Romanenko O K, Pivovarov A S, Bakalkin G Ia
Nauchnye Doki Vyss Shkoly Biol Nauki. 1987(6):50-5.
The opiate antagonist naloxone modifies the electric activity of some identified neurons of the Helix lucorum which have not been preliminary exposed to the effect of exogenous opioids. Some neurons are excited while others are inhibited by naloxone, and in both cases the reaction may have both a short and long latent period. The reactions depend on naloxone dose and become less expressed or are blocked when naloxone is administered together with the agonists of opiate receptor (morphine, D-Ala2, D-Leu5-enkephalin, bremazocine and beta-endorphin). Opioids alone do not produce any effect on neurons. The effect of naloxone on neurons is assumed to be a result of the elimination by the opiate antagonist of the tonic effect of endogenous opioids by their replacing on opiate receptors which are constantly stimulated by endogenous ligands.
阿片拮抗剂纳洛酮可改变尚未预先接触外源性阿片类药物作用的福寿螺某些已确定神经元的电活动。一些神经元被纳洛酮兴奋,而另一些则被抑制,在这两种情况下,反应都可能有短潜伏期和长潜伏期。这些反应取决于纳洛酮的剂量,当纳洛酮与阿片受体激动剂(吗啡、D-丙氨酸2、D-亮氨酸5-脑啡肽、布瑞马佐辛和β-内啡肽)一起给药时,反应减弱或被阻断。单独使用阿片类药物对神经元没有任何影响。纳洛酮对神经元的作用被认为是阿片拮抗剂通过取代内源性配体持续刺激的阿片受体,消除内源性阿片类药物的强直作用的结果。