Cubeddu L X, Hoffmann I S
J Neurochem. 1983 Jul;41(1):94-101. doi: 10.1111/j.1471-4159.1983.tb11818.x.
The release of [3H]dopamine (DA) and [14C]acetylcholine (ACh) was monitored from single slices of the rabbit striatum. In all cases, the evoked overflow of ACh showed a higher peak and was of shorter duration than that of 3H products. For ACh, the release per pulse showed a marked decline with increasing frequency of stimulation, whereas flat frequency-release curves were obtained for DA. At 0.1 and 1 Hz the evoked overflows of ACh were 15 and 7 times greater, respectively, than those of DA. Haloperidol (0.03 microM) and sulpiride (1 microM) produced large increases in the evoked overflow of DA and ACh at 3 and 10 Hz; little effect was observed at lower frequencies. These results indicate that the frequency-release curves for DA and ACh are different and that at high frequencies the slope of the curves is modified by activation of pre- and postsynaptic DA receptors. Apomorphine inhibited in a concentration-dependent fashion the evoked overflow of DA and ACh; greater inhibition was obtained at lower frequencies of stimulation. At 0.3 Hz the DA agonist was two times more potent in inhibiting DA than ACh overflow (IC50: 12.0 +/- 2.2 versus 22.0 +/- 2.8 nM; p less than 0.01). The greater sensitivity of pre- than postsynaptic sites to apomorphine was also seen at higher frequencies (3 Hz). Benztropine (1 microM) reduced the evoked overflow of ACh at 10 Hz, and enhanced that of 3H products at all rates of stimulation (0.3-10 Hz). These results suggest that the release of DA and ACh is regulated by dopaminergic receptors. They also indicate that the effects of DA agonists and antagonists and of uptake inhibitors on DA and ACh release are highly dependent on the frequency of stimulation used.
从兔纹状体的单个切片中监测[3H]多巴胺(DA)和[14C]乙酰胆碱(ACh)的释放。在所有情况下,诱发的ACh溢出显示出更高的峰值,且持续时间比3H产物的短。对于ACh,每个脉冲的释放量随刺激频率增加而显著下降,而DA则获得了平稳的频率-释放曲线。在0.1和1 Hz时,诱发的ACh溢出分别比DA溢出大15倍和7倍。氟哌啶醇(0.03 microM)和舒必利(1 microM)在3和10 Hz时使诱发的DA和ACh溢出大幅增加;在较低频率时观察到的影响较小。这些结果表明,DA和ACh的频率-释放曲线不同,并且在高频时,曲线斜率会因突触前和突触后DA受体的激活而改变。阿扑吗啡以浓度依赖性方式抑制诱发的DA和ACh溢出;在较低刺激频率下获得更大的抑制作用。在0.3 Hz时,DA激动剂抑制DA溢出的效力比抑制ACh溢出的效力高两倍(IC50:12.0 +/- 2.2对22.0 +/- 2.8 nM;p小于0.01)。在较高频率(3 Hz)时也观察到突触前位点比突触后位点对阿扑吗啡更敏感。苯海索(1 microM)在10 Hz时降低了诱发的ACh溢出,并在所有刺激速率(0.3 - 10 Hz)下增强了3H产物的溢出。这些结果表明,DA和ACh的释放受多巴胺能受体调节。它们还表明,DA激动剂、拮抗剂和摄取抑制剂对DA和ACh释放的影响高度依赖于所用的刺激频率。