食品科学 ›› 2025, Vol. 46 ›› Issue (19): 167-176.doi: 10.7506/spkx1002-6630-20250222-105

• 营养卫生 • 上一篇    

基于秀丽隐杆线虫模型的槟榔碱运动神经毒性效应及机制

王玥,邹泽斌,李雅琪,杜冰,黎攀   

  1. (华南农业大学食品学院,广东 广州 510642)
  • 发布日期:2025-09-16
  • 基金资助:
    现代农业产业技术体系建设专项(CARS-21)

Neurotoxic Effects and Mechanism of Arecoline on Locomotor Function in Caenorhabditis elegans as Model Organism

WANG Yue, ZOU Zebin, LI Yaqi, DU Bing, LI Pan   

  1. (College of Food Science, South China Agriculture University, Guangzhou 510642, China)
  • Published:2025-09-16

摘要: 以秀丽隐杆线虫(Caenorhabditis elegans)为模型,通过0.5~4 mg/mL槟榔碱暴露实验,分析其对运动能力、肠屏障、能量代谢、氧化应激及线粒体功能等多维度生理指标的影响,揭示槟榔碱介导的运动神经毒性机制。结果表明:与Control组相比,2 mg/mL AEC-2组线虫运动能力显著降低(P<0.001);线虫体内氧化还原平衡被破坏、脂褐质积累(P<0.01),平均荧光强度提高29.01%;线虫肠道屏障功能的完整性被破坏,影响线虫的产能代谢(P<0.001),其中葡萄糖、丙酮酸、柠檬酸及ATP含量分别下降36.94%、43.11%、37.76%、55.88%;同时本研究发现线虫神经元受到损伤,神经递质的水平显著减少(P<0.01),进一步证实槟榔碱具有神经毒性;线虫体内线粒体数目显著减少(P<0.05)且线粒体功能受损。本研究证实了2 mg/mL槟榔碱通过破坏线虫肠道屏障功能介导产能代谢降低与氧化应激,引发运动能力下降及神经元损伤,揭示了其运动神经毒性机制,可为筛选改善槟榔碱神经毒性的活性物质提供理论支撑。

关键词: 槟榔碱;秀丽隐杆线虫;运动能力;毒性作用

Abstract: This study explored the effects of exposure to arecoline at different concentrations (0.5, 1, 2 and 4 mg/mL) on the locomotor capacity, intestinal barrier function, energy metabolism, oxidative stress and mitochondrial function of the model organism Caenorhabditis elegans, and it also revealed the neurotoxic mechanism of arecoline. The results showed that compared with the control group, exposure to 2 mg/mL arecoline significantly decreased the locomotor capacity of C. elegans (P < 0.001), disrupted the redox balance, resulted in lipofuscin accumulation (P < 0.01) and increased the average fluorescence intensity by 29.01%. Meanwhile, it damaged intestinal barrier integrity and affected energy metabolism (P < 0.001), decreasing the levels of glucose, pyruvate, citric acid and ATP by 36.94%, 43.11%, 37.76% and 55.88%, respectively. Additionally, arecoline exposure caused neuronal damage and significantly decreased neurotransmitter levels (P < 0.01), further confirming its neurotoxicity. It also decreased significantly the number of mitochondria in C. elegans (P < 0.05) and impaired mitochondrial function. In summary, 2 mg/mL arecoline exerts significant motor neurotoxicity in C. elegans mainly by disrupting intestinal barrier function, mediating reduced energy metabolism as well as oxidative stress, and ultimately resulting in reduced locomotor capacity and neuronal damage. These findings elucidate the mechanism of the motor neurotoxicity of arecoline, providing a theoretical basis for screening active substances that mitigates this neurotoxicity.

Key words: arecoline; Caenorhabditis elegans; locomotor capacity; toxic effect

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