Burnstock G, Wong H
Br J Pharmacol. 1978 Feb;62(2):293-302. doi: 10.1111/j.1476-5381.1978.tb08459.x.
1 The responses of the guinea-pig taenia coli, urinary bladder, and the rabbit portal vein to ultraviolet (u.v.) light were compared to those elicited by purinergic nerve stimulation and exogenous adenosine triphosphate (ATP).2 In the presence of sodium nitrite, u.v. light between 340-380 nm produced a maximum relaxation of the taenia coli. The relaxation was reversible and fast in onset. It was unaffected by atropine, guanethidine or low concentrations of phentolamine or propranolol. When the tone was low, the relaxation was usually followed by a ;rebound contraction' upon cessation of stimulation. Thus, the response to u.v. light closely resembles the responses to both purinergic nerve stimulation and exogenously applied ATP.3 U.v. light did not initiate impulses in purinergic nerves since its action was unaffected by tetrodotoxin; nor did it release ATP from nerve terminals (in contrast to its release during purinergic nerve stimulation). The adenosine-uptake inhibitor, dipyridamole, which potentiates the responses to purinergic nerve stimulation and ATP, did not affect the response to u.v. light.4 Agents known to alter postjunctional responses to purinergic nerve stimulation and ATP also altered the response to u.v. light. High concentrations of the 2-substituted imidazoline compounds, antazoline and phentolamine, which antagonize the responses to purinergic nerve stimulation and ATP, reduced the responses to u.v. irradiation. The prostaglandin synthesis inhibitor, indomethacin, which abolishes the ;rebound contraction' following stimulation of purinergic nerves, also blocks the ;rebound ;contraction' following u.v. irradiation. Increases in the K(+) concentration produced parallel changes in the inhibitory responses to u.v. light and purinergic nerve stimulation.5 U.v. light produced relaxation and inhibition of spontaneous activity of the rabbit portal vein (relaxed by ATP), but had no effect on the guinea-pig urinary bladder (contracted by ATP) and ureter (unaffected by ATP).6 It is suggested that u.v. light is acting on some part of the purinergic receptor complex which is involved in the mediation of inhibitory responses to ATP and purinergic nerve stimulation, and may therefore provide a way of investigating the chemistry of inhibitory purinergic receptors.
将豚鼠结肠带、膀胱以及兔门静脉对紫外线(uv)的反应与嘌呤能神经刺激和外源性三磷酸腺苷(ATP)所引发的反应进行了比较。
在亚硝酸钠存在的情况下,340 - 380纳米之间的紫外线使结肠带产生最大程度的松弛。这种松弛是可逆的,且起效迅速。它不受阿托品、胍乙啶或低浓度酚妥拉明或普萘洛尔的影响。当张力较低时,刺激停止后,松弛通常会接着出现“反跳性收缩”。因此,对紫外线的反应与对嘌呤能神经刺激和外源性ATP的反应极为相似。
紫外线不会在嘌呤能神经中引发冲动,因为其作用不受河豚毒素的影响;它也不会从神经末梢释放ATP(与嘌呤能神经刺激期间的释放情况相反)。腺苷摄取抑制剂双嘧达莫可增强对嘌呤能神经刺激和ATP的反应,但对紫外线的反应没有影响。
已知能改变对嘌呤能神经刺激和ATP的节后反应的药物,也会改变对紫外线的反应。高浓度的2 - 取代咪唑啉化合物安他唑啉和酚妥拉明可拮抗对嘌呤能神经刺激和ATP的反应,它们会降低对紫外线照射的反应。前列腺素合成抑制剂吲哚美辛可消除嘌呤能神经刺激后的“反跳性收缩”,它也会阻断紫外线照射后的“反跳性收缩”。钾离子浓度的增加会使对紫外线和嘌呤能神经刺激的抑制反应产生平行变化。
紫外线可使兔门静脉松弛并抑制其自发活动(ATP可使其松弛),但对豚鼠膀胱(ATP可使其收缩)和输尿管(不受ATP影响)没有作用。
有人提出,紫外线作用于嘌呤能受体复合物的某些部分,这些部分参与介导对ATP和嘌呤能神经刺激的抑制反应,因此可能为研究抑制性嘌呤能受体的化学性质提供一种方法。