IGF-1 defends against chronic-stress induced depression in rat models of chronic unpredictable mild stress through the PI3K/Akt/FoxO3a pathway

被引:31
作者
Kuang, Wei-Hong [1 ,2 ]
Dong, Zai-Quan [1 ,2 ]
Tian, Lian-Tian [3 ]
Li, Jin [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Psychiat, 37 Guoxue Xiang, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Mental Hlth Ctr, 37 Guoxue Xiang, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Teaching Hosp 4, West China Sch Publ Hlth, Res Ctr Publ Hlth & Prevent Med, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
IGF-1; Chronic-stress induced depression; Rat models; Chronic unpredictable mild stress; PI3K/Akt/FoxO3a signaling pathway; GROWTH-FACTOR-I; INSULIN; PROLIFERATION;
D O I
10.1016/j.kjms.2018.02.004
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study aims to investigate the role of IGF-1 in chronic-stress induced depression through the PI3K/Akt/FoxO3a pathway. A rat model of chronic unpredictable mild stress (CUMS) was established. In total, 48 rats were randomized into control (normal rats), CUMS (CUMS modeled rats) and CUMS + IGF-1 (injection of IGF-1 before CUMS modeling) groups. Body weight, horizontal (number of horizontal crossing) and vertical activity (rearing times), and sucrose consumption were identified one day before and after the open-field test. The mRNA and protein expression of PI3K, Akt, FoxO3a and Bim in the hippocampus was measured by RT-qPCR and Western blotting, respectively. Compared with the control group, a lower body weight, a decreased number of horizontal crossings, reduced rearing times and lower sucrose consumption were observed in the CUMS and CUMS + IGF-1 groups after the test. However, a higher body weight, number of horizontal crossings, rearing times and sucrose consumption were found in the CUMS + IGF-1 group than those in the CUMS group. Compared with the control group, mRNA and protein expression of PI3K, Akt and FoxO3a was decreased, and Bim mRNA and protein expression was increased in the CUMS + IGF-1 and CUMS groups. Meanwhile, in comparison to the CUMS group, mRNA and protein expression of PI3K, Akt and FoxO3a was elevated, and Bim mRNA and protein expression was reduced in the CUMS + IGF-1 group. The results suggested that IGF-1 exerted an antidepressant-like effect on chronic-stress induced depression through the PI3K/Akt/FoxO3a pathway. Copyright (C) 2018, Kaohsiung Medical University. Published by Elsevier Taiwan LLC.
引用
收藏
页码:370 / 376
页数:7
相关论文
共 28 条
[1]   Behavioural and neurochemical effects induced by chronic mild stress applied to two different rat strains [J].
Bekris, S ;
Antoniou, K ;
Daskas, S ;
Papadopoulou-Daifoti, Z .
BEHAVIOURAL BRAIN RESEARCH, 2005, 161 (01) :45-59
[2]   Alterations of Hair and Nail Content of Selected Trace Elements in Nonoccupationally Exposed Patients with Chronic Depression from Different Geographical Regions [J].
Blazewicz, Anna ;
Liao, Kuan-Yung ;
Liao, Heng-Hsin ;
Nizinski, Przemyslaw ;
Komsta, Lukasz ;
Momcilovic, Berislav ;
Jablonska-Czapla, Magdalena ;
Michalski, Rajmund ;
Prystupa, Andrzej ;
Sak, Jaroslaw J. ;
Kocjan, Ryszard .
BIOMED RESEARCH INTERNATIONAL, 2017, 2017
[3]   Insulin-like growth factor 1 and risk of depression in older people: the English Longitudinal Study of Ageing [J].
Chigogora, S. ;
Zaninotto, P. ;
Kivimaki, M. ;
Steptoe, A. ;
Batty, G. D. .
TRANSLATIONAL PSYCHIATRY, 2016, 6 :e898-e898
[4]   The safety of extended-release drug formulations for the treatment of ADHD [J].
Childress, Ann .
EXPERT OPINION ON DRUG SAFETY, 2017, 16 (05) :603-615
[5]   IGF-1 suppresses Bim expression in multiple myeloma via epigenetic and posttranslational mechanisms [J].
De Bruyne, Elke ;
Bos, Tomas J. ;
Schuit, Frans ;
Van Valckenborgh, Els ;
Menu, Eline ;
Thorrez, Lieven ;
Atadja, Peter ;
Jernberg-Wiklund, Helena ;
Vanderkerken, Karin .
BLOOD, 2010, 115 (12) :2430-2440
[6]   Is unpredictable chronic mild stress (UCMS) a reliable model to study depression-induced neuroinflammation? [J].
Farooq, Rai Khalid ;
Isingrini, Elsa ;
Tanti, Arnaud ;
Le Guisquet, Anne-Marie ;
Arlicot, Nicolas ;
Minier, Frederic ;
Leman, Samuel ;
Chalon, Sylvie ;
Belzung, Catherine ;
Camus, Vincent .
BEHAVIOURAL BRAIN RESEARCH, 2012, 231 (01) :130-137
[7]   Clinical Practice Guidelines for the management of Depression [J].
Gautam, Shiv ;
Jain, Akhilesh ;
Gautam, Manaswi ;
Vahia, Vihang N. ;
Grover, Sandeep .
INDIAN JOURNAL OF PSYCHIATRY, 2017, 59 (05) :S34-S50
[8]   Selegiline Ameliorates Depression-Like Behavior in Mice Lacking the CD157/BST1 Gene, a Risk Factor for Parkinson's Disease [J].
Kasai, Satoka ;
Yoshihara, Toru ;
Lopatina, Olga ;
Ishihara, Katsuhiko ;
Higashida, Haruhiro .
FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 2017, 11
[9]  
Kitagishi Yasuko, 2012, Depress Res Treat, V2012, P752563, DOI [10.1155/2012/236530, 10.1155/2012/752563]
[10]   IGF-I in major depression and antidepressant treatment response [J].
Kopczak, Anna ;
Stalla, Guenter Karl ;
Uhr, Manfred ;
Lucae, Susanne ;
Hennings, Johannes ;
Ising, Marcus ;
Holsboer, Florian ;
Kloiber, Stefan .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2015, 25 (06) :864-872