Please wait a minute...
文章检索
预防医学  2022, Vol. 34 Issue (10): 1069-1074    DOI: 10.19485/j.cnki.issn2096-5087.2022.10.019
  实验技术 本期目录 | 过刊浏览 | 高级检索 |
大鼠肝21种全氟化合物生物利用率和蛋白粉作用研究
蔡德雷, 俞莎, 郑熠斌, 沈海涛, 夏勇, 宋燕华, 姚进, 陈苘
浙江省疾病预防控制中心理化与毒理检验所,浙江 杭州 310051
Effect of protein powder on the bioavailability of 21 types of perfluorochemicals in rat liver
CAI Delei, YU Sha, ZHENG Yibin, SHEN Haitao, XIA Yong, SONG Yanhua, YAO Jin, CHEN Qing
Department of Physicochemical and Toxicology, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, Zhejiang 310051, China
全文: PDF(807 KB)  
输出: BibTeX | EndNote (RIS)      
摘要 目的 检测大鼠肝21种全氟化合物(PFCs)生物利用率并分析蛋白粉的干预作用。方法 24只SD大鼠随机纳入对照组、模型组和蛋白粉组。21种PFCs按10 ng/mL等浓度混合,模型组和蛋白粉组大鼠每日经口灌胃给予PFCs混合物,灌胃体积为5 mL/kg体重。蛋白粉组大鼠经口灌胃给予3.87 g/kg体重的蛋白粉15 mL/kg体重,模型组、对照组分别给予15、20 mL/kg体重的去离子水,持续28 d。采用超高效液相色谱-串联质谱仪内标法定量,检测肝中PFCs含量并计算生物利用率。结果 对照组、模型组和蛋白粉组大鼠体重和肝体比差异均无统计学意义(P>0.05)。蛋白粉组雌、雄性大鼠肝全氟羧酸(PFCA)生物利用率、全氟磺酸(PFSA)生物利用率与模型组相比,差异均无统计学意义(P>0.05)。模型组雄性大鼠肝PFCA(t=-22.266,P<0.001)和PFSA(t=-34.312,P<0.001)总生物利用率均高于雌性大鼠。随碳链长度增加,模型组大鼠肝对PFCA和PFSA的生物利用率先升高后降低。模型组雌性大鼠对全氟正十二酸(PFDoA)和全氟-1-辛烷磺酸钠(L-PFOS)的生物利用率最高,分别为(36.06±2.93)%和(37.11±1.73)%;模型组雄性大鼠对全氟正壬酸(PFNA)和L-PFOS的生物利用率最高,分别为(61.02±2.16)%和(87.16±3.29)%。结论 大鼠肝PFCs生物利用率与PFCs碳链长度、动物性别有关;未发现蛋白粉对大鼠肝21种PFCs生物利用率有明显影响。
服务
把本文推荐给朋友
加入引用管理器
E-mail Alert
RSS
作者相关文章
蔡德雷
俞莎
郑熠斌
沈海涛
夏勇
宋燕华
姚进
陈苘
关键词 全氟化合物生物利用率蛋白粉    
AbstractObjective To detect the bioavailability of 21 types of perfluorochemicals (PFCs) in rat liver and to examine the effect of protein powder. Methods Twenty-four rats of the SD strain were randomly divided into the control group, the model group, and the protein powder group. Twenty-one types of PFCs were mixed at an equal concentration of 10 ng/mL, and rats in the model group and the protein powder group were given by oral administration of PFCs mixtures at a daily dose of 5 mL/kg. Rats in the protein powder group were given protein powder by gavage at a dose of 15 mL/kg, while animals in the model and control groups were given deionized water at doses of 15 and 20 mL/kg for 28 successive days. The PFCs contents were quantified in rat liver using ultra-high performance liquid chromatography-electrospray tandem mass spectrometry (UPLC-MS/MS), and the bioavailability was estimated. Results There were no significant differences in rat body weight or liver/body weight ratio in the control, model and protein powder groups (P>0.05). There were no significant differences in the bioavailability of perfluoroalkylated carboxylic acid (PFCA) or sulfonate (PFSA) in the liver of female and male rats between the protein powder group and the model group (P>0.05), and the gross bioavailability of PFCA (t=-22.266, P<0.001) and PFSA (t=-34.312, P<0.001) was significantly higher in the liver of male rats than in that of female rats in the model group, and the bioavailability of PFCA and PFSA increased followed by a reduction in rat livers with the increase of carbon chain length in the model group. In the model group, the highest bioavailability was measured in perfluorododecanoic acid (PFDoA) and sodium perfluorooctylsulfonate (L-PFOS) in the female rat liver [(36.06±2.93)% and (37.11±1.73)%], and the highest bioavailability was measured in perfluorononanoic acid (PFNA) and L-PFOS in the female rat liver [(61.02±2.16)% and (87.16±3.29)%]. Conclusions The bioavailability of PFCs correlates with the carbon chain length and animal gender in rat livers, and protein powder poses no clear-cut effects on the bioavailability of 21 types of PFCs in rat livers.
Key wordsperfluorochemical    bioavailability    protein powder
收稿日期: 2022-05-11      修回日期: 2022-07-07      出版日期: 2022-10-10
中图分类号:  R992  
  R322  
基金资助:浙江省公益技术应用研究(分析测试)(LGC20B050004)
作者简介: 蔡德雷,硕士,副主任技师,主要从事卫生毒理学研究工作
通信作者: 陈苘,E-mail:qingchen@cdc.zj.cn   
引用本文:   
蔡德雷, 俞莎, 郑熠斌, 沈海涛, 夏勇, 宋燕华, 姚进, 陈苘. 大鼠肝21种全氟化合物生物利用率和蛋白粉作用研究[J]. 预防医学, 2022, 34(10): 1069-1074.
CAI Delei, YU Sha, ZHENG Yibin, SHEN Haitao, XIA Yong, SONG Yanhua, YAO Jin, CHEN Qing. Effect of protein powder on the bioavailability of 21 types of perfluorochemicals in rat liver. Preventive Medicine, 2022, 34(10): 1069-1074.
链接本文:  
https://www.zjyfyxzz.com/CN/10.19485/j.cnki.issn2096-5087.2022.10.019      或      https://www.zjyfyxzz.com/CN/Y2022/V34/I10/1069
[1] WANG T,WANG Y,LIAO C,et al.Perspectives on the inclusion of perfluorooctane sulfonate into the Stockholm Convention on Persistent Organic Pollutants[J].Environ Sci Technol,2009,43:5171-5175.
[2] GEBBINK W A,BERGER U,COUSINS I T.Estimating human exposure to PFOS isomers and PFCA homologues:the relative importance of direct and indirect(precursor)exposure[J].Environ Int,2015,74:160-169.
[3] 吴修鹏,马志远,李志华,等.全氟化合物内分泌干扰作用研究[J].毒理学杂志,2021,35(5):436-439.
WU X P,MA Z Y,LI Z H,et al.Disrupting effect on endocrine of perfluoroalkyl substances[J].J Toxicol,2021,35(5):436-439.
[4] 陈敏燕,汪子夏,田英,等.全氟化合物免疫毒性研究进展[J].环境与职业医学,2022,39(2):223-228,235.
CHEN M Y,WANG Z X,TIAN Y,et al.Advances on immunotoxicities induced by per- and polyfluoroalkylated substances[J].J Environ Occup Med,2022,39(2):223-228,235.
[5] TURNER B D,SLOAN S W,CURRELL G R.Novel remediation of per- and polyfluoroalkyl substances(PFASs)from contaminated groundwater using Cannabis Sativa L.(hemp)protein powder[J].Chemosphere,2019,229:22-31.
[6] LI K,LI C,YU N Y,et al.In vivo bioavailability and in vitro bioaccessibility of perfluorooctanoic acid(PFOA)in food matrices:correlation analysis and method development[J].Environ Sci Technol,2015,49:150-158.
[7] 王杰明,王丽,冯玉静,等.液相色谱—质谱联用分析动物内脏和肌肉组织中的全氟化合物[J].食品科学,2010,31(4):127-131.
WANG J M,WANG L,FENG Y J,et al.High performance liquid chromatography-tandem mass spectrometry for determination of perfluorinated compounds in animal visceral and muscle tissues[J].Food Sci,2010,31(4):127-131.
[8] KJØLHOLT J,JENSEN A A,WARMING M.Short-chain polyfluoroalkyl substances(PFAS):a literature review of information on human health effects and environmental fate and effect aspects of short-chain PFAS[M].Odense:the Danish Environmental Protection Agency,2015.
[9] PIZZURRO D M,SEELEY M,KERPER L E,et al.Interspecies differences in perfluoroalkyl substances(PFAS)toxicokinetics and application to health-based criteria[J].Regul Toxicol Pharmacol,2019,106:239-250.
[10] XIA J,FANG Y,SHI Y,et al.Effect of food matrices on the in vitro bioavailability and oxidative damage in PC12 cells of lead[J].Food Chem,2018,266:397-404.
[11] LAURENT C,FEIDT C,GROVA N,et al.Portal absorption of 14C after ingestion of spiked milk with 14C-phenanthrene,14C-benzo[a] pyrene or 14C-TCDD in growing pigs[J].Chemosphere,2002,48(8):843-848.
[12] CHANG S C,NOKER P E,GORMAN G S,et al.Comparative pharmacokinetics of perfluorooctanesulfonate(PFOS) in rats,mice,and monkeys[J].Reprod Toxicol,2012,33(4):428-440.
[13] CHENGELIS C P,KIRKPATRICK J B,MYERS N R,et al.Comparison of the toxicokinetic behavior of perfluorohexanoic acid(PFHxA) and nonafluorobutane-1-sulfonic acid(PFBS) in cynomolgus monkeys and rats[J].Reprod Toxicol,2009,27(3/4):400-406.
[14] KUDO N,SUZUK E,KATAKURA M,et al.Comparison of the elimination between perflfluorinated fatty acids with different carbon chain length in rats[J].Chem Biol Interact,2001,134:203-216.
[15] KUDO N,KATAKURA M,SATO Y,et al.Sex hormone-regulated renal transport of perflfluorooctanoic acid[J].Chem Biol Interact,2002,139:301-316.
[1] 蔡德雷, 郑熠斌, 夏勇, 张世鑫, 宋燕华, 沈海涛, 姚进, 陈苘. 蛋白粉对大鼠肾脏全氟化合物生物利用率的影响[J]. 预防医学, 2024, 36(3): 268-271.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed