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The objective of the present study is to assess the hepatoprotective activity of Oroxylum indicum Linn. (OI) whole stem extract on antitubercular drug induced liver toxicity in rats. Hepatotoxicity was induced by oral dosing of the combination of antitubercular drugs viz. AKT-4 for 90 days to Wistar rats. After assessing the hepatotoxicity in the animals, treatment with both aqueous and ethanolic whole stem extracts of Oroxylum indicum Linn. (OI) as well as standard marketed drug was done for 30 days. At the end of 30 days the hepatoprotective activity of OI was assessed using serum markers for liver dysfunction and expression of antioxidant enzymes in the liver tissue. Histopathological assessment and mRNA expression profiles for TNFα, IL6, NFkB, P38 MAPK was carried out to evaluate the protection of liver against antitubercular drugs by the extracts. Both the aqueous and ethanolic extracts of OI significantly (p<0.05) restored the serum enzyme levels. Also the various tissue antioxidant enzymes were also restored compared to normal group. Histopathological evaluations showed absence of any remarkable pathological and metabolic changes in the liver sections of treated groups. mRNA expression was significantly increased in disease induced group as compared to normal control. Treatment with extract significantly reduced cytokines and P38 MAPK mRNA expressions.
Drug induced liver injury is responsible for 5% of all hospital admission and 50% of acute liver failure. About 2.3 million new tuberculosis patients were identified in India in the year 2012 which was one 4th of the worldwide tuberculosis population. Introduction of Isoniazid (INH) was considered safe in 1963, The American Thoracic Society recommended INH for a year to tuberculin-positive persons as a chemoprophylaxis treatment regardless of age or duration. A study conducted by United States Public Health Service revealed 1% incidence of hepatitis and 0.06% deaths from hepatitis are due to INH. After introduction of Rifampicin (RMP), several studies inferred that hepatitis was more frequent and severe in patients receiving combination of INH and RMP than in those receiving INH alone. The current treatment of tuberculosis is to start with a combination chemotherapy containing INH, RMP, and Pyrazinamide (PZA) with or without ethambutol for the initial 2 months followed by a continuation phase of 4–6 months of combination of INH and RMP. It is known that anti tuberculosis treatment with INH, RMP and PZA induces hepatotoxicity and has intense adverse drug reactions. Preventive therapy of latent tuberculosis with 2 months course of RMP and PZA has shown fatal and severe hepatotoxicity, than 6 month of INH therapy. To reduce the incidence of hepatotoxicity due to exposure of these offending drugs in latent TB patients, recommendations for patient selection criteria, line of treatment and duration have been revised several times, but to the best of our knowledge no drug has been developed for prevention of hepatotoxicity. Oroxylum indicum Linn. (OI) belongs to the family Bignoniaceae is widely used in Indian Traditional System of medicine for various purposes. The plant is distributed in Indian subcontinents. Different parts of the plant are used for asthma, cough, viral hepatitis, antianorexic, antirheumatic, antibronchitic, anthelmintic and anti-inflammatory. Protection offered by Oroxylum indicum was reported in acetaminophen induced hepatic injury and modulation of liver function in rats at 500 mg/kg. Hence 500 mg/kg dose was selected for the present study. The present study was designed to evaluate the hepatoprotective effect of Oroxylumindicum whole stem, aqueous and ethanolic extracts against combination of INH, RMP, PZA and Ethambutol induced hepatotoxicity in experimental rat model.
The objective of the present study is to assess the hepatoprotective activity of Oroxylum indicum Linn. (OI) whole stem extract on antitubercular drug induced liver toxicity in rats.
Effect of OI on biochemical parameters
As shown in figure 1A, After treatment for 30 days, disease control group showed significant elevated (p<0.001) levels of the biochemical parameters viz. ALT, AST, LDH and T Bil. when compared to normal control group. On the other hand, the animals treated with aqueous and ethanolic extracts of OI (500 mg/kg) as well as standard drug Silymarin (100 mg/kg) showed significant decrease (p<0.01, p<0.001) in the levels of the serum enzyme activity when compared with the disease control group. The TP level was significantly decreased (p<0.001) in the disease control group which is increased significantly (p<0.001) in the groups treated with extracts of OI and standard. Disease control group showed significant increased (p<0.001) value of GDH when compared to the normal control group. Treatment with standard drug and both the extracts of OI showed significant decrease (p<0.001) in the value of GDH.
Effect of OI on Tissue antioxidant enzymes
Effect on Catalase and SOD levels
As shown in figure 1B, there was significant decrease (p<0.001) in Catalase and SOD values in disease control group as compared to normal control group, The Group III treated with standard drug and Group IV and Group V treated with aqueous and ethanolic extracts of OI showed significant (p<0.01, p<0.001) increase in the Catalase and SOD values when compared with the disease control.
Effect on MDA level
The group III treated with standard drug and Group IV and Group V treated with extracts of OI showed significantly decreased (p<0.01, p<0.001) levels of MDA in liver tissue when compared to disease control.
Effect on Reduced Glutathione level
Disease control group showed significant decrease (p<0.001) in GSH level as compare to normal control group. Standard and test drugs treated groups showed significantly increased (p<0.001) values of GSH when compared with disease control after treatment.
As shown in figure 1C, The microscopic examination of liver section from Normal Control group showed normal histo-architecture of hepatic parenchyma with normal cellular features (I). Whereas, Disease Control group showed moderate to severe pathological changes of hepatocytes with distorted hepatic cords along with the marked degenerative and necrobiotic changes with accumulation of fat globules inside the cytoplasm of hepatocytes along with haemorrhages and cellular swelling of hepatocytes (II). Standard drug treated group showed an absence of any remarkable pathological and metabolic change in all the sections of liver. Only minimal changes with focal cellular swelling of hepatocytes and focal congestion were evident in this group (III). Aqueous extract as well as ethanolic extract treated group showed focal cellular swelling of hepatocytes along with the slight congestion of hepatic artery and central vein. There was absence of any remarkable pathological and metabolic changes in all the sections of livers from this group when compared with the disease control group (IV, V).
Effect of OI on mRNA profiles
TNFα mRNA expression
As shown in figure 1D, as compared to normal control, TNFα mRNA level was significantly upregulated (p<0.01) in disease control group, indicating secretion of cytokines due to prolonged intervention of combinational anti-tubercular treatment. In treatment groups, ethanol extract showed significant down-regulation in TNFα mRNA expression (p<0.01), followed by standard and aqueous extract treatment group (p<0.05).
IL6 mRNA expression
As compared to normal control, in disease control group IL6 mRNA expression levels was significantly upregulated (p<0.01), indicating secretion of cytokines. In treatment groups, standard and ethanol extract showed significant reduction in TNFα mRNA expression (p<0.05). Aqueous extract suppressed IL6 mRNA expression levels but was not statistically significant.
NFkB mRNA expression
As compared to normal control, in disease control group NFkB gene was significantly upregulated (p<0.05), indicating appearance of inflammation. There was no significant reduction in NFkB mRNA expression in all the three treatment groups as compared to disease control. Ethanolic and aqueous extract showed relatively suppressed levels of NFkB mRNA expression as compared to standard treatment.
P38 MAPK mRNA expression
As compared to normal control, in disease control group P38 MAPK mRNA was highly upregulated (p<0.001), indicating appearance of cellular stress due to intervention of combinational anti-tubercular treatment. Both ethanolic and aqueous extract suppressed the P38 MAPK mRNA expression significantly (p<0.01) followed by standard treatment (p<0.05) when compared with disease control group.
World Health Organisation has revised its TB control programme and recommended and adapted Directly Observed Treatment Short Course (DOTS) strategy, as the most systematic and cost effective approach in developing and under developed countries (WHO). In the present study, hepatotoxicity induced in animals by combinational anti-tubercular drugs produced liver toxicity of different degrees of degenerative and necrobiotic changes along with alteration in the serum enzyme levels and antioxidant enzymes. Hepatotoxicity increases when taken in the combination. Increased lipid peroxidation and reduced SOD, Catalase and GSH suggested oxidative damage in hepatocytes. This caused damaged to the structural and functional integrity of the liver cells, significantly increased hepatocellular enzymes, as previously described. In the present investigation the total recovery of liver injury was observed after treatment with aqueous and ethanolic extract of OI whole stem. Marked reduction in elevated circulating levels of hepatocellular enzymes, restored total protein levels may be due to the membrane stabilizing effect of the OI extracts. The results obtained for the serum biochemical parameters and tissue antioxidant enzymes are comparable with the standard marketed drug silymarin. Glutamate dehydrogenase (GDH) is also another specific enzyme indicative of liver necrosis. Due to delayed release of GDH in liver toxicity, makes it more specific marker to study the liver necrosis. After administration of both the extracts of OI, circulating levels of GDH reduced significantly in extract intervened groups as compared to disease control group. Depletion of the catalase, SOD and GSH suggests the damage to hepatic parenchymal cells due to depletion in the free radical scavenging capacity of the liver cells caused by oxidative stress. We have observed the significant reduction in the catalase, SOD and GSH levels and significant increase in the LPO level in antitubercular drug treated group. Standard marketed drug silymarin significantly increased the levels of the antioxidant enzymes and results are in line with earlier findings. The animals treated with standard drug and with aqueous and ethanolic extracts of the OI showed minimal pathological changes as compared to disease control and the results are in line with previous findings, these results clearly shows that OI extracts have protective effects towards toxic action of anitubercular drugs. P38 MAPK appears to play a major role in apoptosis, cytokine production and cytoskeletal reorganization. Previous studies suggested the role of P38 MAPK and NFkB transition factor as a key regulators of genes that involved in inflammation, immunity, wound healing, acute phase response and apoptosis. In the present study, role of P38 MAPK and NFkB in liver tissues from normal, disease control and OI extract treated animals were assessed. P38 MAPK signalling plays important role in regulating TNF-α in diseased liver tissue, and was significantly down regulated in OI extract treated animals. NFkB promotes liver regeneration by up-regulating IL-6 and other molecules like hepatocyte growth factors. Though NFkB and IL-6 expressions were upregulated in liver tissue of disease control they were significantly down-regulated in OI extract treated liver tissue. It has been reported that inhibition of P38 MAPK and NFkB may be a useful target to treat pathophysiologic inflammation in liver injury. Hepatocyte death is the major feature of liver injury. In response to hepatic injury certain intracellular processes are initiated to conserve the liver integrity. Inflammatory cytokines including TNFα and IL-6 are key mediators of these processes as they are involved in different cellular response such as activation of proliferation, survival and death. TNFα induces specific signalling pathways in hepatocytes leading to the activation of either pro-survival mediators or effectors of cell death. Our study first time demonstrated that administration of OI stem extracts supressed P38 MAPK activity, NF-KB transcription factor and cytokine mRNA levels in tubercular drug induced hepatotoxicity and preventing further liver damage.
Given these promising findings, we suggest that OI, which is potentially safe and inexpensive for clinical use and may be considered as an effective supplement for the patients taking antitubercular medicaments.
Drugs and Chemicals
The marketed first line antituberculosis drug AKT-4 (Lupin Pharmaceuticals Ltd., India) containing isoniazid 300 mg, rifampicin 450 mg, pyrazinamide 750 mg and ethambutol 800 mg were used to produce the hepatotoxicity. Marketed Silymarin (Microlabs, Bangalore, India) was used as a standard drug. The diagnostic assay kits were procured from Pathozyme diagnostics Ltd., India. All the chemicals used for this study were of analytical grade.
Preparation of plant extracts
The plant was collected from Pune, Maharashtra, India and was authenticated by Botanical Survey of India (BSI/WRC/TECH/2011). The dried stem of OI was cleaned, coarse powder was made and kept in the Soxhlet apparatus for the hot extraction. The aqueous extract (AQOI) and 90% ethanolic extract (ETOI) were concentrated using rotary evaporator under vacuum. The percent yield of both the extracts were determined.
Male and female albino Wistar rats weighing about 150–180 grams were selected for efficacy study. The experiment was conducted as per Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA) guidelines, with prior permission from the Institutional Animal Ethics Committee (IAEC). The animals were housed in the polypropylene cages maintained at the standard laboratory conditions with access to food and water ad libitum.
Animal study protocol
30 Wistar rats (15 male and 15 female respectively) weighing between 150–180 grams were selected for the study. The first group served as Normal Control and remaining 24 animals received the antitubercular treatment of isoniazid 100 mg/kg, rifampicin 150 mg/kg, pyrazinamide 250 mg/kg and ethambutol 265 mg/kg to induce the hepatotoxicity for 3 months. Based on liver function test, animals were randomly divided into subgroups mentioned below followed by standard drug and OI extract treatments for 1 month. In brief animals were distributed in 5 groups viz. 1] Norrmal Control, 2] Disease Control, 3] Standard Control (Silymarin 100 mg/kg), 4] Aqueous extract (AQOI: 500 mg/kg), 5] Ethanolic extract (ETOI: 500 mg/kg).
A day after treatment, animals were euthanized with an overdose of anesthesia and the blood was collected immediately by cardiac puncture for the biochemical assessment. Liver tissues were collected for antioxidant enzyme analysis, histopathology and mRNA expressions.
Serum ALT, AST, TP, LDH and Bilirubin were assessed on 30th day using biochemical kits on semi-automatic biochemistry analyser (Pathozyme, India). Glutamate dehydrogenase (GDH) was estimated spectrophotometrically from serum.
Anti-oxidant enzymes analysis
Catalase [CAT; EC: 18.104.22.168], SOD and GSH were assessed using liver homogenate. A 10% liver homogenate was prepared using 1X PBS. The homogenate was then centrifuged and the supernatant was used for the estimation of antioxidant enzymes. Lipid Peroxidase (LPO) was estimated from the liver homogenate by TBARS method.
A portion of the liver was preserved in 10% formalin solution and histopathology was carried out to assess the histological changes after treatment with standard drug, AQOI and ETOI.
Real time quantitative (RT-PCR) assay
Total RNA was isolated from liver tissue using the RNeasy kit following the manufacturer's instructions (Qiagen, Hilden, Germany). 2 µg total RNA was reverse-transcribed in a total reaction volume of 20 µl using the high capacity cDNA reverse transcriptase kit (Applied Biosystems, Foster City, CA) as described by the manufacturer. Single stranded cDNA products were then analysed by RT-PCR using SYBR Green chemistry (Applied Biosystems, Foster City, CA). Primers were designed using Gene Runner software (version 3.05). Primers were synthesized from Eurofins MWG Operons. The amount of target gene was normalized to the internal standard β-actin and reported as a relative value.
The study was funded by APT Research Foundation, Pune, India.
The authors would like to thank Dr. Sunil Jalapure from Dr. Prabhakar Kore Basic Science Research Centre, KLE University, Belagavi for providing the research facilities to carry out the research work. The authors are also, very thankful to all the staff of National Toxicology Centre, APT Testing and Research Pvt. Ltd. and APT Research Foundation for their encouragement and providing facilities to carry out this work.
The experiment was conducted as per Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA) guidelines, with prior permission from the Institutional Animal Ethics Committee (IAEC).