Roldán G, Bolaños-Badillo E, González-Sánchez H, Quirarte G L, Prado-Alcalá R A
Department of Physiology, Faculty of Medicine, Universidad Nacional Autónoma de México, Mexico.
Neurosci Lett. 1997 Jul 18;230(2):93-6. doi: 10.1016/s0304-3940(97)00489-8.
The effect of three different M1 muscarinic antagonists, pirenzepine, biperiden, and trihexyphenidyl on memory consolidation was investigated. Rats were trained in a one-trial step-through inhibitory avoidance task and injected intraperitoneally immediately afterwards, either with pirenzepine, biperiden, or trihexyphenidyl (dose range from 0 to 16 mg/kg). The non-selective antimuscarinic compound scopolamine, was also administered for comparison. One day later, rats were tested for retention. Results show that biperiden, trihexyphenidyl and scopolamine produced a dose-dependent impairment of inhibitory avoidance consolidation, while pirenzepine had no effect. The amnestic state produced by biperiden and trihexyphenidyl was comparable to that observed after the administration of scopolamine. These results indicate that the selective blockade of the central M1 muscarinic receptors interfere with memory consolidation of inhibitory avoidance and suggest that this receptor subtype is critically involved in mnemonic functions.
研究了三种不同的M1毒蕈碱拮抗剂哌仑西平、比哌立登和苯海索对记忆巩固的影响。大鼠接受单次步入式抑制性回避任务训练,随后立即腹腔注射哌仑西平、比哌立登或苯海索(剂量范围为0至16 mg/kg)。还给予非选择性抗毒蕈碱化合物东莨菪碱作为对照。一天后,测试大鼠的记忆保持情况。结果显示,比哌立登、苯海索和东莨菪碱产生了剂量依赖性的抑制性回避巩固损伤,而哌仑西平没有效果。比哌立登和苯海索产生的遗忘状态与给予东莨菪碱后观察到的相似。这些结果表明,中枢M1毒蕈碱受体的选择性阻断会干扰抑制性回避的记忆巩固,并提示该受体亚型在记忆功能中起关键作用。