4.3 Article

α-adrenoceptor-mediated vasoconstriction is not involved in impaired functional vasodilation in the obese Zucker rat

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出版社

BLACKWELL PUBLISHING
DOI: 10.1111/j.1440-1681.2007.04849.x

关键词

blood flow; functional hyperaemia; metabolic syndrome; microcirculation; vasoconstriction

资金

  1. NHLBI NIH HHS [R01 HL063958-03, F32 HL082438, P01 HL051971-159001, HL-51971, P01 HL051971, HL-082438, F32 HL082438-01, R01 HL160606, R01 HL063958, HL-63958] Funding Source: Medline

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1. Obesity/metabolic syndrome is associated with augmented alpha-adrenoceptor sensitivity and impaired hyperaemic responses to exercise. Thus, it is possible that this elevated alpha-adrenoceptor constriction contributes to the blunted hyperaemic response. 2. Male lean and obese Zucker rats were instrumented for acute measurements of blood pressure (BP) and iliac blood flow (BF). Changes in BP and BF were determined in anaesthetized animals in response to intravenous administration of increasing doses of the alpha(1)-adrenoceptor agonist phenylephrine (PE). Once BF and BP returned to normal, a single bolus of the a-adrenoceptor antagonist phentolamine (0.5 mg) was administered. In separate animals, the spinotrapezius muscle was exteriorized for direct in situ observation of the microcirculation in response to phentolamine and muscle contraction. 3. Administration of PE demonstrated that iliac BF is highly autoregulated in the face of increasing perfusion pressure. Iliac conductance following phentolamine was significantly greater in obese rats. Following phentolamine administration, iliac vascular conductance was significantly greater in obese rats compared with lean animals. However, alpha-adrenoceptor blockade did not significantly alter arteriolar diameter in the spinotrapezius muscle during muscle contraction in either lean or obese animals. 4. These results suggest a greater contribution of the alpha-adrenoceptors in basal hindlimb vascular tone in obese rats. Furthermore, an augmented alpha-adrenoceptor-mediated vasoconstriction may not contribute to the impaired functional dilation in anaesthetized obese rats.

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