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1.
Am J Hypertens ; 27(4): 522-9, 2014 Apr.
Article in English | MEDLINE | ID: mdl-23479073

ABSTRACT

BACKGROUND: Cholinergic enzyme activities are altered in hypertension, reflecting a low-grade inflammation. Regular physical exercise exerts anti-inflammatory effects and has been described as a coadjutant in the treatment of hypertension. In this study, we investigated the effect of 6 weeks of swimming training on cholinergic enzyme activities (acetylcholinesterase and butyrylcholinesterase) in Nω-Nitro-L-arginine methyl ester hydrochloride (L-NAME)-induced hypertensive rats. METHODS: The rats were divided into 4 groups: control (n = 10), exercise (n = 10), L-NAME (n = 10), and exercise L-NAME (n = 10). The animals were trained 5 times per week in an adapted swimming system for 60 minutes with a gradual increase of the workload up to 5% of animal's body weight. Enzyme activities were measured spectrophotometrically in lymphocytes, whole blood, and serum. RESULTS: A significant rise in acetylcholinesterase activity was observed in lymphocytes and whole blood as well as in serum butyrylcholinesterase activity in the L-NAME group when compared with the other groups (P < 0.05), and the increase in cholinesterase activities was positively correlated with the rise in blood pressure (r = 0.5721, r = 0.6121, and r = 0.5811, respectively). Swimming training was efficient in preventing these alterations in the exercise L-NAME group, which displayed values similar to those of the control group. Exercise training demonstrated a significant hypotensive effect in hypertensive rats. CONCLUSIONS: Exercise training was shown to prevent increased cholinesterase related to inflammatory processes in hypertensive rats, providing a new insight about protective exercise mechanisms to avoid hypertension-related inflammation.


Subject(s)
Acetylcholinesterase/blood , Butyrylcholinesterase/blood , Hypertension/physiopathology , Physical Conditioning, Animal , Swimming , Animals , Blood Pressure , Hypertension/blood , Hypertension/chemically induced , Hypertension/therapy , Inflammation/prevention & control , Lymphocytes/enzymology , Male , NG-Nitroarginine Methyl Ester , Rats , Rats, Wistar
2.
Mol Cell Biochem ; 381(1-2): 1-8, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23797318

ABSTRACT

This study investigated the effect of quercetin on nucleoside triphosphate diphosphohydrolase (NTP-Dase), 50-nucleotidase, adenosine deaminase (ADA), and acetylcholinesterase (AChE) activities in synaptosomes from cerebral cortex of adult rats exposed to cadmium (Cd). Rats were exposed to Cd (2.5 mg/Kg) and quercetin (5, 25 or 50 mg/Kg) by gavage for 45 days. Rats were randomly divided into eight groups (n = 8-10): saline/ethanol, saline/Querc 5 mg/kg, saline/Querc 25 mg/kg, saline/Querc 50 mg/kg, Cd/ethanol, Cd/Querc 5 mg/kg, Cd/Querc 25 mg/kg, and Cd/Querc 50 mg/kg. Results demonstrated that AChE activity increased in the Cd/ethanol group when compared to saline/ethanol group. Treatment with quercetin prevented the increase in AChE activity when compared to Cd/ethanol group. Quercetin treatment prevented the cadmium-induced increase in NTPDase, 5-nucleotidase, and ADA activities in Cd/ethanol group when compared to saline/ethanol group. Our data showed that quercetin have a protector effect against Cd intoxication. This way, is a promising candidate among the flavonoids to be investigated as a therapeutic agent to attenuate neurological disorders associated with Cd intoxication.


Subject(s)
5'-Nucleotidase/metabolism , Acetylcholinesterase/metabolism , Cadmium/toxicity , Cerebral Cortex/enzymology , Neuroprotective Agents/pharmacology , Quercetin/pharmacology , Synaptosomes/enzymology , Adenosine Deaminase/metabolism , Animals , Antigens, CD/metabolism , Apyrase/metabolism , Cerebral Cortex/drug effects , Cerebral Cortex/pathology , Hydrolysis , Male , Nucleotides/metabolism , Rats , Rats, Wistar , Synaptosomes/drug effects , Synaptosomes/pathology
3.
Cell Biochem Funct ; 31(2): 136-51, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22961602

ABSTRACT

The present study investigated the effects of a 6-week swimming training on blood pressure, nitric oxide (NO) levels and oxidative stress parameters such as protein and lipid oxidation, antioxidant enzyme activity and endogenous non-enzymatic antioxidant content in kidney and circulating fluids, as well as on serum biochemical parameters (cholesterol, triglycerides, urea and creatinine) from Nω-nitro-L-arginine methyl ester hydrochloride (L-NAME)-induced hypertension treated rats. Animals were divided into four groups (n = 10): Control, Exercise, L-NAME and Exercise L-NAME. Results showed that exercise prevented a decrease in NO levels in hypertensive rats (P < 0·05). An increase in protein and lipid oxidation observed in the L-NAME-treated group was reverted by physical training in serum from the Exercise L-NAME group (P < 0·05). A decrease in the catalase (CAT) and superoxide dismutase (SOD) activities in the L-NAME group was observed when compared with normotensive groups (P < 0·05). In kidney, exercise significantly augmented the CAT and SOD activities in the Exercise L-NAME group when compared with the L-NAME group (P < 0·05). There was a decrease in the non-protein thiols (NPSH) levels in the L-NAME-treated group when compared with the normotensive groups (P < 0·05). In the Exercise L-NAME group, there was an increase in NPSH levels when compared with the L-NAME group (P < 0·05). The elevation in serum cholesterol, triglycerides, urea and creatinine levels observed in the L-NAME group were reverted to levels close to normal by exercise in the Exercise L-NAME group (P < 0·05). Exercise training had hypotensive effect, reducing blood pressure in the Exercise L-NAME group (P < 0·05). These findings suggest that physical training could have a protector effect against oxidative damage and renal injury caused by hypertension.


Subject(s)
Hypertension/pathology , Oxidative Stress , Physical Conditioning, Animal , Animals , Ascorbic Acid/metabolism , Biomarkers/metabolism , Blood Pressure , Body Weight , Catalase/blood , Heart Rate , Hypertension/blood , Hypertension/physiopathology , Kidney/enzymology , Kidney/pathology , Lipid Peroxidation , Lipids/blood , Male , NG-Nitroarginine Methyl Ester , Nitric Oxide/metabolism , Oxidation-Reduction , Protein Carbonylation , Rats , Rats, Wistar , Sulfhydryl Compounds/blood , Superoxide Dismutase/blood , Swimming , Systole , Thiobarbituric Acid Reactive Substances/metabolism
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