Petcoff D W, Cooper D M
Eur J Pharmacol. 1987 Jun 4;137(2-3):269-71. doi: 10.1016/0014-2999(87)90234-2.
The accumulation of inositol-1-phosphate in rat striatal slices was inhibited by the adenosine analogues 5'-N-ethylcarboxamide-adenosine and N6-phenylisopropyladenosine. Maximal inhibition (approximately 20%) was achieved by micromolar concentrations of either compound. Both basal and stimulated values could be inhibited, and the inhibition was reversible by the adenosine receptor antagonist 8-phenyltheophylline (10 microM). The results suggest that adenosine may exert a tonic inhibitory influence on inositol phospholipid-derived second messenger production in the striatum in vivo.
大鼠纹状体切片中肌醇-1-磷酸的积累受到腺苷类似物5'-N-乙基甲酰胺-腺苷和N6-苯基异丙基腺苷的抑制。微摩尔浓度的这两种化合物均可实现最大抑制(约20%)。基础值和刺激值均可被抑制,且腺苷受体拮抗剂8-苯基茶碱(10微摩尔)可逆转这种抑制作用。结果表明,腺苷可能对体内纹状体中肌醇磷脂衍生的第二信使产生具有紧张性抑制作用。