Behavioral Neuropharmacology and Neuroimaging Laboratory on Addictions (BNNLA), Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, United States.
Department of Biomedical Sciences, University at Buffalo, Buffalo, NY, United States.
Front Public Health. 2023 Dec 19;11:1257629. doi: 10.3389/fpubh.2023.1257629. eCollection 2023.
Previous research has outlined the health benefits of exercise including its therapeutic potential for substance use disorders (SUD). These data have already been utilized and it is now common to find exercise as part of SUD treatment and relapse prevention programs. However, we need to better understand different exercise regimens and determine which would be the most beneficial for SUDs. Recently, high intensity interval training (HIIT) has gained attention in comparison with aerobic and resistance exercise. Little is known regarding the neurobiological mechanisms of HIIT, including its effects on dopamine signaling and receptor levels in the brain. The present study examined the effects of chronic HIIT exercise on dopamine signaling as measured by dopamine type 1-like receptor (D1R)-like, dopamine type 2-like receptor (D2R)-like, and tyrosine hydroxylase (TH) quantification in the brains of male and female rats as measured by [H] SCH 23390 and [H] spiperone autoradiography, and TH-immunoreactive optical density values.
Rats were separated in two groups: sedentary and HIIT exercise. Exercise was on a treadmill for 30 min daily (10 3 min cycles) for six weeks with progressive speed increased up to 0.8 mph (21.5 m/min).
Results showed for D2R-like binding, a significant effect across the ventral caudate putamen (V CPU) between sexes, such that mean D2R-like binding was 14% greater for males than females. In the nucleus accumbens shell (Nac Shell), the HIIT Exercise rats showed 16% greater D2R-like binding as compared to the sedentary rats. No significant effects of HIIT exercise were found across groups for brain D1R-like binding levels or TH expression.
These results suggest that HIIT exercise can modulate dopamine signaling by way of increased D2R. These findings support the premise that HIIT exercise plays an important role in dopamine signaling and, may provide a potential mechanism for how HIIT exercise can impact the brain and behavior.
先前的研究已经概述了运动的健康益处,包括其对物质使用障碍(SUD)的治疗潜力。这些数据已经得到了利用,现在在 SUD 治疗和复发预防计划中经常可以找到运动。然而,我们需要更好地了解不同的运动方案,并确定哪些方案对 SUD 最有益。最近,高强度间歇训练(HIIT)与有氧运动和抗阻运动相比受到了关注。关于 HIIT 的神经生物学机制知之甚少,包括其对大脑中多巴胺信号和受体水平的影响。本研究通过 [H]SCH23390 和 [H]spiperone 放射自显影测量多巴胺 1 样受体(D1R)样、多巴胺 2 样受体(D2R)样和酪氨酸羟化酶(TH)的定量,以及通过 [H]SCH23390 和 [H]spiperone 放射自显影测量雄性和雌性大鼠大脑中的多巴胺信号,研究了慢性 HIIT 运动对多巴胺信号的影响,并通过 TH-免疫反应性光密度值进行了测量。
大鼠分为两组:安静组和 HIIT 运动组。运动是在跑步机上进行的,每天 30 分钟(10 个 3 分钟的循环),持续六周,速度逐渐增加到 0.8 英里/小时(21.5 米/分钟)。
结果表明,在腹侧尾壳核(VCPU)中,D2R 样结合存在显著的性别间效应,即雄性的 D2R 样结合比雌性高 14%。在伏隔核壳(Nac Shell)中,HIIT 运动组的 D2R 样结合比安静组高 16%。在大脑 D1R 样结合水平或 TH 表达方面,HIIT 运动组之间没有发现显著的影响。
这些结果表明,HIIT 运动可以通过增加 D2R 来调节多巴胺信号。这些发现支持 HIIT 运动在多巴胺信号中发挥重要作用的前提,并可能为 HIIT 运动如何影响大脑和行为提供潜在机制。