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Therapeutic Methods and Therapies TCIM
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1.
Indian J Exp Biol ; 49(12): 939-45, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22403868

ABSTRACT

Administration of hydroalcoholic extract of Cissampelos pareira roots (CPRE) and standard drug silymarin in rats showed significant hepatoprotective action against CCl4 induced hepatotoxicity. Elevated serum marker enzymes of AST, ALT, ALP and serum bilirubin were significantly reduced to near normal level in CPRE treated rats. Lipid peroxidation level was decreased significantly in CPRE 100, 200, 400 mg/kg doses treatment groups. In case of antioxidant enzymes SOD, catalase levels were increased significantly after CPRE 200, 400 mg/kg doses, similarly it increased the enzyme levels of GST, GPx, and GSH. CPRE 200, 400 mg/kg decreased cholesterol level, and increased triglyceride level. In vitro hepatoprotective activity of the extract was evaluated at 20, 40, 60, 80 and 100 microg/ml concentration against CCl4 (1%) induced toxicity in freshly isolated rat hepatocytes. HepG2 cells showed significant dose dependent increase in percentage viability at the doses 20, 40, 60, 80 and 100 microg/ml of CPRE compared to CCl4 exposed HepG2 cells. Results of this study strongly demonstrate Cissampelos pariera having good hepatoprotective potential.


Subject(s)
Carbon Tetrachloride/toxicity , Chemical and Drug Induced Liver Injury/prevention & control , Cissampelos/chemistry , Liver/drug effects , Plant Extracts/therapeutic use , Protective Agents/therapeutic use , Animals , Cell Survival/drug effects , Chemical and Drug Induced Liver Injury/enzymology , Chemical and Drug Induced Liver Injury/etiology , Chemical and Drug Induced Liver Injury/metabolism , Chemical and Drug Induced Liver Injury/pathology , Hep G2 Cells , Humans , Lipid Peroxidation/drug effects , Liver/enzymology , Liver/metabolism , Liver/pathology , Liver Function Tests , Male , Plant Extracts/isolation & purification , Plant Roots/chemistry , Protective Agents/isolation & purification , Rats , Rats, Sprague-Dawley
2.
J Ethnopharmacol ; 128(2): 537-40, 2010 Mar 24.
Article in English | MEDLINE | ID: mdl-20083180

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Cinnamomum tamala T. Nees & Eberm (Family Lauraceae) is used traditionally in Indian System of Medicine as carminative, anthelmintic, diuretic, and used in colic, dyspepsia, and diarrhea. AIM OF THE STUDY: This study was aimed to evaluate the gastroprotective effects of Cinnamomum tamala leaves. METHODS: Cinnamomum tamala leaves extract (CTE; 50,100 and 200mg/kg body weight) was administered orally, twice daily for 5 days for prevention from ethanol (EtOH)-, cold-restraint stress (CRS)- and pylorus ligation (PL)-induced ulcers. Estimation of H(+)K(+)ATPase activity and gastric wall mucous were performed in EtOH-induced ulcer model, antioxidant enzyme activities was carried out in CRS-induced ulcer model, and various gastric secretion parameters like volume of gastric juice, acid output, and pH value were estimated in PL-induced ulcer model. RESULTS: A significant reduction in lesion index was observed in ulcer-induced animals treated with CTE at different doses when compared with ulcerated rats in all models. A significant decrease occurred in the level of H(+)K(+)ATPase, volume of gastric juice, and acid output. Simultaneously the level of gastric wall mucus and pH were increased significantly. These showed dose-dependent action of CTE. The antioxidant enzyme levels of LPO and SOD were decreased while administering CTE at different doses, compared with their control values. Contrary to this the level of CAT enzyme showed significant increase. CONCLUSIONS: The results of our study showed that Cinnamomum tamala possess significant gastroprotective activity, probably due to its free radical scavenging activity.


Subject(s)
Anti-Ulcer Agents/pharmacology , Cinnamomum/chemistry , Protective Agents/pharmacology , Stomach Ulcer/drug therapy , Stomach/drug effects , Animals , Anti-Ulcer Agents/therapeutic use , Antioxidants/pharmacology , Diarrhea/drug therapy , Duodenal Ulcer/drug therapy , Duodenal Ulcer/pathology , Ethanol/pharmacology , Free Radical Scavengers/pharmacology , Gastric Juice/chemistry , Plant Leaves/chemistry , Protective Agents/therapeutic use , Random Allocation , Rats , Rats, Sprague-Dawley , Stomach/pathology , Stomach Ulcer/chemically induced , Stomach Ulcer/pathology , Superoxide Dismutase/pharmacology
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