Basille M, Gonzalez B J, Fournier A, Vaudry H
Institut Fédératif de Recherches Multidisciplinaires sur les Peptides, Unité INSERM U 413, Unité affilieé au CNRS, Faculté des Sciences, Université de Rouen, Mont-Saint-Aignan, France.
Brain Res Dev Brain Res. 1994 Oct 14;82(1-2):81-9. doi: 10.1016/0165-3806(94)90150-3.
Pituitary adenylate cyclase-activating polypeptide and PACAP receptors are both present in the rat cerebellar cortex, suggesting that PACAP may play an important role in the cerebellum. In the present study, the variation of the concentration of PACAP binding sites in the rat cerebellum was investigated during postnatal development by means of quantitative autoradiography, using [125I]PACAP27 as a radioligand. In the external granule cell layer and the medulla, the density of PACAP binding sites was high at birth, markedly decreased from postnatal day 8 (P8) to P25 and finally vanished at the end of the third postnatal week. In the internal granule cell layer and molecular layer, PACAP binding sites were first detected at P8. In the internal granule cell layer, the density of binding sites slightly decreased during development but remained elevated in adults. Conversely, in the molecular layer, PACAP binding sites rapidly decreased during the second and third postnatal weeks and virtually disappeared after P25. In all four layers of the cerebellar cortex, the autoradiographic labeling was displaced by PACAP27 (IC50 close to 10(-8) M), but was not affected by VIP. No significant changes in IC50 and Hill coefficient were noticed in the various layers throughout development. The present study shows that all four layers of the cerebellar cortex express PACAP binding sites during development. The evolution of the receptor concentration exhibited differential profiles in the various layers but the specificity characteristics of the recognition sites were identical in all four structures.(ABSTRACT TRUNCATED AT 250 WORDS)
垂体腺苷酸环化酶激活多肽(PACAP)及其受体均存在于大鼠小脑皮质中,这表明PACAP可能在小脑中发挥重要作用。在本研究中,以[125I]PACAP27作为放射性配体,采用定量放射自显影术研究了大鼠小脑在出生后发育过程中PACAP结合位点浓度的变化。在外部颗粒细胞层和髓质中,PACAP结合位点的密度在出生时较高,从出生后第8天(P8)到P25显著降低,最终在出生后第三周结束时消失。在内部颗粒细胞层和分子层中,PACAP结合位点在P8时首次被检测到。在内部颗粒细胞层中,结合位点的密度在发育过程中略有下降,但在成年后仍保持升高。相反,在分子层中,PACAP结合位点在出生后第二和第三周迅速减少,在P25后几乎消失。在小脑皮质的所有四层中,放射自显影标记被PACAP27取代(IC50接近10^(-8) M),但不受血管活性肠肽(VIP)影响。在整个发育过程中,各层的IC50和希尔系数均未发现显著变化。本研究表明,小脑皮质的所有四层在发育过程中均表达PACAP结合位点。受体浓度的演变在各层中呈现出不同的模式,但识别位点的特异性特征在所有四个结构中是相同的。(摘要截断于250字)