RESUMO
Eleven men with diabetes mellitus were compared with 45 male controls for platelet alpha-adrenergic binding sites by using [3H]dihydroergocryptine (DHE) as the radioligand antagonist. There was no difference between the two for binding affinity, but the number of sites was 430 +/- 30 (means +/- SEM) for diabetic subjects and 574 +/- 29 for controls (P = .005). Decreased sites were related to increased glycosylated hemoglobin levels (P = .002). There was no relationship between the decreased sites and catecholamine levels, duration of disease, body weight, or fasting blood sugar. Hence, binding sites were inversely related to control, but further studies are needed to define the pathophysiologic significance of this.
Assuntos
Plaquetas/análise , Diabetes Mellitus/sangue , Receptores Adrenérgicos alfa/análise , Adulto , Idoso , Glicemia/análise , Catecolaminas/sangue , Di-Hidroergotoxina , Hemoglobinas Glicadas/análise , Humanos , Masculino , Pessoa de Meia-Idade , Ensaio RadioliganteRESUMO
Prostacyclin (PGI2) infusion was studied in patients during cardiopulmonary bypass for coronary artery bypass grafting to assess its capacity to protect platelet hemostatic function. Twelve patients received PGI2 at doses ranging from 20 to 70 ng/kg/min by continuous infusion directly into the bubble oxygenator. Nine control patients were also studied. Platelet counts were not different in the two groups; the platelet count at the completion of the operation was decreased by a mean of 29% in treated patients and 40% in control patients (p greater than 0.15). Bleeding times were uniformly greater than 30 minutes following 30 minutes on bypass in both groups (p greater than 0.5). Also there was no difference in the bleeding times between the treated and untreated groups in the immediate postbypass period (p greater than 0.05). In addition, no difference in transfusion requirements was observed between the treated and control groups. However, plasma levels of platelet factor 4 were lower in the treated patients (p less than 0.05), and, more significantly, blood pressure was lower at all time points in the treated patients (p less than 0.001) despite the greater use of vasopressors. We conclude that PGI2 infusion in this study was of no hemostatic benefit but produced significant hypotension, a potential source of morbidity.
Assuntos
Plaquetas/efeitos dos fármacos , Ponte de Artéria Coronária , Epoprostenol/administração & dosagem , Hemostasia Cirúrgica/métodos , Adulto , Idoso , Tempo de Sangramento , Pressão Sanguínea/efeitos dos fármacos , Creatinina/urina , Avaliação de Medicamentos , Feminino , Humanos , Hipotensão/induzido quimicamente , Infusões Parenterais , Masculino , Pessoa de Meia-Idade , Fator de Ativação de Plaquetas/análise , Contagem de Plaquetas , Fator Plaquetário 4/análise , Fatores de Tempo , beta-Tromboglobulina/análiseRESUMO
Platelets adenine nucleotide levels were determined in 11 patients with Dacron bifemoral aortic prostheses using high performance liquid chromatography. Total platelet and dense granule adenine nucleotide levels were measured in neutralized perchloric acid extracts prepared from gel-filtered platelet suspensions and from platelet supernatants following thrombin-induced release of granule constituents respectively. Dense granule adenine nucleotide levels were significantly decreased in the patient group compared with age and sex-matched controls (p less than 0.01), whereas no differences in cytoplasmic adenine nucleotide levels were observed (p greater than 0.2). Platelet survival measurements were made on 3 patients; when grouped with control subjects, a positive correlation was observed between platelet survival and platelet dense granule ADP (r = 0.96; p less than 0.01). These results suggest that platelet dense granule adenine nucleotide content may be a clinically significant indicator of vascular graft thrombogenesis.
Assuntos
Nucleotídeos de Adenina/sangue , Aorta/cirurgia , Plaquetas/metabolismo , Polietilenotereftalatos , Próteses e Implantes/efeitos adversos , Difosfato de Adenosina/sangue , Trifosfato de Adenosina/sangue , Adulto , Idoso , Plaquetas/ultraestrutura , Grânulos Citoplasmáticos/análise , Humanos , Masculino , Pessoa de Meia-Idade , Contagem de PlaquetasAssuntos
Transtornos Plaquetários/fisiopatologia , Plaquetas/fisiologia , Alcoolismo/fisiopatologia , Amiloidose/fisiopatologia , Antibacterianos/farmacologia , Aspirina/efeitos adversos , Transtornos Plaquetários/terapia , Transfusão de Sangue , Produtos de Degradação da Fibrina e do Fibrinogênio/metabolismo , Heparina/efeitos adversos , Humanos , Adesividade Plaquetária , Agregação Plaquetária , Transfusão de Plaquetas , Serotonina/fisiologia , Trombocitopenia/fisiopatologia , Uremia/fisiopatologiaRESUMO
Cardiopulmonary bypass in baboons produced transient severe platelet dysfunction (bleeding times prolonged to 27.8 +/- 1.4 min compared with 3.9 +/- 0.7 baseline) that was associated with a parallel release of platelet alpha-granule proteins into plasma (platelet factor 4 and beta-thromboglobulin levels of 28.8 +/- 9.3 and 20.0 +/- 1.8 ng/ml, respectively) and their clearance into urine with a reciprocal depletion from circulating platelets. In contrast, platelet-dense granules did not undergo significant release. The bleeding times normalized rapidly following bypass (8.5 +/- 1.4 min at 1 hr). The infusion of prostacyclin (PGI2) into the bubble oxygenator during bypass (40--80 ng/kg/min) prevented the prolongation in bleeding time (p less than 0.01 compared with untreated control values) but did not block the release of alpha-granule proteins. Dosages outside this range were associated with prolonged bleeding times. These results show that transient platelet dysfunction occurring during cardiopulmonary bypass represents activation of platelets independent of alpha or dense granule release and is blocked by potent short-acting inhibition of platelet function using PGI2 infused into the oxygenator apparatus at optimal therapeutic doses.
Assuntos
Ponte Cardiopulmonar , Epoprostenol/uso terapêutico , Hemostasia , Prostaglandinas/uso terapêutico , Animais , Tempo de Sangramento , Grânulos Citoplasmáticos/metabolismo , Heparina/farmacologia , Oxigenadores , Papio , Contagem de Plaquetas , Serotonina/metabolismoRESUMO
Platelet-derived growth factor (PDGF) is a potent mitogen for many cultured connective tissue cells. It is present in concentrated form within the platelet alpha-granules and is believed to be released during platelet degranulation at sites of vascular injury. We have used a sensitive radioreceptor assay to measure PDGF levels in whole blood serum from normal humans [17.5 +/- 3.1 (SD) ng/mL] and baboons (2.7 +/- 1.2 ng/mL). PDGF was not detected in plasma from either species. In addition, plasma was found to substantially reduce the ability of added purified PDGF to bind to the cell surface PDGF receptor on cultured cells, suggesting that plasma may contain a PDGF-binding protein that would serve to inactivate PDGF released into plasma. Calculations of PDGF concentrations in serum have been corrected for the effects of the binding protein. 125I-PDGF injected intravenously into normal baboons was cleared rapidly from the plasma (t1/2 = two minutes). The rapid clearance of 125I-PDGF did not result from iodination damage, as purified unlabeled PDGF was cleared with comparable kinetics. The rapid clearance of purified and iodinated PDGF did not result from changes in PDGF structure during purification or from removal of PDGF-associated proteins during purification, as PDGF present in freeze-thaw lysates of fresh platelets was cleared equally rapidly. We conclude that release of PDGF at sites of vascular injury would greatly increase the local concentration of PDGF and that PDGF not localized to the site of injury would be rapidly cleared from the circulation.
Assuntos
Fator de Crescimento Derivado de Plaquetas/sangue , Animais , Ligação Competitiva , Células Sanguíneas/metabolismo , Plaquetas/fisiologia , Sobrevivência Celular , Humanos , Cinética , Papio , Fator Plaquetário 4/análise , Fator Plaquetário 4/metabolismo , Transfusão de Plaquetas , Fator de Crescimento Derivado de Plaquetas/farmacologia , Protaminas/farmacologia , Ensaio Radioligante , Receptores de Superfície Celular/análise , Receptores de Superfície Celular/efeitos dos fármacos , Receptores do Fator de Crescimento Derivado de Plaquetas , beta-Tromboglobulina/análiseRESUMO
Nine patients with myelodysplasia or myeloproliferative syndrome were studied with respect to platelet count and volume, 51Cr and 14C-serotonin platelet kinetics, bleeding time, and platelet dense and alpha-granule contents. Platelet counts ranged from 45,000 to 293,000 platelets/microliters. The bleeding time was significantly longer (greater than 4 minutes) than the predicted value in seven of nine patients. All patients had significant dense granule storage pool depletion (thrombin-releasable ADP was 0.59 +/- 0.30 vs. 2.41 +/- 0.20 mumol per 10(11) platelets in patients compared with normal volunteers; total platelet ADP was 0.97 +/- 0.29 vs. 2.72 +/- 0.15, and total platelet ATP/ADP was 4.77 +/- 1.89 vs. 1.65 +/- 0.11). The prolongation in bleeding time correlated inversely with thrombin-releasable ADP (r = -0.637, p less than 0.01) and with total ADP (r = -0.832, p less than 0.005), and directly with the ATP/ADP ratio (r = 0.781, p less than 0.005). When autologous platelets were doubly labeled with 14C-serotonin and 51Cr to test for loss of dense granule contents, marked preferential shortening of the 14C-serotonin platelet disappearance curve with relation to 51Cr platelet survival was observed in five of the six patients (six normal participants uniformly showed 14C-serotonin platelet disappearance patterns that were 15% to 20% longer than 51Cr platelet survivals). Reduction in alpha-granule contents was less striking and occurred less frequently than dense granule depletion (two of nine values were significantly reduced for platelet factor 4 content, whereas all patients had significantly reduced dense granule ADP levels). Mean plasma levels of both platelet factor 4 and beta-thromboglobulin were elevated in patients compared with normal participants (4.1 +/- 3.2 and 26.6 +/- 12.3 vs. 1.8 +/- 1.0 and 6.0 +/- 3.6 ng/ml; p less than 0.01 and p less than 0.01, respectively). Two patients had elevated urinary platelet factor 4. There was no correlation between platelet factor 4 content and thrombin-releasable platelet ADP levels (r = 0.167, p greater than 0.1). These patients had acquired storage pool deficiency of platelet dense granule ADP that correlated directly with platelet dysfunction, as measured by prolongation of bleeding time. The reduction in dense granule constituents appears to be the consequence of an ongoing loss of dense granule contents from circulating platelets.
Assuntos
Difosfato de Adenosina/sangue , Tempo de Sangramento , Plaquetas/metabolismo , Transtornos Mieloproliferativos/sangue , Testes de Função Plaquetária , Trifosfato de Adenosina/sangue , Plaquetas/patologia , Grânulos Citoplasmáticos/metabolismo , Meia-Vida , Humanos , Cinética , Transtornos Mieloproliferativos/urina , Contagem de Plaquetas , Fator Plaquetário 4/análise , Serotonina/sangue , beta-Tromboglobulina/análiseRESUMO
Experimental evidence suggests that the fibroblastic proliferation often associated with the myeloproliferative disorders is not part of the neoplastic process, but is secondary to an unknown stimulus. This stimulus may be a factor derived from platelets which promotes the proliferation of fibroblasts in vitro (PDGF). Platelet-derived growth factor is localized to platelet alpha-granules together with PF4 and beta-TG. As an indicator of alpha-granule release, we have measured PF4 levels in plasma, platelets and urine in 46 normal subjects and 49 patients with myeloproliferative disorders, secondary thrombocytosis and miscellaneous malignancies. All 11 patients with elevated urinary PF4 excretion exhibited myelofibrosis, whereas 11 of 22 patients with documented myelofibrosis had urinary PF4 excretion in the normal range. No correlation was seen between marrow fibrosis and plasma levels or the platelet content of PF4. The data are consistent with the possibility that release of mitogen(s) from platelet or megakaryocyte alpha-granules in some patients with myeloproliferative disorders is pathogenetically related to the development of marrow fibrosis.