Hösli E, Hösli L
Department of Physiology, University of Basel, Switzerland.
Neuroscience. 1988 Feb;24(2):621-8. doi: 10.1016/0306-4522(88)90355-7.
The cellular localization of the uptake of [3H]adenosine and of binding of labelled adenosine analogues was studied in explant cultures of rat cerebellum and spinal cord by means of autoradiography. [3H]Adenosine was taken up by many neurons and astrocytes in both cerebellar and spinal cord cultures. The uptake of adenosine was inhibited in the absence of sodium or at 0 degrees C, suggesting an active transport mechanism. In both types of cultures, a great number of neurons showed binding sites for the A1-receptor agonist [3H]R-N6-phenylisopropyladenosine and for the mixed A1/A2-agonist [3H]N(ethyl)carboxamidoadenosine. Binding sites for both radioligands were also found on astrocytes, suggesting that these cells have receptors for the purinergic neurotransmitter adenosine. This suggestion is further supported by recent electrophysiological studies from our laboratory demonstrating that adenosine and its analogues produce hyperpolarizations of astrocytes which are blocked by the adenosine antagonist theophylline.
通过放射自显影术,研究了大鼠小脑和脊髓外植体培养物中[3H]腺苷摄取及标记腺苷类似物结合的细胞定位。在小脑和脊髓培养物中,许多神经元和星形胶质细胞都摄取了[3H]腺苷。在无钠或0℃条件下,腺苷摄取受到抑制,提示存在主动转运机制。在这两种培养物中,大量神经元显示出A1受体激动剂[3H]R-N6-苯基异丙基腺苷及混合A1/A2激动剂[3H]N(乙基)羧酰胺腺苷的结合位点。在星形胶质细胞上也发现了这两种放射性配体的结合位点,表明这些细胞具有嘌呤能神经递质腺苷的受体。我们实验室最近的电生理研究进一步支持了这一观点,该研究表明腺苷及其类似物可使星形胶质细胞超极化,而这种超极化可被腺苷拮抗剂茶碱阻断。