Burnstock G, Warland J J
Br J Pharmacol. 1987 Jan;90(1):111-20. doi: 10.1111/j.1476-5381.1987.tb16830.x.
Mechanical responses to transmural electrical stimulation were recorded in isolated transverse ring preparations of rabbit saphenous artery. Electrical stimulation for a period of 1 s produced a rapid monophasic contraction and, for a period of 1 min, a biphasic contraction consisting of a rapid constriction followed by a slower sustained constriction. All contractions were abolished in the presence of tetrodotoxin (1 microgram ml-1) or guanethidine (4 microM). After desensitization of the P2-purinoceptor with alpha,beta-methylene ATP, contractions to electrical stimulation for 1 s were reduced significantly at all frequencies tested: responses evoked by stimulation at 4 Hz were usually almost completely inhibited, whereas those evoked by stimulation at 64 Hz were only partially inhibited. On the other hand, in the presence of the alpha-adrenoceptor antagonist, prazosin, neurogenic contractions were only partially reduced: at 4 Hz there was no significant reduction in the neurogenic contractions while at 32 and 64 Hz, contractions were reduced by an average of 20 and 28% respectively. Usually all contractions were abolished by a combination of the two drugs. Prazosin antagonized contractions of the vessel to exogenously applied noradrenaline but not to ATP, whereas desensitization of the P2-purinoceptor with alpha,beta-methylene ATP blocked responses to ATP but not those to noradrenaline. The concentration response curve to histamine was not affected by treatment of the vessel with prazosin, or after desensitization of the P2-purinoceptor with alpha,beta-methylene ATP. These results suggest that noradrenaline and ATP are co-released from sympathetic nerves supplying the rabbit saphenous artery, both substances being involved in the mechanical contractions of this tissue. Further, the ratio of ATP to noradrenaline involved in these mechanical contractions is dependent upon the frequency of stimulation, but at all frequencies tested the purinergic component is greater than the adrenergic component.
在兔隐动脉的离体横向环制备物中记录对跨壁电刺激的机械反应。持续1秒的电刺激产生快速单相收缩,持续1分钟的电刺激产生双相收缩,包括快速收缩后接着缓慢持续收缩。在存在河豚毒素(1微克/毫升)或胍乙啶(4微摩尔)时,所有收缩均被消除。用α,β-亚甲基ATP使P2嘌呤受体脱敏后,在所有测试频率下,持续1秒的电刺激引起的收缩均显著降低:4赫兹刺激引起的反应通常几乎完全被抑制,而64赫兹刺激引起的反应仅部分被抑制。另一方面,在存在α-肾上腺素能受体拮抗剂哌唑嗪的情况下,神经源性收缩仅部分降低:在4赫兹时,神经源性收缩无显著降低,而在32和64赫兹时,收缩分别平均降低20%和28%。通常,两种药物联合使用可消除所有收缩。哌唑嗪可拮抗血管对外源性去甲肾上腺素的收缩,但对ATP无作用,而用α,β-亚甲基ATP使P2嘌呤受体脱敏可阻断对ATP的反应,但不阻断对去甲肾上腺素的反应。用哌唑嗪处理血管或用α,β-亚甲基ATP使P2嘌呤受体脱敏后,对组胺的浓度反应曲线不受影响。这些结果表明,去甲肾上腺素和ATP从供应兔隐动脉的交感神经共同释放,这两种物质均参与该组织的机械收缩。此外,参与这些机械收缩的ATP与去甲肾上腺素的比例取决于刺激频率,但在所有测试频率下,嘌呤能成分均大于肾上腺素能成分。