Kovàcs G L, Bohus B, De Wied D
Psychoneuroendocrinology. 1983;8(4):411-9. doi: 10.1016/0306-4530(83)90020-3.
The effects on retrieval of a one-trial learning inhibitory avoidance response of beta-endorphin, alpha-endorphin, and gamma-endorphin, given prior to test have been studied in rats. beta-Endorphin (beta-LPH 61-91) in a relatively low dose (1.56 micrograms sc. or 50 ng icv.) facilitated inhibitory avoidance behavior, while a higher dose (10 micrograms sc. or 100 ng icv.) caused bimodal changes (facilitation in 50% of the animals and attenuation in another 40%. Peripheral injection of gamma-endorphin attenuated inhibitory avoidance behaviour in a dose-dependent manner. The C-terminus of beta-endorphin (beta-LPH 78-91) was ineffective. alpha-Endorphin facilitated inhibitory avoidance behavior in a dose dependent manner. Naltrexone pretreatment antagonized the bimodal effect of beta-endorphin: following pretreatment with the opiate antagonist the low latency component disappeared, but the facilitatory effect of the neuropeptide remained the same. It is suggested that beta-endorphin carries more than one bit of behavioral information. Inherent activities either related or unrelated to naltrexone-sensitive opiate as well as biotransformation into alpha- and gamma-endorphin may contribute to the multiple behavioral effects of this neuropeptide.
研究了在大鼠测试前给予β-内啡肽、α-内啡肽和γ-内啡肽单次学习抑制性回避反应对记忆提取的影响。相对低剂量(皮下注射1.56微克或脑室内注射50纳克)的β-内啡肽(β-促脂解素61-91)促进了抑制性回避行为,而较高剂量(皮下注射10微克或脑室内注射100纳克)则引起双峰变化(50%的动物表现为促进,另外40%表现为减弱)。外周注射γ-内啡肽以剂量依赖性方式减弱抑制性回避行为。β-内啡肽的C末端(β-促脂解素78-91)无效。α-内啡肽以剂量依赖性方式促进抑制性回避行为。纳曲酮预处理拮抗了β-内啡肽的双峰效应:用阿片拮抗剂预处理后,低潜伏期成分消失,但神经肽的促进作用保持不变。提示β-内啡肽携带不止一种行为信息。与纳曲酮敏感的阿片相关或不相关的固有活性以及向α-和γ-内啡肽的生物转化可能导致这种神经肽的多种行为效应。