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1.
China Journal of Chinese Materia Medica ; (24): 2178-2186, 2022.
Article in Chinese | WPRIM | ID: wpr-928158

ABSTRACT

The present study investigated the main components of fenugreek(Trigonella foenum-graecum L.) leaf flavonoids(FLFs) and their antioxidant activity. FLFs were prepared and enriched by solvent extraction, and the flavonoids were characterized by high-performance liquid chromatography-quadrupole-time-of-flight tandem mass spectrometry(HPLC-Q-TOF-MS/MS). The protective effect of FLFs against H_2O_2-induced stress damage to L02 hepatocytes was also investigated. Firstly, the cell viability was measured by MTT assay. The oxidative stress injury model was induced by H_2O_2 in L02 cells. The release of lactate dehydrogenase(LDH), the content of reduced glutathione(GSH) and malondialdehyde(MDA), and the activities of superoxide dismutase(SOD) and catalase(CAT) were measured by assay kits. Hoechst fluorescence staining was performed to observe the cell apoptosis. The expression levels of c-Jun N-terminal kinase(JNK), extracellular signal-regulated kinase 1/2(ERK1/2), nuclear factor erythroid-2 related factor 2(Nrf2), heme oxygenase 1(HO-1), and their phosphorylated proteins were detected by Western blot. Based on the MS fragment ion information and data in databases, FLFs contained eight flavonoids with quercetin and kaempferol as the main aglycons. The cell viabi-lity assay revealed that as compared with the conditions in the H_2O_2 treatment group, 3.125-25 μg·mL~(-1) FLFs could increase the viability of L02 cells, reduce LDH release and MDA content in a dose-dependent manner, potentiate the activities of SOD, CAT, and GSH, decrease the phosphorylation of JNK and ERK1/2 proteins, and up-regulate the expression of Nrf2 and HO-1. The results of fluorescence staining showed that the nucleus of the H_2O_2 treatment group showed concentrated and dense strong blue fluorescence, while the blue fluorescence intensity of the FLFs group decreased significantly. FLFs showed a protective effect against H_2O_2-induced oxidative damage in L02 cells, and the underlying mechanism is associated with the enhancement of cell capability in clearing oxygen free radicals and the inhibition of apoptosis by the activation of the MAPKs/Nrf2/HO-1 signaling pathway. The antioxidant effect of fenugreek leaf is related to its rich flavonoids.


Subject(s)
Antioxidants/pharmacology , Apoptosis , Flavonoids/pharmacology , Hepatocytes/metabolism , NF-E2-Related Factor 2/metabolism , Oxidative Stress , Plant Leaves/metabolism , Superoxide Dismutase/metabolism , Tandem Mass Spectrometry , Trigonella/metabolism
2.
Indian J Biochem Biophys ; 2010 Aug; 47(4): 227-233
Article in English | IMSEAR | ID: sea-135270

ABSTRACT

Diabetes is an oxidative stress disorder and oxidative damage to tissues such as heart, kidney, liver and other organs may be a contributory factor to several diabetic complications. Momordica charantia (family: Cucurbitaceae) and Trigonella foenum graecum (family: Fabaceae) are used traditionally in Indian folk medicine to manage diabetes mellitus. In the present study, the anti-hyperglycemic and anti-oxidative potential of aqueous extracts of M. charantia pulp and seed powder of T. foenum graecum were assessed in alloxan (150 mg/kg body weight) induced diabetic rats. Alloxan treatment to the rats could induce diabetes as the fasting blood glucose (FBG) levels were >280 mg/dl. Treatment of diabetic rats for 30 days with M. charantia and T. foenum graecum could significantly (p<0.001) improve the FBG levels to near normal glucose levels. Antioxidant activities (superoxide dismutase, catalase, reduced glutathione content and glutathione-s-transferase) and lipid peroxidation levels were measured in heart, kidney and liver tissues of normal, diabetic and experimental animals (diabetics + treatment). TBARS levels were significantly (p<0.001) higher and anti-oxidative activities were found low in diabetic group, as compared to the control group. Significant (p<0.001) improvement in both the TBARS levels and antioxidant activities were observed when M. charantia and T. foenum graecum were given to diabetic rats. Our results clearly demonstrate that M. charantia and T. foenum graecum are not only useful in controlling the blood glucose levels, but also have antioxidant potential to protect vital organs such as heart and kidney against damage caused due to diabetes induced oxidative stress.


Subject(s)
Alloxan/chemistry , Animals , Antioxidants/chemistry , Antioxidants/pharmacology , Diabetes Mellitus, Experimental/drug therapy , Glutathione/chemistry , Hypoglycemic Agents/pharmacology , Male , Momordica charantia/metabolism , Oxidative Stress , Plant Extracts/chemistry , Rats , Rats, Wistar , Seeds/chemistry , Thiobarbituric Acid Reactive Substances/chemistry , Trigonella/metabolism
3.
DARU-Journal of Faculty of Pharmacy Tehran University of Medical Sciences. 2006; 14 (1): 1-5
in English | IMEMR | ID: emr-76403

ABSTRACT

Some ion channels like voltage-operated calcium channels [VOCC] within the plasma membrane of vascular muscle cells from the walls of resistance arteries and arterioles play a central role in the regulation of vascular tone. On the basis of reports about the beneficial attenuating effect of fenugreek [Trigonella foenum-graecum L.; TFG] on the contractile reactivity of aortic rings of diabetic rats, this study was carried out to evaluate the possible involvement of L-type voltage-operated calcium channels in the vascular effect of this medicinal plant. For this purpose, male Wistar rats were made diabetic using streptozotocin [STZ, 60 mg/Kg, i.p]. The extract-treated control and diabetic rats received aqueous leaf extract of TFG [200 mg/Kg, i.p.] every other day for two months. At the end of the study, contractile response of isolated aortic rings to KC1 and noreadrenaline [NA] was determined in the absence and presence of the calcium channel blocker nifedipine. The results showed that aortic rings from diabetic rats are more responsive to the effect of KC1 and NA than those of controls, TFG extract treatment could attenuate the enhanced contractile response of aortic rings of diabetic rats, and nifedipine pretreatment could partially neutralize the beneficial effect of this extract. It is concluded that TFG extract attenuates the enhanced vascular reactivity in chronic diabetic rats and voltage-operated calcium channels are in part responsible for this effect of TFG extract


Subject(s)
Animals, Laboratory , Calcium Channels , Trigonella/metabolism , Rats, Wistar , Diabetes Mellitus, Experimental , Aorta
4.
J Biosci ; 2005 Sep; 30(4): 483-90
Article in English | IMSEAR | ID: sea-110765

ABSTRACT

Trigonella foenum graecum seed powder (TSP) and sodium orthovanadate (SOV) have been reported to have antidiabetic effects. However, SOV exerts hypoglycemic effects at relatively high doses with several toxic effects. We used low doses of vanadate in combination with TSP and evaluated their antidiabetic effects on anti-oxidant enzymes and membrane-linked functions in diabetic rat brains. In rats, diabetes was induced by alloxan monohydrate (15 mg/100 g body wt.) and they were treated with 2 IU insulin, 0.6 mg/ml SOV, 5% TSP and a combination of 0.2 mg/ml SOV with 5% TSP for 21 days. Blood glucose levels, activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), Na+/K+ ATPase, membrane lipid peroxidation and fluidity were determined in different fractions of whole brain after 21 days of treatment. Diabetic rats showed high blood glucose (P less than 0.001), decreased activities of SOD, catalase and Na+/K+ ATPase (P less than 0.01, P less than 0.001 and P less than 0.01), increased levels of GPx and MDA (P less than 0.01 and P less than 0.001) and decreased membrane fluidity (P less than 0.01). Treatment with different antidiabetic compounds restored the above-altered parameters. Combined dose of Trigonella and vanadate was found to be the most effective treatment in normalizing these alterations. Lower doses of vanadate could be used in combination with TSP to effectively counter diabetic alterations without any toxic effects.


Subject(s)
Animals , Brain/drug effects , Cell Membrane/drug effects , Diabetes Mellitus, Experimental/drug therapy , Female , Lipid Peroxidation/drug effects , Oxidative Stress/drug effects , Rats , Rats, Wistar , Seeds , Sodium-Potassium-Exchanging ATPase/antagonists & inhibitors , Trace Elements/pharmacology , Trigonella/metabolism , Vanadates/pharmacology , Vanadium/pharmacology
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