1. Caffeic acid treatment alters the extracellular adenine nucleotide hydrolysis in platelets and lymphocytes of adult rats.
- Author
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Anwar J, Spanevello RM, Pimentel VC, Gutierres J, Thomé G, Cardoso A, Zanini D, Martins C, Palma HE, Bagatini MD, Baldissarelli J, Schmatz R, Leal CA, da Costa P, Morsch VM, and Schetinger MR
- Subjects
- Adenosine Deaminase metabolism, Adenosine Triphosphatases metabolism, Animals, Blood Platelets enzymology, Dose-Response Relationship, Drug, Hydrolysis, Lymphocytes enzymology, Male, Phosphoric Diester Hydrolases metabolism, Platelet Aggregation drug effects, Pyrophosphatases metabolism, Rats, Rats, Wistar, Adenine Nucleotides metabolism, Blood Platelets drug effects, Caffeic Acids pharmacology, Lymphocytes drug effects
- Abstract
This study evaluated the effects of caffeic acid on ectonucleotidase activities such as NTPDase (nucleoside triphosphate diphosphohydrolase), Ecto-NPP (nucleotide pyrophosphatase/phosphodiesterase), 5'-nucleotidase and adenosine deaminase (ADA) in platelets and lymphocytes of rats, as well as in the profile of platelet aggregation. Animals were divided into five groups: I (control); II (oil); III (caffeic acid 10 mg/kg); IV (caffeic acid 50 mg/kg); and V (caffeic acid 100 mg/kg). Animals were treated with caffeic acid diluted in oil for 30 days. In platelets, caffeic acid decreased the ATP hydrolysis and increased ADP hydrolysis in groups III, IV and V when compared to control (P<0.05). The 5'-nucleotidase activity was decreased, while E-NPP and ADA activities were increased in platelets of rats of groups III, IV and V (P<0.05). Caffeic acid reduced significantly the platelet aggregation in the animals of groups III, IV and V in relation to group I (P<0.05). In lymphocytes, the NTPDase and ADA activities were increased in all groups treated with caffeic acid when compared to control (P<0.05). These findings demonstrated that the enzymes were altered in tissues by caffeic acid and this compound decreased the platelet aggregation suggesting that caffeic acid should be considered a potentially therapeutic agent in disorders related to the purinergic system., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2013
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