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1.
Biometals ; 32(2): 241-249, 2019 04.
Article in English | MEDLINE | ID: mdl-30649636

ABSTRACT

Silver catfish (Rhamdia quelen) is a fish species with neotropical distribution, and is a potential model organism to study polluted environment. The aim of this study is to analyze the response of silver catfish to environmental concentrations of waterborne zinc (Zn) over 96 h. Significant metal accumulation was seen in gill, intestine and liver tissues. No significant accumulation was seen in muscle tissue. Lipid peroxidation increased in the brain, and decreased in the muscle and liver at all levels of exposure. Zinc exposure led to decreased protein carbonyl levels in the brain and increased levels in the liver. The activity of catalase in the liver was reduced for all exposed groups. Glutathione S-transferase activity decreased in the brain at the highest level of exposure and in the liver at all Zn concentrations tested. Non-protein thiols increased in the muscle and in the gills after exposure. Ascorbic acid levels increased in the brain and in the gills. Exposure to Zn also altered the metabolic parameters, causing decreased lactate and ammonia levels in the muscle, and decreased glycogen in the liver. Zinc exposure increased ammonia and amino acid levels in the liver, and increase glycogen and amino acid levels in muscle tissue. Our results demonstrate that exposure to environmentally relevant concentrations of Zn led to accumulation of metals in the tissues of silver catfish, with significant changes in biochemical parameters.


Subject(s)
Catfishes/anatomy & histology , Catfishes/metabolism , Gills/metabolism , Intestines/chemistry , Liver/metabolism , Water Pollutants, Chemical/metabolism , Zinc/metabolism , Animals , Gills/chemistry , Liver/chemistry , Tissue Distribution
2.
Psychopharmacology (Berl) ; 236(2): 641-655, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30377748

ABSTRACT

Alzheimer's disease (AD) is a progressive and irreversible neurodegenerative disease. The present study investigated the effects of 50 and 100 mg/kg berberine (BRB) on recognition memory, oxidative stress, and purinergic neurotransmission, in a model of sporadic dementia of the Alzheimer's type induced by intracerebroventricular (ICV) injection of streptozotocin (STZ) in rats. Rats were submitted to ICV-STZ 3 mg/kg or saline, and 3 days later, were started on a treatment of BRB or saline for 21 days. The results demonstrated that BRB was effective in protecting against memory impairment, increased reactive oxygen species, and the subsequent increase in protein and lipid oxidation in the cerebral cortex and hippocampus, as well as δ-aminolevulinate dehydratase inhibition in the cerebral cortex. Moreover, the decrease in total thiols, and the reduced glutathione and glutathione S-transferase activity in the cerebral cortex and hippocampus of ICV-STZ rats, was prevented by BRB treatment. Besides an antioxidant effect, BRB treatment was capable of preventing decreases in ecto-nucleoside triphosphate diphosphohydrolase (NTPDase), 5'-nucleotidase (EC-5'-Nt), and adenosine deaminase (ADA) activities in synaptosomes of the cerebral cortex and hippocampus. Thus, our data suggest that BRB exerts a neuroprotective effect on recognition memory, as well as on oxidative stress and oxidative stress-related damage, such as dysfunction of the purinergic system. This suggests that BRB may act as a promising multipotent agent for the treatment of AD.


Subject(s)
Berberine/pharmacology , Brain/drug effects , Neuroprotective Agents/pharmacology , Oxidative Stress/drug effects , Recognition, Psychology/drug effects , 5'-Nucleotidase/drug effects , 5'-Nucleotidase/metabolism , Adenosine Deaminase/drug effects , Adenosine Deaminase/metabolism , Alzheimer Disease/psychology , Animals , Antibiotics, Antineoplastic/toxicity , Antioxidants , Brain/metabolism , Cerebral Cortex/drug effects , Cerebral Cortex/metabolism , Disease Models, Animal , Glutathione , Glutathione Transferase/drug effects , Glutathione Transferase/metabolism , Hippocampus/drug effects , Hippocampus/metabolism , Injections, Intraventricular , Lipid Metabolism/drug effects , Male , Memory/drug effects , Memory Disorders/chemically induced , Oxidation-Reduction/drug effects , Pyrophosphatases/drug effects , Pyrophosphatases/metabolism , Rats , Rats, Wistar , Reactive Oxygen Species/metabolism , Streptozocin/toxicity , Synaptosomes/drug effects , Synaptosomes/enzymology
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