Blazynski C
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110.
J Neurochem. 1990 Feb;54(2):648-55. doi: 10.1111/j.1471-4159.1990.tb01920.x.
Binding sites for both the adenosine A1 receptor agonists [3H]phenylisopropyladenosine and [3H]cyclohexyladenosine and the mixed A1-A2 agonist N-[3H]ethylcarboxamidoadenosine [( 3H]NECA) were localized in rabbit and mouse retinas using autoradiographic techniques. These two classes of agonists bound to very different regions of mammalian retinas. A1 agonist binding was localized to the inner retina, particularly over the inner plexiform layer. The binding of [3H]NECA was observed primarily over the retinal pigmented epithelium and the outer and inner segments of photoreceptors. [3H]NECA labeling was not affected either by including a low concentration of unlabeled A1 agonist or by pretreating tissue with N-ethylmaleimide to inhibit ligand binding at A1 sites. While virtually all of the [3H]NECA binding was displaced by an excess of unlabeled NECA, displacement with antagonist or a large excess of cyclohexyladenosine revealed that approximately 30% of the [3H]NECA binding was at non-A1,A2 sites. The majority of the binding in the outer retina thus labeled A2 receptor sites. The unique localizations of the two classes of adenosine receptors suggest different functions in visual processing.
利用放射自显影技术,在兔和小鼠视网膜中定位了腺苷A1受体激动剂[3H]苯异丙基腺苷和[3H]环己基腺苷以及混合A1 - A2激动剂N - [3H]乙基羧酰胺腺苷[(3H)NECA]的结合位点。这两类激动剂与哺乳动物视网膜的非常不同的区域结合。A1激动剂结合定位于视网膜内层,特别是在内网状层上。[3H]NECA的结合主要在视网膜色素上皮以及光感受器的外段和内段观察到。[3H]NECA标记不受低浓度未标记A1激动剂的影响,也不受用N - 乙基马来酰亚胺预处理组织以抑制A1位点配体结合的影响。虽然几乎所有的[3H]NECA结合都被过量的未标记NECA取代,但用拮抗剂或大量过量的环己基腺苷取代表明,约30%的[3H]NECA结合位于非A1、A2位点。因此,在外层视网膜中标记的大部分结合为A2受体位点。两类腺苷受体的独特定位表明在视觉处理中具有不同的功能。