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Naloxone and β-endorphin alter the effects of post-training epinephrine on memory

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Abstract

These experiments examined the involvement of opioid peptides in the memory-modulating effects of post-training epinephrine (Epi). Mice were trained on inhibitory avoidance (IA) and Y-maze discrimination (YMD) tasks and given post-training injections followed by retention tests 24 h later. In the IA task retention was enhanced by low doses of Epi and impaired by high doses. In both tasks, naloxone facilitated retention and blocked the memory-impairing effects of Epi. These findings are consistent with other evidence suggesting that the memory-impairing effects of β-endorphin are mediated by the release of opioid peptides. Previous studies have shown that a novel exploratory experience given 1 h prior to training blocks the release of brain β-endorphin and blocks the memory-enhancing effects of post-training naloxone. In the present study we found that a novel experience given 1 h prior to training blocked the memory-impairing effect of post-training Epi otherwise obtained in both tasks. The effects of a low, memory-enhancing dose of Epi appear not to involve the release of opioid peptides: a low dose of Epi blocked the memory-impairing effect of β-endorphin. Further, low doses of Epi and naloxone, which were ineffective when administered alone, significantly enhanced retention when administered together. We interpret these findings as indicating that the memory-enhancing and memory-impairing effects of Epi are mediated by different mechanisms.

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References

  • Arbilla H, Langer SZ (1978) Morphine and beta-endorphin inhibit release of noradrenaline from cerebral cortex but not of dopamine from rat striatum. Nature 271:559–561

    Google Scholar 

  • Baratti CM, Introini IB, Huygens P (1984) Possible interaction between central cholinergic muscarinic and opioid peptidergic systems during memory consolidation in mice. Behav Neural Biol 40:155–169

    Google Scholar 

  • Borrell J, de Kloet ER, Versteeg DHG, Bohus B (1983) The role of adrenomedullary catecholamines in the modulation of memory by vasopressin. In: Endroczi E, de Wied D, Angelucci L, Scapagnini V (eds) Integrative neurohumoral mechanisms: developments in neuroscience. Elsevier/North Holland, Amsterdam, pp 85–90

    Google Scholar 

  • Carrasco MA, Dias RD, Perry MLS, Wofchuk ST, Souza DO, Izquierdo I (1982) Effect of morphine, ACTH, epinephrine, Met-, Leu- and des-Tyr-Met-enkephalin on beta-endorphin-like immunoreactivity of rat brain. Psychoneuroendocrinology 7:229–234

    Google Scholar 

  • Castellano C (1975) Effects of morphine and heroin on discrimination learning and consolidation in mice. Psychopharmacologia 42:235–242

    Google Scholar 

  • Fanelli RJ, Rosenberg RA, Gallagher M (1986) Role of noradrenergic function in the opiate antagonist facilitation of spatial memory. Behav Neurosci (in press)

  • Gallagher M, Kapp BS (1978) Manipulation of opiate activity in the amygdala alters memory processes. Life Sci 23:1973–1978

    Google Scholar 

  • Gallagher M, King RA, Young NB (1983) Opiate antagonists improve spatial memory. Science 221:975–976

    Google Scholar 

  • Gallagher M, Rapp PR, Fanelli RJ (1985) Opiate antagonist facilitation of time-dependent memory processes: Dependence upon intact norepinephrine function. Brain Res 347:284–290

    Google Scholar 

  • Gold PE, van Buskirk R (1975) Facilitation of time-dependent memory processes with postrial epinephrine injections. Behav Biol 13:145–153

    Google Scholar 

  • Gold PE, Zornetzer SF (1983) The mnemon and its juices: Neuromodulation of memory processes. Behav Neural Biol 38:151–189

    Google Scholar 

  • Gold PE, McCarty R, Sternberg DB (1982) Peripheral catecholamines and memory modulation. In: Marsan CA, Matthies H (eds) Neuronal plasticity and memory formation. Raven, New York, pp 327–338

    Google Scholar 

  • Introini-Collison IB, Baratti CM (1986) Opioid peptidergic systems may modulate the activity of β-adrenergic mechanisms during memory consolidation processes. Behav Neural Biol 46:227–241

    Google Scholar 

  • Introini-Collison I, McGaugh JL (1986) Epinephrine modulates long-term retention of an aversively-motivated discrimination task. Behav Neural Biol 45:358–365

    Google Scholar 

  • Introini IB, McGaugh JL, Baratti CM (1985) Pharmacological evidence of a central effect of naltrexone, morphine and beta-endorphin and a peripheral effect of Met-and Leu-enkephalin on retention of an inhibitory response in mice. Behav Neural Biol 44:434–446

    Google Scholar 

  • Izquierdo I (1979) Effect of naloxone and morphine on various forms of memory in the rat: Possible role of endogenous opiate mechanisms in memory consolidation. Psychopharmacology 66:199–203

    Google Scholar 

  • Izquierdo I (1982) Beta-endorphin and forgetting. TIPS 3:455–457

    Google Scholar 

  • Izquierdo I, Graudenz M (1980) Memory facilitation by naloxone is due to release of dopaminergic and beta-adrenergic systems from tonic inhibition. Psychopharmacology 67:265–268

    Google Scholar 

  • Izquierdo I, Dias RD (1983a) Memory as a state dependent phenomenon: Role of ACTH and epinephrine. Behav Neural Biol 38:144–151

    Google Scholar 

  • Izquierdo I, Dias RD (1983b) Effect of ACTH, epinephrine, β-endorphin, naloxone, and of the combination of naloxone or β-endorphin with ACTH or epinephrine on memory consolidation. Psychoneuroendocrinology 8:81–87

    Google Scholar 

  • Izquierdo I, McGaugh JL (1985) Effect of a novel experience prior to training or testing on retention of an inhibitory avoidance response in mice: Involvement of an opioid system. Behav Neural Biol 44:228–238

    Google Scholar 

  • Izquierdo I, Souza DO, Dias RD, Carrasco MA, Perry ML, Eisinger S, Elisabetsky E, Vendite DA (1980) Beta-endorphin causes retrograde amnesia and is released from the rat brain by various forms of training and stimulation. Psychopharmacology 70:173–177

    Google Scholar 

  • Izquierdo I, Perry MLS, Dias RD, Orsinger OA, Carrasco MA (1981) Effect of training and testing rats in two different behavioral paradigms on brain beta-endorphin immunoreactivity. Arqu Biol Tecnol (Parana) 24:327–331

    Google Scholar 

  • Izquierdo I, Souza DO, Dias RD, Carrasco MA, Vokmer N, Perry MLS, Netto CA (1984) Effect of various behavioral training and testing procedures on brain beta-endorphin-like immunoreactivity, and the possible role of beta-endorphin in behavioral regulation. Psychoneuroendocrinology 9:381–389

    Google Scholar 

  • Izquierdo I, Netto CA, Carrasco MA, Dias RD, Volkmer N (1985) Time course of the decrease of hypothalamic β-endorphin induced by training, and the development of the effect of β-endorphin on retrieval of inhibitory avoidance in rats. Brazil J Med Biol Res 18:391–395

    Google Scholar 

  • Jaim-Etcheverry G, Zieher LM (1980) DSP-4 a novel compound with neurotoxic effects on noradrenergic neurons of adults and developing rats. Brain Res 188:513–523

    Google Scholar 

  • Jonsson G, Hallman H, Ponzio F, Ross SB (1981) DSP 4 (N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine). A useful denervation tool for central and peripheral noradrenaline neurons. Eu J Pharmacol 72:173–188

    Google Scholar 

  • Lader MH, Tyrer PJ (1972) Central and peripheral effects of propranolol and sotalol in normal subjects. Br J Pharmacol 45:557–560

    Google Scholar 

  • Liang KC, McGaugh JL (1983) Lesions of the stria terminalis attenuate the enhancing effect of posttraining epinephrine on retention of an inhibitory avoidance response. Behav Brain Res 9:49–58

    Google Scholar 

  • Liang KC, Juler R, McGaugh JL (1986) Modulating effects of posttraining epinephrine on memory: Involvement of the amygdala noradrenergic system. Brain Res 368:125–133

    Google Scholar 

  • Lucion AB, Rosito G, Sapper D, Palmini A, Izquierdo I (1982) Intracerebroventricular administration of nanogram amounts of beta-endorphin and Met-enkephalin causes retrograde amnesia in rats. Behav Brain Res 4:111–115

    Google Scholar 

  • McGaugh JL (1983) Hormonal influences on memory. Annu Rev Psychol 34:297–323

    Google Scholar 

  • McGaugh JL, Gold PE (1986) Hormonal modulation of memory. In: Brush RB, Levine S (eds) Psychoendocrinology. Academic, New York

    Google Scholar 

  • McGaugh JL, Landfield PW (1970) Delayed development of amnesia following electroconvulsive shock. Physiol Behav 5:1109–1111

    Google Scholar 

  • McGaugh JL, Introini-Collison IB, Juler RG, Izquierdo I (1986) Stria terminalis lesions attenuate the effects of posttraining naloxone and β-endorphin on retention. Behav Neurosci 100:839–844

    Google Scholar 

  • Messing RB, Jensen RA, Martinez Jr JL, Spiehler VR, Vasquez BJ, Soumireu-Mourat B, Liang KC, McGaugh JL (1979) Naloxone enhancement of memory. Behav Neural Biol 27:266–275

    Google Scholar 

  • Sternberg DB, Korol D, Novack GD, McGaugh JL (1986) Epinephrine-induced memory facilitation: Attenuation by adrenergic receptor antagonists. Eur J Pharmacol 129:189–193

    Google Scholar 

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Introini-Collison, I.B., McGaugh, J.L. Naloxone and β-endorphin alter the effects of post-training epinephrine on memory. Psychopharmacology 92, 229–235 (1987). https://doi.org/10.1007/BF00177921

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  • DOI: https://doi.org/10.1007/BF00177921

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