Bonifacj J F, Hasni H, Laborit H
Laboratoire d'Eutonologie, Hôpital Boucicaut, Paris, France.
Res Commun Chem Pathol Pharmacol. 1990 Jun;68(3):299-305.
N6(amido-3-propyl) adenosine (Agr 529) has central properties analogous to those of adenosine. It increases plasma corticosterone levels in rats as a function of dose and of time. A plateau is reached at the dose of 10 mg.kg-1 one hour after intraperitoneal injection. Treatment with a blocker of adenosine receptors, 8-(p-sulfophenyl)-theophylline, which does not cross the blood-brain barrier, inhibits the increase of plasma corticosterone induced by Agr 529. This increase is also absent in hypophysectomized rats and in rats receiving Agr 529 intracerebroventricularly. Thus it is consistent to believe that Agr 529 increases plasma corticosterone in normal rats by acting on adenosine A2 receptors in the pituitary.
N6-(氨基-3-丙基)腺苷(Agr 529)具有与腺苷类似的中枢特性。它可使大鼠血浆皮质酮水平随剂量和时间而升高。腹腔注射1小时后,剂量达10 mg·kg-1时达到平台期。用不能透过血脑屏障的腺苷受体阻断剂8-(对磺基苯基)茶碱处理,可抑制Agr 529诱导的血浆皮质酮升高。垂体切除的大鼠以及脑室内注射Agr 529的大鼠也不会出现这种升高。因此,可以认为Agr 529通过作用于垂体中的腺苷A2受体来增加正常大鼠的血浆皮质酮。