Functional interaction between 5-HT6 receptors and hypothalamic-pituitary-adrenal axis:: Cognitive implications

被引:34
作者
Marcos, B. [1 ]
Aisa, B. [1 ]
Ramirez, M. J. [1 ]
机构
[1] Univ Navarra, Dept Pharmacol, Sch Med, Pamplona 31008, Spain
关键词
maternal separation; adrenalectomy; glucocorticoid receptor; SB271046; cognitive deficits; depression;
D O I
10.1016/j.neuropharm.2007.11.019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The serotonin 5-HT6 receptor has become a promising target for the treatment of neuropsychological diseases, such as affective disorders. Increasing evidence implicates stress and its effector system, the hypothalamic-pituitary-adrenal (HPA) axis, in the neurobiology of depression. In addition, there are important memory disturbances in stress-related psychiatric disorders that have been associated to an impairment of the HPA axis reactivity. The aim of the present work is to study the functional interactions between 5-HT6 receptors and HPA axis. In a situation of increased HPA axis responsiveness (maternal separation, MS) no differences were found in the expression of 5-HT6 gene in the hippocampus or frontal cortex, although serotonin levels were higher in the frontal cortex of MS rats. 5-HT6 receptor mRNA expression increased significantly in the hippocampus in a situation of decreased glucocorticoid levels, such as adrenalectomy. Cognitive deficits associated to HPA dysfunction, such those found in the MS model, were fully reversed by administration of SB271046, a selective 5-HT6 receptor antagonist. A chronic treatment with SB271046 did not modify CRF mRNA levels in the hypothalamus, but there was a higher glucocorticoid receptor density in the hippocampus compared to control. In contrast, in the frontal cortex, treatment with SB271046 induced a significant decrease in glucocorticoid receptor density. These data suggest that expression of 5-HT6 receptors might be differentially regulated depending on levels of circulating adrenal corticoids. These results are discussed in terms of therapeutical approaches to the treatment of behavioral (depressive-like) and cognitive disturbances associated to an altered response to stress. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:708 / 714
页数:7
相关论文
共 52 条
[1]   Cognitive impairment associated to HPA axis hyperactivity after maternal separation in rats [J].
Aisa, Barbara ;
Tordera, Rosa ;
Lasheras, Berta ;
Del Rio, Joaquin ;
Ramirez, Maria J. .
PSYCHONEUROENDOCRINOLOGY, 2007, 32 (03) :256-266
[2]   The role of corticotropin-releasing factor in depression and anxiety disorders [J].
Arborelius, L ;
Owens, MJ ;
Plotsky, PM ;
Nemeroff, CB .
JOURNAL OF ENDOCRINOLOGY, 1999, 160 (01) :1-12
[3]   Investigation of stretching behaviour induced by the selective 5-HT6 receptor antagonist, Ro 04-6790, in rats [J].
Bentley, JC ;
Bourson, A ;
Boess, FG ;
Fone, KCF ;
Marsden, CA ;
Petit, N ;
Sleight, AJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 126 (07) :1537-1542
[4]   New approaches to antidepressant drug discovery: beyond monoamines [J].
Berton, O ;
Nestler, EJ .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (02) :137-151
[5]   Functional and radioligand binding characterization of rat 5-HT6 receptors stably expressed in HEK293 cells [J].
Boess, FG ;
Monsma, FJ ;
Carolo, C ;
Meyer, V ;
Rudler, A ;
Zwingelstein, C ;
Sleight, AJ .
NEUROPHARMACOLOGY, 1997, 36 (4-5) :713-720
[6]  
BOURSON A, 1995, J PHARMACOL EXP THER, V274, P173
[7]  
Bremner J Douglas, 2003, Psychopharmacol Bull, V37, P6
[8]   The effects of stress on memory and the hippocampus throughout the life cycle: Implications for childhood development and aging [J].
Bremner, JD ;
Narayan, M .
DEVELOPMENT AND PSYCHOPATHOLOGY, 1998, 10 (04) :871-885
[9]   Recognition memory: What are the roles of the perirhinal cortex and hippocampus? [J].
Brown, MW ;
Aggleton, JP .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (01) :51-61
[10]   Maternal separation in rats leads to anxiety-like behavior and a blunted ACTH response and altered neurotransmitter levels in response to a subsequent stressor [J].
Daniels, WMU ;
Pietersen, CY ;
Carstens, ME ;
Stein, DJ .
METABOLIC BRAIN DISEASE, 2004, 19 (1-2) :3-14