Huston J P, Hasenöhrl R U, Boix F, Gerhardt P, Schwarting R K
Institute of Physiological Psychology I, Heinrich-Heine-University of Düsseldorf, Germany.
Psychopharmacology (Berl). 1993;112(2-3):147-62. doi: 10.1007/BF02244906.
There is ample evidence that the neurokinin substance P (SP) can have neurotrophic as well as memory-promoting effects. This paper outlines a recent series of experiments dealing with the effects of SP and its N- and C-terminal fragments on memory, reinforcement, and brain monoamine metabolism. It was shown that SP, when applied peripherally (IP), promotes memory (inhibitory avoidance learning) and is reinforcing (place preference task) at the same dose of 37 nmol/kg. Most important, however, is the finding that these effects seemed to be encoded by different SP sequences, since the N-terminal SP1-7 (185 nmol/kg) enhanced memory, whereas C-terminal hepta- and hexapeptide sequences of SP proved to be reinforcing in a dose equimolar to SP. These differential behavioral effects were paralleled by selective and site-specific changes in dopamine (DA) activity, as both SP and its C-, but not N-terminus, increased extracellular DA in the nucleus accumbens (NAc), but not in the neostriatum. The neurochemical changes lasted at least 2 h after injection. These results show that the reinforcing action of peripheral administered SP may be mediated by its C-terminal sequence, and that this effect could be related to DA activity in the NAc. Direct application of SP (0.74 pmol) into the region of the nucleus basalis magnocellularis (NBM) was also memory-promoting and reinforcing, and again, these effects were differentially produced by the N-terminus and C-terminus, supporting the proposed structure-activity relationship for SP's effects on memory and reinfrocement. These results may provide a hypothetical link between the memory-modulating and reinforcing effects of SP and the impairment in associative functioning accompanying certain neurodegenerative processes.
有充分证据表明,神经激肽P物质(SP)具有神经营养以及促进记忆的作用。本文概述了最近一系列关于SP及其N端和C端片段对记忆、强化作用和脑单胺代谢影响的实验。结果表明,外周注射(腹腔注射)SP时,在37 nmol/kg的相同剂量下可促进记忆(抑制性回避学习)并具有强化作用(位置偏爱任务)。然而,最重要的是发现这些作用似乎由不同的SP序列编码,因为N端的SP1-7(185 nmol/kg)增强记忆,而SP的C端七肽和六肽序列在与SP等摩尔剂量时被证明具有强化作用。这些不同的行为效应与多巴胺(DA)活性的选择性和位点特异性变化平行,因为SP及其C端而非N端均增加伏隔核(NAc)而非新纹状体的细胞外DA。注射后神经化学变化至少持续2小时。这些结果表明,外周给予的SP的强化作用可能由其C端序列介导,且这种作用可能与NAc中的DA活性有关。将SP(0.74 pmol)直接注射到基底大细胞核(NBM)区域也具有促进记忆和强化作用,同样,这些作用由N端和C端差异产生,支持了所提出的SP对记忆和强化作用的构效关系。这些结果可能为SP的记忆调节和强化作用与某些神经退行性过程中伴随的联想功能损害之间提供一个假设性联系。