Neal H, Keane P E
Electroencephalogr Clin Neurophysiol. 1978 Nov;45(5):655-65. doi: 10.1016/0013-4694(78)90166-9.
The effects of various opiate compounds have been studied on the electrocorticogram (ECoG) of the rat following local injection into various brain areas. Injections of all compounds studied into both the caudate-putamen and the basal forebrain, in particular the olfactory tubercles, induced changes in the ECoG. Injections of saline vehicle into these areas were ineffective as were injections of morphine into the corpus callosum. Potency was etorphine greater than morphine = codeine greater than thebaine. Naloxone alone was inactive following injection but if combined with morphine markedly attenuated the normal morphine response and reversed the morphine response if injected following morphine. The endogenous opiate compound enkephalin and the synthetic analogue D-ala2-met5-encamide also induced electrocortical changes which were naloxone sensitive. The results are similar to those following systemic administration of opiates. It is possible that the areas studied represent the site of action of systemically applied opiates. It is suggested that the opiates and enkephalins produce their actions by acting at the same site. Since the areas studied are rich in dopaminergic terminals an interaction may exist between dopaminergic and opiate mechanism to bring about the observed changes.
在将各种阿片类化合物局部注射到大鼠不同脑区后,研究了它们对大鼠脑电图(ECoG)的影响。将所有研究的化合物注射到尾状核 - 壳核以及基底前脑,特别是嗅结节,均会引起ECoG的变化。向这些区域注射生理盐水载体无效,向胼胝体注射吗啡也无效。效力顺序为埃托啡大于吗啡 = 可待因大于蒂巴因。单独注射纳洛酮无活性,但如果与吗啡联合注射,则会显著减弱正常的吗啡反应,并且如果在注射吗啡后再注射纳洛酮,则会逆转吗啡反应。内源性阿片类化合物脑啡肽和合成类似物D - ala2 - met5 - 脑酰胺也会引起对纳洛酮敏感的皮层电变化。这些结果与全身给予阿片类药物后的结果相似。所研究的区域可能代表全身应用阿片类药物的作用部位。有人提出,阿片类药物和脑啡肽通过作用于同一部位来产生作用。由于所研究的区域富含多巴胺能终末,多巴胺能和阿片类机制之间可能存在相互作用,从而导致观察到的变化。