Activation of mineralocorticoid receptors facilitate the acquisition of fear memory extinction and impair the generalization of fear memory in diabetic animals

被引:7
|
作者
Ribeiro, Thiago Oliari [1 ]
Bueno-de-Camargo, Leticia Morais [2 ]
Farias Waltrick, Ana Paula [1 ]
de Oliveira, Amanda Ribeiro [3 ,4 ,5 ]
Brandao, Marcus Lira [4 ,5 ]
Munhoz, Carolina Demarchi [2 ]
Zanoveli, Janaina Menezes [1 ,4 ,5 ]
机构
[1] Univ Fed Parana, Dept Pharmacol, Biol Sci Bldg, Rua Coronel H dos Santos S-N,POB 19031, BR-81540990 Curitiba, Parana, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Pharmacol, BR-05508900 Sao Paulo, SP, Brazil
[3] Univ Fed Sao Carlos, Ctr Educ & Human Sci, Dept Psychol, BR-13565905 Sao Carlos, SP, Brazil
[4] Univ Sao Paulo, Inst Neurosci & Behav, Fac Philosophy Sci & Letters, BR-14040900 Ribeirao Preto, SP, Brazil
[5] Univ Sao Paulo, Lab Neuropsychopharmacol, Fac Philosophy Sci & Letters, BR-14040900 Ribeirao Preto, SP, Brazil
关键词
Streptozotocin; Diabetes; Hippocampus; Prefrontal cortex; Glucocorticoid receptor; Aversive memory; Anxiety; Contextual conditioned fear; DEPRESSIVE-LIKE BEHAVIOR; PITUITARY-ADRENAL AXIS; POSTTRAUMATIC-STRESS-DISORDER; ELEVATED PLUS-MAZE; ANXIETY DISORDERS; GLUCOCORTICOID-RECEPTORS; BASOLATERAL AMYGDALA; VENTRAL HIPPOCAMPUS; PREFRONTAL CORTEX; CONDITIONED FEAR;
D O I
10.1007/s00213-019-05388-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale Studies point out a higher prevalence of posttraumatic stress disorder (PTSD) in individuals with diabetes mellitus. It is known that glucocorticoid (GR) and mineralocorticoid (MR) receptors are implicated in fear memory processes and PTSD. However, there is no preclinical studies addressing the involvement of these receptors on abnormal fear memories related to diabetic condition. Objectives By inducing a contextual conditioned fear memory, we generate a suitable condition to investigate the extinction and the generalization of the fear memory in streptozotocin-induced diabetic (DBT) rats alongside the expression of the cytosolic and nuclear GR and MR in the hippocampus (HIP) and prefrontal cortex (PFC). Moreover, we investigated the involvement of the MR or GR on the acquisition of fear memory extinction and on the generalization of this fear memory. When appropriate, anxiety-related behavior was evaluated. Methods Male Wistar rats received one injection of steptozotocin (i.p.) to induce diabetes. After 4 weeks, the animals (DBTs and non-DBTs) were subjected to a conditioned contextual fear protocol. Results The expression of MR and GR in the HIP and PFC was similar among all the groups. The single injection of MR agonist was able to facilitate the acquisition of the impaired fear memory extinction in DBTs animals together with the impairment of its generalization. However, the GR antagonism impaired only the generalization of this fear memory which was blocked by the previous injection of the MR antagonist. All treatments were able to exert anxiolytic-like effects. Conclusions The results indicate that MR activation in DBT animals disrupts the overconsolidation of aversive memory, without discarding the involvement of emotional behavior in these processes.
引用
收藏
页码:529 / 542
页数:14
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