Malec D, Michalska E, Pikulicka J
Department of Pharmacodynamics, Medical Academy, Lublin, Poland.
Pol J Pharmacol. 1996 Nov-Dec;48(6):583-8.
The influence of adenosine, its analogs: (-)N6-(R-phenylisopropyl)-adenosine (R-PIA), N6-cyclohexyladenosine (CHA), 5-(N-ethylcarboxamido)-adenosine (NECA), adenosine uptake inhibitor-dipyridamole, and theophylline and caffeine (adenosine receptor antagonists) on ethanol withdrawal syndrome was investigated in rats. Adenosine (100 mg/kg ip), all adenosine analogs and dipyridamole (30 mg/kg ip) reduced the number of rats in which audiogenic convulsions appeared. Caffeine and theophylline (5-25 mg/kg ip) did not influence significantly the audiogenic seizures, but they antagonized the depressing effects of adenosine analogs on these withdrawal symptoms. The results suggest that adenosine mechanisms in the brain may be implicated in the development of ethanol withdrawal syndrome.
(-)N6-(R-苯异丙基)-腺苷(R-PIA)、N6-环己基腺苷(CHA)、5-(N-乙基甲酰胺基)-腺苷(NECA)、腺苷摄取抑制剂双嘧达莫以及茶碱和咖啡因(腺苷受体拮抗剂)对大鼠乙醇戒断综合征的影响。腹腔注射腺苷(100mg/kg)、所有腺苷类似物和双嘧达莫(30mg/kg)可减少出现听源性惊厥的大鼠数量。腹腔注射咖啡因和茶碱(5-25mg/kg)对听源性惊厥无显著影响,但它们可拮抗腺苷类似物对这些戒断症状的抑制作用。结果表明,大脑中的腺苷机制可能与乙醇戒断综合征的发生有关。