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Shedding of TNF-α receptors, blood pressure, and insulin sensitivity in type 2 diabetes mellitus

  • José Manuel Fernandez-Real
  • , Begoña Lainez
  • , Joan Vendrell
  • , Mercedes Rigla
  • , Antoni Castro
  • , Georgina Peñarroja
  • , Montserrat Broch
  • , Antonio Pérez
  • , Cristobal Richart
  • , Pablo Engel
  • , Wifredo Ricart
  • University of Girona
  • University Hospital of Tarragona
  • Institut d'Estudis Avançats
  • University of Barcelona
  • Hospital de La Santa Creu I Sant Pau

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66 Cites (Scopus)

Resum

Tumor necrosis factor-α (TNF-α) is increasingly recognized as a key component in the development of insulin resistance and increased blood pressure. In a sample of 368 individuals, the ratio of soluble TNF-α receptors (sTNFR2/sTNFR1) correlated positively with systolic and diastolic blood pressure (P < 0.01). This ratio was significantly greater in type 2 diabetic subjects (DM-2) than in type 1 diabetic patients and was greater than in control nondiabetic subjects (P < 0.00001). The TNF-α receptor 1 (TNFR1) density in peripheral blood monocytes was similar in DM-2 patients and in nondiabetic subjects. After phorbol 12-myristate 13-acetate, TNFR1 shedding was significantly decreased in DM-2 compared with control subjects, and it was directly associated with insulin sensitivity (r = 0.54, P = 0.03). Serum sTNFR1 concentration was also linked to the vasodilatory response to glyceryltrinitrate (P = 0.01). Conversely, TNF-α receptor 2 shedding was negatively associated with insulin sensitivity (r = -0.54, P = 0.03), whereas shedding of L-selectin showed no significant association. After exercise-induced lowering of blood pressure, a parallel decrease in sTNFR2/sTNFR1 was observed in DM-2 patients. Our findings suggest that insulin resistance and blood pressure are linked to altered shedding of TNF-α receptors in DM-2. The latter seems reversible and is not genetically determined.

Idioma originalAnglès
Pàgines (de-a)E952-E959
RevistaAmerican Journal of Physiology - Endocrinology and Metabolism
Volum282
Número4 45-4
DOIs
Estat de la publicacióData de publicació - 2002
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