Eva C, Fusco M, Bono C, Tria M A, Ricci Gamalero S, Leon A, Genazzani E
Istituto di Farmacologia e Terapia Sperimentale, Università di Torino, Italy.
Brain Res Mol Brain Res. 1992 Aug;14(4):344-51. doi: 10.1016/0169-328x(92)90102-h.
The effect of nerve growth factor (NGF) on muscarinic receptor subtypes was investigated in a primary culture of telencephalic neurons prepared from neonatal rats. The treatment with 100 ng/ml of NGF significantly enhanced choline acetyltransferase (ChAT) activity and intracellular acetylcholine (ACh) content during cultivation. The same treatment induced an early transient increase of the number of muscarinic cholinergic receptors (mAChR), as measured by [3H]quinuclidinyl benzilate binding to cell homogenate, that was followed by a dramatic decrease of the receptor density from the 9th day of culture. Atropine completely prevented the decrease of the maximal number of muscarinic recognition sites induced by NGF. Prolonged exposure of telencephalic neurons to NGF also induced a significant reduction of the relative content of the messenger RNA (mRNA) encoding m1 and m3 receptors, while the m4 transcript was increased by the treatment. We suggest that the prolonged stimulation of cholinergic neurons by NGF induces a downregulation of m1 and m3 mAChR and their mRNAs on the postsynaptic site, while it increases the synthesis of the functionally distinct m4 receptor subtype, which might be presynaptically localized on cholinergic neurons. The transient increase of the receptor number that occurs at the first days of culture was not paralleled by changes in the relative content of mAChR mRNAs and might be associated with the trophic activity of NGF on cholinergic synapses during early development.
在新生大鼠制备的端脑神经元原代培养物中,研究了神经生长因子(NGF)对毒蕈碱受体亚型的影响。在培养过程中,用100 ng/ml的NGF处理可显著增强胆碱乙酰转移酶(ChAT)活性和细胞内乙酰胆碱(ACh)含量。同样的处理诱导了毒蕈碱胆碱能受体(mAChR)数量的早期短暂增加,这通过[3H]喹核醇基苯甲酸酯与细胞匀浆结合来测量,随后从培养的第9天起受体密度急剧下降。阿托品完全阻止了NGF诱导的毒蕈碱识别位点最大数量的减少。将端脑神经元长时间暴露于NGF也诱导了编码m1和m3受体的信使核糖核酸(mRNA)相对含量的显著降低,而m4转录本则因该处理而增加。我们认为,NGF对胆碱能神经元的长期刺激会诱导突触后位点m1和m3 mAChR及其mRNA的下调,同时增加功能不同的m4受体亚型的合成,m4受体亚型可能在胆碱能神经元上突触前定位。培养初期出现的受体数量短暂增加与mAChR mRNA相对含量的变化并不平行,可能与早期发育过程中NGF对胆碱能突触的营养活性有关。