat wherein hepatotoxicity was induced by CCl4.14Observation in the current investigation that thegeneral architecture of the liver nearly remained nor- mal in groups C D and E which were pretreated with EEP. These results are comparable to earlier reports in which treatment of rats with CCL4 caused degenerat- ion and disintegration of liver architecture;14 in this study hepatic lesions were characterized by massive hepatic necrosis and large vacuolation; it was also re- ported earlier that pretreatment with propolis extract showed restoration of liver to normal lobular pattern with well form polygonal hepatocytes having conspi- cuous nuclei in experimental modules using rats.14 It was seen in the current investigation that the number of Kupffer cells which increased in group B and these were restored to nearly control level in groups D and E treated with EEP for 20 and 30 days. These results are in accord with previous studies in which it was postu- lated that depletion of Kupffer cells protect the liver injury from alkylating agent for example melphelan19 and the industrial chemical thioacetamide20 kupffer cells activators however are reported to markedly en- hance hepatotoxicity induced by acetaminophen alco- hol and halobenzenes.21In the current investigations INH in group B cau- sed statistically significant degree of necrosis pyknosis and periportal inflammation when compared with the control (p-value less than 0.001); these were indicative of de- generative changes and toxic effects of INH on liver. Pyknosis is the irreversible condensation of chromatin of the nucleus leading onto apoptosis; these nuclei appear as dark and condensed chromatin material.Evidences of regeneration were present in propolis treated groups. Multinucleated hepatocytes (mostly binucleated) with prominent nucleoli and increasedcytoplasmic eosinophilia are regarded as the evidence of regeneration9. In current study in groups C D and E there were many binucleated hepatocytes present which corroborated with the early reported work in which pretreatment with propolis extract for 5 days after CCl4 administration for three weeks showed binu- cleated hepatocytes with no evidence of neutrophilic infiltration and fatty changes.14 These changes are in- dicative of hepatoprotective effect.Hydrazine is the toxic metabolite of isoniazid whi- ch is metabolized and subsequently detoxified by cyto- chrome P-450 system in liver. Hepatotoxicity could be due to any disturbance in cytochrome P-450 system or in detoxification pathway.222 It was reported that ani- mals receiving isoniazid showed periportal inflammat- ion fatty changes liver cell necrosis ballooning dege- neration vascular congestion pyknosis and apoptosis; these histopathological changes were reversed by vari- ous drugs and herbs such as cimetidine Pisonia Acu- leate (Nyctaginaceae) Jetepar (Glucometamine gluco- diamine nicotinamide ascorbate) Embelia Tsjeriam Cottam fruit Vitex negundo (five leaved chaste tree) leaf extract and aqueous extract of Azadirachta indica (Neem leaves) respectively.51823-26 INH produces oxi- dative stress and free radicals which are quenched by these antioxidants. Similarly it is proposed that pro- polis being an antioxidant prevented isoniazid indu- ced hepatic injury.Further trials are necessary regarding dose route of administration formulation and duration to assessits full benefits.It is Concluded that the present study is the first in which ethanolic extract of propolis was studied agai- nst isoniazid induced hepatotoxicity. The investigat- ions provide an efficient cheap and affordable hepato- protective natural protection for INH produce hepato- toxicity.
ACKNOWLEDGEMENTSWe are grateful to the HEC for providing research gra- nt for the project. We are obliged to PCSIR laboratory FBRC department Lahore for the preparation of etha- nolic extract of propolis. REFERENCES1. Ravi V. Patel S. S. Verma N. K. Dutta D and Saleem T.S. M. Hepatoprotective activity of bombax ceiba Linn against isoniazid and rifampicin induced toxicity in experimental rats. IJARNP. 2010; 3: 19-26.2. Tostmann A. Boeree M. J. Aarnouts R. E. Dekhuijzen R. Antituberculosis drug induced hepatotoxicity. J. Gastroenterol. Hepatol. 2008; 23: 192-202.3. Pal R. Vaiphei K. Sikander A. Singh K. Rana S. V. Eff- ect of garlic on isoniazid and rifampicin induced hepa- tic injury in rats. World J. Gastroenterol. 2006a; 12:636-639.4. Saukkonen J. J. Cohn D. Jasmer R M. Schenker S. Jereb J. A. Nolan C. M. et al. An official ATS statement: Hepatotoxicity of antituberculosis therapy. Am. J. Res- pir. Crit. Care Med. 2006; 174: 935-952.5. Kalra B. S. Aggarwal S. Khurana N. Gupta U. Effect of cimetidine on hepatotoxicity induced by isoniazid-rifa- mpicin combination in rabbits. Indian J. Gastroenterol.2007; 26: 18-21.6. Tariq S. Khan T. S. Malik S. Anwar M. S. Rashid A.Frequency of anti-tuberculous therapy induced hepa- totoxicity in patients and their outcome. J. Ayub. Med. Coll. Abbottabad 2009; 21: 50-52.7. Jehangir A. Nagi A. H. Shahzad M. Zia A. The hepato- protective effect of Cassia fistula (amaltas) leaves in iso- niazid and rifampicin induced hepatotoxicity in rodents. Biomedica. 2010; 26: 2529.8. Russo A. Longo R. Vanella A. Antioxidant activity of propolis: role of caffeic acid phenethyl ester and galan- gin. Fitoterapia. 2002; 73: 2129.9. Attalla F. El- Kott. Owayss A. A. Protective effects of propolis against the amitraz hepatotoxicity in mice. J. Pharmacol. Toxicol. 2008; 3: 402-408.10. Burdock G. A. Review of the biological properties and toxicity of bee propolis. Food Chem. Toxicol. 1998; 36:347-363.11. Marcucci M. C. Propolis: chemical composition biolo- gical properties and therapeutic activity. Apidologie.1995; 26: 83-99.12. Abo-Salem O. A. El-Edel R. H. Harisa G. E. El-Hala- wany N. Ghonaim M. M. Experimental diabetic nephro- pathy can be prevented by propolis: Effect on metabolic disturbances and renal oxidative parameters. Pak. J. Pharm. Sci. 2009; 22: 205-210.13. Liu C. F. Lin C. H. Lin C. C. Lin Y. H. Chen C. F. Lin S. C. Protective effect of propolis ethanol extract on eth- anol induced renal toxicity: an in vivo study. AMJ Chi- nese Med 2005; 33: 779-786.14. Bhadauria M. Nirala S. K. Shukla S. Hepatoprotective efficacy of propolis extract: A biochemical and histopa- thological approach. IJPT 2007; 6: 145-154.
15. Seo K. W. Park W. Song Y. J. Kim S. J. Yoon K. R. The protective effects of propolis on hepatic injury and its mechanism. Phytother. Res. 2003; 17: 250253.16. Rao G. N. Lindamood C. Heath J. E. Farnell D. R. Gi- les H. D. Sub chronic toxicity of human immunodefici- ency virus and tuberculosis combination therapies in B6C3F1 Mice. Toxicol. Sci. 1998; 45: 113-127.17. Cynamon M. H. Sklaney M. Gatifloxacin and ethiona- mide as the foundation for therapy of tuberculosis. Anti- microb. Agents. CH ASM 2003; 47: 24422444.18. Anbarasu C. Rajkapoor B. Kalpana J. Protective effect of Pisonia aculeate on rifampicin and isoniazid induced hepatotoxicity in rats. Inter. J. Phytomed. 2011; 3: 75-83.19. Kresse M. Latta M. KA1/4nstle G. Riehle H. M. Van Rooi- jen N. Hentze H. Kupffer cell expressed membrane- bound TNF mediates melphalan hepatotoxicity via acti- vation of both TNF receptors. J. Immuno. 2005; 175:4076-83.20. AndrACopyrights D. D. Sanchez Reus II. Bautista M. M. Cas- cales M. M. Depletion of kupffer cell function by gadoli- nium chloride attenuates thioacetamide induced he- patotoxicity. Biochem. Pharmacol. 2003; 66: 917-26.21. Buchweitz J. P. Sneed R. A. Jean P. A. Ganey P. E.Pentoxifylline attenuates bacterial lipopolysaccharide- induced enhancement of allyl alcohol hepatotoxicity. Toxicol. Sci. 2000; 56: 203-10.22. Noorani A. A. Saini N. Saini K. Kale M. K. Hepatopro- tective effect of rimonabant against isoniazid induced liver damage in albino wistar rats. IJPBA 2010; 1: 473- 477.23. Maryam S. Aziz K. Bhatti A. S. A. Shahzad A. W. Effe- cts of jetepar (glucometamine glucodiamine and nicoti- namide ascorbate) on isoniazid induced hepatotoxicity in rabbits. ANNUALS 2010a; 16: 37-42.24. Sambrekar S. N. Patil P. A. Kangralkar V. A. Protective effect of Embelia Tsjeriam Cottam fruit extracts on isoniazid induced hepatotoxicity in wistar rats. IJPSR2010; 4: 136- 139.
25. Tandon V. R. Khajuria V. Kapoor B. Kour D. Gupta S.Hepatoprotective activity of Vitex negundo leaf extract against anti-tubercular drugs induced hepatoxicity. Fito- terapia. 2008; 79: 533-538.26. Kale B. P. Kothekar M. A. Tayade H. P. Jaju J. B. Ma- teen-ud-Din M. Effect of aqueous extract of azadirachtaindica leaves on hepatotoxicity induced by anti-tuber- cular drugs in rats. Indian. J. Pharmacol. 2003; 35: 177-180.
|Printer friendly Cite/link Email Feedback|
|Date:||Jun 30, 2014|
|Previous Article:||COMPARATIVE STUDY OF CINNAMON AND GARLIC ON DIFFERENT PARAMETERS IN RATS.|
|Next Article:||A STUDY ON THE PATTERN OF SUICIDE IN KARACHI PAKISTAN.|