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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:
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.
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页码:4491 / 4504
页数:14
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