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1.
Redox Rep ; 19(5): 206-13, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24725132

ABSTRACT

OBJECTIVE: This study aimed to investigate the effect of the leaf extracts of Syzygium jambos and Solanum guaraniticum on the δ-aminolevulinate dehydratase (δ-ALA-D) activity, their antioxidant activity and potential protective action on oxidatively stressed erythrocytes, in order to demonstrate the safety or toxicity of the plant. METHODS: In erythrocyte samples, the effect of both extracts on δ-ALA-D activity, H2O2-induced oxidative stress, and 2,2'azobis (2-amidinopropane) (AAPH)-induced hemolysis was evaluated, as well as some antioxidant mechanisms. RESULTS: Both extracts inhibited δ-ALA-D activity (S. guaraniticum > S. jambos), and an involvement of the zinc ion of the δ-ALA-D structure on the inhibition of enzyme activity was verified. S. jambos leaf extract showed marked efficiency in countering H2O2-induced lipid peroxidation and in maintaining cellular integrity against AAPH-induced hemolysis. Furthermore, S. jambos exhibited greater H2O2 scavenging activity and stronger reduction power than S. guaraniticum. DISCUSSION: Both extracts bear potent antioxidant property as an important beneficial effect. However, the inhibition of δ-ALA-D activity suggests a possible harmful effect of these vegetal preparations and indicates the need for further investigation regarding their toxicological properties. All together, these data represent a significant contribution to the knowledge of these plants, both to the scientific community and to the folk medicine.


Subject(s)
Erythrocytes/drug effects , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Plant Leaves/chemistry , Porphobilinogen Synthase/metabolism , Solanum/chemistry , Syzygium/chemistry , Amidines/pharmacology , Antioxidants/metabolism , Erythrocytes/enzymology , Hemolysis/drug effects , Humans , Hydrogen Peroxide/pharmacology , Lipid Peroxidation/drug effects , Oxidants/pharmacology , Oxidation-Reduction
2.
Basic Clin Pharmacol Toxicol ; 104(5): 408-13, 2009 May.
Article in English | MEDLINE | ID: mdl-19413661

ABSTRACT

Adenosine plays an important neuromodulatory role in the central nervous system, and adenosine deaminase is an important enzyme in the degradation of adenine nucleotides. Methylmercury is the most prevalent form of mercury found in the environment. Methylmercury neurotoxicity has been correlated to the production of reactive oxygen species. In this study, its potential pathogenic effects were investigated in vitro in cerebral cortex and hippocampus of rats. We first observed that adenosine deaminase activity was higher in young rat brains when compared to the 60-day-old rats and was higher in hippocampus when compared to the cortex. Methylmercury (0.1, 1.0, 20 microM) inhibited adenosine deaminase activity in 7- and 60-day-old rats in a concentration-dependent manner. We have demonstrated that methylmercury-induced inhibition was antagonized by garlic alcoholic extract, but sodium selenate did not alter enzyme activity. In addition, glutathione and dithiothreitol restored the methylmercury-induced decrease of adenosine deaminase activity. These results demonstrated that there are age-related changes in adenosine deaminase activity and that thiol agents may contribute to the maintenance of adenosine deaminase activity and may be important in the neuromodulation of adenosine. Garlic alcoholic extract may be effective in reducing the effect of methylmercury-induced adenosine deaminase, which may be due to its sulphur-containing compounds.


Subject(s)
Adenosine Deaminase/metabolism , Aging/metabolism , Cerebral Cortex/drug effects , Garlic/chemistry , Hippocampus/drug effects , Metals, Heavy/toxicity , Methylmercury Compounds/toxicity , Plant Extracts/pharmacology , Adenosine Deaminase Inhibitors , Aging/drug effects , Animals , Antioxidants/pharmacology , Cerebral Cortex/enzymology , Dose-Response Relationship, Drug , Hippocampus/enzymology , Male , Plant Extracts/isolation & purification , Rats , Rats, Wistar , Selenic Acid , Selenium Compounds/pharmacology , Sulfhydryl Compounds/metabolism , Sulfhydryl Compounds/pharmacology
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