Walsh Martin P, Marshall Janice M
Department of Physiology, The Medical School, Birmingham B15 2TT, UK.
J Physiol. 2006 Aug 15;575(Pt 1):277-89. doi: 10.1113/jphysiol.2006.108779. Epub 2006 May 11.
Experiments were performed on anaesthetized normoxic (N) rats and chronically hypoxic rats that had been exposed to 12% O2 for 1, 3 or 7 days (1, 3 or 7CH rats). The adenosine A1 receptor antagonist DPCPX did not affect the resting hyperventilation of 1-7CH rats breathing 12% O2 and increased resting heart rate (HR) in 1CH rats only. DPCPX partially restored the decreased baseline arterial pressure (ABP) and increased femoral vascular conductance (FVC) of 1 and 3CH rats, but had no effect in N or 7CH rats. DPCPX also attenuated the decrease in arterial blood pressure (ABP) and increase in FVC evoked by acute hypoxia in N and 1-7CH rats. The non-selective adenosine receptor antagonist 8-SPT had no further effect on baselines or cardiovascular responses to acute hypoxia, but attenuated the hypoxia-evoked increase in respiratory frequency in 1-7CH rats. In N, and 1 and 3CH rats, the inducible nitric oxide synthase (iNOS) inhibitor aminoguanidine had no effect on baselines or increases in FVC evoked by acetylcholine. We propose: (i) that tonically released adenosine acting on A1 receptors reduces HR in 1CH rats and stimulates endothelial NOS in 1 and 3CH rats to decrease ABP and increase FVC, the remaining NO-dependent tonic vasodilatation being independent of iNOS activity; (ii) that in 7CH rats, tonic adenosine release has waned; (iii) that in 1-7CH rats, adenosine released by acute hypoxia stimulates A1 but not A2 receptors to produce muscle vasodilatation, and stimulates carotid body A2 receptors to increase respiration.
实验在麻醉的常氧(N)大鼠和慢性低氧大鼠身上进行,慢性低氧大鼠暴露于12%氧气环境1、3或7天(分别为1CH、3CH或7CH大鼠)。腺苷A1受体拮抗剂DPCPX对呼吸12%氧气的1 - 7CH大鼠的静息过度通气无影响,仅使1CH大鼠的静息心率(HR)增加。DPCPX部分恢复了1CH和3CH大鼠降低的基线动脉血压(ABP)并增加了股血管传导性(FVC),但对N大鼠或7CH大鼠无影响。DPCPX还减弱了N大鼠和1 - 7CH大鼠急性低氧诱发的动脉血压(ABP)降低和FVC增加。非选择性腺苷受体拮抗剂8 - SPT对基线或急性低氧的心血管反应无进一步影响,但减弱了1 - 7CH大鼠低氧诱发的呼吸频率增加。在N大鼠以及1CH和3CH大鼠中,诱导型一氧化氮合酶(iNOS)抑制剂氨基胍对基线或乙酰胆碱诱发的FVC增加无影响。我们提出:(i)持续释放的腺苷作用于A1受体降低1CH大鼠的心率,并刺激1CH和3CH大鼠的内皮型一氧化氮合酶以降低ABP并增加FVC,其余依赖一氧化氮的持续性血管舒张独立于iNOS活性;(ii)在7CH大鼠中,腺苷的持续释放已经减弱;(iii)在1 - 7CH大鼠中,急性低氧释放的腺苷刺激A1而非A2受体以产生肌肉血管舒张,并刺激颈动脉体A2受体以增加呼吸。