Literature DB >> 22915168

Exercise training prevents ecto-nucleotidases alterations in platelets of hypertensive rats.

Andréia Machado Cardoso1, Margarete Dulce Bagatini, Caroline Curry Martins, Fátima Hussein Abdalla, Daniela Zanini, Roberta Schmatz, Jessié Gutierres, Victor Camera Pimentel, Gustavo Thomé, Claudio Alberto Martins Leal, Juliano Marchi Vieira, Naiara Stefanello, Fernando da Silva Fiorin, Jucimara Baldissareli, Luiz Fernando Freire Royes, Adriane Bello Klein, Vera Maria Morsch, Maria Rosa Chitolina Schetinger.   

Abstract

In this study, we investigated the effect of 6 weeks of swimming training on the ecto-nucleotidase activities and platelet aggregation from rats that developed hypertension in response to oral administration of L-NAME. The rats were divided into four groups: control (n = 10), exercise (n = 10), L-NAME (n = 10), and exercise L-NAME (n = 10). The animals were trained five times per week in an adapted swimming system for 60 min with a gradual increase of the workload up to 5 % of animal's body weight. The results showed an increase in ATP, ADP, AMP, and adenosine hydrolysis, indicating an augment in NTPDase (from 35.3 ± 8.1 to 53.0 ± 15.1 nmol Pi/min/mg protein for ATP; and from 21.7 ± 7.0 to 46.4 ± 15.6 nmol Pi/min/mg protein for ADP as substrate), ecto-5'-nucleotidase (from 8.0 ± 5.7 to 28.1 ± 6.9 nmol Pi/min/mg protein), and ADA (from 0.8 ± 0.5 to 3.9 ± 0.8 U/L) activities in platelets from L-NAME-treated rats when compared to other groups (p < 0.05). A significant augment on platelet aggregation in L-NAME group was also observed. Exercise training was efficient in preventing these alterations in the exercise L-NAME group, besides showing a significant hypotensive effect. In conclusion, our results clearly indicated a protector action of moderate intensity exercise on nucleotides and nucleoside hydrolysis and on platelet aggregation, which highlights the exercise training effect to avoid hypertension complications related to ecto-nucleotidase activities.

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Year:  2012        PMID: 22915168     DOI: 10.1007/s11010-012-1431-7

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  42 in total

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