Brain-Derived Neurotrophic Factor Prevents Depressive-Like Behaviors in Early-Symptomatic YAC128 Huntington's Disease Mice

被引:15
|
作者
da Fonseca, Victor Silva [1 ]
da Silva Colla, Andre R. [2 ]
Nascimento-Castro, Cristine de Paula [1 ]
Placido, Evelini [1 ]
Rosa, Julia Macedo [2 ]
Farina, Marcelo [2 ]
Gil-Mohapel, Joana [3 ]
Rodrigues, Ana Lucia S. [2 ]
Brocardo, Patricia S. [1 ]
机构
[1] Univ Fed Santa Catarina, Ctr Biol Sci, Dept Morphol Sci, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Santa Catarina, Ctr Biol Sci, Dept Biochem, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Victoria, Div Med Sci, UBC Isl Med Program, Victoria, BC V8W 2Y2, Canada
关键词
Huntington's disease; Brain-derived neurotrophic factor (BDNF); Depression; Hippocampus; Neurogenesis; YAC128 transgenic mice; TRANSGENIC MOUSE MODEL; CHRONIC MILD STRESS; HIPPOCAMPAL DENTATE GYRUS; TAIL SUSPENSION TEST; ADULT NEUROGENESIS; ANTIDEPRESSANT TREATMENT; ANIMAL-MODEL; ENVIRONMENTAL ENRICHMENT; INCREASES NEUROGENESIS; PSYCHIATRIC-SYMPTOMS;
D O I
10.1007/s12035-018-0890-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Huntington disease (HD) is a neurodegenerative disorder caused by an expanded CAG repeat in the Huntington disease gene. The symptomatic stage of the disease is defined by the onset of motor symptoms. However, psychiatric disturbances, including depression, are common features of HD and can occur a decade before the manifestation of motor symptoms. We used the YAC128 transgenic mice (which develop motor deficits at a later stage, allowing more time to study depressive behaviors without the confounding effects of motor impairment) to test the effects of intranasal brain-derived neurotrophic factor (BDNF) treatment for 15 days in the occurrence of depressive-like behaviors. Using multiple well-validated behavioral tests, we found that BDNF treatment alleviated anhedonic and depressive-like behaviors in the YAC128 HD mice. Furthermore, we also investigated whether the antidepressant-like effects of BDNF were associated with an increase in adult hippocampal neurogenesis. However, BDNF treatment only increased cell proliferation and neuronal differentiation in the hippocampal dentate gyrus (DG) of wild-type (WT) mice, without altering these parameters in their YAC128 counterparts. Moreover, BDNF treatment did not cause an increase in the number of dendritic branches in the hippocampal DG when compared with animals treated with vehicle. In conclusion, our results suggest that non-invasive administration of BDNF via the intranasal route may have important therapeutic potential for treating mood disturbances in early-symptomatic HD patients.
引用
收藏
页码:7201 / 7215
页数:15
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