首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Spironolactone and low-dose dexamethasone enhance extinction of contextual fear conditioning.
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Spironolactone and low-dose dexamethasone enhance extinction of contextual fear conditioning.

机译:螺内酯和小剂量地塞米松可增强背景恐惧条件的消退。

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摘要

Glucocorticoids play a role in memory formation, and they may contribute to memory changes in stress-related mental disorders, such as posttraumatic stress disorder. Cortisol may act through mineralocorticoid (MR) or glucocorticoid (GR) receptors, and the objective of the present study was to evaluate the effects of the MR antagonist spironolactone, the GR antagonist mifepristone, the MR agonist fludrocortisone, and the GR agonist dexamethasone on the extinction of contextually conditioned fear in rats. Propranolol was used as a positive control. As expected, propranolol administered before the test session increased memory extinction. Pre-test administration of spironolactone and low-dose dexamethasone also increased the extinction of an aversive memory, whereas fludrocortisone impaired extinction. High-dose dexamethasone and mifepristone were found to have no effect in this model. Post-test spironolactone treatment impaired aversive memory extinction. These results indicate that MR and GR are related to extinction of aversive memories, and MR blockade may be a promising candidate for the treatment of stress-related memory disorders.
机译:糖皮质激素在记忆形成中起作用,它们可能导致与压力有关的精神障碍(例如创伤后应激障碍)的记忆变化。皮质醇可能通过盐皮质激素(MR)或糖皮质激素(GR)受体起作用,本研究的目的是评估MR拮抗剂螺内酯,GR拮抗剂米非司酮,MR激动剂氟可的松和GR激动剂地塞米松的作用。在大鼠中因环境条件而产生的恐惧的消除。普萘洛尔用作阳性对照。如预期的那样,在试验前服用普萘洛尔可增加记忆消失。螺内酯和小剂量地塞米松的预试验给药也增加了厌恶记忆的消退,而氟可的松则损害了消退。发现高剂量地塞米松和米非司酮在该模型中没有作用。测试后螺内酯治疗会损害厌恶性记忆的消失。这些结果表明,MR和GR与厌恶性记忆的消退有关,而MR阻滞可能是治疗与压力有关的记忆障碍的有前途的候选者。

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