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Cyclooxygenase products sensitize muscle mechanoreceptors in humans with heart failure.
Middlekauff, Holly R; Chiu, Josephine; Hamilton, Michele A; Fonarow, Gregg C; Maclellan, W Robb; Hage, Antoine; Moriguchi, Jaime; Patel, Jignesh.
Afiliação
  • Middlekauff HR; Dept. of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA. hmiddlekauff@mednet.ucla.edu
Am J Physiol Heart Circ Physiol ; 294(4): H1956-62, 2008 Apr.
Article em En | MEDLINE | ID: mdl-18296564
Prior work in animals and humans suggests that muscle mechanoreceptor control of sympathetic activation [muscle sympathetic nerve activity (MSNA)] during exercise in heart failure (HF) patients is heightened compared with that of healthy humans and that muscle mechanoreceptors are sensitized by metabolic by-products. We sought to determine whether cyclooxygenase products and/or endogenous adenosine, two metabolites of ischemic exercise, sensitize muscle mechanoreceptors during rhythmic handgrip (RHG) exercise in HF patients. Indomethacin, which inhibits the production of prostaglandins, and saline control were infused in 12 HF patients. In a different protocol, aminophylline, which inhibits adenosine receptors, and saline control were infused in 12 different HF patients. MSNA was recorded (microneurography). During exercise following saline, MSNA increased in the first minute of exercise, consistent with baseline heightened mechanoreceptor sensitivity. MSNA continued to increase during 3 min of RHG, indicative that muscle mechanoreceptors are sensitized by ischemia metabolites. Indomethacin, but not aminophylline, markedly attenuated the increase in MSNA during the entire 3 min of low-level rhythmic exercise, consistent with the sensitization of muscle mechanoreceptors by cyclooxygenase products. Interestingly, even the early increase in MSNA was abolished by indomethacin infusion, indicative of the very early generation of cyclooxygenase products after the onset of exercise in HF patients. In conclusion, muscle mechanoreceptors mediate the increase in MSNA during low-level RHG exercise in HF. Cyclooxygenase products, but not endogenous adenosine, play a central role in muscle mechanoreceptor sensitization. Finally, muscle mechanoreceptors in patients with HF have heightened basal sensitivity to mechanical stimuli, which also appears to be mediated by the early generation of cyclooxygenase products, resulting in exaggerated early increases in MSNA.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Reflexo / Sistema Nervoso Simpático / Prostaglandina-Endoperóxido Sintases / Músculo Esquelético / Mecanotransdução Celular / Insuficiência Cardíaca / Mecanorreceptores / Contração Muscular Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Physiol Heart Circ Physiol Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Reflexo / Sistema Nervoso Simpático / Prostaglandina-Endoperóxido Sintases / Músculo Esquelético / Mecanotransdução Celular / Insuficiência Cardíaca / Mecanorreceptores / Contração Muscular Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Physiol Heart Circ Physiol Ano de publicação: 2008 Tipo de documento: Article