el-Etr M, Lombes M, Baulieu E E, Erlanger B F
INSERM U.33, Lab Hormones, Kremlin-Bicêtre, France.
Neurosci Lett. 1992 Sep 28;145(1):15-8. doi: 10.1016/0304-3940(92)90192-a.
To determine which subtype of adenosine receptor mediates the potentiating effect of 2-chloroadenosine on the noradrenaline-induced inositol-phosphate formation, we used the monoclonal anti-idiotypic antibody AA1 that acts as an 'internal image' of adenosine and specifically recognizes the A1 adenosine receptor. In cultured mouse striatal astrocytes, AA1 increased the noradrenaline-evoked inositol phosphate (IP) accumulation, thus demonstrating a biological activity of an anti-idiotypic antibody. This effect was inhibited by PACPX, a selective A1 antagonist. Inhibitors of phospholipase A2 activity prevented the potentiation. These results establish the involvement of A1 adenosine receptors in the modulation of phospholipase C activity.
为了确定哪种亚型的腺苷受体介导2-氯腺苷对去甲肾上腺素诱导的肌醇磷酸形成的增强作用,我们使用了单克隆抗独特型抗体AA1,它作为腺苷的“内影像”,特异性识别A1腺苷受体。在培养的小鼠纹状体星形胶质细胞中,AA1增加了去甲肾上腺素诱发的肌醇磷酸(IP)积累,从而证明了抗独特型抗体的生物学活性。这种作用被选择性A1拮抗剂PACPX抑制。磷脂酶A2活性抑制剂可阻止这种增强作用。这些结果证实了A1腺苷受体参与了磷脂酶C活性的调节。