Moylan R D, Westfall T C
Blood Vessels. 1979;16(6):302-10. doi: 10.1159/000158220.
This study examined the effect of exogenously applied adenosine on the release of 3H-norepinephrine from the field-stimulated, superfused rat portal vein. Adenosine was found to inhibit the field-stimulated release of 3H-norepinephrine in a dose-dependent manner in 50- to 1,000-microM concentrations. The effect was reversed when adenosine was washed out. The inhibitory effects of adenosine were antagonized by theophylline (10-4 M) which by itself showed a slight enhancement of stimulated 3H-norepinephrine release. ATP was found to inhibit 3H-norepinephrine release at the same concentration as adenosine while inosine was inactive. When adenosine was tested in the presence of the muscarinic and alpha-adrenergic blocking agents atropine and phenoxybenzamine along with indomethacin, a prostaglandin synthesis inhibitor, its inhibotory effect on the stimulated release of 3H-norepinephrine persisted. It is concluded that adenosine and/or ATP can modulate the nerve-stimulated induced release of norepinephrine presumably by an action on the adrenergic nerve terminals.
本研究检测了外源性应用腺苷对电场刺激的、灌流的大鼠门静脉释放3H-去甲肾上腺素的影响。发现在50至1000微摩尔浓度范围内,腺苷以剂量依赖的方式抑制电场刺激的3H-去甲肾上腺素释放。当腺苷被洗脱时,该作用被逆转。腺苷的抑制作用被茶碱(10-4 M)拮抗,而茶碱本身显示出对刺激的3H-去甲肾上腺素释放有轻微增强作用。发现ATP在与腺苷相同的浓度下抑制3H-去甲肾上腺素释放,而肌苷无活性。当在毒蕈碱和α-肾上腺素能阻断剂阿托品和酚苄明以及前列腺素合成抑制剂吲哚美辛存在的情况下检测腺苷时,其对刺激的3H-去甲肾上腺素释放的抑制作用持续存在。得出的结论是,腺苷和/或ATP可能通过作用于肾上腺素能神经末梢来调节神经刺激诱导的去甲肾上腺素释放。