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Platelet Apoptotic Response May Be Associated With the Capacity of Aspirin to Inhibit Platelets.
Zamorano-León, José J; Gascón, Martin; Martínez, Carlos H; Freixer, Gala; Guerra, Redy; Zekri-Nechar, Khaoula; Bernardo, Esther; Serna-Soto, Mariano de la; Segura, Antonio; Giner, Manel; García-Fernández, Miguel A; Macaya, Carlos; López-Farré, Antonio J.
Afiliação
  • Zamorano-León JJ; Department of Public Health and Maternal and Child Health, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Gascón M; Health Care Department, General Headquarters, Spanish Navy, Madrid, Spain.
  • Martínez CH; Department of Medicine, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Freixer G; Department of Medicine, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Guerra R; Cardiology Department, Hospital Clínico San Carlos, Madrid, Spain.
  • Zekri-Nechar K; Department of Medicine, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Bernardo E; Cardiology Department, Hospital Clínico San Carlos, Madrid, Spain.
  • Serna-Soto M; Department of Medicine, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Segura A; Department of Health and Social Affairs, Health Institute of Talavera de la Reina, Toledo, Spain; and.
  • Giner M; Department of Surgery, School of Medicine, Universidad Complutense, Madrid, Spain.
  • García-Fernández MA; Department of Medicine, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Macaya C; Cardiology Department, Hospital Clínico San Carlos, Madrid, Spain.
  • López-Farré AJ; Department of Medicine, School of Medicine, Universidad Complutense, Madrid, Spain.
J Cardiovasc Pharmacol ; 76(5): 584-591, 2020 11.
Article em En | MEDLINE | ID: mdl-33170592
ABSTRACT
An inadequate platelet response to aspirin (ASA) has been identified in some patients under chronic ASA treatment. The aim of this study was to analyze if ASA-sensitive and ASA-resistant platelets have differences in their apoptotic capability. Clinically stable ischemic coronary patients who had been taking ASA (100 mg/d) for at least 9 months before inclusion were divided into ASA-resistant (n = 11) and ASA-sensitive (n = 13) groups as defined by the PFA-100 test. Platelets from ASA-sensitive patients showed higher expression of the proapoptotic proteins Bak and Bax than those from ASA-resistant patients, although only Bak protein remained different when the results were adjusted by age. In resting platelets, neither caspase-3 activity nor cytosolic cytochrome C levels were different between both experimental groups. Stimulation of platelets with calcium ionophore (10 nmol/L, A23187) increased caspase-3 activity (1.91-fold higher; P < 0.05) and cytosolic cytochrome C levels (1.84-fold higher; P < 0.05) to a higher degree in ASA-sensitive than in ASA-resistant platelets. In conclusion, ASA-sensitive platelets seem to be better prepared to undergo apoptosis during robust platelet activation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plaquetas / Inibidores da Agregação Plaquetária / Aspirina / Isquemia Miocárdica / Apoptose / Proteínas Reguladoras de Apoptose Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plaquetas / Inibidores da Agregação Plaquetária / Aspirina / Isquemia Miocárdica / Apoptose / Proteínas Reguladoras de Apoptose Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article