食品科学 ›› 2026, Vol. 47 ›› Issue (10): 167-179.doi: 10.7506/spkx1002-6630-20251111-074

• 营养卫生 • 上一篇    下一篇

多组学方法探究叶绿素对镉诱导小鼠肝肾损伤的缓解作用

张志敏,王元楷,黄起阳,王藩龙,赖东京,蔡甜,陈科伟   

  1. (1.西南大学食品科学学院,重庆 400715;2.中匈食品科学合作研究中心,重庆 400715;3.西南大学化学化工学院,重庆 400715;4.川渝共建特色食品重庆市重点实验室,重庆 400715)
  • 出版日期:2026-05-25 发布日期:2026-06-10
  • 基金资助:
    “十四五”国家重点研发计划重点专项(2023YFE0116100); 重庆市科技局新重庆青年创新人才项目(CSTB2025YITP-QCRCX0008); 重庆市人社局留学回国人员创业创新项目(cx2025086)

Multi-omic Investigation of the Alleviation of Cadmium-Induced Liver and Kidney Injury in Mice by Chlorophyll

ZHANG Zhimin, WANG Yuankai, HUANG Qiyang, WANG Fanlong, LAI Dongjing, CAI Tian, CHEN Kewei   

  1. (1. College of Food Science, Southwest University, Chongqing 400715, China; 2. Chinese-Hungarian Cooperative Research Centre for Food Science, Chongqing 400715, China; 3. School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China; 4. Chongqing Key Laboratory of Specialty Food Co-Built by Sichuan and Chongqing, Chongqing 400715, China)
  • Online:2026-05-25 Published:2026-06-10

摘要: 目的:探讨叶绿素对镉(Cd)诱导小鼠肝肾损伤的缓解作用及其潜在机制。方法:以C57BL/6J雄性小鼠为模型,连续8 周经饮水暴露100 mg/L CdCl2建立镉暴露模型,饲料中分别添加高、低剂量叶绿素(0.09 mg/g与0.045 mg/g)。检测血清丙氨酸氨基转移酶(alanine aminotransferase,ALT)、天冬氨酸氨基转移酶(aspartate aminotransferase,AST)、碱性磷酸酶(alkaline phosphatase,ALP)、尿素、尿酸(uric acid,UA)、肌酐(creatinine,CREA)水平以及肝肾组织中的超氧化物歧化酶(superoxide dismutase,SOD)、谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)、丙二醛(malondialdehyde,MDA)水平,并结合苏木精-伊红染色、转录组学和非靶向代谢组学分析叶绿素对镉诱导的小鼠肝肾损伤的缓解作用。结果:与Cd组(100 mg/L CdCl2溶液)相比,叶绿素干预后肝脏抗氧化防御能力得到改善,表现为SOD、GSH-Px活性升高而MDA水平降低。同时,血清AST、尿素与CREA水平均显著下调(P<0.05),肝细胞水样变性与肾小球萎缩等组织学损伤得到缓解。利用代谢组学分析从肝脏、肾脏中分别鉴定出52、49 种差异显著代谢物,主要涉及甘油磷脂、亚油酸及苯丙氨酸代谢通路。利用转录组学分析从肝脏、肾脏中分别鉴定出799、1 778 个差异显著基因,富集于氧化磷酸化、磷脂酰肌3-激酶/蛋白激酶B及脂质代谢等通路。综合分析表明,叶绿素可能通过减轻线粒体DNA损伤、调节能量代谢及恢复脂质与氨基酸代谢稳态,显著缓解镉诱导的肝肾氧化损伤。结论:紫菜叶绿素具有显著的抗氧化与解毒作用,可作为防控重金属镉毒性的潜在膳食功能因子,本研究可为高镉暴露人群的营养干预提供科学依据。

关键词: 镉;叶绿素;非靶向代谢组学;转录组学;氧化损伤

Abstract: Objective: This study investigated the alleviating effect of chlorophyll on Cd-induced liver and kidney damage in mice and explored its potential mechanisms. Methods: Male C57BL/6J mice were exposed to 100 mg/L CdCl2 via drinking water for 8 consecutive weeks to establish a cadmium exposure model. High-dose (0.09 mg/g) and low-dose (0.045 mg/g) chlorophyll were added to the diet. Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) activities, as well as urea, uric acid (UA), and creatinine (CREA) levels were measured. In addition, the levels of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) in liver and kidney tissues were determined. Lastly, the alleviating effect of chlorophyll on cadmium-induced liver and kidney injury in mice was elucidated through hematoxylin and eosin (HE) staining, transcriptomics, and non-targeted metabolomic analysis. Results: Compared with the Cd group (100 mg/L CdCl2 solution), chlorophyll intervention improved hepatic antioxidant defense, as evidenced by increased SOD and GSH-Px activities and decreased MDA levels. Meanwhile, the serum levels of AST, urea, and CREA were significantly reduced (P < 0.05), and histopathological lesions such as hepatocellular hydropic degeneration and glomerular atrophy were alleviated. Metabolomics identified 52 differential metabolites in the liver and 49 in the kidney. These metabolites were primarily involved in glycerophospholipid, linoleic acid, and phenylalanine metabolic pathways. Transcriptomics identified 799 differential genes in the liver and 1 778 in the kidney. These genes were enriched in oxidative phosphorylation, phosphoinositide 3-kinase/protein kinase B (PI3K-Akt), and lipid metabolism pathways. Collectively, chlorophyll significantly alleviates cadmium-induced oxidative damage in the liver and kidney by mitigating mitochondrial DNA damage, regulating energy metabolism, and restoring lipid and amino acid metabolic homeostasis. Conclusion: Chlorophyll from purple laver exhibits potent antioxidant and detoxifying effects, positioning it as a potential dietary functional factor for controlling cadmium toxicity. This provides a scientific rationale for nutritional intervention in populations exposed to high cadmium levels.

Key words: cadmium; chlorophylls; untargeted metabolomics; transcriptomics; oxidative damage

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