Incensole acetate reduces depressive-like behavior and modulates hippocampal BDNF and CRF expression of submissive animals

被引:35
作者
Moussaieff, Arieh [1 ]
Gross, Moshe [1 ,2 ,3 ]
Nesher, Elimelech [1 ,2 ]
Tikhonov, Tatiana [1 ]
Yadid, Gal [2 ]
Pinhasov, Albert [1 ,3 ]
机构
[1] Ariel Univ Ctr Samaria, Dept Mol Biol, IL-40700 Ariel, Israel
[2] Bar Ilan Univ, Dept Life Sci, Ramat Gan, Israel
[3] Samaria & Jordan Rift Res & Dev Ctr, Ariel, Israel
关键词
Incensole acetate; depression; dominant-submissive relationship (DSR); corticotrophin releasing factor (CRF); brain derived neurotrophic factor (BDNF); corticosterone; CORTICOTROPIN-RELEASING-FACTOR; NEUROTROPHIC FACTOR TRANSCRIPTS; ANTIDEPRESSANT DRUG ACTIVITY; PLACEBO-CONTROLLED TRIAL; ADULT-RAT HIPPOCAMPUS; MAJOR DEPRESSION; DIFFERENTIAL REGULATION; PARAVENTRICULAR NUCLEUS; NEUROSECRETORY NEURONS; PROTEIN EXPRESSION;
D O I
10.1177/0269881112458729
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Incensole acetate (IA), a constituent of Boswellia resin ('frankincense'), was previously demonstrated to exhibit an antidepressive-like effect in the Forced Swim Test (FST) in mice following single dose administration (50 mg/kg). Here, we show that acute administration of considerably lower dose (10 mg/kg) IA to selectively bred mice, showing prominent submissive behavior, exerted significant antidepressant-like effects in the FST. Furthermore, chronic administration of 1 or 5 mg/kg per day of IA for three consecutive weeks dose- and time-dependently reduced the submissiveness of the mice in the Dominant-Submissive Relationship test, developed to screen the chronic effect of antidepressants. This behavioral effect was concomitant to reduced serum corticosterone levels, dose-dependent down-regulation of corticotropin releasing factor and up-regulation of brain derived neurotrophic factor transcripts IV and VI expression in the hippocampus. These data suggest that IA modulates the hypothalamic-pituitary-adrenal (HPA) axis and influences hippocampal gene expression, leading to beneficial behavioral effects supporting its potential as a novel treatment of depressive-like disorders.
引用
收藏
页码:1584 / 1593
页数:10
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