Chapal J, Loubatieres-Mariani M M
Eur J Pharmacol. 1981 Sep 11;74(2-3):127-34. doi: 10.1016/0014-2999(81)90522-7.
An attempt was made to antagonize the stimulatory effect of ATP on insulin secretion from the isolated perfused rat pancreas. The insulin secretory effect of ATP does not seem to be mediated by cholinergic or beta-adrenergic receptors since neither atropine 0.3 micro mol/1 nor propranolol 1 micro mol/1 had any antagonistic action on insulin secretion induced by ATP (16.5 micro mol/1). Theophylline (50 micro mol/1) did not antagonize the insulin secretion evoked by ATP (16.5 micro mol/1). Apamin (10 nmol/1) was also without antagonistic action. 2-2'Pyridylisatogen tosylate (5 micro mol/1) had not effect on insulin secretion induced by glucose )8.33 mmol/1) or acetylcholine (0.5 micro mol/1 and 0.1 micro mol/1) but inhibited the insulin secretory effect of ATP (16.5 micro mol/1). Thus, the antagonism of 2-2'pyridylisatogen for ATP seems selective. We conclude that a purinoceptor of the P2-type is likely to be present on the B-cell of the rat pancreas.
人们试图拮抗ATP对离体灌注大鼠胰腺胰岛素分泌的刺激作用。ATP的胰岛素分泌作用似乎不是由胆碱能或β-肾上腺素能受体介导的,因为0.3微摩尔/升的阿托品和1微摩尔/升的普萘洛尔对ATP(16.5微摩尔/升)诱导的胰岛素分泌均无拮抗作用。茶碱(50微摩尔/升)也不能拮抗ATP(16.5微摩尔/升)诱发的胰岛素分泌。蜂毒明肽(10纳摩尔/升)同样没有拮抗作用。2-2'吡啶异硫氰酸酯甲苯磺酸盐(5微摩尔/升)对葡萄糖(8.33毫摩尔/升)或乙酰胆碱(0.5微摩尔/升和0.1微摩尔/升)诱导的胰岛素分泌没有影响,但能抑制ATP(16.5微摩尔/升)的胰岛素分泌作用。因此,2-2'吡啶异硫氰酸酯对ATP的拮抗作用似乎具有选择性。我们得出结论,大鼠胰腺β细胞上可能存在P2型嘌呤受体。