在诱导神经发生方面,高强度间歇运动比中等强度运动更有效。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Marvin Lambertus, Samuel Geiseler, Cecilie Morland
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引用次数: 0

摘要

在衰老过程中,大脑的神经源潜力会下降,而患神经退行性疾病和中风的风险则会上升。这就造成了神经元丢失速度与大脑替代能力之间的不匹配。成人神经发生主要发生在粒下区(SGZ)和脑室-脑室下区(V-SVZ)。运动能增强 SGZ 神经发生,我们以前的研究表明,V-SVZ 神经发生是通过激活乳酸受体 HCA1 由运动诱导的。在这里,我们研究了高强度间歇训练(HIIT)和中等强度间歇训练(MIIT)如何影响这些龛位的神经发生。野生型(WT)和 HCA1 基因敲除(KO)小鼠被随机分配到静坐、HIIT 或 MIIT(每组 n = 5-8)训练中,为期 3 周。在SGZ中,HIIT使WT小鼠的双皮质素(DCX)阳性细胞密度增加了85%(5.77±1.76 vs. 3.12±1.54个细胞/100微米,P = 0.013),KO小鼠的双皮质素阳性细胞密度增加了67%(7.91±2.92 vs. 4.73±1.63个细胞/100微米,P = 0.004)。MIIT没有改变两种基因型中DCX阳性细胞的密度。HIIT 仅增加了 KO 小鼠 Ki-67 阳性细胞的密度(P = 0.038),而在 nestin 阳性细胞中未观察到差异。在 V-SVZ 中,HIIT 使 WT 小鼠的 DCX 阳性细胞密度增加了 155% (117.79±39.72 vs. 46.25±19.96 cells/100 µm,P 1),在 V-SVZ 神经发生中发挥了关键作用。要点:大脑的神经源潜能会随着年龄的增长而降低,而神经退行性疾病和中风的风险却在增加,这凸显了神经元损失和替代能力之间的不匹配。运动能增强粒细胞下区和脑室-脑室下区的神经元生成。高强度间歇运动比中等强度间歇运动更能促进野生型小鼠粒细胞下区和心室-室下区的神经发生。中强度和高强度间歇运动能够诱导野生型小鼠的神经发生,而 HCA1 基因敲除小鼠则没有这种效果,这证明脑室-室下区神经发生的增强依赖于 HCA1 受体的激活。相比之下,粒细胞下区的神经发生与 HCA1 受体的激活无关,这突出表明这两大神经发生龛的神经发生受到不同的调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-intensity interval exercise is more efficient than medium intensity exercise at inducing neurogenesis

High-intensity interval exercise is more efficient than medium intensity exercise at inducing neurogenesis
The neurogenic potential of the brain decreases during ageing, whereas the risk of neurodegenerative diseases and stroke rises. This creates a mismatch between the rate of neuron loss and the brain's capacity for replacement. Adult neurogenesis primarily occurs in the subgranular zone (SGZ) and the ventricular-subventricular zone (V-SVZ). Exercise enhances SGZ neurogenesis, and we previously showed that V-SVZ neurogenesis is induced by exercise via activation of the lactate receptor HCA1. Here, we investigated how high-intensity interval training (HIIT) and medium-intensity interval training (MIIT) affect neurogenesis in these niches. Wild-type (WT) and HCA1 knockout (KO) mice were randomized to sedentary, HIIT or MIIT (n = 5–8 per group) for 3 weeks. In the SGZ, HIIT increased the density of doublecortin (DCX)-positive cells in WT mice by 85% (5.77±1.76 vs. 3.12±1.54 cells/100 µm, P = 0.013) and KO mice (67% increase; 7.91±2.92 vs. 4.73±1.63 cells/100 µm, P = 0.004). MIIT did not alter the density of DCX-positive cells in either genotype. HIIT increased the density of Ki-67-positive cells only in KO mice (P = 0.038), whereas no differences in nestin-positive cells were observed. In the V-SVZ, HIIT increased the density of DCX-positive cells in WT mice by 155% (117.79±39.72 vs. 46.25±19.96 cells/100 µm, < 0.001) and MIIT increased the density of DCX-positive cells by 80% (83.26±39.48 vs. 46.25±19.96 cells/100µm, P = 0.027). No exercise-induced changes were observed in KO mice. Similar patterns were noted for Ki-67 positive and DCX/Ki-67 double-positive cells in the V-SVZ. These findings suggest that HIIT enhances neurogenesis more robustly than MIIT in both niches, with HCA1 playing a crucial role in V-SVZ neurogenesis.

Key points

  • The neurogenic potential of the brain decreases with age, whereas the risk of neurodegenerative diseases and stroke increases, highlighting a mismatch between neuronal loss and replacement capacity.
  • Exercise enhances neurogenesis in both the subgranular zone and the ventricular-subventricular zone.
  • High-intensity interval exercise is more effective than medium-intensity interval exercise at promoting neurogenesis in both the subgranular zone and the ventricular-subventricular zone of wild-type mice.
  • The enhancement of neurogenesis in the ventricular-subventricular zone is dependent on the activation of the HCA1 receptor, as evidenced by the ability of medium- and high-intensity interval exercise to induce neurogenesis in wild-type mice and the lack of this effect in HCA1 knockout mice.
  • By contrast, neurogenesis in the subgranular zone is independent on the activation of the HCA1 receptor, highlighting that neurogenesis in the two major neurogenic niches are regulated differently.
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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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