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1.
Asian Pacific Journal of Tropical Medicine ; (12): 426-432, 2013.
Article in English | WPRIM | ID: wpr-820027

ABSTRACT

OBJECTIVE@#To evaluate the antioxidant activity of aqueous extract of Moringa oleifera (M. oleifera) young leaves by in vivo as well as in vitro assays.@*METHODS@#In vitro study included estimation of total phenolic, total flavonol, total flavonoid and total antioxidant power (FRAP assay). In addition, in vivo study was done with the identified most effective dose of 200 mg/kg of its lyophilized powder on normal and diabetic rats. Its effect on different oxidative free radical scavenging enzymes,viz, superoxide dismutase (SOD), catalase (CAT), glutathione-S-transferase (GST), lipid peroxide (LPO) contents were measured.@*RESULTS@#Significant increase in activities of SOD, CAT, GST while, a decrease in LPO content was observed. Whereas, total phenolic, flavonoid and flavonol contents in the extract were found to be 120 mg/g of GAE, 40.5 mg/g of QE and 12.12 mg/g of QE, respectively. On the other hand, FRAP assay results of M. oleifera leaves was (85.00 ± 5.00) μM/g of extract powder.@*CONCLUSIONS@#The significant antioxidant activities of M. oleifera leaves from both in vivo as well as in vitro studies suggests that the regular intake of its leaves through diet can protect normal as well as diabetic patients against oxidative damage.


Subject(s)
Animals , Male , Rats , Analysis of Variance , Antioxidants , Pharmacology , Catalase , Metabolism , Diabetes Mellitus, Experimental , Drug Therapy , Metabolism , Flavonoids , Glutathione Transferase , Metabolism , Lipid Peroxides , Metabolism , Moringa oleifera , Chemistry , Organ Specificity , Oxidative Stress , Phenols , Plant Extracts , Pharmacology , Plant Leaves , Chemistry , Rats, Wistar , Superoxide Dismutase , Metabolism
2.
The Korean Journal of Internal Medicine ; : 573-578, 2013.
Article in English | WPRIM | ID: wpr-175092

ABSTRACT

BACKGROUND/AIMS: The higher incidence of gallbladder cancer (GBC) in females has been accredited to the involvement of hormones. The clinical implications of sex hormone receptors in GBC are well established. Cysteine proteases (such as caspase-3-9, etc.) are known to play a central role in the apoptotic pathway. Of these, the downstream enzyme caspase-3 is often activated in the apoptotic pathway. The aim of this work was to examine the status of apoptosis (which directly correlated with the level of active caspase-3) in hormone-responsive GBC. METHODS: We used 10 androgen receptor (AR)-positive, 14 estrogen receptor (ER)-positive, 12 HER/neu-positive, eight triple positive, and 10 triple negative malignant GBC human tissue samples. We isolated the total cellular protein from tumor tissues and carried out Western blotting using antipro-caspase-3 and anti-activated caspase-3 antibodies. RESULTS: ER and HER/neu-positive GBC exhibited high caspase-3 activity and low procaspase-3 activity, whereas AR-positive GBC showed no significant level of apoptosis. We also evaluated the apoptosis status of triple positive GBC and triple negative GBC, and found significant apoptosis in triple positive GBC. CONCLUSIONS: The results indicate that ER and HER/neu-positive GBCs had active apoptosis, whereas AR-positive GBC was highly resistant to apoptosis.


Subject(s)
Humans , Antineoplastic Agents, Hormonal/therapeutic use , Apoptosis/drug effects , Blotting, Western , Carcinoma/drug therapy , Caspase 3/analysis , Drug Resistance, Neoplasm , Enzyme Activation , Gallbladder Neoplasms/drug therapy , Neoplasms, Hormone-Dependent/drug therapy , Receptor, ErbB-2/analysis , Receptors, Androgen/analysis , Receptors, Estrogen/analysis , Biomarkers, Tumor/analysis
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