Loiacono R E, Story D F
Naunyn Schmiedebergs Arch Pharmacol. 1986 Sep;334(1):40-7. doi: 10.1007/BF00498738.
Evidence was sought for the existence on cholinergic nerve terminals in guinea-pig atria of alpha-adrenoceptors subserving inhibition of acetylcholine release. The experiments were performed with atria which had been incubated with 3H-choline and transmitter release was deduced from the efflux of radioactivity elicited by field stimulation. In preparations which had been incubated with 3H-choline, field stimulation (60 pulses, 2 Hz) evoked release and radioactivity which was inhibited by 1.0 mumol/l noradrenaline, in the presence of propranolol (1.0 mumol/l), but was unaltered by clonidine (1.0 and 10.0 mumol/l). The inhibitory effect noradrenaline on the stimulation-induced efflux of radioactivity was blocked by idazoxan (0.3 mumol/l), and phentolamine (1.0 mumol/l) but not by prazosin (0.3 mumol/l). In the presence of propranolol (1.0 mumol/l), neither phentolamine (1.0 mumol/l), idazoxan (0.3 mumol/l) nor prazosin (0.3 mumol/l) had any effect on stimulation-induced efflux of radioactivity. Stimulation of the extrinsic vagus nerve of atrial preparations with trains of pulses at frequencies of 2, 4, 8, and 16 Hz produced graded decreases in the rate of atrial beating. The negative chronotropic responses to vagus stimulation were unaffected by noradrenaline (1.0 mumol/l) in the presence of propranolol (1.0 mumol/l). These findings indicate that the release of acetylcholine from the cholinergic terminals in guinea-pig atria can be inhibited by a mechanism apparently involving prejunctional alpha 2-adrenoceptors. However, under the experimental conditions used here the chronotropic responses of atria to stimulation of the extrinsic vagus nerve was not affected by activation of the prejunctional alpha 2-adrenoceptors associated with the cholinergic terminals.
在豚鼠心房的胆碱能神经末梢上,寻找有助于抑制乙酰胆碱释放的α-肾上腺素能受体存在的证据。实验使用预先用³H-胆碱孵育过的心房进行,通过场刺激引发的放射性流出量来推断递质释放。在用³H-胆碱孵育过的标本中,场刺激(60个脉冲,2赫兹)诱发释放和放射性,在普萘洛尔(1.0微摩尔/升)存在的情况下,1.0微摩尔/升去甲肾上腺素可抑制这种释放和放射性,但可乐定(1.0和10.0微摩尔/升)对其无影响。去甲肾上腺素对刺激诱导的放射性流出的抑制作用可被咪唑克生(0.3微摩尔/升)和酚妥拉明(1.0微摩尔/升)阻断,但不被哌唑嗪(0.3微摩尔/升)阻断。在普萘洛尔(1.0微摩尔/升)存在的情况下,酚妥拉明(1.0微摩尔/升)、咪唑克生(0.3微摩尔/升)和哌唑嗪(0.3微摩尔/升)对刺激诱导的放射性流出均无影响。用频率为2、4、8和16赫兹的脉冲串刺激心房标本的外在迷走神经,可使心房跳动速率逐渐降低。在普萘洛尔(1.0微摩尔/升)存在的情况下,去甲肾上腺素(1.0微摩尔/升)不影响迷走神经刺激引起的负性变时反应。这些发现表明,豚鼠心房胆碱能末梢释放乙酰胆碱可被一种显然涉及节前α₂-肾上腺素能受体的机制所抑制。然而,在此处使用的实验条件下,心房对刺激外在迷走神经的变时反应不受与胆碱能末梢相关的节前α₂-肾上腺素能受体激活的影响。