Ray Clare J, Marshall Janice M
University of Birmingham, UK.
J Physiol. 2009 Apr 1;587(Pt 7):1579-91. doi: 10.1113/jphysiol.2008.163691. Epub 2009 Feb 9.
Exercise hyperaemia is partly mediated by adenosine A(2A)-receptors. Adenosine can evoke nitric oxide (NO) release via endothelial A(2A)-receptors, but the role for NO in exercise hyperaemia is controversial. We have investigated the contribution of NO to hyperaemia evoked by isometric twitch contractions in its own right and in interaction with adenosine. In three groups of anaesthetized rats the effect of A(2A)-receptor inhibition with ZM241385 on femoral vascular conductance (FVC) and hindlimb O(2) consumption at rest and during isometric twitch contractions (4 Hz) was tested (i) after NO synthase inhibition with l-NAME, and when FVC had been restored by infusion of (ii) an NO donor (SNAP) or (iii) cell-permeant cGMP. Exercise hyperaemia was significantly reduced (32%) by l-NAME and further significantly attenuated by ZM241385 (60% from control). After restoring FVC with SNAP or 8-bromo-cGMP, l-NAME did not affect exercise hyperaemia, but ZM241385 still significantly reduced the hyperaemia by 25%. There was no evidence that NO limited muscle during contraction. These results indicate that NO is not required for adenosine release during contraction and that adenosine released during contraction does not depend on new synthesis of NO to produce vasodilatation. They also substantiate our general hypothesis that the mechanisms by which adenosine contributes to muscle vasodilatation during systemic hypoxia and exercise are different: we propose that, during muscle contraction, adenosine is released from skeletal muscle fibres independently of NO and acts directly on A(2A)-receptors on the vascular smooth muscle to cause vasodilatation.
运动性充血部分由腺苷A(2A)受体介导。腺苷可通过内皮A(2A)受体引发一氧化氮(NO)释放,但NO在运动性充血中的作用存在争议。我们研究了NO本身以及与腺苷相互作用时对等长收缩诱发的充血的贡献。在三组麻醉大鼠中,测试了用ZM241385抑制A(2A)受体对静息和等长收缩(4 Hz)期间股血管传导(FVC)和后肢O(2)消耗的影响:(i)在用l-NAME抑制一氧化氮合酶后,以及当通过输注(ii)NO供体(SNAP)或(iii)细胞渗透性cGMP恢复FVC后。l-NAME使运动性充血显著减少(32%),而ZM241385使其进一步显著减弱(比对照减少60%)。在用SNAP或8-溴-cGMP恢复FVC后,l-NAME不影响运动性充血,但ZM241385仍使充血显著减少25%。没有证据表明NO在收缩过程中限制肌肉。这些结果表明,收缩过程中腺苷释放不需要NO,且收缩过程中释放的腺苷产生血管舒张不依赖于NO的新合成。它们还证实了我们的一般假设,即腺苷在全身缺氧和运动期间促成肌肉血管舒张的机制不同:我们提出,在肌肉收缩期间,腺苷从骨骼肌纤维中释放,独立于NO,并直接作用于血管平滑肌上的A(2A)受体以引起血管舒张。