Downregulation of growth hormone 1 gene in the cerebellum and prefrontal cortex of rats with depressive-like behavior

被引:11
作者
Yamamoto, Yuta [1 ]
Ueyama, Takashi [1 ]
Ito, Takao [1 ]
Tsuruo, Yoshihiro [1 ]
机构
[1] Wakayama Med Univ, Sch Med, Dept Anat & Cell Biol, Wakayama 6418509, Japan
关键词
depression; growth hormone 1; forced swimming test; brain; microarray analysis; Ingenuity Pathway Analysis; INDIVIDUAL-DIFFERENCES; ANIMAL-MODELS; EXPRESSION; HIPPOCAMPUS; STRESS; MECHANISMS; AMYGDALA; ANXIETY; BRAIN; MICE;
D O I
10.1152/physiolgenomics.00119.2014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Depressive-like behaviors in animals are usually assessed by standardized behavioral tests such as the forced swimming test (FST). However, individual variation in test performance may obscure group differences and thereby hinder the discovery of genes responsible for depression. Few reports have shown the influence of individual variability in identifying the genes associated with depressive-like behaviors. In this study, we conducted microarray analysis to identify genes differentially expressed in the prefrontal cortex (PFC) and cerebellum of rats stratified by FST immobility ratio (% immobility in 5 min) into a control group [immobility ratio: --1 to + 1 standard deviation (SD) from the mean] and a depressive group (immobility ratio: -1 to + 2 SDs above the mean). Genes differentially expressed in both the cerebellum and PFC of the depressive group were Alas2, Gh1, Hba-a2, Hbb, Hbb-b1, Hbe2, LOC689064, Mrps10, Mybpc, Olf6415, and Pfkb1. Ingenuity Pathway Analysis identified Gh1 as a hub gene in the networks of differentially expressed genes in both brain regions. This study indicates that the depressive-like behavior may be related to the decrease of Gh1 expression in the cerebellum and PFC.
引用
收藏
页码:170 / 176
页数:7
相关论文
共 33 条
[11]  
Hallberg M, 2012, OPEN ENDOCRINOL J, V6, P27, DOI DOI 10.2174/1874216501206010027
[12]   Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis [J].
Herman, JP ;
Ostrander, MM ;
Mueller, NK ;
Figueiredo, H .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2005, 29 (08) :1201-1213
[13]   GROWTH-HORMONE (GH) IMMUNOREACTIVITY IN THE RODENT AND PRIMATE CNS - DISTRIBUTION, CHARACTERIZATION AND PRESENCE POST-HYPOPHYSECTOMY [J].
HOJVAT, S ;
BAKER, G ;
KIRSTEINS, L ;
LAWRENCE, AM .
BRAIN RESEARCH, 1982, 239 (02) :543-557
[14]   A TEST FOR NORMALITY OF OBSERVATIONS AND REGRESSION RESIDUALS [J].
JARQUE, CM ;
BERA, AK .
INTERNATIONAL STATISTICAL REVIEW, 1987, 55 (02) :163-172
[15]   Neuroendocrinology of coping styles: Towards understanding the biology of individual variation [J].
Koolhaas, J. M. ;
de Boer, S. F. ;
Coppens, C. M. ;
Buwalda, B. .
FRONTIERS IN NEUROENDOCRINOLOGY, 2010, 31 (03) :307-321
[16]   Chronic Gestational Stress Leads to Depressive-Like Behavior and Compromises Medial Prefrontal Cortex Structure and Function during the Postpartum Period [J].
Leuner, Benedetta ;
Fredericks, Peter J. ;
Nealer, Connor ;
Albin-Brooks, Christopher .
PLOS ONE, 2014, 9 (03)
[17]   Dominant-submissive behavior as models of mania and depression [J].
Malatynska, E ;
Knapp, RJ .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2005, 29 (4-5) :715-737
[18]   THE KOLMOGOROV-SMIRNOV TEST FOR GOODNESS OF FIT [J].
MASSEY, FJ .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1951, 46 (253) :68-78
[19]   Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala [J].
Murray, Elisabeth A. ;
Wise, Steven P. ;
Drevets, Wayne C. .
BIOLOGICAL PSYCHIATRY, 2011, 69 (12) :E43-E54
[20]   Neurobiology of depression [J].
Nestler, EJ ;
Barrot, M ;
DiLeone, RJ ;
Eisch, AJ ;
Gold, SJ ;
Monteggia, LM .
NEURON, 2002, 34 (01) :13-25