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Inhibition of noradrenaline release by adenosine.

机译:腺苷抑制去甲肾上腺素释放。

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摘要

1. Release of [3H]noradrenaline evoked by stimulation (5 Hz) of the pre-labelled rat vas deferens was reduced to 50% by adenosine (10(-6) g/ml.). Inhibition of release was dependent on the concentration of adenosine and was inversely related to the frequency of stimulation. Phenoxybenzamine did not interfere with the action of adenosine on release. 2. Exposure of the pre-labelled rat vas deferens to 135 mM-K+ released almost 10 times more [3H]noradrenaline than exposure to 45 mM-K+. Release induced by 45 mM-K+ was almost abolished by adenosine (10(-6) g/ml.) but that induced by 135 mM-K+ was reduced to only 45%. 3. Inhibition of [3H]noradrenaline release was observed in salivary gland, heart and portal vein of the rat, and in the guinea-pig heart and vas deferens. A very high concentration of adenosine (10(-4) g/ml.) reduced the release (about 50%) in the rabbit heart, but the cat heart was totally insensitive to the inhibitory action of adenosine. 4. Aminophylline (2 x 10(-4) g/ml.) antagonized the inhibitory action of adenosine (10(-6) g/ml.) on the release of [3H]noradrenaline in the phenoxybenzamine-treated vas deferens. 5. Tetraethylammonium (8 x 10(-4) g/ml.) enhanced stimulation-evoked release in the rat salivary gland by almost tenfold. In the presence of tetraethylammonium, even higher concentrations (2 x 10(-5) g/ml.) of adenosine failed to interfere with release. 6. Elevation of external K+ (19 mM) blocked stimulation-evoked release in the rat vas deferens by about 55%. Combination of high K+ and adenosine (10(-6) g/ml.), which blocked release by about 40%, caused still greater inhibition (80%) of the release. 7. The possible mechanism of action of the inhibitory effect of adenosine on the stimulation-evoked release of noradrenaline is discussed in relation to the calcium hypothesis.
机译:1.腺苷(10(-6)g / ml)将预先标记的大鼠输精管的刺激(5 Hz)引起的[3H]去甲肾上腺素的释放降低至50%。释放的抑制取决于腺苷的浓度,并且与刺激的频率成反比。苯氧基苯甲胺不干扰腺苷释放的作用。 2.将预先标记的大鼠输精管暴露于135 mM-K +,释放的[3H]去甲肾上腺素比暴露于45 mM-K +几乎多10倍。腺苷(10(-6)g / ml。)几乎消除了由45 mM-K +诱导的释放,但由135 mM-K +诱导的释放降低至仅45%。 3.在大鼠的唾液腺,心脏和门静脉以及豚鼠的心脏和输精管中观察到[3 H]去甲肾上腺素释放的抑制作用。很高浓度的腺苷(10(-4)g / ml。)减少了兔心脏中的释放(约50%),但猫心脏对腺苷的抑制作用完全不敏感。 4.氨茶碱(2 x 10(-4)g / ml。)拮抗腺苷(10(-6)g / ml。)对苯氧基苯扎明处理的输精管中[3H]去甲肾上腺素释放的抑制作用。 5.四乙铵(8 x 10(-4)g / ml。)将大鼠唾液腺中刺激诱发的释放增强了近十倍。在存在四乙铵的情况下,甚至更高浓度(2 x 10(-5)g / mL。)的腺苷也无法干扰释放。 6.外部K +(19 mM)升高阻止了大鼠输精管中刺激诱发的释放约55%。高K +和腺苷(10(-6)g / ml。)的组合,阻止了约40%的释放,导致更大的释放抑制(80%)。 7.结合钙假说,讨论了腺苷抑制去甲肾上腺素刺激释放释放的可能作用机理。

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