Tasca C I, Cardoso L F, Vendite D, Souza D O
Departamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, Florianópolis, Brasil.
Neurochem Res. 1999 Aug;24(8):1067-74. doi: 10.1023/a:1021017112717.
Binding properties of the subtypes of adenosine A2 receptors in membrane preparations and the effects of adenosine receptor ligands on cAMP accumulation in slices from the optic tectum of neonatal chicks have been investigated. [3H]2-[4-(2-p-carboxyethyl)phenylamino]-5'-N-ethylcarboxaminoadenosin e (CGS 21680), a selective ligand for adenosine A2a receptors, did not bind to optic tectal membranes, as observed with rat striatal membranes. CGS 21680 also did not induce cyclic AMP accumulation in optic tectum slices. However, 5'-N-ethylcarboxamidoadenosine (NECA), 2-chloro-adenosine or adenosine induced a 2.5- to 3-fold increase on cyclic AMP accumulation in this preparation. [3H]NECA binds to fresh non-washed-membranes obtained from optic tectum of chicks, displaying one population of binding sites, which can be displaced by NECA, 8-phenyltheophylline, 2-chloro-adenosine, but is not affected by CGS 21680. The estimated K(D) value was 400.90 +/- 80.50 nM and the Bmax was estimated to be 2.51 +/- 0.54 pmol/mg protein. Guanine nucleotides, which modulate G-proteins activity intracellularly, are also involved in the inhibition of glutamate responses by acting extracellularly. Moreover, we have previously reported that guanine nucleotides potentiate, while glutamate inhibits, adenosine-induced cyclic AMP accumulation in slices from optic tectum of chicks. However, the guanine nucleotides, GMP or GppNHp and the metabotropic glutamate receptors agonist, 1S,3R-ACPD did not alter the [3H]NECA binding observed in fresh non-washed-membranes. Therefore, the adenosine A2 receptor found in the optic tectum must be the adenosine A2b receptor which is available only in fresh membrane preparations, and its not modulated by guanine nucleotides or glutamate analogs.
研究了腺苷A2受体亚型在膜制剂中的结合特性,以及腺苷受体配体对新生雏鸡视顶盖切片中cAMP积累的影响。[3H]2-[4-(2-对羧乙基)phenylamino]-5'-N-乙基羧氨基腺苷(CGS 21680)是腺苷A2a受体的选择性配体,与大鼠纹状体膜的情况一样,它不与视顶盖膜结合。CGS 21680也不会在视顶盖切片中诱导环磷酸腺苷积累。然而,5'-N-乙基羧酰胺腺苷(NECA)、2-氯腺苷或腺苷会使该制剂中的环磷酸腺苷积累增加2.5至3倍。[3H]NECA与从雏鸡视顶盖获得的新鲜未洗涤膜结合,显示出一群结合位点,可被NECA、8-苯基茶碱、2-氯腺苷取代,但不受CGS 21680影响。估计的K(D)值为400.90±80.50 nM,Bmax估计为2.51±0.54 pmol/mg蛋白质。鸟嘌呤核苷酸在细胞内调节G蛋白活性,也通过细胞外作用参与谷氨酸反应的抑制。此外,我们之前报道过,鸟嘌呤核苷酸增强,而谷氨酸抑制雏鸡视顶盖切片中腺苷诱导的环磷酸腺苷积累。然而,鸟嘌呤核苷酸、GMP或GppNHp以及代谢型谷氨酸受体激动剂1S,3R-ACPD并没有改变在新鲜未洗涤膜中观察到的[3H]NECA结合。因此,在视顶盖中发现的腺苷A2受体一定是仅在新鲜膜制剂中存在的腺苷A2b受体,并且它不受鸟嘌呤核苷酸或谷氨酸类似物的调节。