Effects of repeated treatment with a delta opioid receptor agonist KNT-127 on hyperemotionality in olfactory-bulbectomized rats

被引:19
|
作者
Gotoh, Leo [1 ]
Saitoh, Akiyoshi [1 ]
Yamada, Misa [1 ]
Fujii, Hideaki [2 ]
Nagase, Hiroshi [3 ]
Yamada, Mitsuhiko [1 ]
机构
[1] Natl Inst Mental Hlth, Natl Ctr Neurol & Psychiat, Dept Neuropsychopharmacol, 4-1-1 Ogawahigashimachi, Kodaira, Tokyo 1878553, Japan
[2] Kitasato Univ, Sch Pharm, Med Chem Lab, Tokyo 1088641, Japan
[3] Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
Olfactory bulbectomy; Delta opioid; Animal model; Antidepressant; KNT-127; Depression; ANTIDEPRESSANT-LIKE; DEPRESSION; MODEL; MICE; DISORDERS; BW373U86; BEHAVIOR; DRUGS; SNC80;
D O I
10.1016/j.bbr.2016.11.008
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
We previously demonstrated that a single treatment of a non-peptidic delta opioid receptor agonist, KNT-127, has an antidepressant-like effect in rodents in the forced swim test. Here we evaluated the effect of repeated administration of the potential antidepressant KNT-127 in an olfactory-bulbectomized (OBX) rat model. Male Wistar rats (8-12 weeks old) underwent olfactory bulbectomy. From 14 days after surgery each was weighed and administered either KNT-127 (3 mg kg(-1)/day), the selective serotonin reuptake inhibitor (SSRI) fluoxetine (10 mg kg(-1)/day), or vehicle, daily for 14 days. Hyperemotionality was measured on days 3, 5, 7, 10, and 14. Repeated administration of KNT-127 significantly decreased total and individual hyperemotionality scores (attack, startle, struggle and fight) over the entire period. Conversely, fluoxetine did not show any significant effect on days 3, 5, 7, or 14 but significantly reduced the total score on day 10. The inhibitory effects of KNT-127 were greater than those of fluoxetine. The KNT-127 and control groups both gained weight, while the fluoxetine group lost weight. Our results suggest that KNT-127 is a potential lead compound for antidepressant therapy, with high efficacy, a relatively rapid onset of therapeutic effect, and without the possible adverse effects of weight loss caused by SSRIs. 2016 Published by Elsevier B.V.
引用
收藏
页码:11 / 14
页数:4
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