Literature DB >> 16731646

Effects of sympathetically induced vasomotion on tissue-capillary fluid exchange.

Terumi Sakurai1, Naohito Terui.   

Abstract

The spontaneous and rhythmic constriction of peripheral arterioles, which is not associated with the cardiac or respiratory cycles, is called vasomotion. Vasomotion is observed in various tissues of various species, but the physiological role of vasomotion has not been clarified because of the difficulty in controlling the appearance of vasomotion in in vivo preparations. We developed a method of controlling vasomotion in in vivo experiments. The electrical stimulation of the cervical sympathetic nerve could reproducibly evoke vasomotion in rabbit ear skin. The frequencies of the evoked vasomotion were 0.04-0.07 Hz, which corresponded to spontaneously occurring vasomotion that has been reported before. Vasomotion was always evoked between 25 and 35 degrees C. At lower than 17 degrees C or higher than 37 degrees C, vasomotion was not evoked. With the use of this method of evoking vasomotion in vivo, the role of vasomotion in tissue perfusion was examined. A tracer (Cr-EDTA) was injected into the ear tissue, and tracer fading was then measured by using a camera. The rates of fading (clearance) of the tracer with vasomotion were significantly greater (1.7 to 8.1 times) than those without vasomotion. These results provided evidence that vasomotion enhanced tissue perfusion.

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Year:  2006        PMID: 16731646     DOI: 10.1152/ajpheart.00280.2006

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  15 in total

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5.  The role of perfusion in the oxygen extraction capability of skin and skeletal muscle.

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8.  Differential effect of calcium-activated potassium and chloride channels on rat basilar artery vasomotion.

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9.  Skin vasodilator function and vasomotion in patients with morbid obesity: effects of gastric bypass surgery.

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10.  Spontaneous Rhythmic Contractions (Vasomotion) of the Isolated, Pressurized Ductus Arteriosus of Preterm, but Not Term, Fetal Mice.

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