基于血清脂肪酸代谢轮廓的化学肝损伤评价研究

刘晓杰, 黎红维, 胡聪, 吴琳静, 熊印华

中国药学杂志 ›› 2021, Vol. 56 ›› Issue (8) : 647-653.

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中国药学杂志 ›› 2021, Vol. 56 ›› Issue (8) : 647-653. DOI: 10.11669/cpj.2021.08.007
论著

基于血清脂肪酸代谢轮廓的化学肝损伤评价研究

  • 刘晓杰a, 黎红维a, 胡聪a, 吴琳静a, 熊印华a,b*
作者信息 +

Evaluation of Chemical Liver Injury Based on Metabolic Profiling of Serum Fatty Acids

  • LIU Xiao-jiea, LI Hong-weia, HU Conga, WU Lin-jinga, XIONG Yin-huaa,b*
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文章历史 +

摘要

目的 从血清脂肪酸代谢轮廓的角度评价四氯化碳(carbon tetrachloride, CCl4)和α-异硫氰酸萘酯(α-naphthalene isothiocyanate, ANIT)诱导的化学肝损伤。方法 采用气相-质谱联用技术测定CCl4对照组、CCl4给药组、ANIT对照组和ANIT给药组的大鼠血清中15种游离脂肪酸和酯化脂肪酸的含量,该定量方法的主要参数为毛细管色谱柱DB-225MS、程序升温、电子轰击离子源(70 eV)和选择离子扫描模式(监测m/z 55、67、74、79)。采用偏最小二乘法-判别分析和主成分分析等方法分析大鼠肝损伤后血清脂肪酸代谢轮廓的变化,运用Pearson和典型相关分析方法分析化学肝损伤与脂肪酸代谢的相关性。结果 CCl4给药组和ANIT给药组的大鼠血清脂肪酸代谢轮廓明显偏离对照组,且能完全互相区分开;亚油酸、二十二碳六烯酸、油酸、花生四烯酸和硬脂酸对CCl4和ANIT诱导的化学肝损伤具有重要贡献,且这5个游离脂肪酸与丙氨酸氨基转移酶、天冬氨酸氨基转移酶和碱性磷酸酶具有良好的正相关性(P<0.05,P<0.01)。结论 血清脂肪酸代谢轮廓与CCl4和ANIT诱导的化学肝损伤密切相关。

Abstract

OBJECTIVE To evaluate the chemical liver injury induced by carbon tetrachloride (CCl4) and α-naphthalene isothiocyanate (ANIT). METHODS The serum concentrations of 15 kinds of free and esterified fatty acids in rats in CCl4 control group, CCl4 treatment group, ANIT control group and ANIT treatment group were determined by gas chromatography-mass spectrometry. DB-225MS capillary column was used with programmed temperature increase, and electron impact ion source of 70 eV and selective ion scanning mode (monitoring at m/z 55, 67, 74, 79) were used. The metabolic profiles of serum fatty acids in rats after liver injury were measured by chemometrics such as partial least squares-discriminant analysis and principal component analysis. Pearson and canonical correlation analyses were used to analyze the relationship between chemical liver injury and fatty acid metabolism. RESULTS The metabolic profiles of fatty acids in the serum of CCl4-treated and ANIT-treated rats obviously deviated from those of the control rats, and could be completely distinguished from each other. Linoleic acid, docosahexaenoic acid, oleic acid, arachidonic acid and stearic acid played an important role in the chemical liver injury induced by CCl4 and ANIT. Furthermore, these five free fatty acids were positively correlated with aspartate aminotransferase, alanine aminotransferase and alkaline phosphatase (P<0.05, P<0.01). CONCLUSION The metabolic profile of serum fatty acids is closely related to CCl4-induced and ANIT-induced chemical liver injuries.

关键词

化学肝损伤 / 四氯化碳 / α-异硫氰酸萘酯 / 脂肪酸 / 代谢轮廓

Key words

chemical liver injury / CCl4 / ANIT / fatty acid / metabolic profiling

引用本文

导出引用
刘晓杰, 黎红维, 胡聪, 吴琳静, 熊印华. 基于血清脂肪酸代谢轮廓的化学肝损伤评价研究[J]. 中国药学杂志, 2021, 56(8): 647-653 https://doi.org/10.11669/cpj.2021.08.007
LIU Xiao-jie, LI Hong-wei, HU Cong, WU Lin-jing, XIONG Yin-hua. Evaluation of Chemical Liver Injury Based on Metabolic Profiling of Serum Fatty Acids[J]. Chinese Pharmaceutical Journal, 2021, 56(8): 647-653 https://doi.org/10.11669/cpj.2021.08.007
中图分类号: R965   

参考文献

[1] TEMPLE R J, HIMMEL M H. Safety of newly approved drugs: implication for prescribing[J]. JAMA, 2002, 287(17):2273-2275.
[2] KOHLROSER J, MATHAI J, REICHHELD J, et al. Hepatotoxicity due to troglitazone: report of two cases and review of adverse events reported to the United States Food and Drug Administration[J]. Am J Gastroenterol, 2000, 95(1):272-276.
[3] BEGER R D, SUN J L. Metabolomics approaches for discovering biomarkers of drug-induced hepatotoxicity and nephrotoxicity[J]. Toxicol Appl Pharmacol, 2010, 243(2):154-166.
[4] STIRNIMANN G, KESSEBOHM K, LAUTERBURG B. Liver injury caused by drugs: an update[J]. Swiss Med Wkly, 2010, 140(8):w13080.
[5] CLAYTON T A, LINDON J C, CLOAREC O, et al. Pharmaco-metabonomic phenotyping and personalized drug treatment[J]. Nature, 2006, 440(7087):1073-1077.
[6] LI F, ZHAO Y, LIN R, et al. Research progress on the effective substances and the mechanism of traditional Chinese medicine compound[J]. Chin Pharm J(中国药学杂志), 2019, 54(13):1037-1044.
[7] LINDON J C, HOLMES E, NICHOLSON J K. Metabonomics techniques and applications to pharmaceutical research & development[J]. Pharm Res, 2006, 23(6):1075-1088.
[8] EBBELS T, KEUNT I C, BEEKONERT O P. Prediction and classification of drug toxicity using probabilistic modeling of temporal metabolic data: the consortium on metabonomic toxicology screening approach[J]. J Proteome Res, 2007, 6(11):4407-4422.
[9] XIONG Y H, LIU X J, WANG X T, et al. Evaluation of Toosendan Fructus-induced hepatotoxicity based on metabolic profile of fatty acids[J]. Chin Tradit Herb Drugs(中草药), 2017, 48(15):3104-3109.
[10] XIONG Y H, XU Y, YANG L, et al. The metabolic profile of serum fatty acids in rats with Rhizoma Dioscoreae Bulbiferae-induced liver injure[J]. Acta Pharm Sin (药学学报), 2017, 52 (5):753-759.
[11] SCHMOCKER C, WEYLANDT K H, KAHLKE L, et al. ω-3 fatty acids alleviate chemically induced acute hepatitis by suppression of cytokines[J]. Hepatology, 2007, 45(4):864-869.
[12] LIU Y, CHEN Z G, SHANG E C, et al. Controlling arachidonic acid metabolic network: from single-to multi-target inhibitors of key enzymes[J]. Acta Pharm Sin (药学学报), 2009, 44(3):231-241.
[13] EL-MOWAFY A M, KATARY M M, PYE C, et al. Novel molecular triggers underlie valproate-induced liver injury and its alleviation by the omega-3 fatty acid DHA: role of inflammation and apoptosis[J]. Heliyon, 2016, 2(7):e00130.
[14] LIU X J, LI H W, XIONG Y H. Evaluation on D-galactosamine-induced liver injury based on fatty acid metabolic profiling[J]. J Jiangxi Sci Technol Normal Univ (江西科技师范大学学报), 2017, (6): 71-76.
[15] CHEN C, KRAUSZ K W, SHAH Y M, et al. Serum metabolomics reveals irreversible inhibition of fatty acid beta-oxidation through the suppression of PPARa activation as a contributing mechanism of acetaminophen-induced hepatotoxicity[J]. Chem Res Toxicol, 2009, 22(4):699-707.
[16] CAO W R, GE J Q, XIE X, et al. Protective effects of petroleum ether extracts of Herpetospermum caudigerum against α-naphthylisothiocyanate-induced acute cholestasis of rats[J]. J Ethnopharmacol, 2017, 198: 139-147.
[17] YANG J, ZHU D, JU B, et al. Hepatoprotective effects of Gentianella turkestanerum extracts on acute liver injury induced by carbon tetrachloride in mice[J]. Am J Transl Res, 2017, 9(2):569-579.
[18] AI G, HUANG Z M, LIU Q C, et al. The protective effect of total phenolics from Oenanthe Javanica on acute liver failure induced by D-galactosamine[J]. J Ethnopharmacol, 2016, 186: 53-60.

基金

国家自然科学基金项目资助(81660692);江西省教育厅科学技术研究项目资助(GJJ170683);江西省药物分子设计与评价重点实验室项目资助(20171BCD40015)
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