Butt C M, Pauly J R, Wilkins L H, Dwoskin L P, Debski E A
School of Biological Sciences, University of Kentucky, 101 T. H. Morgan Building, Lexington, KY 40506-0225, USA.
Neuroscience. 2001;104(1):161-79. doi: 10.1016/s0306-4522(01)00048-3.
Visually evoked behaviors mediated by the frog optic tectum require cholinergic activity, but the receptor subtypes through which acetylcholine acts are not yet identified. Using quantitative autoradiography and scintillation spectrometry, we examined the binding of [3H]pirenzepine and [3H]AF-DX 384 in the laminated optic tectum of the frog. In mammalian systems, these substances bind excitatory (m1 and m3 subtypes) and inhibitory (m2 and m4 subtypes) muscarinic acetylcholine receptors, respectively. Pharmacological analyses, including the use of specific muscarinic toxins, confirmed the subtype selectivity of the radioligands in the frog brain. Binding sites for [3H]pirenzepine were distinct from those for [3H]AF-DX 384. In the adult tectum, [3H]pirenzepine demonstrated specific binding in tectal layers 5-9. [3H]Pirenzepine binding was also present in tadpoles as young as stage V, but all sampled stages of tadpole tectum had significantly less binding when compared to adults. Lesioning of the optic nerve had no effect on [3H]pirenzepine binding. Specific [3H]AF-DX 384 binding was found in all layers of the adult tectum. All sampled tadpole stages exhibited binding sites for [3H]AF-DX 384, but the densities of these sites were also significantly higher in adults than they were in developing stages. Short-term lesions of the optic nerve reduced [3H]AF-DX 384 binding in all tectal layers of the deafferented lobe when compared to the afferented one. Long-term lesions decreased [3H]AF-DX 384 sites in both lobes.These results indicate that multiple muscarinic acetylcholine receptor binding sites reside in the frog optic tectum at all stages of development, and their pharmacology resembles that of mammalian m1/m3, m2 and m4 subtypes. Our data indicate that few, if any, of these receptors are likely to be located on retinal ganglion cell terminals. Furthermore, the expression of inhibitory muscarinic subtypes seems to be regulated by different mechanisms than that for excitatory subtypes.
由青蛙视顶盖介导的视觉诱发行为需要胆碱能活性,但乙酰胆碱发挥作用的受体亚型尚未确定。我们使用定量放射自显影术和闪烁光谱法,研究了[3H]哌仑西平和[3H]AF-DX 384在青蛙分层视顶盖中的结合情况。在哺乳动物系统中,这些物质分别与兴奋性(m1和m3亚型)和抑制性(m2和m4亚型)毒蕈碱型乙酰胆碱受体结合。药理学分析,包括使用特定的毒蕈碱毒素,证实了放射性配体在青蛙大脑中的亚型选择性。[3H]哌仑西平的结合位点与[3H]AF-DX 384的不同。在成年顶盖中,[3H]哌仑西平在顶盖第5 - 9层显示出特异性结合。[3H]哌仑西平结合在V期幼体蝌蚪中也存在,但与成年个体相比,所有取样阶段的蝌蚪顶盖结合量都显著减少。视神经损伤对[3H]哌仑西平结合没有影响。在成年顶盖的所有层中都发现了特异性的[3H]AF-DX 384结合。所有取样的蝌蚪阶段都表现出[3H]AF-DX 384的结合位点,但这些位点的密度在成年个体中也显著高于发育阶段。与传入叶相比,视神经的短期损伤降低了去传入叶所有顶盖层中[3H]AF-DX 384的结合。长期损伤使两个叶中的[3H]AF-DX 384位点减少。这些结果表明,在青蛙发育的所有阶段,视顶盖中都存在多个毒蕈碱型乙酰胆碱受体结合位点,它们的药理学特性类似于哺乳动物的m1/m3、m2和m4亚型。我们的数据表明,这些受体中即使有也很少可能位于视网膜神经节细胞终末。此外,抑制性毒蕈碱亚型的表达似乎受与兴奋性亚型不同的机制调控。