Grailhe Régis, Cardona Ana, Even Naïla, Seif Isabelle, Changeux Jean-Pierre, Cloëz-Tayarani Isabelle
Institut Pasteur URA CNRS D 2182, 28 rue du Docteur Roux, 75015 Paris, France.
Brain Res Bull. 2009 Mar 30;78(6):283-9. doi: 10.1016/j.brainresbull.2008.12.004. Epub 2008 Dec 25.
Elevated brain monoamine concentrations resulting from monoamine oxidase A genetic ablation (MAOA knock-out mice) lead to changes in other neurotransmitter systems. To investigate the consequences of MAOA deficiency on the cholinergic system, we measured ligand binding to the high-affinity choline transporter (CHT1) and to muscarinic and nicotinic receptors in brain sections of MAOA knock-out (KO) and wild-type mice. A twofold increase in [(3)H]-hemicholinium-3 ([(3)H]-HC-3) binding to CHT1 was observed in the caudate putamen, nucleus accumbens, and motor cortex in MAOA KO mice as compared with wild-type (WT) mice. There was no difference in [(3)H]-HC-3 labeling in the hippocampus (dentate gyrus) between the two genotypes. Binding of [(125)I]-epibatidine ([(125)I]-Epi), [(125)I]-alpha-bungarotoxin ([(125)I]-BGT), [(3)H]-pirenzepine ([(3)H]-PZR), and [(3)H]-AFDX-384 ([(3)H]-AFX), which respectively label high- and low-affinity nicotinic receptors, M1 and M2 muscarinic cholinergic receptors, was not modified in the caudate putamen, nucleus accumbens, and motor cortex. A small but significant decrease of 19% in M1 binding densities was observed in the hippocampus (CA1 field) of KO mice. Next, we tested acetylcholinesterase activity and found that it was decreased by 25% in the striatum of KO mice as compared with WT mice. Our data suggest that genetic deficiency in MAOA enzyme is associated with changes in cholinergic activity, which may account for some of the behavioral alterations observed in mice and humans lacking MAOA.
单胺氧化酶A基因敲除(MAOA基因敲除小鼠)导致脑内单胺浓度升高,进而引起其他神经递质系统的变化。为了研究MAOA缺乏对胆碱能系统的影响,我们测定了MAOA基因敲除(KO)小鼠和野生型小鼠脑切片中高亲和力胆碱转运体(CHT1)以及毒蕈碱型和烟碱型受体的配体结合情况。与野生型(WT)小鼠相比,MAOA基因敲除小鼠的尾壳核、伏隔核和运动皮层中,[(3)H]-半胱氨酸三甲铵([(3)H]-HC-3)与CHT1的结合增加了两倍。两种基因型小鼠海马体(齿状回)的[(3)H]-HC-3标记没有差异。[(125)I]-埃博霉素([(125)I]-Epi)、[(125)I]-α-银环蛇毒素([(125)I]-BGT)、[(3)H]-哌仑西平([(3)H]-PZR)和[(3)H]-AFDX-384([(3)H]-AFX)分别标记高亲和力和低亲和力烟碱型受体、M1和M2毒蕈碱型胆碱能受体,其在尾壳核、伏隔核和运动皮层中的结合未发生改变。在基因敲除小鼠的海马体(CA1区)中,M1结合密度有小幅但显著的19%的下降。接下来,我们检测了乙酰胆碱酯酶活性,发现与野生型小鼠相比,基因敲除小鼠纹状体中的乙酰胆碱酯酶活性降低了25%。我们的数据表明,MAOA酶的基因缺陷与胆碱能活性的变化有关,这可能解释了在缺乏MAOA的小鼠和人类中观察到的一些行为改变。