Germany A, Villar M, Quijada L, Contreras E
Departamento de Ciencias Fisiológicas, Facultad de Ciencias Biológicas y de Recursos Naturales, Universidad de Concepción, Chile.
Cell Mol Biol. 1990;36(4):409-14.
A number of adenosine agonists were investigated for possible actions on tolerance to morphine withdrawal in mice. The induction of tolerance to a sustained release preparation of morphine was assessed by measuring the analgesic effect induced by a test dose of the drug. The concomitant treatment with L- and D-phenylisopropyl adenosine, (L- and D-PIA), cyclopentyladenosine (CPA) or chloroadenosine (CADO) during the period of morphine absorption did not alter the induction of the process. In contrast cyclohexyladenosine (CHA) significantly decreased the intensity of tolerance. The administration of naloxone 30 hrs, after the priming dose of morphine induced an intense withdrawal reaction. The intensity of the abstinence syndrome was decreased by the administration of L-PIA, CHA or CADO; CPA and D-PIA were ineffective. These results suggest that adenosine analogs may interfere with the known morphine effects on calcium disposition in nerve terminals.
研究了多种腺苷激动剂对小鼠吗啡戒断耐受性的可能作用。通过测量试验剂量药物诱导的镇痛作用来评估对吗啡缓释制剂耐受性的诱导情况。在吗啡吸收期间,同时给予L-和D-苯异丙基腺苷(L-和D-PIA)、环戊基腺苷(CPA)或氯腺苷(CADO),并未改变该过程的诱导。相比之下,环己基腺苷(CHA)显著降低了耐受性的强度。在给予吗啡启动剂量30小时后给予纳洛酮,会引发强烈的戒断反应。给予L-PIA、CHA或CADO可降低戒断综合征的强度;CPA和D-PIA无效。这些结果表明,腺苷类似物可能会干扰吗啡对神经末梢钙分布的已知作用。