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Nitric oxide contribution to vascular wall oxygen consumption in arterioles.
Shibata, M; Yamakoshi, T; Yamakoshi, K.
Afiliación
  • Shibata M; Biomedical Engineering, University of Tokyo Bunkyo-ku Tokyo, Japan. shibatam@m.u-tokyo.ac.jp
Conf Proc IEEE Eng Med Biol Soc ; Suppl: 6703-6, 2006.
Article en En | MEDLINE | ID: mdl-17959491
To study the role of nitric oxide (NO) in regulating oxygen consumption by vessel walls, the oxygen consumption rate of arteriolar walls in rat cremaster muscle was measured in vivo during flow-induced vasodilation and after inhibiting NO synthesis. The oxygen consumption rate of arteriolar was calculated based on the intra- and peri-vascular oxygen tension (P0(2)) values measured by phosphorescence quenching laser microscopy. The peri-vascular PO(2) value of the arterioles during vasodilation was significantly higher than under control conditions, although the intravascular PO(2) values under both conditions were approximately the same. On the other hand, inhibition of NO synthesis caused a significant decrease in both the intra- and peri-vascular P0(2) values of the arterioles. The inhibition of NO synthesis increased the oxygen consumption rate of the walls by 42%, whereas enhancement of flow-induced NO release decreased it by 34%. These results suggest that NO plays an important role not only as a regulator of peripheral vascular tone, but also as a modulator of tissue oxygen consumption by reducing oxygen consumption by vessel walls.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Consumo de Oxígeno / Arteriolas / Vasodilatación / Músculos / Óxido Nítrico Límite: Animals Idioma: En Revista: Conf Proc IEEE Eng Med Biol Soc Asunto de la revista: ENGENHARIA BIOMEDICA Año: 2006 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Consumo de Oxígeno / Arteriolas / Vasodilatación / Músculos / Óxido Nítrico Límite: Animals Idioma: En Revista: Conf Proc IEEE Eng Med Biol Soc Asunto de la revista: ENGENHARIA BIOMEDICA Año: 2006 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos