Galanin (1-15) enhances the antidepressant effects of the 5-HT1A receptor agonist 8-OH-DPAT: involvement of the raphe-hippocampal 5-HT neuron system

被引:34
|
作者
Millon, Carmelo [1 ]
Flores-Burgess, Antonio [1 ]
Narvaez, Manuel [1 ]
Borroto-Escuela, Dasiel O. [2 ]
Santin, Luis [3 ]
Gago, Belen [1 ]
Angel Narvaez, Jose [1 ]
Fuxe, Kjell [2 ]
Diaz-Cabiale, Zaida [1 ]
机构
[1] Univ Malaga, Inst Invest Biomed Malaga, Fac Med, Dept Fisiol, Campus Teatinos S-N, Malaga 29071, Spain
[2] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
[3] Univ Malaga, Inst Invest Biomed Malaga, Dept Psicobiol, Fac Psicol, Campus Teatinos S-N, E-29071 Malaga, Spain
来源
BRAIN STRUCTURE & FUNCTION | 2016年 / 221卷 / 09期
基金
英国医学研究理事会;
关键词
Galanin; Galanin (1-15); 5-HT1A receptors; Heteroreceptor complexes; Depression; FORCED SWIMMING TEST; CENTRAL CARDIOVASCULAR CONTROL; VENTRAL LIMBIC CORTEX; INTRAVENTRICULAR GALANIN; DORSAL RAPHE; RAT-BRAIN; BINDING-SITES; DEPRESSION; AUTORECEPTOR; SUBTYPES;
D O I
10.1007/s00429-015-1180-y
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Galanin N-terminal fragment (1-15) [GAL(1-15)] is associated with depression-related and anxiogenic-like effects in rats. In this study, we analyzed the ability of GAL(1-15) to modulate 5-HT1A receptors (5-HT1AR), a key receptor in depression. GAL(1-15) enhanced the antidepressant effects induced by the 5-HT1AR agonist 8-OH-DPAT in the forced swimming test. These effects were stronger than the ones induced by Galanin (GAL). This action involved interactions at receptor level since GAL(1-15) affected the binding characteristics and the mRNA levels of 5-HT1AR in the dorsal hippocampus and dorsal raphe. The involvement of the GALR2 was demonstrated with the GALR2 antagonist M871. Proximity ligation assay experiments indicated that 5-HT1AR are in close proximity with GALR1 and GALR2 in both regions and in raphe RN33B cells. The current results indicate that GAL(1-15) enhances the antidepressant effects induced by 8-OH-DPAT acting on 5-HT1AR operating as postjunctional or as autoreceptors. These results may give the basis for the development of drugs targeting potential GALR1-GALR2-5-HT1AR heteroreceptor complexes linked to the raphe-hippocampal 5-HT neurons for the treatment of depression.
引用
收藏
页码:4491 / 4504
页数:14
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