Protective role of Phyllanthus niruri against nimesulide induced hepatic damage
被引:16
|
作者:
Chatterjee M.
论文数: 0引用数: 0
h-index: 0
机构:
Department of Chemistry, Bose Institute, Kolkata-700009, 93/1, Acharya Prafulla Chandra RoadDepartment of Chemistry, Bose Institute, Kolkata-700009, 93/1, Acharya Prafulla Chandra Road
Chatterjee M.
[1
]
Sil P.C.
论文数: 0引用数: 0
h-index: 0
机构:
Department of Chemistry, Bose Institute, Kolkata-700009, 93/1, Acharya Prafulla Chandra Road
Department of Chemistry, Bose Institute, Calcutta-700009 West Bengal, 93/1, A.P.C. RoadDepartment of Chemistry, Bose Institute, Kolkata-700009, 93/1, Acharya Prafulla Chandra Road
Sil P.C.
[1
,2
]
机构:
[1] Department of Chemistry, Bose Institute, Kolkata-700009, 93/1, Acharya Prafulla Chandra Road
[2] Department of Chemistry, Bose Institute, Calcutta-700009 West Bengal, 93/1, A.P.C. Road
Present study aimed to evaluate the protective role of the aqueous extract of Phyllanthus niruri (P. niruri) against nimesulide-induced hepatic disorder in mice by determining levels of glutamate oxaloacetate transaminase (GOT), glutamate pyruvate transaminase (GPT) and alkaline phosphatase (ALP) in serum and also by measuring the hepatic content of the antioxidant enzymes, superoxide dismitase (SOD) and catalase (CAT); the free radical scavenger, reduced glutathione (GSH) and thiobarbituric acid reacting substances (TBARS). Aqueous extract of P. niruri was administered either orally or intraperitoneally in different doses and times as needed for the experiments. Intraperitoneal pretreatment of the extract (100 mg/kg body weight for seven days) reduced nimesulide (750 mg/kg body weight for 3 days) induced increased levels of GOT (37.0 ± 1.8 units/ml in control group vs. 91.8 ± 2.0 units/ml in nimesulide treated group vs. 35.0 ± 1.0 units/ml in extract treated group), GPT (30.0 ± 2.1 units/ml in control group vs. 88.4 ± 2.9 units/ml in nimesulide treated group vs. 34.1 ± 1.8 units/ml in extract treated group), and ALP (7.86 ± 0.47 KA units /ml in control group vs. 23.80 ± 0.60 KA units /ml in nimesulide treated group vs. 7.30 ± 0.40 KA units/ml in extract treated group) to almost normal. In addition, P. niruri restored the nimesulide induced alterations of hepatic SOD (550 ± 20 units/mg total protein in control group vs. 310 ± 13 units/mg total protein in nimesulide treated group vs. 515 ± 10 units/mg total protein in extract treated group), CAT (99.5 ± 2 units/mg total protein in control group vs. 25.0 ± 1.5 units/mg total protein in nimesulide treated group vs. 81.0 ± 0.8 units/mg total protein in extract treated group), GSH (90 ± 3 nmoles/mg total protein in control group vs. 17 ± 4.2 nmoles/mg total protein in nimesulide treated group vs. 81 ± 1 nmoles/mg total protein in extract treated group) and TBARS (measured as MDA, 36.6 ± 3.0 nmoles/g liver tissue in control group vs. 96.3 ± 5.2 nmoles/g liver tissue in nimesulide treated group vs. 41.2 ± 1.7 nmoles/g liver tissue in extract treated group) contents. Dose-dependent studies showed that the herb could protect liver even if the nimesulide-induced injury is severe. Intraperitoneal administration of the extract showed better protective effect than oral administration. Combining all, the data suggest that P. niruri possesses hepatoprotective activity against nimesulide-induced liver toxicity and probably acts via an antioxidant defense mechanism. To the best of our knowledge, this is the first report of the hepatoprotective action of P. niruri against nimesulide induced liver damage.
机构:
Seth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
King Edward Mem Hosp, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, IndiaSeth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
Panchabhai, T. S.
Ambarkhane, S. V.
论文数: 0引用数: 0
h-index: 0
机构:
Seth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
King Edward Mem Hosp, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, IndiaSeth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
Ambarkhane, S. V.
Joshi, A. S.
论文数: 0引用数: 0
h-index: 0
机构:
Seth GS Med Coll, Dept Pathol, Bombay, Maharashtra, India
King Edward Mem Hosp, Dept Pathol, Bombay, Maharashtra, IndiaSeth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
Joshi, A. S.
Samant, B. D.
论文数: 0引用数: 0
h-index: 0
机构:
Seth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
King Edward Mem Hosp, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, IndiaSeth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
Samant, B. D.
Rege, N. N.
论文数: 0引用数: 0
h-index: 0
机构:
Seth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
King Edward Mem Hosp, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, IndiaSeth GS Med Coll, Dept Pharmacol & Therapeut, Ayurveda Res Ctr, Bombay, Maharashtra, India
机构:
Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Farmaceut, Lab Pesquisa Farmacognosia & Controle Qualidade F, Porto Alegre, RS, BrazilUniv Vale Itajai UNIVALI, Programa Posgrad Ciencias Farmaceut, Itajai, Brazil
Henriques, Amelia T.
Andrade, Sergio F.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Vale Itajai UNIVALI, Programa Posgrad Ciencias Farmaceut, Itajai, Brazil
Univ Vale Itajai UNIVALI, Nucleo Invest Quim Farmaceut NIQFAR, Itajai, BrazilUniv Vale Itajai UNIVALI, Programa Posgrad Ciencias Farmaceut, Itajai, Brazil
Andrade, Sergio F.
Cechinel-Filho, Valdir
论文数: 0引用数: 0
h-index: 0
机构:
Univ Vale Itajai UNIVALI, Programa Posgrad Ciencias Farmaceut, Itajai, Brazil
Univ Vale Itajai UNIVALI, Nucleo Invest Quim Farmaceut NIQFAR, Itajai, BrazilUniv Vale Itajai UNIVALI, Programa Posgrad Ciencias Farmaceut, Itajai, Brazil