Department of Environmental Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Department of Sports and Exercise Science, Zhejiang University, Hangzhou, China.
Ecotoxicol Environ Saf. 2023 Jun 15;258:114986. doi: 10.1016/j.ecoenv.2023.114986. Epub 2023 May 8.
Cadmium (Cd) is a well-known environmental pollutant with high toxicity. Despite a variety of studies have demonstrated that Cd exposure induces multiple organ damages in humans, there is still a lack of knowledge of Cd induced skeletal muscle impairment. Exercise is a non-invasive, effective intervention to improve human health and combat diseases. In this study, we aimed to evaluate the toxic effects of Cd exposure on skeletal muscle function and explore the possibility of exercise for attenuating skeletal muscle toxicity of chronic Cd exposure. C57BL/6J mice were exposed to Cd via drinking water containing CdCl 10 mg/dL for 8 weeks while a moderate exercise was daily induced by a motorized treadmill to mice. It was found that Cd exposure significantly reduced the ratio of gastrocnemius and body weight, decreased mouse exercise capacity, weakened muscle strength, promoted lipid accumulation and up-regulated pro-apoptotic genes in the skeletal muscle. Non-targeted lipidomics analysis indicated that Cd exposure disturbed lipid metabolism, altered lipid signatures and elevated pro-inflammatory lipid species in the skeletal muscle. Moreover, Cd exposure evoked an intense inflammatory response in the skeletal muscle by up-regulating pro-inflammatory cytokine production such as Eotaxin (CCL11), TNF-α, IL-1β, IL-6, RANTES (CCL5) and so on. Notably, treadmill exercise effectively protected against Cd induced skeletal muscle impairment indicated by the effects of inhibiting lipid metabolism disturbance, suppressing pro-inflammatory cytokine production and preserving skeletal muscle function. These results demonstrated that environment relevant Cd exposure impairs skeletal muscle function and exercise effectively antagonizes the Cd toxicity in the skeletal muscle and preserves skeletal muscle function. This study provided the novel evidence for unraveling Cd toxicity on the skeletal muscle function and highlighted the possibility of considering exercise as a countermeasure for Cd induced skeletal muscle impairment at population level.
镉(Cd)是一种毒性很强的环境污染物。尽管有大量研究表明,镉暴露会导致人体多器官损伤,但对于镉诱导的骨骼肌损伤机制仍知之甚少。运动是一种非侵入性的、有效的干预手段,可以改善人类健康,防治疾病。在本研究中,我们旨在评估镉暴露对骨骼肌功能的毒性作用,并探讨运动对缓解慢性镉暴露引起的骨骼肌毒性的可能性。通过给 C57BL/6J 小鼠饮用含 10mg/dL CdCl 的水,使小鼠暴露于镉中 8 周,同时每天用电动跑步机对小鼠进行适度运动。结果发现,镉暴露显著降低了比目鱼肌与体重的比值,降低了小鼠的运动能力,减弱了肌肉力量,促进了脂质在骨骼肌中的积累,并上调了骨骼肌中的促凋亡基因。非靶向脂质组学分析表明,镉暴露扰乱了脂质代谢,改变了骨骼肌中的脂质特征,并增加了促炎脂质种类。此外,镉暴露通过上调促炎细胞因子如 Eotaxin(CCL11)、TNF-α、IL-1β、IL-6、RANTES(CCL5)等的产生,在骨骼肌中引发强烈的炎症反应。值得注意的是,跑步机运动有效地防止了镉引起的骨骼肌损伤,其作用包括抑制脂质代谢紊乱、抑制促炎细胞因子的产生和保护骨骼肌功能。这些结果表明,环境相关的镉暴露会损害骨骼肌功能,而运动则能有效拮抗镉对骨骼肌的毒性作用,保护骨骼肌功能。本研究为揭示镉对骨骼肌功能的毒性作用提供了新的证据,并强调了在人群水平上考虑运动作为对抗镉诱导的骨骼肌损伤的对策的可能性。