Kato A C, Collier B, Ilson D, Wright J M
Can J Physiol Pharmacol. 1975 Dec;53(6):1050-7. doi: 10.1139/y75-146.
Atropine is known to increase the release of acetylcholine (ACh) from cerebral cortex, and the present experiments tested the effect of this drug upon ACh release in the superior cervical ganglion of the cat. The release of ACh was measured by a radio-enzymic method, which was shown to provide an estimate of the ACh content of samples collected from perfused ganglia that was similar (102%) to that obtained by the method of bioassay more usually used . Atropine (3 X 10(-6) M) increased (3.5 to 4-fold) the amount of ACh released by rat's sliced cerebral cortex incubated in a high (23 mM) potassium medium. However atropine (3 X 10(-6)-3 X 10(-5) M) did not change the amount of ACh released by ganglia during preganglionic nerve stimulation (5-10 Hz). It is concluded that cholinergic nerve terminals in different tissues appear to have different pharmacological properties.
已知阿托品可增加大脑皮层乙酰胆碱(ACh)的释放,本实验测试了该药物对猫颈上神经节中ACh释放的影响。采用放射酶法测定ACh的释放,结果表明该方法对从灌注神经节收集的样本中ACh含量的估计与通常使用的生物测定法相似(102%)。阿托品(3×10⁻⁶ M)可使在高钾(23 mM)培养基中孵育的大鼠大脑皮层切片释放的ACh量增加(3.5至4倍)。然而,阿托品(3×10⁻⁶ - 3×10⁻⁵ M)在节前神经刺激(5 - 10 Hz)期间并未改变神经节释放的ACh量。由此得出结论,不同组织中的胆碱能神经末梢似乎具有不同的药理学特性。