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A(2A) 腺苷受体亚型在麻醉猫后肢功能性充血中的作用。

The role of the A(2A) adenosine receptor subtype in functional hyperaemia in the hindlimb of anaesthetized cats.

作者信息

Poucher S M

机构信息

Cardiovascular and Metabolism Department, Zeneca Pharmaceuticals, Macclesfield, Cheshire, UK.

出版信息

J Physiol. 1996 Apr 15;492 ( Pt 2)(Pt 2):495-503. doi: 10.1113/jphysiol.1996.sp021324.

Abstract
  1. The present study was designed to investigate the contribution of the A(2A) adenosine receptor subtype in the functional hyperaemia response during muscle contraction. 2. In cats anaesthetized with sodium pentobarbitone and breathing spontaneously following tracheotomy, the left sciatic and femoral nerves were electrically stimulated at 3 Hz for 20 min to induce muscle contraction, and hindlimb blood flow was measured with a flow probe. The contribution of the A(2A) adenosine receptor subtype was assessed using ZM 241385, a potent and selective A(2A) adenosine receptor antagonist. 3. In a control group, the muscle isometric tension measured in the extensor digitorum longus-tibialis anterior muscle group was 6.64 +/- 0.66 kg (100 g muscle mass)(-1) and hindlimb vascular conductance was 0.22 +/- 0.03 ml mmHg(-1)(kg body mass)(-1) at 20 min of contraction. Administration of vehicle did not affect these parameters upon a second contraction period: 6.31 +/- 0.61 kg (100 g muscle mass)(-1) and 0.23 +/- 0.03 ml mmHg(-1) (kg body mass)(-1), respectively. Total hindlimb conductance during contraction was unaffected (5.5 +/- 3.7% decrease). 4. ZM 241385 (1.0 mg kg(-1)) did not alter the amount of force produced by the muscle at 20 min of contraction. Hindlimb conductance response was reduced by 27.1 +/- 4.8% following the A(2A) selective adenosine receptor antagonist, similar to that observed with the non-selective antagonist 8-phenyltheophylline. 5. These results show that adenosine acting at the A(2A) subtype receptor can contribute up to 30% of the functional hyperaemia response in the hindlimb of anaesthetized cats.
摘要
  1. 本研究旨在探讨A(2A)腺苷受体亚型在肌肉收缩期间功能性充血反应中的作用。2. 在经戊巴比妥钠麻醉并在气管切开后自主呼吸的猫中,以3 Hz的频率对左坐骨神经和股神经进行20分钟的电刺激以诱导肌肉收缩,并用血流探头测量后肢血流量。使用强效选择性A(2A)腺苷受体拮抗剂ZM 241385评估A(2A)腺苷受体亚型的作用。3. 在对照组中,在收缩20分钟时,在趾长伸肌 - 胫骨前肌组中测量的肌肉等长张力为6.64±0.66 kg(100 g肌肉质量)(-1),后肢血管传导率为0.22±0.03 ml mmHg(-1)(kg体重)(-1)。在第二个收缩期给予赋形剂不影响这些参数:分别为6.31±0.61 kg(100 g肌肉质量)(-1)和0.23±0.03 ml mmHg(-1)(kg体重)(-1)。收缩期间总的后肢传导率未受影响(下降5.5±3.7%)。4. ZM 241385(1.0 mg kg(-1))在收缩20分钟时未改变肌肉产生的力量大小。在给予A(2A)选择性腺苷受体拮抗剂后,后肢传导率反应降低了27.1±4.8%,这与非选择性拮抗剂8 - 苯基茶碱观察到的情况相似。5. 这些结果表明,作用于A(2A)亚型受体的腺苷可在麻醉猫的后肢功能性充血反应中贡献高达30%。

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