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1.
Biochem Biophys Res Commun ; 392(1): 47-52, 2010 Jan 29.
Artigo em Inglês | MEDLINE | ID: mdl-20051227

RESUMO

A prothrombotic state in obesity may be partially responsible for the higher incidence of atherosclerotic complications. However the factors responsible for this prothrombotic state, linked with high levels of plasminogen activator inhibitor-1 (PAI-1), are not fully known. Leptin is elevated in obesity and studies have shown a positive correlation between leptin and PAI-1 levels in human subjects, along with a negative correlation with tissue-type plasminogen activator (tPA). We tested the hypothesis that leptin induces PAI-1 and inhibits tPA expression using human coronary artery endothelial cells (HCAEC) in culture as these cells play an important role in atherosclerosis. We demonstrate that leptin induces the transcription and translation of PAI-1 in HCAEC. The leptin dependent upregulation of PAI-1 mRNA and protein was comparable to insulin-induced PAI-1 expression. We show leptin concentration (0-150 ng/ml) dependent increases in PAI-1 mRNA and protein after 6 and 12h of leptin administration, respectively. Increased intracellular PAI-1 expression correlates with increased PAI-1 activity in conditioned media and inhibition of specific ERK1/2 pathway by treatment with PD98059 (20-40 microM) inhibits leptin dependent PAI-1 expression. However no changes in tPA expression were seen with time or increasing concentrations of leptin. Also leptin treatment did not alter total tPA concentration or tPA activity in conditioned media. In conclusion, our study shows that leptin upregulates the expression of PAI-1 in vascular endothelial cells via activation of ERK1/2 but does not regulate tPA expression. These studies demonstrate a novel mechanism for the prothrombotic role of leptin in development of atherosclerosis.


Assuntos
Aterosclerose/metabolismo , Endotélio Vascular/metabolismo , Leptina/metabolismo , Obesidade/metabolismo , Inibidor 1 de Ativador de Plasminogênio/biossíntese , Aterosclerose/etiologia , Células Cultivadas , Endotélio Vascular/efeitos dos fármacos , Flavonoides/farmacologia , Humanos , Leptina/farmacologia , Proteína Quinase 1 Ativada por Mitógeno/antagonistas & inibidores , Proteína Quinase 1 Ativada por Mitógeno/metabolismo , Proteína Quinase 3 Ativada por Mitógeno/antagonistas & inibidores , Proteína Quinase 3 Ativada por Mitógeno/metabolismo , Obesidade/complicações , Inibidor 1 de Ativador de Plasminogênio/genética , Inibidores de Proteínas Quinases/farmacologia , Trombose/etiologia , Trombose/metabolismo , Regulação para Cima
2.
Am J Hosp Palliat Care ; 23(3): 185-91, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17060277

RESUMO

There has been much research documenting the impact of having a loved one diagnosed with advanced cancer, but little is known about how to reduce care-giver burden. In this randomized controlled trial, the authors examined the potential relationship of an advanced cancer patient's participation in an 8-session, structured, multidisciplinary intervention on the care-giver's burden and quality of life (QOL). Although the patients randomly assigned to the intervention (n = 54) demonstrated improved QOL compared to the control condition (n = 49) participants (P < .05), there was no evidence that improving the patient's QOL made an impact on the caregiver's level of burden or the care-giver's QOL. Further investigation is warranted in this area, including interventions specifically designed and targeted to both reduce caregiver burden and to improve caregiver QOL.


Assuntos
Cuidadores/psicologia , Relações Interpessoais , Neoplasias/enfermagem , Cuidados Paliativos/métodos , Qualidade de Vida , Adaptação Psicológica , Adulto , Humanos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Neoplasias/psicologia , Apoio Social , Espiritualidade , Estresse Psicológico , Inquéritos e Questionários
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