CHANGES IN SPONTANEOUS CONTRACTILE ACTIVITY OF SMOOTH MUSCLES IN THE GASTROINTESTINAL TRACT OF RATS UNDER LONG-TERM INTAKE OF A MIXTURE OF POLYPROPYLENE NANOPARTICLES AND MICROPARTICLES

Maria Shulha, Oleksandr Chunikhin, Volodymyr Malyshev, Andrij Sybirnyy, Oleksandr Savchenko, Sergij Mandryk, Khrystyna Sholota, Oleksandr Artemenko, Olga Tsymbalyuk


DOI: http://dx.doi.org/10.30970/sbi.2001.874

Abstract


Background. Plastic is the most common pollutant in the environment. In natural conditions, plastic undergoes mechanical and photochemical degradation, forming micro- and nanoparticles that are accumulated by living organisms. Regular intake of plastic micro- and nanoparticles (MNP) in the gastrointestinal tract (GIT) leads to the development of inflammatory processes in the alimentary canal walls and disrupts intestinal microbiota. However, the contractile activity of smooth muscles in the GIT under these conditions is yet to be studied.
The aim of the study was to investigate the spontaneous contractile activity of circular smooth muscles of the antrum and caecum of rats under long-term peroral intake of MNP of one of the most common plastic pollutants for the environment, polypropylene (PP).
Materials and Methods. The suspension of polypropylene particles was prepared using disposable dishes by Roursgaard’s method with slight modifications. The determination of the average hydrodynamic diameter of PP particles in the aqueous suspension involved the method of dynamic light scattering. The animals in the experimental group received the PP suspension in their drinking water (at a daily dose of 2.5 mg/kg) for 6 weeks. The tenzometric experiments were conducted in the isometric mode of registration, using isolated circular smooth muscle preparations from the antrum and caecum of rats. The spontaneous contractions were analyzed by mechanokinetic analysis with the estimation of force, time, velocity, and impulse parameters.
Results. The polypropylene suspension contained particles of up to 4 µm, 34.1 % of which were < 1 µm. Long-term peroral intake of PP into the organism was accompanied by the impairment of the spontaneous contractile activity of smooth muscles in the antrum and caecum: a decrease in the frequency and modulation of mechanokinetic parameters of some contractions. In case of the antrum muscles, there was an increase in force and velocity parameters, time parameters were below the control ones, while the impulse parameters remained unchanged. Under the effect of PP, the mechanokinetic parameters of contractions in the caecum demonstrated the following changes: there was a considerable increase in force parameters for the amplitude and phase of contraction, as well as all the time and impulse parameters, whereas velocity parameters were considerably decreased.
Conclusions. Prolonged intake of polypropylene MNP into the organism causes changes in the frequency of spontaneous smooth muscles contractions, likely due to impaired functioning of pacemaker cells; whereas changes in amplitude parameters are likely due to MNP’s action on smooth muscle cells.


Keywords


mixture of nano- and microplastics, polypropylene, smooth muscles, antrum, caecum, spontaneous contractions, mechanokinetic parameters

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Al-Shboul, O., & Mustafa, A. (2015). Effect of oxidative stress on Rho kinase II and smooth muscle contraction in rat stomach. Canadian Journal of Physiology and Pharmacology, 93(6), 405-411. doi:10.1139/cjpp-2014-0505
CrossrefPubMedGoogle Scholar

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(19), e2417104122. doi:10.1073/pnas.2417104122
CrossrefPubMedPMCGoogle Scholar

Bora, S. S., Gogoi, R., Sharma, M. R., Anshu, Borah, M. P., Deka, P., Bora, J., Naorem, R. S., Das, J., & Teli, A. B. (2024). Microplastics and human health: unveiling the gut microbiome disruption and chronic disease risks. Frontiers in Cellular and Infection Microbiology, 14, 1492759. doi:10.3389/fcimb.2024.1492759
CrossrefPubMedPMCGoogle Scholar

Chi, J., Patterson, J. S., Jin, Y., Kim, K. J., Lalime, N., Hawley, D., Lewis, F., Li, L., Wang, X., Campen, M. J., Cui, J. Y., & Gu, H. (2025). Metabolic reprogramming in gut microbiota exposed to polystyrene microplastics. Biomedicines, 13(2), 446. doi:10.3390/biomedicines13020446
CrossrefPubMedPMCGoogle Scholar

Claassen, V. (1994). Food and water intake. In Techniques in the behavioral and neural sciences (Vol. 12, pp. 267-287). Amsterdam: Elsevier. doi:10.1016/b978-0-444-81871-3.50019-9
CrossrefGoogle Scholar

da Silva Brito, W. A., Mutter, F., Wende, K., Cecchini, A. L., Schmidt, A., & Bekeschus, S. (2022). Consequences of nano and microplastic exposure in rodent models: the known and unknown. Particle and Fibre Toxicology, 19(1), 28. doi:10.1186/s12989-022-00473-y
CrossrefPubMedPMCGoogle Scholar

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(1), 46687. doi:10.1038/srep46687
CrossrefPubMedPMCGoogle Scholar

Di Natale, M. R., Wang, X., Hunne, B., Wraight, M., Liu, Z., Han, M. N., & Furness, J. B. (2025). Regional specialisations of innervation and musculature of the rat stomach. Journal of Anatomy. doi:10.1111/joa.7010540
CrossrefPubMedGoogle Scholar

Donisi, I., Colloca, A., Anastasio, C., Balestrieri, M. L., & D'Onofrio, N. (2024). Micro(nano)plastics: an emerging burden for human health. International Journal of Biological Sciences, 20(14), 5779-5792. doi:10.7150/ijbs.99556
CrossrefPubMedPMCGoogle Scholar

Dube, E., & Okuthe, G. E. (2023). Plastics and micro/nano-plastics (MNPs) in the environment: occurrence, impact, and toxicity. International Journal of Environmental Research and Public Health, 20(17), 6667. doi:10.3390/ijerph20176667
CrossrefPubMedPMCGoogle Scholar

Fackelmann, G., & Sommer, S. (2019). Microplastics and the gut microbiome: how chronically exposed species may suffer from gut dysbiosis. Marine Pollution Bulletin, 143, 193-203. doi:10.1016/j.marpolbul.2019.04.030
CrossrefPubMedGoogle Scholar

Forte, M., Iachetta, G., Tussellino, M., Carotenuto, R., Prisco, M., De Falco, M., Laforgia, V., & Valiante, S. (2016). Polystyrene nanoparticles internalization in human gastric adenocarcinoma cells. Toxicology in Vitro, 31, 126-136. doi:10.1016/j.tiv.2015.11.006
CrossrefPubMedGoogle Scholar

Gopinath, P. M., Parvathi, V. D., Yoghalakshmi, N., Kumar, S. M., Athulya, P. A., Mukherjee, A., & Chandrasekaran, N. (2022). Plastic particles in medicine: a systematic review of exposure and effects to human health. Chemosphere, 303, 135227. doi:10.1016/j.chemosphere.2022.135227
CrossrefPubMedGoogle Scholar

Hwang, S. J., Kwon, J. G., Beckett, E. A. H., Kim, M., Herbert, T., Sanders, K. M., & Ward, S. M. (2025). Functional roles of interstitial cells of Cajal in the GI tract of rats. American Journal of Physiology-Gastrointestinal and Liver Physiology, 328(6), G677-G695. doi:10.1152/ajpgi.00036.2025
CrossrefPubMedPMCGoogle Scholar

Jani, P., Halbert, G. W., Langridge, J., & Florence, A. T. (1990). Nanoparticle uptake by the rat gastrointestinal mucosa: quantitation and particle size dependency. Journal of Pharmacy and Pharmacology, 42(12), 821-826. doi:10.1111/j.2042-7158.1990.tb07033.x
CrossrefPubMedGoogle Scholar

Jeon, B. J., Ko, Y. J., Cha, J. J., Kim, C., Seo, M. Y., Lee, S. H., Park, J. Y., Bae, J. H., & Tae, B. S. (2024). Examining the relationship between polystyrene microplastics and male fertility: insights from an in vivo study and in vitro Sertoli cell culture. Journal of Korean Medical Science, 39(38), e259. doi:10.3346/jkms.2024.39.e259
CrossrefPubMedPMCGoogle Scholar

Jin, Y., Lu, L., Tu, W., Luo, T., & Fu, Z. (2019). Impacts of polystyrene microplastic on the gut barrier, microbiota and metabolism of mice. Science of The Total Environment, 649, 308-317. doi:10.1016/j.scitotenv.2018.08.353
CrossrefPubMedGoogle Scholar

Kiran, B. R., Kopperi, H., & Venkata Mohan, S. (2022). Micro/nano-plastics occurrence, identification, risk analysis and mitigation: challenges and perspectives. Reviews in Environmental Science and Bio/Technology, 21(1), 169-203. doi:10.1007/s11157-021-09609-6
CrossrefPubMedPMCGoogle Scholar

Kopatz, V., Wen, K., Kovács, T., Keimowitz, A. S., Pichler, V., Widder, J., Vethaak, A. D., Hollóczki, O., & Kenner, L. (2023). Micro- and nanoplastics breach the blood-brain barrier (BBB): biomolecular corona's role revealed. Nanomaterials, 13(8), 1404. doi:10.3390/nano13081404
CrossrefPubMedPMCGoogle Scholar

Kosterin, S., Tsymbalyuk, O., & Holden, O. (2021). Multiparameter analysis of mechanokinetics of the contractile response of smooth muscles. Series on Biomechanics, 35(1), 14-30.
Google Scholar

Li, Z., Zhu, S., Liu, Q., Wei, J., Jin, Y., Wang, X., & Zhang, L. (2020). Polystyrene microplastics cause cardiac fibrosis by activating Wnt/β-catenin signaling pathway and promoting cardiomyocyte apoptosis in rats. Environmental Pollution, 265, 115025. doi:10.1016/j.envpol.2020.115025
CrossrefPubMedGoogle Scholar

Liu, X., Yang, K., Jia, Y., Yeertai, Y., Wu, C., Wang, X., Jia, Q., Gu, Z., Cong, J., & Ling, J. (2025). Chaihushugan powder regulates the gut microbiota to alleviate mitochondrial oxidative stress in the gastric tissues of rats with functional dyspepsia. Frontiers in Immunology, 16, 1549554. doi:10.3389/fimmu.2025.1549554
CrossrefPubMedPMCGoogle Scholar

Mahavadi, S., Sriwai, W., Manion, O., Grider, J. R., & Murthy, K. S. (2017). Diabetes-induced oxidative stress mediates upregulation of RhoA/Rho kinase pathway and hypercontractility of gastric smooth muscle. PloS One, 12(7), e0178574. doi:10.1371/journal.pone.0178574
CrossrefPubMedPMCGoogle Scholar

Paul, M. B., Stock, V., Cara-Carmona, J., Lisicki, E., Shopova, S., Fessard, V., Braeuning, A., Sieg, H., & Böhmert, L. (2020). Micro- and nanoplastics - current state of knowledge with the focus on oral uptake and toxicity. Nanoscale Advances, 2(10), 4350-4367. doi:10.1039/d0na00539h
CrossrefPubMedPMCGoogle Scholar

Persiani, E., Cecchettini, A., Amato, S., Ceccherini, E., Gisone, I., Sgalippa, A., Ippolito, C., Castelvetro, V., Lomonaco, T., & Vozzi, F. (2025). Virgin and photo-degraded microplastics induce the activation of human vascular smooth muscle cells. Scientific Reports, 15(1), 4263. doi:10.1038/s41598-025-89006-z
CrossrefPubMedPMCGoogle Scholar

Pradel, A., Catrouillet, C., & Gigault, J. (2023). The environmental fate of nanoplastics: what we know and what we need to know about aggregation. NanoImpact, 29, 100453. doi:10.1016/j.impact.2023.100453
CrossrefPubMedGoogle Scholar

Roursgaard, M., Hezareh Rothmann, M., Schulte, J., Karadimou, I., Marinelli, E., & Møller, P. (2022). Genotoxicity of particles from grinded plastic items in Caco-2 and HepG2 cells. Frontiers in Public Health, 10, 906430. doi:10.3389/fpubh.2022.906430
CrossrefPubMedPMCGoogle Scholar

Sadri, S. S., & Thompson, R. C. (2014). On the quantity and composition of floating plastic debris entering and leaving the Tamar Estuary, Southwest England. Marine Pollution Bulletin, 81(1), 55-60. doi:10.1016/j.marpolbul.2014.02.020
CrossrefPubMedGoogle Scholar

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. Journal of Hazardous Materials, 404, 124004. doi:10.1016/j.jhazmat.2020.124004
CrossrefPubMedGoogle Scholar

Shan, S., Zhang, Y., Zhao, H., Zeng, T., & Zhao, X. (2022). Polystyrene nanoplastics penetrate across the blood-brain barrier and induce activation of microglia in the brain of mice. Chemosphere, 298, 134261. doi:10.1016/j.chemosphere.2022.134261
CrossrefPubMedGoogle Scholar

Simon, L., Warren, I., & Dayan, A. D. (1997). Effect of solid and liquid diet on uptake of large particulates across intestinal epithelium in rats. Digestive Diseases and Sciences, 42(7), 1519-1523. doi:10.1023/a:1018883230764
CrossrefPubMedGoogle Scholar

Smith, T. K., Reed, J. B., & Sanders, K. M. (1987). Interaction of two electrical pacemakers in muscularis of canine proximal colon. American Journal of Physiology-Cell Physiology, 252(3), C290-C299. doi:10.1152/ajpcell.1987.252.3.c290
CrossrefPubMedGoogle Scholar

Sun, J., Sun, L., Li, J., Xu, J., Wan, Z., Ouyang, Z., Liang, L., Li, S., & Zeng, D. (2018). A multi-functional polymeric carrier for simultaneous positron emission tomography imaging and combination therapy. Acta Biomaterialia, 75, 312-322. do:10.1016/j.actbio.2018.06.010
CrossrefPubMedPMCGoogle Scholar

Wang, M., Xing, N., Wu, L., Huang, W.-C., Xu, Z., & Liu, G. (2018). Regulation of spontaneous contractions in intact rat bladder strips and the effects of hydrogen peroxide. BioMed Research International, 2018, 2925985. doi:10.1155/2018/2925985
CrossrefPubMedPMCGoogle Scholar

Wieland, S., Balmes, A., Bender, J., Kitzinger, J., Meyer, F., Ramsperger, A. F., Roeder, F., Tengelmann, C., Wimmer, B. H., Laforsch, C., & Kress, H. (2022). From properties to toxicity: comparing microplastics to other airborne microparticles. Journal of Hazardous Materials, 428, 128151. doi:10.1016/j.jhazmat.2021.128151
CrossrefPubMedGoogle Scholar

Wu, X., Leung, T., Jima, D. D., Iyangbe, M., & Bang, J. (2025). Developing a feasible fast-track testing method for developmental neurotoxicity studies: alternative model for risk assessment of micro- and nanoplastics. Frontiers in Toxicology, 7, 1567225. doi:10.3389/ftox.2025.1567225
CrossrefPubMedPMCGoogle Scholar

Xie, X., Wang, K., Shen, X., Li, X., Wang, S., Yuan, S., Li, B., & Wang, Z. (2024). Potential mechanisms of aortic medial degeneration promoted by co-exposure to microplastics and lead. Journal of Hazardous Materials, 475, 134854. doi:10.1016/j.jhazmat.2024.134854
CrossrefPubMedGoogle Scholar

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(3), 468-485. doi:10.1007/s40726-023-00273-8
CrossrefGoogle Scholar

Yu, J., Qiu, H., Yin, S., Wang, H., & Li, Y. (2021). Polymeric drug delivery system based on pluronics for cancer treatment. Molecules, 26(12), 3610. doi:10.3390/molecules26123610
CrossrefPubMedPMCGoogle Scholar

Zhang, M., Shi, J., Pan, H., Zhu, J., Wang, X., Song, L., & Deng, H. (2024). A novel tiRNA-Glu-CTC induces nanoplastics accelerated vascular smooth muscle cell phenotypic switching and vascular injury through mitochondrial damage. Science of The Total Environment, 912, 169515. doi:10.1016/j.scitotenv.2023.169515
CrossrefPubMedGoogle Scholar

Zhao, Q., Fang, Z., Wang, P., Qian, Z., Yang, Y., Ran, L., Zheng, J., Tang, Y., Cui, X., Li, Y.-Y., Zhang, Z., & Jiang, H. (2025). Polylactic acid micro/nanoplastic exposure induces male reproductive toxicity by disrupting spermatogenesis and mitochondrial dysfunction in mice. ACS Nano, 19(5), 5589-5603. doi:10.1021/acsnano.4c15112
CrossrefPubMedGoogle Scholar

Zhu, X., Wang, C., Duan, X., Liang, B., Genbo Xu, E., & Huang, Z. (2023). Micro- and nanoplastics: a new cardiovascular risk factor? Environment International, 171, 107662. doi:10.1016/j.envint.2022.107662
CrossrefPubMedGoogle Scholar

Zurub, R. E., Cariaco, Y., Wade, M. G., & Bainbridge, S. A. (2024). Microplastics exposure: implications for human fertility, pregnancy and child health. Frontiers in Endocrinology, 14, 1330396. doi:10.3389/fendo.2023.1330396
CrossrefPubMedPMCGoogle Scholar


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