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Antidepressive and BDNF effects of enriched environment treatment across ages in mice lacking BDNF expression through promoter IV

机译:通过启动子IV对缺乏BDNF表达的小鼠进行多年龄的丰富环境治疗具有抗抑郁和BDNF的作用

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摘要

Reduced promoter IV-driven expression of brain-derived neurotrophic factor (BDNF) is implicated in stress and major depression. We previously reported that defective promoter IV (KIV) caused depression-like behavior in young adult mice, which was reversed more effectively by enriched environment treatment (EET) than antidepressants. The effects of promoter IV-BDNF deficiency and EET over the life stages remain unknown. Since early-life development (ED) involves dynamic epigenetic processes, we hypothesized that EET during ED would provide maximum antidepressive effects that would persist later in life due to enhanced, long-lasting BDNF induction. We tested this hypothesis by determining EET effects across three life stages: ED (0–2 months), young adult (2–4 months), and old adult (12–14 months). KIV mice at all life stages showed depression-like behavior in the open-field and tail-suspension tests compared with wild-type mice. Two months of EET reduced depression-like behavior in ED and young adult, but not old adult mice, with the largest effect in ED KIV mice. This effect lasted for 1 month after discontinuance of EET only in ED mice. BDNF protein induction by EET in the hippocampus and frontal cortex was also the largest in ED mice and persisted only in the hippocampus of ED KIV mice after discontinuance of EET. No gender-specific effects were observed. The results suggest that defective promoter IV causes depression-like behavior, regardless of age and gender, and that EET during ED is particularly beneficial to individuals with promoter IV-BDNF deficiency, while additional treatment may be needed for older adults.
机译:脑源性神经营养因子(BDNF)的启动子IV驱动的表达减少与压力和严重抑郁有关。我们先前曾报道缺陷启动子IV(KIV)在年轻成年小鼠中引起抑郁样行为,与抗抑郁药相比,通过富集环境治疗(EET)更有效地逆转了这种行为。启动子IV-BDNF缺乏和EET在整个生命周期中的作用仍然未知。由于早期生命发展(ED)涉及动态表观遗传过程,因此我们假设ED期间的EET将提供最大的抗抑郁作用,由于增强的BDNF持久诱导,该抗抑郁作用将在生命的后期持续存在。我们通过确定三个生命阶段的EET影响来检验这一假设:ED(0–2个月),年轻人(2–4个月)和成年人(12–14个月)。与野生型小鼠相比,在所有生命阶段的KIV小鼠在开放视野和尾部悬挂测试中均表现出抑郁样行为。两个月的EET可以降低ED和成年小鼠的抑郁样行为,但不能降低成年成年小鼠的抑郁症行为,对ED KIV小鼠的影响最大。仅在ED小鼠中,EET中断后,这种作用持续了1个月。 EET在海马和额叶皮层中对BDNF蛋白的诱导也是ED小鼠中最大的,并且在EET中断后仅在ED KIV小鼠的海马中持续存在。没有观察到针对性别的影响。结果表明,有缺陷的启动子IV不论年龄和性别,都会引起抑郁样行为,并且在ED期间EET对具有启动子IV-BDNF缺乏症的个体特别有益,而老年人可能需要额外的治疗。

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