Hillaire-Buys D, Bertrand G, Gross R, Loubatières-Mariani M M
Eur J Pharmacol. 1987 Apr 7;136(1):109-12. doi: 10.1016/0014-2999(87)90786-2.
The effects of L- and D-phenylisopropyladenosine (L- and D-PIA) were studied on glucose-induced insulin secretion from the isolated perfused rat pancreas. L-PIA at the low dose of 16.5 nM inhibited insulin secretion by 50%. In contrast, D-PIA at 16.5 and 82.5 nM was ineffective. D-PIA used at a 100-fold higher concentration (1.65 microM) than L-PIA induced a similar inhibition of insulin secretion. The inhibitory effect of L-PIA was abolished by 8-phenyltheophylline (1 microM), a potent P1 purinoceptor antagonist. The present experiments provide evidence for an adenosine receptor of the A1 subtype on the insulin-secreting pancreatic cell of rats.
研究了L-和D-苯异丙基腺苷(L-和D-PIA)对离体灌注大鼠胰腺葡萄糖诱导的胰岛素分泌的影响。低剂量16.5 nM的L-PIA可抑制胰岛素分泌50%。相比之下,16.5 nM和82.5 nM的D-PIA无效。D-PIA使用的浓度比L-PIA高100倍(1.65 microM)时,可诱导类似的胰岛素分泌抑制作用。L-PIA的抑制作用被强效P1嘌呤受体拮抗剂8-苯基茶碱(1 microM)消除。本实验为大鼠胰岛素分泌胰腺细胞上存在A1亚型腺苷受体提供了证据。