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1.
Biomed Pharmacother ; 88: 19-26, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28092841

ABSTRACT

Liver and kidney diseases are a global concern, therefore considerable efforts to obtain fine herbs useful as drugs from medicinal plants are currently in progress. The aim of this work was to study the antioxidant effects of previous supplementation with fenugreek seeds (FS) against carbon tetrachloride (CCl4) toxicity in the liver and kidney. CCl4 toxicity was induced by one dose (i.g. 5ml CCl4/kg of body weight, 50% CCl4 in olive oil) after 7 weeks of normal diet or diet rich in 10% of grinded fenugreek seeds (20g of pellet rat food/rat/day). 24h after the treatment with CCl4, all animals were scarified and biological analyses were performed. A phytochemical study of fenugreek seed extract (FSE) was also carried out. The phytochemical analysis of FS and FSE revealed the presence of polyphenols (5.92±0.02mg EGA/g DM), flavonoids (0.44±0.19mg ER/g DM), polysaccharides and trace elements. DPPH radical-scavenging activity of FSE showed an EC50 of 285.59±2.01µg/ml. In vivo, CCl4 administration significantly (p<0.05) induced an increase liver and kidney biomarkers. A significant (p<0.05) alteration of the antioxidant enzyme activities was also observed. In animals pretreated with FS, the studied parameters were much less shifted. These results indicate that the supplementation with fenugreek seeds is significantly effective in protecting the liver and kidneys from CCl4 toxicity.


Subject(s)
Carbon Tetrachloride/toxicity , Kidney/pathology , Liver/pathology , Phytochemicals/pharmacology , Protective Agents/pharmacology , Seeds/chemistry , Trigonella/chemistry , Animals , Antioxidants/metabolism , Flavonoids/analysis , Free Radical Scavengers/pharmacology , Kidney/drug effects , Lipid Peroxidation/drug effects , Liver/drug effects , Male , Phenols/analysis , Plant Extracts/pharmacology , Rats, Wistar , Spectrophotometry, Ultraviolet , Thiobarbituric Acid Reactive Substances/metabolism , Tissue Extracts
2.
J Oleo Sci ; 65(8): 701-12, 2016 Aug 01.
Article in English | MEDLINE | ID: mdl-27430382

ABSTRACT

Aromatic and medicinal plants are sources of natural antioxidants thanks to their secondary metabolites. Administration of Pinus halepensis L. (Pinaceae family) in previous studies was found to alleviate deleterious effects of aspirin-induced damage on liver and kidney. The present study, carried out on female rats, evaluates the effects of P. halepensis L. essential oil (EOP) on aspirin (A)-induced damage to liver and kidney. The animals used in this study were rats (n=28) divided into 4 groups of 7 each: (1) a control group (C); (2) a group given NaCl for 56 days then treated with (A) (600 mg/kg) for 4 days (A); (3) a group fed with (EOP) for 56 days then (A) for 4 days; and a group fed with only (EOP) for 56 days and given NaCl for 4 days. Estimations of biochemical parameters in blood were determined using kit methods (Spinreact). Lipid peroxidation levels (TBARS), superoxide dismutase (SOD) and catalase (CAT), glutathione peroxidase (GPx) activities were determined. Histopathological study was done by immersing pieces of both organs in a fixative solution followed by paraffin embeddeding and hematoxylin-eosin staining. Under our experimental conditions, Aspirin at dose 600 mg/kg body weight induced an increase of serum biochemical parameters as well as an oxidative stress in both organs. An increase occurred in TBARS by 108% and 55%, a decrease in SOD by 78% and 53%, CAT by 53% and 78%, and GPx by 78% and 51% in liver and kidney, respectively, compared to control. Administration of EOP given to rats enabled correction in these parameters. It could be concluded that the treatment with P. halepensis L. essential oil inhibited aspirin-induced liver and kidney damage.


Subject(s)
Aspirin/adverse effects , Chemical and Drug Induced Liver Injury/prevention & control , Kidney Diseases/prevention & control , Kidney/drug effects , Liver/drug effects , Oils, Volatile/pharmacology , Pinus/chemistry , Protective Agents/pharmacology , Acute Disease , Albinism , Animals , Chemical and Drug Induced Liver Injury/pathology , Female , Kidney/metabolism , Kidney/pathology , Kidney Diseases/chemically induced , Kidney Diseases/pathology , Liver/metabolism , Liver/pathology , Oils, Volatile/administration & dosage , Oils, Volatile/isolation & purification , Oxidative Stress/drug effects , Protective Agents/administration & dosage , Protective Agents/isolation & purification , Rats , Rats, Wistar
3.
Bosn J Basic Med Sci ; 14(2): 99-104, 2014 05.
Article in English | MEDLINE | ID: mdl-24856382

ABSTRACT

Plants have historically been used in treating many diseases. Eucalyptus globules, a rich source of bioactive compounds, and have been shown to possess antioxidative properties. The purpose of this study, carried out on male Wistar rats, was to evaluate the beneficial effects of Eucalyptus globulus extract upon acetaminophen-induced damages in kidney. Our study is realized in the Department of Biology, Faculty of Sciences of Sfax (Tunisia). 32 Wistar male rats; were divided into 4 batches: a control group (n=8), a group of rats treated with acetaminophen (900 mg/kg) by intraperitoneal injection during 4 days (n=8), a group receiving Eucalyptus globulus extract (130 mg of dry leaves/kg/day) in drinking water during 42 days after 2 hours of acetaminophen administration (during 4 days) (n=8) and group received only Eucalyptus (n=8) during 42 days. After 6 weeks, animals from each group were rapidly sacrificed by decapitation. Blood serum was obtained by centrifugation. Under our experimental conditions, acetaminophen poisoning resulted in an oxidative stress evidenced by statistically significant losses in the activities of catalase (CAT), superoxide-dismutase (SOD), glutathione-peroxidase (GPX) activities and an increase in lipids peroxidation level in renal tissue of acetaminophen-treated group compared with the control group. Acetaminophen also caused kidney damage as evident by statistically significant (p<0.05) increase in levels of creatinine and urea and decreased levels of uric acid and proteins in blood. Histological analysis demonstrated alteration of proximal tubules, atrophy of the glomerule and dilatation of urinary space. Previous administration of plant extract is found to alleviate this acetaminophen-induced damage.


Subject(s)
Acetaminophen/toxicity , Analgesics, Non-Narcotic/toxicity , Eucalyptus , Kidney Diseases/chemically induced , Kidney Diseases/prevention & control , Phytotherapy , Animals , Kidney Diseases/pathology , Male , Oxidative Stress , Plant Extracts/therapeutic use , Plant Leaves , Rats , Rats, Wistar
4.
Gen Physiol Biophys ; 32(1): 115-27, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23531841

ABSTRACT

Rhus tripartitum (sumac) is an Anacardiaceae tree with a wide phytotherapeutic application including the use of its roots in the management of gastric ulcer. In the present study the Rhus tripartitum root barks extract (RTE) was phytochemical studied, in vitro tested for their potential antioxidant activity using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and reducing power assay and in vivo evaluated for its ability to prevent ethanol-induced gastric ulcer in rats. The RTE was rich in phenolics, flavonoids, tannins and polysaccharide contents and exhibited a low but not weak in vitro antioxidant activity when compared with (+)-catechin. Pre-treatment with RTE at oral doses 50, 200 and 400 mg/kg body weight was found to provide a dose-dependent protection against ethanol-induced ulcer by averting the deep ulcer lesions of the gastric epithelium, by reducing gastric juice and acid output, by enhancing gastric mucus production by preserving normal antioxidant enzymes activities, and inhibiting the lipid peroxidation. The antiulcerogenic activity of RTE might be due to a possible synergistic antioxidant and antisecretory effects.


Subject(s)
Plant Bark/chemistry , Plant Extracts/pharmacology , Plant Roots/chemistry , Rhus/chemistry , Ulcer/drug therapy , Animals , Anti-Ulcer Agents/pharmacology , Antioxidants/chemistry , Antioxidants/pharmacology , Chromatography, High Pressure Liquid , Dose-Response Relationship, Drug , Ethanol/adverse effects , Flavonoids/chemistry , Male , Phenol/chemistry , Phytotherapy/methods , Plant Extracts/chemistry , Polysaccharides/chemistry , Rats , Rats, Wistar , Spectrophotometry, Infrared , Spectroscopy, Fourier Transform Infrared , Tannins/chemistry , Time Factors
5.
Gen Physiol Biophys ; 31(3): 335-42, 2012 Sep.
Article in English | MEDLINE | ID: mdl-23047946

ABSTRACT

The aim of our present study is to investigate the effect of Opuntia ficus indica f. inermis prickly pear juice (PPJ) against ethanol-induced liver injury in rats. Chronic ethanol administration (3 g/kg b.w.) during 90 days to Wistar rats, significantly (p < 0.01) increased the liver lipid and protein oxidation, reduced the glutathione content and the activities of liver antioxidant enzymes such as superoxide dismutase, catalase, glutathione peroxidase and conversely elevated the liver injury biochemical markers like aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, gamma glutamyl transferase, lactate dehydrogenase, cholesterol, triglycerides and caused a severe histopathologic injuries. Conversely pre-treatment of ethanol-fed rats with PPJ (20 and 40 ml/kg b.w., orally), interestingly reduced liver lipid and protein oxidation, histopathologic lesions and inhibited the alterations of antioxidant enzymes and the release of biochemical markers. The hepatoprotective effect of PPJ could be due to their capacity to end free radicals chain reactions or to enhance the endogenous antioxidants activities.


Subject(s)
Caryophyllaceae/chemistry , Chemical and Drug Induced Liver Injury/metabolism , Chemical and Drug Induced Liver Injury/prevention & control , Ethanol/toxicity , Phytotherapy/methods , Plant Extracts/administration & dosage , Reactive Oxygen Species/metabolism , Animals , Beverages , Chemical and Drug Induced Liver Injury/etiology , Fruit/chemistry , Male , Rats , Rats, Wistar , Treatment Outcome
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