請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/105040完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 林靖愉 | zh_TW |
| dc.contributor.advisor | Ching-Yu Lin | en |
| dc.contributor.author | 葉宇庭 | zh_TW |
| dc.contributor.author | Yu-Ting Yeh | en |
| dc.date.accessioned | 2026-09-07T16:36:47Z | - |
| dc.date.available | 2026-09-08 | - |
| dc.date.copyright | 2026-09-07 | - |
| dc.date.issued | 2026 | - |
| dc.date.submitted | 2026-08-13 14:07:35 | - |
| dc.identifier.citation | Adeva-Andany, María M., Pérez-Felpete, N., Fernández-Fernández, C., Donapetry-García, C., & Pazos-García, C. (2016). Liver glucose metabolism in humans. Bioscience Reports, 36. https://doi.org/10.1042/bsr20160385
Akhtar, A., Xu, H., Gulzar, S., Wei, J., Liu, L., Yang, M., Batool, U., Bakar, A., Nawaz, M., Sun, J., & Shen, Z. (2026). Lifetime exposure to microplastics: From consumption to distribution in the body. Journal of Hazardous Materials Advances, 21, 101077. https://doi.org/10.1016/j.hazadv.2026.101077 Albillos, A., de Gottardi, A., & Rescigno, M. (2020). The gut-liver axis in liver disease: Pathophysiological basis for therapy. J Hepatol, 72, 558–577. https://doi.org/10.1016/j.jhep.2019.10.003 Alvim, C. B., Bes-Piá, M. A., & Mendoza-Roca, J. A. (2020). Separation and identification of microplastics from primary and secondary effluents and activated sludge from wastewater treatment plants. Chemical Engineering Journal, 402, 126293. https://doi.org/10.1016/j.cej.2020.126293 Andersson, E. R., Bayless, A. L., Brua, R. B., Casu, F., Cheng, L. L., Choo, M., Edison, A. S., Eghbalnia, H. R., Fleischer, C. C., Gouveia, G. J., Hoch, J. C., Kaur, G., Li, D.-W., Pathmasiri, W., Pelczer, I., Probert, F., Raftery, D., Rovnyak, D., Secreto, M.,…Gebregiworgis, T. (2025). Securing the Future of NMR Metabolomics Reproducibility: A Call for Standardized Reporting. Analytical Chemistry, 97, 20655–20666. https://doi.org/10.1021/acs.analchem.5c03274 Aristizabal, M., Jiménez-Orrego, K. V., Caicedo-León, M. D., Páez-Cárdenas, L. S., Castellanos-García, I., Villalba-Moreno, D. L., Ramírez-Zuluaga, L. V., Hsu, J. T. S., Jaller, J., & Gold, M. (2024). Microplastics in dermatology: Potential effects on skin homeostasis. J Cosmet Dermatol, 23, 766–772. https://doi.org/10.1111/jocd.16167 Baliou, S., Adamaki, M., Ioannou, P., Pappa, A., Panayiotidis, M. I., Spandidos, D. A., Christodoulou, I., Kyriakopoulos, A. M., & Zoumpourlis, V. (2021). Protective role of taurine against oxidative stress (Review). Mol Med Rep, 24. https://doi.org/10.3892/mmr.2021.12242 Bao, L., Cui, X., Zeng, T., Liu, G., Lai, W., Zhao, H., Gao, F., Wu, J., Leong, K. W., & Chen, C. (2025). Incorporation of polylactic acid microplastics into the carbon cycle as a carbon source to remodel the endogenous metabolism of the gut. Proceedings of the National Academy of Sciences, 122, e2417104122. https://doi.org/doi:10.1073/pnas.2417104122 Bashirova, N., Poppitz, D., Klüver, N., Scholz, S., Matysik, J., & Alia, A. (2023). A mechanistic understanding of the effects of polyethylene terephthalate nanoplastics in the zebrafish (Danio rerio) embryo. Scientific Reports, 13, 1891. https://doi.org/10.1038/s41598-023-28712-y Beckonert, O., Keun, H. C., Ebbels, T. M. D., Bundy, J., Holmes, E., Lindon, J. C., & Nicholson, J. K. (2007). Metabolic profiling, metabolomic and metabonomic procedures for NMR spectroscopy of urine, plasma, serum and tissue extracts. Nature protocols, 2, 2692–2703. https://doi.org/10.1038/nprot.2007.376 Bedia, C. (2022). Metabolomics in environmental toxicology: Applications and challenges. Trends in Environmental Analytical Chemistry, 34, e00161. https://doi.org/10.1016/j.teac.2022.e00161 Bligh, E. G., & Dyer, W. J. (1959). A rapid method of total lipid extraction and purification. Can J Biochem Physiol, 37, 911–917. https://doi.org/10.1139/o59-099 Bodzek, M., Pohl, A., & Rosik-Dulewska, C. (2024). Microplastics in Wastewater Treatment Plants: Characteristics, Occurrence and Removal Technologies. Water, 16, 3574. https://doi.org/10.3390/ma15072683 Brooks, G. A. (2018). The Science and Translation of Lactate Shuttle Theory. Cell Metabolism, 27, 757–785. https://doi.org/10.1016/j.cmet.2018.03.008 Camici, M., Garcia-Gil, M., & Tozzi, M. G. (2018). The Inside Story of Adenosine. International Journal of Molecular Sciences, 19, 784. Canfora, E. E., Meex, R. C. R., Venema, K., & Blaak, E. E. (2019). Gut microbial metabolites in obesity, NAFLD and T2DM. Nature Reviews Endocrinology, 15, 261–273. https://doi.org/10.1038/s41574-019-0156-z Chelakkot, C., Ghim, J., & Ryu, S. H. (2018). Mechanisms regulating intestinal barrier integrity and its pathological implications. Experimental & Molecular Medicine, 50, 1–9. https://doi.org/10.1038/s12276-018-0126-x Chicco, D., Sichenze, A., & Jurman, G. (2025). A simple guide to the use of Student’s t-test, Mann-Whitney U test, Chi-squared test, and Kruskal-Wallis test in biostatistics. BioData Mining, 18, 56. https://doi.org/10.1186/s13040-025-00465-6 Choi, H., Kaneko, S., Suzuki, Y., Inamura, K., Nishikawa, M., & Sakai, Y. (2024). Size-Dependent Internalization of Microplastics and Nanoplastics Using In Vitro Model of the Human Intestine-Contribution of Each Cell in the Tri-Culture Models. Nanomaterials (Basel), 14. https://doi.org/10.3390/nano14171435 Cicero, A. F. G., Fogacci, F., Di Micoli, V., Angeloni, C., Giovannini, M., & Borghi, C. (2023). Purine Metabolism Dysfunctions: Experimental Methods of Detection and Diagnostic Potential. International Journal of Molecular Sciences, 24, 7027. Cox, K. D., Covernton, G. A., Davies, H. L., Dower, J. F., Juanes, F., & Dudas, S. E. (2019). Human Consumption of Microplastics. Environmental Science & Technology, 53, 7068–7074. https://doi.org/10.1021/acs.est.9b01517 Debik, J., Sangermani, M., Wang, F., Madssen, T. S., & Giskeødegård, G. F. (2022). Multivariate analysis of NMR-based metabolomic data. NMR Biomed, 35, e4638. https://doi.org/10.1002/nbm.4638 Deng, Y., Zhang, Y., Lemos, B., & Ren, H. (2017). Tissue accumulation of microplastics in mice and biomarker responses suggest widespread health risks of exposure. Scientific Reports, 7, 10, 46687. https://doi.org/10.1038/srep46687 Dong, C.-D., Chen, C.-W., Chen, Y.-C., Chen, H.-H., Lee, J.-S., & Lin, C.-H. (2020). Polystyrene microplastic particles: In vitro pulmonary toxicity assessment. Journal of Hazardous Materials, 385, 121575. https://doi.org/10.1016/j.jhazmat.2019.121575 Du, B., Li, T., He, H., Xu, X., Zhang, C., Lu, X., Wang, Y., Cao, J., Lu, Y., Liu, Y., Hu, S., Li, J., Li, L., & Shi, M. (2024). Analysis of Biodistribution and in vivo Toxicity of Varying Sized Polystyrene Micro and Nanoplastics in Mice. Int J Nanomedicine, 19, 7617–7630. https://doi.org/10.2147/ijn.S466258 Du, F., Cai, H., Zhang, Q., Chen, Q., & Shi, H. (2020). Microplastics in take-out food containers. Journal of Hazardous Materials, 399, 122969. https://doi.org/10.1016/j.jhazmat.2020.122969 Eberhard, T., Casillas, G., Zarus, G. M., & Barr, D. B. (2024). Systematic review of microplastics and nanoplastics in indoor and outdoor air: identifying a framework and data needs for quantifying human inhalation exposures. Journal of Exposure Science & Environmental Epidemiology, 34, 185–196. https://doi.org/10.1038/s41370-023-00634-x EFSA. (2016). Presence of microplastics and nanoplastics in food, with particular focus on seafood. Efsa j, 14, e04501. https://doi.org/10.2903/j.efsa.2016.4501 Emwas, A.-H., Saccenti, E., Gao, X., McKay, R. T., dos Santos, V. A. P. M., Roy, R., & Wishart, D. S. (2018). Recommended strategies for spectral processing and post-processing of 1D 1H-NMR data of biofluids with a particular focus on urine. Metabolomics, 14, 31. https://doi.org/10.1007/s11306-018-1321-4 Eskandrani, A., Abdel-Rahman Mohamed, A., Alotaibi, B. S., Abd El-Hakim, Y. M., Khamis, T., E. Noreldin, A., E Abdelhamid, A., Alsubaie, N., & Alqahtani, L. S. (2025). Palliative effect of taurine against hepatic injury induced by polystyrene microplastics through antioxidant and metabolic pathway modulation in mice. Frontiers in Pharmacology, Volume 16 - 2025. https://doi.org/10.3389/fphar.2025.1665161 Fan, J., Qu, Y., Qu, L., Shen, D., Liu, H., & Nie, Z. (2025). Oral exposure to PLA microplastics induces time-dependent nanotoxicity via the gut-liver axis. Journal of Hazardous Materials, 495, 138931. https://doi.org/10.1016/j.jhazmat.2025.138931 Feng, Y., Wang, Y., Wang, P., Huang, Y., & Wang, F. (2018). Short-Chain Fatty Acids Manifest Stimulative and Protective Effects on Intestinal Barrier Function Through the Inhibition of NLRP3 Inflammasome and Autophagy. Cell Physiol Biochem, 49, 190–205. https://doi.org/10.1159/000492853 Gigault, J., El Hadri, H., Nguyen, B., Grassl, B., Rowenczyk, L., Tufenkji, N., Feng, S., & Wiesner, M. (2021). Nanoplastics are neither microplastics nor engineered nanoparticles. Nature Nanotechnology, 16, 501–507. https://doi.org/10.1038/s41565-021-00886-4 Gigault, J., Halle, A. t., Baudrimont, M., Pascal, P.-Y., Gauffre, F., Phi, T.-L., El Hadri, H., Grassl, B., & Reynaud, S. (2018). Current opinion: What is a nanoplastic? Environmental Pollution, 235, 1030–1034. https://doi.org/10.1016/j.envpol.2018.01.024 Gopinath, P. M., Twayana, K. S., Ravanan, P., John, T., Mukherjee, A., Jenkins, D. F., & Chandrasekaran, N. (2021). Prospects on the nano-plastic particles internalization and induction of cellular response in human keratinocytes. Part Fibre Toxicol, 18, 35. https://doi.org/10.1186/s12989-021-00428-9 Hahladakis, J. N., Velis, C. A., Weber, R., Iacovidou, E., & Purnell, P. (2018). An overview of chemical additives present in plastics: Migration, release, fate and environmental impact during their use, disposal and recycling. J Hazard Mater, 344, 179–199. https://doi.org/10.1016/j.jhazmat.2017.10.014 Han, W., Cui, J., Sun, G., Miao, X., Pufang, Z., & nannan, L. (2024). Nano-sized microplastics exposure induces skin cell senescence via triggering the mitochondrial localization of GSDMD. Environmental Pollution, 349, 123874. https://doi.org/10.1016/j.envpol.2024.123874 Hardie, D. G., Ross, F. A., & Hawley, S. A. (2012). AMPK: a nutrient and energy sensor that maintains energy homeostasis. Nature Reviews Molecular Cell Biology, 13, 251–262. https://doi.org/10.1038/nrm3311 Hernandez, L. M., Xu, E. G., Larsson, H. C. E., Tahara, R., Maisuria, V. B., & Tufenkji, N. (2019). Plastic Teabags Release Billions of Microparticles and Nanoparticles into Tea. Environmental Science & Technology, 53, 12300–12310. https://doi.org/10.1021/acs.est.9b02540 Ho, K. T., Bjorkland, R., & Burgess, R. M. (2024). Comparing the definitions of microplastics based on size range: Scientific and policy implications. Mar Pollut Bull, 207, 116907. https://doi.org/10.1016/j.marpolbul.2024.116907 Hollenbeck, C. B. (2010). The importance of being choline. J Am Diet Assoc, 110, 1162–1165. https://doi.org/10.1016/j.jada.2010.05.012 Hong, Y.-S., Ahn, Y.-T., Park, J.-C., Lee, J.-H., Lee, H., Huh, C.-S., Kim, D.-H., Ryu, D. H., & Hwang, G.-S. (2010). 1H NMR-based metabonomic assessment of probiotic effects in a colitis mouse model. Archives of Pharmacal Research, 33, 1091–1101. https://doi.org/10.1007/s12272-010-0716-1 Horvatits, T., Tamminga, M., Liu, B., Sebode, M., Carambia, A., Fischer, L., Püschel, K., Huber, S., & Fischer, E. K. (2022). Microplastics detected in cirrhotic liver tissue. EBioMedicine, 82, 104147. https://doi.org/10.1016/j.ebiom.2022.104147 Hughes, E. R., Winter, M. G., Duerkop, B. A., Spiga, L., Furtado de Carvalho, T., Zhu, W., Gillis, C. C., Büttner, L., Smoot, M. P., Behrendt, C. L., Cherry, S., Santos, R. L., Hooper, L. V., & Winter, S. E. (2017). Microbial Respiration and Formate Oxidation as Metabolic Signatures of Inflammation-Associated Dysbiosis. Cell Host & Microbe, 21, 208–219. https://doi.org/10.1016/j.chom.2017.01.005 Hussain, K. A., Romanova, S., Okur, I., Zhang, D., Kuebler, J., Huang, X., Wang, B., Fernandez-Ballester, L., Lu, Y., Schubert, M., & Li, Y. (2023). Assessing the Release of Microplastics and Nanoplastics from Plastic Containers and Reusable Food Pouches: Implications for Human Health. Environmental Science & Technology, 57, 9782–9792. https://doi.org/10.1021/acs.est.3c01942 Ibrahim, N., Rahman, A. M. N. A. A., Shafiq, M. D., Lockman, Z., Jaafar, M., & Kameda, Y. (2025). Microplastic Pollution: Sources, Degradation Mechanisms, Analytical Advances, and Mitigation Strategies for Environmental Sustainability. Reviews of Environmental Contamination and Toxicology, 263, 27. https://doi.org/10.1007/s44169-025-00098-0 Ibrahim, Y. S., Tuan Anuar, S., Azmi, A. A., Wan Mohd Khalik, W. M. A., Lehata, S., Hamzah, S. R., Ismail, D., Ma, Z. F., Dzulkarnaen, A., Zakaria, Z., Mustaffa, N., Tuan Sharif, S. E., & Lee, Y. Y. (2021). Detection of microplastics in human colectomy specimens. JGH Open, 5, 116–121. https://doi.org/10.1002/jgh3.12457 Jamalinia, M., Saeian, S., Nikkhoo, N., Nazerian, A., & Lankarani, K. B. (2025). Sex and gender differences in MASLD: pathophysiological mechanisms, clinical implications, and future directions. Metabolism and Target Organ Damage, 5, 60. Jiménez-Arroyo, C., Tamargo, A., Molinero, N., & Moreno-Arribas, M. V. (2023). The gut microbiota, a key to understanding the health implications of micro(nano)plastics and their biodegradation. Microb Biotechnol, 16, 34–53. https://doi.org/10.1111/1751-7915.14182 Jin, T., Liu, Y., Lyu, H., He, Y., Sun, H., Tang, J., & Xing, B. (2024). Plastic takeaway food containers may cause human intestinal damage in routine life usage: Microplastics formation and cytotoxic effect. Journal of Hazardous Materials, 475, 134866. https://doi.org/10.1016/j.jhazmat.2024.134866 Jin, Y., Lu, L., Tu, W., Luo, T., & Fu, Z. (2019). Impacts of polystyrene microplastic on the gut barrier, microbiota and metabolism of mice. Sci Total Environ, 649, 308–317. https://doi.org/10.1016/j.scitotenv.2018.08.353 Jung, J. Y., Kim, I. Y., Kim, Y. N., Kim, J. S., Shin, J. H., Jang, Z. H., & Seong, J. K. (2012). 1H NMR-based metabolite profiling of diet-induced obesity in a mouse mode. BMB Reports (Biochemistry and Molecular Biology Reports), 45, 419–424. https://doi.org/10.5483/bmbrep.2012.45.7.248 Kajani, S., Laker, R. C., Ratkova, E., Will, S., & Rhodes, C. J. (2024). Hepatic glucagon action: beyond glucose mobilization. Physiological Reviews, 104, 1021–1060. https://doi.org/10.1152/physrev.00028.2023 Kannan, K., & Vimalkumar, K. (2021). A Review of Human Exposure to Microplastics and Insights Into Microplastics as Obesogens. Frontiers in Endocrinology, Volume 12 - 2021. https://doi.org/10.3389/fendo.2021.724989 Kek, H. Y., Tan, H., Othman, M. H. D., Nyakuma, B. B., Ho, W. S., Sheng, D. D. C. V., Kang, H. S., Chan, Y. T., Lim, N. H. A. S., Leng, P. C., Wahab, N. H. A., & Wong, K. Y. (2024). Critical review on airborne microplastics: An indoor air contaminant of emerging concern. Environmental Research, 245, 118055. https://doi.org/10.1016/j.envres.2023.118055 Klein, J. (2000). Membrane breakdown in acute and chronic neurodegeneration: focus on choline-containing phospholipids. Journal of Neural Transmission, 107, 1027–1063. https://doi.org/10.1007/s007020070051 Koelmans, A. A., Redondo-Hasselerharm, P. E., Nor, N. H. M., de Ruijter, V. N., Mintenig, S. M., & Kooi, M. (2022). Risk assessment of microplastic particles. Nature Reviews Materials, 7, 138–152. https://doi.org/10.1038/s41578-021-00411-y Lamarre, S. G., Morrow, G., Macmillan, L., Brosnan, M. E., & Brosnan, J. T. (2013). Formate: an essential metabolite, a biomarker, or more? Clinical Chemistry and Laboratory Medicine, 51, 571–578. https://doi.org/doi:10.1515/cclm-2012-0552 Lee, S.-H., Lin, W.-Y., & Cheng, T.-J. (2024). Microbiota-mediated metabolic perturbations in the gut and brain of mice after microplastic exposure. Chemosphere, 350, 141026. https://doi.org/10.1016/j.chemosphere.2023.141026 Leslie, H. A., van Velzen, M. J. M., Brandsma, S. H., Vethaak, A. D., Garcia-Vallejo, J. J., & Lamoree, M. H. (2022). Discovery and quantification of plastic particle pollution in human blood. Environment International, 163, 107199. https://doi.org/10.1016/j.envint.2022.107199 Li, D., Shi, Y., Yang, L., Xiao, L., Kehoe, D. K., Gun’ko, Y. K., Boland, J. J., & Wang, J. J. (2020). Microplastic release from the degradation of polypropylene feeding bottles during infant formula preparation. Nature Food, 1, 746–754. https://doi.org/10.1038/s43016-020-00171-y Li, X., Feng, L., Kuang, Q., Wang, X., Yang, J., Niu, X., Gao, L., Huang, L., Luo, P., & Li, L. (2024). Microplastics cause hepatotoxicity in diabetic mice by disrupting glucolipid metabolism via PP2A/AMPK/HNF4A and promoting fibrosis via the Wnt/β-catenin pathway. Environ Toxicol, 39, 1018–1030. https://doi.org/10.1002/tox.24034 Liang, B., Zhong, Y., Huang, Y., Lin, X., Liu, J., Lin, L., Hu, M., Jiang, J., Dai, M., Wang, B., Zhang, B., Meng, H., Lelaka, J. J. J., Sui, H., Yang, X., & Huang, Z. (2021). Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis. Particle and Fibre Toxicology, 18, 20. https://doi.org/10.1186/s12989-021-00414-1 Lin, C.-Y., Huang, L.-H., Deng, D.-F., Lee, S.-H., Liang, H.-J., & Hung, S. S. O. (2019). Metabolic adaptation to feed restriction on the green sturgeon (Acipenser medirostris) fingerlings. Science of the Total Environment, 684, 78–88. https://doi.org/10.1016/j.scitotenv.2019.05.044 Lin, C. Y., Wu, H., Tjeerdema, R. S., & Viant, M. R. (2007). Evaluation of metabolite extraction strategies from tissue samples using NMR metabolomics. Metabolomics, 3, 55–67. https://doi.org/10.1007/s11306-006-0043-1 Lin, S., Zhang, H., Wang, C., Su, X. L., Song, Y., Wu, P., Yang, Z., Wong, M. H., Cai, Z., & Zheng, C. (2022). Metabolomics Reveal Nanoplastic-Induced Mitochondrial Damage in Human Liver and Lung Cells. Environ Sci Technol, 56, 12483–12493. https://doi.org/10.1021/acs.est.2c03980 Lu, L., Wan, Z., Luo, T., Fu, Z., & Jin, Y. (2018). Polystyrene microplastics induce gut microbiota dysbiosis and hepatic lipid metabolism disorder in mice. Science of the Total Environment, 631-632, 449–458. https://doi.org/10.1016/j.scitotenv.2018.03.051 Mahmod, I. F., Jeyasimman, S., Mispan, M. S., Supandi, F., Khatib, A., & Saiman, M. Z. (2023). Comparative Metabolomics Analysis of Weedy Rice (Oryza spp.) across Peninsular Malaysia. Agriculture, 13, 1230. Marfella, R., Prattichizzo, F., Sardu, C., Fulgenzi, G., Graciotti, L., Spadoni, T., D'Onofrio, N., Scisciola, L., La Grotta, R., Frigé, C., Pellegrini, V., Municinò, M., Siniscalchi, M., Spinetti, F., Vigliotti, G., Vecchione, C., Carrizzo, A., Accarino, G., Squillante, A.,…Paolisso, G. (2024). Microplastics and Nanoplastics in Atheromas and Cardiovascular Events. N Engl J Med, 390, 900–910. https://doi.org/10.1056/NEJMoa2309822 Marino, C., Zhang, S., De Simone, G., Grimaldi, M., Di Maio, A., Iasevoli, F., Errico, F., D’Ursi, A. M., de Bartolomeis, A., & Usiello, A. (2026). Untargeted 1H NMR-based metabolomics unveils distinct circulating biochemical signatures between treatment-resistant and non-treatment-resistant schizophrenia patients: a pilot study. Translational Psychiatry, 16, 108. https://doi.org/10.1038/s41398-026-03853-6 McLean, P., Christopher, E. A., Sleeuwenhoek, A., Lofty, M., Dixon, K., & Galea, K. S. (2025). Dermal exposure, review of current knowledge on the uptake of micro-and nano-plastics. Microplastics and Nanoplastics, 6, 12. https://doi.org/10.1186/s43591-025-00163-4 Menéndez-Pedriza, A., & Jaumot, J. (2020). Interaction of Environmental Pollutants with Microplastics: A Critical Review of Sorption Factors, Bioaccumulation and Ecotoxicological Effects. Toxics, 8. https://doi.org/10.3390/toxics8020040 Moco, S. (2022). Studying Metabolism by NMR-Based Metabolomics. Front Mol Biosci, 9, 882487. https://doi.org/10.3389/fmolb.2022.882487 Montano, L., Giorgini, E., Notarstefano, V., Notari, T., Ricciardi, M., Piscopo, M., & Motta, O. (2023). Raman Microspectroscopy evidence of microplastics in human semen. Sci Total Environ, 901, 165922. https://doi.org/10.1016/j.scitotenv.2023.165922 Montano, L., Raimondo, S., Piscopo, M., Ricciardi, M., Guglielmino, A., Chamayou, S., Gentile, R., Gentile, M., Rapisarda, P., Oliveri Conti, G., Ferrante, M., & Motta, O. (2025). First evidence of microplastics in human ovarian follicular fluid: An emerging threat to female fertility. Ecotoxicol Environ Saf, 291, 117868. https://doi.org/10.1016/j.ecoenv.2025.117868 Neinast, M. D., Jang, C., Hui, S., Murashige, D. S., Chu, Q., Morscher, R. J., Li, X., Zhan, L., White, E., Anthony, T. G., Rabinowitz, J. D., & Arany, Z. (2019). Quantitative Analysis of the Whole-Body Metabolic Fate of Branched-Chain Amino Acids. Cell Metab, 29, 417–429.e414. https://doi.org/10.1016/j.cmet.2018.10.013 Nelson, K. L., & Voruganti, V. S. (2025). Implication of xanthine oxidoreductase in oxidative stress-related chronic diseases. Front Endocrinol (Lausanne), 16, 1662037. https://doi.org/10.3389/fendo.2025.1662037 Neurath, M. F., Artis, D., & Becker, C. (2025). The intestinal barrier: a pivotal role in health, inflammation, and cancer. The Lancet Gastroenterology & Hepatology, 10, 573–592. https://doi.org/10.1016/S2468-1253(24)00390-X Nihart, A., Garcia, M., El Hayek, E., Liu, R., Olewine, M., Kingston, J., Castillo, E., Gullapalli, R., Howard, T., Bleske, B., Scott, J., Gonzalez-Estrella, J., Gross, J., Spilde, M., Adolphi, N., Gallego, D., Jarrell, H., Dvorscak, G., Zuluaga-Ruiz, M.,…Campen, M. (2025). Bioaccumulation of microplastics in decedent human brains. Nature Medicine, 31, 16. https://doi.org/10.1038/s41591-024-03453-1 Özsoy, S., Gündogdu, S., Sezigen, S., Tasalp, E., Ikiz, D. A., & Kideys, A. E. (2024). Presence of microplastics in human stomachs. Forensic Science International, 364, 112246. https://doi.org/10.1016/j.forsciint.2024.112246 Parada Venegas, D., De la Fuente, M. K., Landskron, G., González, M. J., Quera, R., Dijkstra, G., Harmsen, H. J. M., Faber, K. N., & Hermoso, M. A. (2019). Short Chain Fatty Acids (SCFAs)-Mediated Gut Epithelial and Immune Regulation and Its Relevance for Inflammatory Bowel Diseases. Frontiers in Immunology, Volume 10 - 2019. https://doi.org/10.3389/fimmu.2019.00277 Park, S., Kim, M. J., Shin, J. H., Kim, E., Son, M., & Lee, S. (2026). Chronic PET-Microplastic Exposure: Disruption of Gut-Liver Homeostasis and Risk of Hepatic Steatosis. Adv Sci (Weinh), 13, e12030. https://doi.org/10.1002/advs.202512030 Patti, G. J., Yanes, O., & Siuzdak, G. (2012). Innovation: Metabolomics: the apogee of the omics trilogy. Nat Rev Mol Cell Biol, 13, 263–269. https://doi.org/10.1038/nrm3314 Pfohl, P., Wagner, M., Meyer, L., Domercq, P., Praetorius, A., Hüffer, T., Hofmann, T., & Wohlleben, W. (2022). Environmental Degradation of Microplastics: How to Measure Fragmentation Rates to Secondary Micro- and Nanoplastic Fragments and Dissociation into Dissolved Organics. Environmental Science & Technology, 56, 11323–11334. https://doi.org/10.1021/acs.est.2c01228 Pironti, C., Notarstefano, V., Ricciardi, M., Motta, O., Giorgini, E., & Montano, L. (2023). First Evidence of Microplastics in Human Urine, a Preliminary Study of Intake in the Human Body. Toxics, 11, 40. https://doi.org/10.3390/toxics11010040 Prata, J. C. (2018). Airborne microplastics: Consequences to human health? Environmental Pollution, 234, 115–126. https://doi.org/10.1016/j.envpol.2017.11.043 Prata, J. C. (2023). Microplastics and human health: Integrating pharmacokinetics. Critical Reviews in Environmental Science and Technology, 53, 1489–1511. https://doi.org/10.1080/10643389.2023.2195798 Prata, J. C., da Costa, J. P., Lopes, I., Duarte, A. C., & Rocha-Santos, T. (2020). Environmental exposure to microplastics: An overview on possible human health effects. Sci Total Environ, 702, 134455. https://doi.org/10.1016/j.scitotenv.2019.134455 Ra, Y. E., & Bang, Y.-J. (2024). Balancing Act of the Intestinal Antimicrobial Proteins on Gut Microbiota and Health. Journal of Microbiology, 62, 167–179. https://doi.org/10.1007/s12275-024-00122-3 Ragusa, A., Svelato, A., Santacroce, C., Catalano, P., Notarstefano, V., Carnevali, O., Papa, F., Rongioletti, M. C. A., Baiocco, F., Draghi, S., D'Amore, E., Rinaldo, D., Matta, M., & Giorgini, E. (2021). Plasticenta: First evidence of microplastics in human placenta. Environment International, 146, 106274. https://doi.org/10.1016/j.envint.2020.106274 Rahman, S., Saha, W., Maysha, T. I., Sarker, P., Datta, T. R., Rahman, S., & Chacrabati, R. (2026). Prevalence and health risks of microplastics in bottled water and beverages: A food safety concern. Journal of Hazardous Materials: Plastics, 2, 100024. https://doi.org/10.1016/j.hazmp.2025.100024 Refosco, A., Dierkes, J., Kögel, T., Dankel, S. N., Laupsa-Borge, J., Gomiero, A., & Daniel, D. B. (2025). Microplastics in human feces: a pilot study exploring links with dietary habits. Microplastics and Nanoplastics, 5, 22. https://doi.org/10.1186/s43591-025-00129-6 Reichardt, F., Lucas, L. N., Okyere, L., Choi, J., Amador-Noguez, D., Gaulke, C. A., & Anakk, S. (2025). Portal bile acid composition and microbiota along the murine intestinal tract exhibit sex differences in physiology. Gut Microbes, 17, 2540483. https://doi.org/10.1080/19490976.2025.2540483 Ridlon, J. M., Harris, S. C., Bhowmik, S., Kang, D.-J., & Hylemon, P. B. (2016). Consequences of bile salt biotransformations by intestinal bacteria. Gut Microbes, 7, 22–39. https://doi.org/10.1080/19490976.2015.1127483 Ripps, H., & Shen, W. (2012). Review: taurine: a "very essential" amino acid. Mol Vis, 18, 2673–2686. Rochman, C. M., Brookson, C., Bikker, J., Djuric, N., Earn, A., Bucci, K., Athey, S., Huntington, A., McIlwraith, H., Munno, K., De Frond, H., Kolomijeca, A., Erdle, L., Grbic, J., Bayoumi, M., Borrelle, S. B., Wu, T., Santoro, S., Werbowski, L. M.,…Hung, C. (2019). Rethinking microplastics as a diverse contaminant suite. Environ Toxicol Chem, 38, 703–711. https://doi.org/10.1002/etc.4371 Rochman, C. M., Hoh, E., Hentschel, B. T., & Kaye, S. (2013). Long-term field measurement of sorption of organic contaminants to five types of plastic pellets: implications for plastic marine debris. Environ Sci Technol, 47, 1646–1654. https://doi.org/10.1021/es303700s Roh, Y., Kim, J., Song, H., Seol, A., Kim, T., Park, E., Park, K., Lim, S., Wang, S., Jung, Y., Kim, H., Lim, Y., & Hwang, D. (2024). Impact of the Oral Administration of Polystyrene Microplastics on Hepatic Lipid, Glucose, and Amino Acid Metabolism in C57BL/6Korl and C57BL/6-Lep(em1hwl)/Korl Mice. Int J Mol Sci, 25. https://doi.org/10.3390/ijms25094964 Roslan, N. S., Lee, Y. Y., Ibrahim, Y. S., Tuan Anuar, S., Yusof, K., Lai, L. A., & Brentnall, T. (2024). Detection of microplastics in human tissues and organs: A scoping review. J Glob Health, 14, 04179. https://doi.org/10.7189/jogh.14.04179 Šaravanja, A., Pušić, T., & Dekanić, T. (2022). Microplastics in Wastewater by Washing Polyester Fabrics. Materials, 15, 2683. Schwabl, P., Köppel, S., Königshofer, P., Bucsics, T., Trauner, M., Reiberger, T., & Liebmann, B. (2019). Detection of Various Microplastics in Human Stool. Annals of Internal Medicine, 171, 453–457. https://doi.org/10.7326/M19-0618 Senathirajah, K., Attwood, S., Bhagwat, G., Carbery, M., Wilson, S., & Palanisami, T. (2021). Estimation of the mass of microplastics ingested - A pivotal first step towards human health risk assessment. J Hazard Mater, 404, 124004. https://doi.org/10.1016/j.jhazmat.2020.124004 Seneff, S., & Kyriakopoulos, A. M. (2025). Taurine prevents mitochondrial dysfunction and protects mitochondria from reactive oxygen species and deuterium toxicity. Amino Acids, 57, 6. https://doi.org/10.1007/s00726-024-03440-3 Simó, C., & García-Cañas, V. (2020). Dietary bioactive ingredients to modulate the gut microbiota-derived metabolite TMAO. New opportunities for functional food development. Food Funct, 11, 6745–6776. https://doi.org/10.1039/d0fo01237h Smith, M., Love, D. C., Rochman, C. M., & Neff, R. A. (2018). Microplastics in Seafood and the Implications for Human Health. Current Environmental Health Reports, 5, 375–386. https://doi.org/10.1007/s40572-018-0206-z Soltani, N. S., Taylor, M. P., & Wilson, S. P. (2021). Quantification and exposure assessment of microplastics in Australian indoor house dust. Environmental Pollution, 283, 117064. https://doi.org/10.1016/j.envpol.2021.117064 Song, J., Wang, C., & Li, G. (2024). Defining Primary and Secondary Microplastics: A Connotation Analysis. ACS ES&T Water, 4, 2330–2332. https://doi.org/10.1021/acsestwater.4c00316 Steinberg, G. R., & Hardie, D. G. (2023). New insights into activation and function of the AMPK. Nature Reviews Molecular Cell Biology, 24, 255–272. https://doi.org/10.1038/s41580-022-00547-x Stock, V., Böhmert, L., Lisicki, E., Block, R., Cara-Carmona, J., Pack, L. K., Selb, R., Lichtenstein, D., Voss, L., Henderson, C. J., Zabinsky, E., Sieg, H., Braeuning, A., & Lampen, A. (2019). Uptake and effects of orally ingested polystyrene microplastic particles in vitro and in vivo. Archives of Toxicology, 93, 1817–1833. https://doi.org/10.1007/s00204-019-02478-7 Su, Q. L., Wu, J., Tan, S. W., Guo, X. Y., Zou, D. Z., & Kang, K. (2024). The impact of microplastics polystyrene on the microscopic structure of mouse intestine, tight junction genes and gut microbiota. PLOS One, 19, e0304686. https://doi.org/10.1371/journal.pone.0304686 Surugihalli, C., Muralidaran, V., Ryan, C. E., Patel, K., Zhao, D., & Sunny, N. E. (2023). Branched-chain amino acids alter cellular redox to induce lipid oxidation and reduce de novo lipogenesis in the liver. Am J Physiol Endocrinol Metab, 324, E299–e313. https://doi.org/10.1152/ajpendo.00307.2022 Tan, E., Saha, S., & Niebel, D. (2025). Plastics in dermatology: A review and solutions. Journal of the European Academy of Dermatology and Venereology, 39, 1715–1724. https://doi.org/10.1111/jdv.20537 Teuten, E. L., Saquing, J. M., Knappe, D. R., Barlaz, M. A., Jonsson, S., Björn, A., Rowland, S. J., Thompson, R. C., Galloway, T. S., Yamashita, R., Ochi, D., Watanuki, Y., Moore, C., Viet, P. H., Tana, T. S., Prudente, M., Boonyatumanond, R., Zakaria, M. P., Akkhavong, K.,…Takada, H. (2009). Transport and release of chemicals from plastics to the environment and to wildlife. Philos Trans R Soc Lond B Biol Sci, 364, 2027–2045. https://doi.org/10.1098/rstb.2008.0284 Thakur, R., Joshi, V., Sahoo, G. C., Jindal, N., Tiwari, R. R., & Rana, S. (2025). Review of mechanisms and impacts of nanoplastic toxicity in aquatic organisms and potential impacts on human health. Toxicol Rep, 14, 102013. https://doi.org/10.1016/j.toxrep.2025.102013 Tretter, L., Patocs, A., & Chinopoulos, C. (2016). Succinate, an intermediate in metabolism, signal transduction, ROS, hypoxia, and tumorigenesis. Biochim Biophys Acta, 1857, 1086–1101. https://doi.org/10.1016/j.bbabio.2016.03.012 Tripathi, A., Debelius, J., Brenner, D. A., Karin, M., Loomba, R., Schnabl, B., & Knight, R. (2018). The gut-liver axis and the intersection with the microbiome. Nat Rev Gastroenterol Hepatol, 15, 397–411. https://doi.org/10.1038/s41575-018-0011-z Tsochatzis, E. D., Gika, H., Theodoridis, G., Maragou, N., Thomaidis, N., & Corredig, M. (2024). Microplastics and nanoplastics: Exposure and toxicological effects require important analysis considerations. Heliyon, 10, e32261. https://doi.org/10.1016/j.heliyon.2024.e32261 Unuofin, J. O., & Igwaran, A. (2023). Microplastics in seafood: Implications for food security, safety, and human health. Journal of Sea Research, 194, 102410. https://doi.org/10.1016/j.seares.2023.102410 van den Berg, R. A., Hoefsloot, H. C. J., Westerhuis, J. A., Smilde, A. K., & van der Werf, M. J. (2006). Centering, scaling, and transformations: improving the biological information content of metabolomics data. BMC Genomics, 7, 142. https://doi.org/10.1186/1471-2164-7-142 Vancamelbeke, M., & Vermeire, S. (2017). The intestinal barrier: a fundamental role in health and disease. Expert Rev Gastroenterol Hepatol, 11, 821–834. https://doi.org/10.1080/17474124.2017.1343143 Wallimann, T., Tokarska-Schlattner, M., & Schlattner, U. (2011). The creatine kinase system and pleiotropic effects of creatine. Amino Acids, 40, 1271–1296. https://doi.org/10.1007/s00726-011-0877-3 Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., Dugar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y. M., Wu, Y., Schauer, P., Smith, J. D., Allayee, H., Tang, W. H., DiDonato, J. A., Lusis, A. J., & Hazen, S. L. (2011). Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease. Nature, 472, 57–63. https://doi.org/10.1038/nature09922 Waxman, D. J., & Holloway, M. G. (2009). Sex differences in the expression of hepatic drug metabolizing enzymes. Mol Pharmacol, 76, 215–228. https://doi.org/10.1124/mol.109.056705 Westerhuis, J. A., Hoefsloot, H. C. J., Smit, S., Vis, D. J., Smilde, A. K., van Velzen, E. J. J., van Duijnhoven, J. P. M., & van Dorsten, F. A. (2008). Assessment of PLSDA cross validation. Metabolomics, 4, 81–89. https://doi.org/10.1007/s11306-007-0099-6 Winston, J. A., & Theriot, C. M. (2020). Diversification of host bile acids by members of the gut microbiota. Gut Microbes, 11, 158–171. https://doi.org/10.1080/19490976.2019.1674124 World Health Organization. (2022). Dietary and inhalation exposure to nano- and microplastic particles and potential implications for human health. https://www.who.int/publications/i/item/9789240054608 Wu, P., Lin, S., Cao, G., Wu, J., Jin, H., Wang, C., Wong, M. H., Yang, Z., & Cai, Z. (2022). Absorption, distribution, metabolism, excretion and toxicity of microplastics in the human body and health implications. J Hazard Mater, 437, 129361. https://doi.org/10.1016/j.jhazmat.2022.129361 Xu, C., Zhang, B., Gu, C., Shen, C., Yin, S., Aamir, M., & Li, F. (2020). Are we underestimating the sources of microplastic pollution in terrestrial environment? Journal of Hazardous Materials, 400, 123228. https://doi.org/10.1016/j.jhazmat.2020.123228 Xu, Y., & Goodacre, R. (2025). Mind your Ps and Qs – Caveats in metabolomics data analysis. TrAC Trends in Analytical Chemistry, 183, 118064. https://doi.org/10.1016/j.trac.2024.118064 Yakovenko, N., Pérez-Serrano, L., Segur, T., Hagelskjaer, O., Margenat, H., Le Roux, G., & Sonke, J. E. (2025). Human exposure to PM10 microplastics in indoor air. PLOS One, 20, e0328011. https://doi.org/10.1371/journal.pone.0328011 Yang, Z., Wang, M., Feng, Z., Wang, Z., Lv, M., Chang, J., Chen, L., & Wang, C. (2023). Human Microplastics Exposure and Potential Health Risks to Target Organs by Different Routes: A Review. Current Pollution Reports, 9, 468–485. https://doi.org/10.1007/s40726-023-00273-8 Yee, M. S.-L., Hii, L.-W., Looi, C. K., Lim, W.-M., Wong, S.-F., Kok, Y.-Y., Tan, B.-K., Wong, C.-Y., & Leong, C.-O. (2021). Impact of Microplastics and Nanoplastics on Human Health. Nanomaterials, 11, 496. https://doi.org/10.3390/nano11020496 Yong, C. Q. Y., Valiyaveettil, S., & Tang, B. L. (2020). Toxicity of Microplastics and Nanoplastics in Mammalian Systems. International Journal of Environmental Research and Public Health, 17, 1509. https://doi.org/10.3390/ijerph17051509 Zeisel, S. H., & da Costa, K. A. (2009). Choline: an essential nutrient for public health. Nutr Rev, 67, 615–623. https://doi.org/10.1111/j.1753-4887.2009.00246.x Zhang, A., Sun, H., Wang, P., Han, Y., & Wang, X. (2012). Modern analytical techniques in metabolomics analysis. Analyst, 137, 293–300. https://doi.org/10.1039/c1an15605e Zhang, Y., Zhao, H., Liu, B., Shu, H., Zhang, L., Bao, M., Yi, W., Tan, Y., Ji, X., Zhang, C., Zhao, N., Pang, G., He, D., Wang, Y., Li, L., Yi, J., & Lu, C. (2021). Human serum metabolomic analysis reveals progression for high blood pressure in type 2 diabetes mellitus. BMJ Open Diabetes Research & Care, 9, e002337. https://doi.org/10.1136/bmjdrc-2021-002337 Zhang, Z., Chen, W., Chan, H., Peng, J., Zhu, P., Li, J., Jiang, X., Zhang, Z., Wang, Y., Tan, Z., Peng, Y., Zhang, S., Lin, K., & Yung, K. K. (2024). Polystyrene microplastics induce size-dependent multi-organ damage in mice: Insights into gut microbiota and fecal metabolites. J Hazard Mater, 461, 132503. https://doi.org/10.1016/j.jhazmat.2023.132503 Zhao, B., Rehati, P., Yang, Z., Cai, Z., Guo, C., & Li, Y. (2024). The potential toxicity of microplastics on human health. Sci Total Environ, 912, 168946. https://doi.org/10.1016/j.scitotenv.2023.168946 Zhao, Q., Zhu, L., Weng, J., Jin, Z., Cao, Y., Jiang, H., & Zhang, Z. (2023). Detection and characterization of microplastics in the human testis and semen. Sci Total Environ, 877, 162713. https://doi.org/10.1016/j.scitotenv.2023.162713 Ziajahromi, S., Lu, H.-C., Drapper, D., Hornbuckle, A., & Leusch, F. D. L. (2023). Microplastics and Tire Wear Particles in Urban Stormwater: Abundance, Characteristics, and Potential Mitigation Strategies. Environmental Science & Technology, 57, 12829–12837. https://doi.org/10.1021/acs.est.3c03949 | - |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/105040 | - |
| dc.description.abstract | 塑膠微粒(microplastics, MPs)泛指尺寸小於 5 毫米的塑膠顆粒。塑膠材料進入環境後,受到物理、化學及生物性作用影響,可持續破碎形成尺寸較小的塑膠微粒,並進一步產生粒徑低於 1000 奈米的次微米塑膠微粒(sub-microplastics),甚至形成小於 100 奈米的奈米塑膠微粒(nanoplastics)。由於塑膠微粒具有高度持久性且廣泛存在於各類環境介質中,已普遍分布於海洋、河川、土壤及大氣等環境。人類可能經由受污染的飲用水、食物及空氣等途徑接觸塑膠微粒。近年研究顯示,部分塑膠微粒可能跨越生物屏障並分布於不同組織與器官,進而與氧化壓力、發炎反應及代謝失衡等生物效應相關。然而,不同粒徑塑膠微粒對體內代謝體的影響仍有待釐清,尤其缺乏同時考量粒徑、性別、器官及暴露時間之系統性研究。
本研究選用聚苯乙烯次微米與奈米塑膠微粒作為暴露物質,並透過核磁共振(nuclear magnetic resonance, NMR)代謝體學分析,探討其對小鼠小腸與肝臟代謝體之影響。實驗使用八週齡雄性與雌性小鼠,分別暴露於 50 nm 與 500 nm 聚苯乙烯粒子懸浮液,並以二次水作為對照。小鼠每週以胃管灌食兩次,劑量為 10 mL/kg 體重,相當於 10 mg/kg 體重之暴露劑量,暴露時間分為一個月與三個月。暴露結束後採集小腸及肝臟組織進行 NMR 代謝體分析,以比較不同粒徑、暴露時間與性別下的代謝反應。 研究結果顯示,各組相對體重均未呈現顯著差異,但部分暴露組的相對器官重量有所改變。暴露三個月後,50 nm 組雌性小鼠的相對小腸重量顯著降低;肝臟方面,暴露一個月後,50 nm 與 500 nm 組雌性小鼠,以及 500 nm 組雄性小鼠的相對肝臟重量皆顯著低於相應對照組。NMR 代謝體分析進一步顯示,50 nm 與 500 nm 聚苯乙烯粒子暴露後,小腸與肝臟呈現不同程度的代謝變化,且其反應模式隨粒徑、性別及暴露時間而異。在小腸中,代謝反應以雄性小鼠較為明顯,尤其在三個月暴露後,主要涉及能量代謝、核苷酸代謝、腸道菌相相關代謝物及膽汁酸相關代謝。相較之下,雌性小鼠的小腸代謝變化較少,主要呈現與腸道菌相來源有機酸相關的變化。肝臟方面,雄性小鼠的代謝反應相對有限,主要涉及能量與嘌呤相關代謝;雌性小鼠則在一個月與三個月暴露後皆呈現較廣泛的代謝變化,其中以 500 nm 組暴露一個月後的變化較為明顯,主要涉及葡萄糖與能量代謝、胺基酸代謝、膽鹼與磷脂代謝及核苷酸代謝。整體而言,50 nm 與 500 nm 粒子在不同器官中呈現不同的代謝反應模式,顯示聚苯乙烯次微米與奈米塑膠微粒暴露所產生的代謝變化可能受到粒徑與組織類型等因素影響。 綜合本研究結果,聚苯乙烯次微米與奈米塑膠微粒暴露所伴隨的代謝反應具有器官、粒徑、性別及暴露時間上的差異,並未呈現單一且一致的反應模式。儘管相對體重與器官重量的變化相對有限,NMR代謝體分析仍可辨識不同暴露條件下的代謝差異。這些變化主要涉及葡萄糖與能量代謝、胺基酸代謝、核苷酸代謝、膽鹼與磷脂代謝,以及腸道菌相相關代謝過程。未來若能結合脂質體學、腸道菌相分析及其他多體學方法,並延長暴露時間,將有助於進一步釐清聚苯乙烯次微米與奈米塑膠微粒暴露相關的生物作用機制,並提供評估其潛在人類健康影響之科學依據。 | zh_TW |
| dc.description.abstract | Microplastics (MPs) are generally defined as plastic particles smaller than 5 mm. Environmental weathering through physical, chemical, and biological processes can progressively fragment plastic materials into smaller particles, including sub-microplastics (<1000 nm) and nanoplastics (<100 nm). Because of their environmental persistence and widespread occurrence, MPs are present across diverse environmental compartments, including marine and freshwater systems, terrestrial environments, and the atmosphere. Human exposure can therefore occur through multiple routes, including the consumption of contaminated food and drinking water and the inhalation of airborne particles. Recent evidence further indicates that some MPs may cross biological barriers and become distributed in different tissues and organs, where they have been associated with oxidative stress, inflammatory responses, and metabolic alterations. Nevertheless, the metabolic responses associated with different particle sizes remain insufficiently characterized, particularly with respect to the combined influences of particle size, biological sex, target organ, and exposure duration.
In this study, polystyrene sub-microplastics and nanoplastics were investigated using nuclear magnetic resonance (NMR)-based metabolomics to characterize metabolic responses in the small intestine and liver of mice. Eight-week-old male and female mice received 50 nm or 500 nm polystyrene particle suspensions (0.1%, w/v) by oral gavage twice weekly at 10 mL/kg body weight, corresponding to a dose of 10 mg/kg body weight. Control animals received double-distilled water. Exposure periods of 1 and 3 months were evaluated. At the end of each exposure period, small intestinal and liver tissues were collected for NMR-based metabolomic profiling to compare metabolic responses across particle sizes, exposure durations, and sexes. The results showed that relative body weight remained comparable across treatment groups, while changes in relative organ weights were observed only in specific groups. After three months of exposure, female mice receiving 50 nm particles showed a lower relative intestinal weight than controls. Lower relative liver weights were also found in female mice exposed to either particle size for one month and in male mice exposed to 500 nm particles for one month. Despite these relatively limited changes in conventional physiological measures, NMR-based metabolomic profiling revealed substantial alterations in the small intestine and liver, with distinct response patterns according to particle size, sex, and exposure duration. In the small intestine, metabolic changes were more evident in male mice, especially after three months of exposure, and were associated mainly with energy and nucleotide metabolism, gut microbiota-related metabolism, and bile acid-related pathways. Female mice showed comparatively fewer intestinal metabolic changes, primarily involving microbiota-derived organic acids. In the liver, male mice exhibited relatively restricted metabolic responses, mainly involving energy- and nucleotide-related metabolites. Female mice showed a wider range of metabolic changes at both exposure durations, with particularly prominent alterations following one month of exposure to 500 nm particles. These changes were associated mainly with glucose, amino acid, choline/phospholipid, and nucleotide metabolism. Taken together, the findings suggest that 50 nm particles were associated more prominently with intestinal metabolic alterations, whereas 500 nm particles produced broader hepatic metabolic responses, although these patterns varied according to sex and exposure duration. In conclusion, exposure to PS sub-MPs and NPs produced distinct metabolic responses across organs, particle sizes, sexes, and exposure durations rather than a uniform toxicological pattern. Despite relatively limited changes in body and organ weights, substantial metabolic alterations were observed, demonstrating that metabolomic profiling can reveal biological responses that may not be apparent from conventional physiological endpoints alone. The affected metabolic processes encompassed glucose and energy metabolism, amino acid metabolism, nucleotide metabolism, choline/phospholipid metabolism, and gut microbiota-related metabolism, with response patterns differing between the small intestine and liver. Collectively, these findings provide a basis for future studies integrating lipidomics, gut microbiome profiling, and other multi-omics approaches to further elucidate the mechanisms of PS-MNP toxicity and improve understanding of the potential long-term implications for human health. | en |
| dc.description.provenance | Submitted by admin ntu (admin@lib.ntu.edu.tw) on 2026-09-07T16:36:47Z No. of bitstreams: 0 | en |
| dc.description.provenance | Made available in DSpace on 2026-09-07T16:36:47Z (GMT). No. of bitstreams: 0 | en |
| dc.description.tableofcontents | 口試委員會審定書 #
誌謝 i 中文摘要 ii ABSTRACT iv CONTENTS vii LIST OF TABLES xiii Chapter 1 Introduction 1 1.1 Microplastics (MPs) 1 1.2 Exposure routes of micro- and nanoplastics 3 1.2.1 Ingestion 3 1.2.2 Inhalation 5 1.2.3 Dermal contact 5 1.3 Physicochemical properties influencing MNP toxicity 6 1.4 Absorption, distribution, metabolism, and excretion of MNPs 7 1.4.1 Absorption 7 1.4.2 Distribution 8 1.4.3 Metabolism and excretion 9 1.5 Adverse health effects in MNP exposure 10 1.6 Nuclear magnetic resonance (NMR)-based metabolomics 14 1.6.1 Fundamentals of metabolomics 14 1.6.2 Metabolomics analysis 14 1.6.3 Application of metabolomics in MNP exposure studies 15 1.7 Study aims 17 Chapter 2 Materials and methods 18 2.1 Experimental framework 18 2.2 PS-MNPs particles 19 2.3 Animal experiment and sample collection 19 2.4 Metabolomic analysis 20 2.4.1 Sample preparation 20 2.4.2 NMR-Based Metabolic Profiling 21 2.4.3 Spectral processing 23 2.5 Statistical analysis 23 2.6 Metabolite identification 25 Chapter 3 Results 26 3.1 Effects of MNPs on Body and Organ Weights 26 3.2 Metabolic profiling and metabolic alterations in mouse intestine following MNP exposure 26 3.2.1 NMR-based metabolic profiling of mouse intestine 26 3.2.2 PCA of intestinal metabolites 27 3.2.3 PLS-DA of intestinal metabolites 28 3.2.4 Effects of exposure duration on intestinal metabolites (1 month vs 3 months) 28 3.2.5 Effects of particle size on intestinal metabolites (Control, 50 nm, 500 nm) 29 3.3 Metabolic profiling and metabolic alterations in mouse liver following MNP exposure 30 3.3.1 NMR-based metabolic profiling of mouse liver 30 3.3.2 PCA of liver metabolites 30 3.3.3 PLS-DA of liver metabolites 31 3.3.4 Effects of exposure duration on liver metabolites (1 month vs 3 months) 32 3.3.5 Effects of particle size on liver metabolites (Control, 50 nm, 500 nm) 33 3.4 Overview and cross-tissue comparison of metabolic alterations following MNP exposure 34 Chapter 4 Discussion 35 4.1 Overview of metabolic responses to PS-MNP exposure 35 4.2 Intestinal metabolic responses to PS-MNP exposure 36 4.2.1 Gut microbiota-related metabolism and intestinal barrier function 37 4.2.2 Intestinal energy metabolism and purine metabolism 39 4.3 Hepatic metabolic responses to PS-MNP exposure 41 4.3.1 Hepatic glucose and energy metabolism 42 4.3.2 Hepatic choline and phospholipid metabolism 43 4.3.3 Alterations in amino acid metabolism 45 4.4 Comparative analysis of PS-MNP-induced metabolic responses 47 4.4.1 Comparison between the intestine and liver 47 4.4.2 Comparison between 50 nm and 500 nm PS-MNPs 49 4.4.3 Comparison between male and female mice 50 4.4.4 Comparison between 1-month and 3-month exposure 50 4.4.5 Overall implications of PS-MNP-induced metabolic alterations 52 4.5 Strength and limitation 52 Chapter 5 Conclusion 55 | - |
| dc.language.iso | en | - |
| dc.subject | 塑膠微粒 | - |
| dc.subject | 次微米塑膠微粒 | - |
| dc.subject | 奈米微粒 | - |
| dc.subject | 肝臟 | - |
| dc.subject | 小腸 | - |
| dc.subject | 核磁共振光譜儀 | - |
| dc.subject | 代謝體學 | - |
| dc.subject | microplastics | - |
| dc.subject | sub-microplastics | - |
| dc.subject | nanoplastics | - |
| dc.subject | liver | - |
| dc.subject | intestine | - |
| dc.subject | nuclear magnetic resonance | - |
| dc.subject | metabolomics | - |
| dc.title | 利用核磁共振光譜儀探討塑膠微粒暴露對小鼠肝臟與小腸之代謝體影響 | zh_TW |
| dc.title | Investigating the Effects of Microplastic Exposure on the Metabolome of Mouse Liver and Intestine Using Nuclear Magnetic Resonance | en |
| dc.type | Thesis | - |
| dc.date.schoolyear | 114-2 | - |
| dc.description.degree | 碩士 | - |
| dc.contributor.oralexamcommittee | 李昇翰;羅宇軒;唐川禾 | zh_TW |
| dc.contributor.oralexamcommittee | Sheng-Han Lee;Yu-Syuan Luo;Chuan-Ho Tang | en |
| dc.subject.keyword | 塑膠微粒; 次微米塑膠微粒; 奈米微粒; 肝臟; 小腸; 核磁共振光譜儀; 代謝體學 | zh_TW |
| dc.subject.keyword | microplastics; sub-microplastics; nanoplastics; liver; intestine; nuclear magnetic resonance; metabolomics | en |
| dc.relation.page | 110 | - |
| dc.identifier.doi | 10.6342/NTU202603969 | - |
| dc.rights.note | 同意授權(限校園內公開) | - |
| dc.date.accepted | 2026-08-13 | - |
| dc.contributor.author-college | 公共衛生學院 | - |
| dc.contributor.author-dept | 環境與職業健康科學研究所 | - |
| dc.date.embargo-lift | 2031-08-10 | - |
| 顯示於系所單位: | 環境與職業健康科學研究所 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-114-2.pdf 未授權公開取用 | 8.07 MB | Adobe PDF | 檢視/開啟 |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
