Gulya K, Budai D, Kása P
Central Research Laboratory, Albert Szent-Györgyi Medical University, Szeged, Hungary.
Neurochem Int. 1989;15(2):153-6. doi: 10.1016/0197-0186(89)90094-6.
The effects of atropine, pirenzepine and AF-DX 116 on the high K(+)-evoked release of endogenous ACh from rat hippocampal slices were compared. As expected, atropine in concentrations of 10(?5) and 10(?6)M increased the release of acetylcholine, to 128 and 157% of the control value, respectively. While AF-DX 116 was also able to increase the release to 148 and 156% of the control value at the above concentrations, pirenzepine had no effect on the release. This may indicate that no M(1) receptors are involved in the control of presynaptic acetylcholine release, probably because of their postsynaptic localization, and that the presynaptic muscarinic cholinergic autoreceptors are equivalent to the M(2) receptors in rat hippocampus.
比较了阿托品、哌仑西平和AF-DX 116对高钾诱发大鼠海马切片内源性乙酰胆碱释放的影响。正如预期的那样,浓度为10⁻⁵和10⁻⁶M的阿托品分别将乙酰胆碱的释放增加至对照值的128%和157%。虽然在上述浓度下AF-DX 116也能够将释放增加至对照值的148%和156%,但哌仑西平对释放没有影响。这可能表明,M₁受体不参与突触前乙酰胆碱释放的控制,可能是因为它们位于突触后,并且突触前毒蕈碱胆碱能自身受体等同于大鼠海马中的M₂受体。