The immunomodulatory tellurium compound ammonium trichloro (dioxoethylene-O,O) tellurate reduces anxiety-like behavior and corticosterone levels of submissive mice

被引:10
|
作者
Gross, Moshe [1 ]
Stanciu, Emanuel [1 ,2 ]
Kenigsbuch-Sredni, Dvora [3 ]
Sredni, Benjamin [2 ]
Pinhasov, Albert [1 ]
机构
[1] Ariel Univ, Dept Mol Biol, IL-40700 Ariel, Israel
[2] Mina & Everard Goodman Fac Life Sci, CAIR Inst, Safdie AIDS & Immunol Res Ctr, Ramat Gan, Israel
[3] Bar Ilan Univ, Interdisciplinary Dept, Fac Social Sci, Ramat Gan, Israel
来源
BEHAVIOURAL PHARMACOLOGY | 2017年 / 28卷 / 06期
关键词
anxiety; ammonium trichloro (dioxoethylene-O; O) tellurate; brain-derived neurotrophic factor; corticosterone; submissive mice; ELEVATED PLUS-MAZE; GENE-ENVIRONMENT INTERACTIONS; ENDOGENOUS CONTROL GENES; DIFFERENTIAL EXPRESSION; PSYCHOLOGICAL STRESS; NEUROTROPHIC FACTOR; CANCER-PATIENTS; MILD STRESS; AS101; MODELS;
D O I
10.1097/FBP.0000000000000319
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Ammonium trichloro (dioxoethylene-O,O) tellurate (AS101) is a synthetic organotellurium compound with potent immunomodulatory and neuroprotective properties shown to inhibit the function of integrin v3, a presynaptic cell-surface-adhesion receptor. As partial deletion of v3 downregulated reuptake of serotonin by the serotonin transporter, we hypothesized that AS101 may influence pathways regulating anxiety. AS101 was tested in the modulation of anxiety-like behavior using the selectively bred Submissive (Sub) mouse strain that develop anxiety-like behavior in response to an i.p. injection. Mice were treated daily with AS101 (i.p., 125 or 200g/kg) or vehicle for 3 weeks, after which their anxiety-like behavior was measured in the elevated plus maze. Animals were then culled for the measurement of serum corticosterone levels by ELISA and hippocampal expression of brain-derived neurotrophic factor (BDNF) by RT-PCR. Chronic administration of AS101 significantly reduced anxiety-like behavior of Sub mice in the elevated plus maze, according to both time spent and entries to open arms, relative to vehicle-treated controls. AS101 also markedly reduced serum corticosterone levels of the treated mice and increased their hippocampal BDNF expression. Anxiolytic-like effects of AS101 may be attributed to the modulation of the regulatory influence integrin of v3 upon the serotonin transporter, suggesting a multifaceted mechanism by which AS101 buffers the hypothalamic-pituitary-adrenal axis response to injection stress, enabling recovery of hippocampal BDNF expression and anxiety-like behavior in Sub mice. Further studies should advance the potential of AS101 in the context of anxiety-related disorders. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:458 / 465
页数:8
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