MIKRO- VA NANOPLASTIKLAR – OZIQ-OVQAT MAHSULOTLARIDAGI KONTAMINANTLARNING IMMUN TIZIMGA TA’SIRI
Keywords:
Kalit so‘zlarL Mikroplastiklar, nanoplastiklar, immun tizimi, yallig‘lanish, oksidlovchi stress, sitokinlar, oshqozon-ichak tizimi, jigar.Abstract
Ushbu maqolada mikro- va nanoplastiklarning (MP va NP) atrof-muhitda keng
tarqalishi hamda ularning inson organizmiga, xususan immun tizimiga ta’siri tahlil
qilingan. Tadqiqotlarda MP va NP oziq-ovqat mahsulotlari, ichimlik suvi va atmosfera
orqali inson organizmiga kirishi, oshqozon-ichak tizimi, o‘pka va boshqa organlarda
to‘planishi mumkinligi ko‘rsatilgan. Ushbu zarrachalar hujayra darajasida oksidlovchi
stress, yallig‘lanish jarayonlari va immunoregulyatsiya buzilishlarini keltirib chiqarishi
aniqlangan. MP va NP makrofaglar faolligini o‘zgartirishi, proyallig‘lanish sitokinlari
(IL-1β, IL-6, TNF-α va boshqalar) ishlab chiqarilishini kuchaytirishi hamda immun
tizimining turli signal yo‘llarini faollashtirishi mumkin. Eksperimental tadqiqotlar
mikroplastiklarning ichak mikroflorasi tarkibini o‘zgartirishi, to‘qimalarda
yallig‘lanish jarayonlarini kuchaytirishi va immun tizimi hujayralari faoliyatiga ta’sir
ko‘rsatishini ko‘rsatadi. Shuningdek, MP va NP ning reproduktiv tizim va metabolik
jarayonlarga ta’siri ham qayd etilgan. Natijalar mikro- va nanoplastiklarning
organizmda aseptik surunkali yallig‘lanish rivojlanishiga olib kelishi mumkinligini
ko‘rsatadi. Shu sababli ularning inson salomatligiga ta’sir mexanizmlarini chuqur
o‘rganish va xavfsizlik bahosini aniqlash dolzarb ilmiy muammo hisoblanadi.
References
Foydalanilgan adabiyotlar
1. Lehner R., Weder C., Petri-Fink A., Rothen-Rutishauser B. Emergence of
nanoplastic in the environment and possible impact on human health. Environ Sci
Technol. 2019; 53 (4): 1748–65. DOI: https://doi. org/10.1021/acs.est.8b05512
2. Prata J.C., da Costa J.P., Lopes I., Duarte A.C., Rocha-Santos T. Environmental
exposure to microplastics: an overview on possible human health eff ects. Sci Total
Environ. 2020; 702: 134455. DOI: https://doi.
org/10.1016/j.scitotenv.2019.134455
3. Rochman C.M., Brookson C., Bikker J., Djuric N., Earn A., Bucci K., et al.
Rethinking microplastics as a diverse contaminant suite. Environ Toxicol Chem.
2019; 38 (4): 703–11. DOI: https://doi.org/10.1002/etc.4371
4. Lebreton L., Slat B., Ferrari F., Sainte-Rose B., Aitken J., Marthouse R., et al.
Evidence that the Great Pacifi c Garbage Patch is rapidly accumulating plastic. Sci
Rep. 2018; 8 (1): 4666. DOI: https://doi. org/10.1038/s41598-018-22939-w
5. Amobonye A., Bhagwat P., Raveendran S., Singh S., Pillai S. Environmental
impacts of microplastics and nanoplastics: a current overview. Front Microbiol.
2021; 12: 768297. DOI: https://doi.org/10.3389/ fmicb.2021.768297
6. Gigault J., El Hadri H., Nguyen B., Grassl B., Rowenczyk L., Tufenkji N., et al.
Nanoplastics are neither microplastics nor engineered nanoparticles. Nat
Nanotechnol. 2021; 16 (5): 501–7. DOI: https://doi. org/10.1038/s41565-021-
00886-4
7. Toussaint B., Raff ael B., Angers-Loustau A., Gilliland D., Kestens V., Petrillo M.,
et al. Review of micro- and nanoplastic contamination in the food chain. Food
Addit Contam Part A Chem Anal Control Expo Risk Assess. 2019; 36 (5): 639–
73. DOI: https://doi.org/10.3389/ fmicb.2021.768297
8. Allan J., Belz S., Hoeveler A., Hugas M., Okuda H., Patri A., et al. Regulatory
landscape of nanotechnology and nanoplastics from a global perspective. Regul
Toxicol Pharmacol. 2021; 122 (8): 104885. DOI:
https://doi.org/10.1016/j.yrtph.2021.104885
9. Xu B., Liu F., Cryder Z., Huang D., Lu Z., He Y., et al. Microplastics in the soil
environment: occurrence, risks, interactions and fate – a review. Crit Rev Environ
Sci Technol. 2020; 50 (21): 2175–222. DOI: https://
doi.org/10.1080/10643389.2019.1694822
10. Wang J., Liu X., Li Y., Powell T., Wang X., Wang G., et al. Microplastics as
contaminants in the soil environment: a mini-review. Sci Total Environ. 2019; 691:
848–57. DOI: https://doi.org/10.1016/j.scitotenv.2019.07.209
11. Corradini F., Meza P., Eguiluz R., Casado F., Huerta-Lwanga E., Geissen V.
Evidence of microplastic accumulation in agricultural soils from sewage sludge
disposal. Sci Total Environ. 2019; 671: 411–20. DOI:
https://doi.org/10.1016/j.scitotenv.2019.03.368
12. Alimba C.G, Faggio C. Microplastics in the marine environment: current trends in
environmental pollution and mechanisms of toxicological profi le. Environ Toxicol
Pharmacol. 2019; 68: 61–74. DOI: https:// doi.org/10.1016/j.etap.2019.03.001
13. Peeken I., Primpke S., Beyer B., Gütermann J., Katlein C., Krumpen T., et al.
Arctic Sea ice is an important temporal sink and means of transport for
microplastic. Nat Commun. 2018; 9 (1): 1505. DOI: https://doi.
org/10.1038/s41467-018-03825-5
14. Schwarz A.E., Ligthart T.N., Boukris E., van Harmelen T. Sources, transport, and
accumulation of diff erent types of plastic litter in aquatic environments: a review
study. Mar Pollut Bull. 2019; 143 (1–2): 92–100. DOI:
https://doi.org/10.1016/j.marpolbul.2019.04.029
15. Lambert S., Wagner M. Microplastics are contaminants of emerging concern in
freshwater environments: an overview. In: Wagner M., Lambert S. (eds).
Freshwater Microplastics. The Handbook of Environmental Chemistry. Vol. 58.
Cham: Springer, 2018: 1–23. DOI: https:// doi.org/10.1007/978-3-319-61615-5_1
16. Koelmans A.A., Mohamed Nor N.H., Hermsen E., Kooi M., Mintenig S.M., De
France J. Microplastics in freshwaters and drinking water: critical review and
assessment of data quality. Water Res. 2019; 155; 410–22. DOI:
https://doi.org/10.1016/j.watres.2019.02.054
17. Danopoulos E., Twiddy M., Rotchell J.M. Microplastic contamination of drinking
water: a systematic review. PLoS One. 2020; 15 (7): 0236838. DOI:
https://doi.org/10.1371/journal.pone.0236838
18. Smith M., Love D.C., Rochman C.M., Neff R.A. Microplastics in seafood and the
implications for human health. Curr Environ Health Rep. 2018; 5 (3): 375–86.
DOI: https://doi.org/10.1007/s40572-018-
0206-z
19. Hantoro I., Löhr A.J., Van Belleghem F.G.A.J., Widianarko B., Ragas A.M.J.
Microplastics in coastal areas and seafood: implications for food safety. Food
Addit Contam Part A Chem Anal Control Expo
Risk Assess. 2019; 36 (5): 674–711. DOI: https://doi.org/10.1080/1944
0049.2019.1585581
20. Liebezeit G., Liebezeit E. Non-pollen particulates in honey and sugar.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2013;
30 (12): 2136–40. DOI: https://doi.org/10.1080/19440049.2013.843025
21. Gündoğdu S. Contamination of table salts from Turkey with microplastics. Food
Addit Contam Part A Chem Anal Control Expo Risk Assess.
2018; 35 (5): 1006–14. DOI: https://doi.org/10.1080/19440049.2018. 1447694
22. Liebezeit G., Liebezeit E. Synthetic particles as contaminants in German beers.
Food Addit Contam Part A Chem Anal Control Expo
Risk Assess. 2014; 31 (9): 1574–78. DOI: https://doi.org/10.1080/19440
049.2014.945099
23. Chen G., Feng Q., Wang J. Mini-review of microplastics in the atmosphere and
their risks to humans. Sci Total Environ. 2020; 703: 135504. DOI:
https://doi.org/10.1016/j.scitotenv.2019.135504
24. Wright S.L., Ulke J., Font A., Chan K.L.A., Kelly F.J. Atmospheric microplastic
deposition in an urban environment and an evaluation of transport. Environ Int.
2020; 136: 105411. DOI: https://doi. org/10.1016/j.envint.2019.105411
25. Hirt N., Body-Malapel M. Immunotoxicity and intestinal eff ects of nano- and
microplastics: a review of the literature. Part Fibre Toxicol.
2020; 17 (1): 57. DOI: https://doi.org/10.1186/s12989-020-00387-7
26. Leslie H.A., van Velzen M.J.M., Brandsma S.H., Vethaak A.D., GarciaVallejo J.J.,
Lamoree M.H. Discovery and quantifi cation of plastic particle pollution in human
blood. Environ Int. 2022; 163: 107199. DOI:
https://doi.org/10.1016/j.envint.2022.107199
27. Khan A., Jia Z. Recent insights into uptake, toxicity, and molecular targets of
microplastics and nanoplastics relevant to human health impacts. iScience. 2023;
26 (2): 106061. DOI: https://doi.org/10.1016/ j.isci.2023.106061
28. Liu S., Shi J., Wang J., Dai Y., Li H., Li J., et al. Interactions between microplastics
and heavy metals in aquatic environments: a review. Front Microbiol. 2021; 12:
652520. DOI: https://doi.org/10.3389/ fmicb.2021.652520
29. Prüst M., Meij er J., Westerink R.H.S. The plastic brain: neurotoxicity of micro-
and nanoplastics. Part Fibre Toxicol. 2020; 17: 1–16. DOI:
https://doi.org/10.1186/s12989-020-00358-y
30. Zhang P., Wang Y., Zhao X., Ji Y., Mei R., Fu L., et al. Surfaceenhanced Raman
scattering labeled nanoplastic models for reliable
bio-nano interaction investigations. J Hazard Mater. 2022; 425: 127959. DOI:
https://doi.org/ 10.1016/j.jhazmat.2021.127959
31. Shen R., Yang K., Cheng X., Guo C., Xing X., Sun H., et al. Accumulation of
polystyrene microplastics induces liver fi brosis by activating cGAS/STING
pathway. Environ Pollut. 2022; 300: 118986. DOI:
https://doi.org/10.1016/j.envpol.2022.118986
32. Lundqvist M., Stigler J., Elia G., Lynch I., Cedervall T., Dawson K.A.
Nanoparticle size and surface properties determine the protein corona with possible
implications for biological impacts. Proc Natl Acad Sci USA. 2008; 105: 14 265–
70. DOI: https://doi.org/10.1073/ pnas.0805135105
33. Yang W., Jannatun N., Zeng Y., Liu T., Zhang G., Chen C., Li Y. Impacts of
microplastics on immunity. Front Toxicol. 2022; 4: 956885.
DOI: https://doi.org/10.3389/ftox. 2022.956885
34. Abihssira-Garcia I.S., Park Y., Kiron V., Olsvik P.A. Fluorescent microplastic
uptake by immune cells of atlantic salmon (Salmo salar L.). Front Environ. 2020;
8: 233. DOI: https://doi.org/10.3389/ fenvs.2020.560206
35. Yee M.S.L., Hii L.W., Looi C.K., Lim W.M., Wong S.F., Kok Y.Y., et al. Impact
of microplastics and nanoplastics on human health. Nanomaterials. 2021; 11: 496.
DOI: https://doi.org/10.3390/nano11020496
36. Mani I., Pandey K.N. Emerging concepts of receptor endocytosis and concurrent
intracellular signaling: mechanisms of guanylyl cyclase/natriuretic peptide
receptor-A activation and traffi cking. Cell Signal. 2019; 60: 17–30. DOI:
https://doi.org/10.1016/j.cellsig.2019. 03.022
37. Xu D., Ma Y., Han X., Chen Y. Systematic toxicity evaluation of polystyrene
nanoplastics on mice and molecular mechanism investigation about their
internalization into Caco-2 cells. J Hazard Mater. 2021; 417: 126092. DOI:
https://doi.org/10.1016/j.jhazmat.2021.126092
38. Powell J.J, Faria N., Thomas-McKay E., Pele L.C. Origin and fate of dietary
nanoparticles and microparticles in the gastrointestinal tract. J Autoimmun. 2010;
34: J226–33. DOI: https://doi.org/10.1016/j. jaut.2009.11.006
39. Lu K., Lai K.P., Stoeger T., Ji S., Lin Z., Lin X., et al. Detrimental eff ects of
microplastic exposure on normal and asthmatic pulmonary physiology. J Hazard
Mater. 2021; 416: 126069. DOI: https://doi. org/10.1016/j.jhazmat.2021.126069
40. Zhang Q., Zhao Y., Du F., Cai H., Wang G., Shi H. Microplastic fallout in diff
erent indoor environments. Environ Sci Technol. 2020; 54: 6530–9. DOI:
https://doi.org/10.1021/acs.est.0c00087
41. Xu M., Halimu G., Zhang Q., Song Y., Fu X., Li Y., et al. Internalization and
toxicity: a preliminary study of eff ects of nanoplastic particles on human lung
epithelial cell. Sci Total Environ. 2019; 694: 133794.
DOI: https://doi.org/10.1016/j.scitotenv.2019.133794
42. Ensign L.M., Cone R., Hanes J. Oral drug delivery with polymeric nanoparticles:
the gastrointestinal mucus barriers. Adv Drug Deliv Rev.
2012; 64: 557–70. DOI: https://doi.org/10.1016/j.addr.2011.12.009
43. Coméra C., Cartier C., Gaultier E., Catrice O., Panouille Q., Hamdi S.E., et al.
Jejunal villus absorption and paracellular tight junction permeability are major
routes for early intestinal uptake of food-grade TiO 2 particles: an in vivo and ex
vivo study in mice. Part Fibre Toxicol. 2020; 17: 1–15. DOI:
https://doi.org/10.1186/s12989-020-00357-z
44. Smith M.W., Thomas N.W., Jenkins P.G., Miller N.G., Cremaschi D., Porta C.
Selective transport of microparticles across Peyer’s patch follicle-associated M
cells from mice and rats. Exp Physiol. 1995; 80: 735–43. DOI:
https://doi.org/10.1113/expphysiol.1995.sp003882
45. Feng X., Zhang Y., Zhang C., Lai X., Zhang Y., Wu J., et al. Nanomaterial-
mediated autophagy: coexisting hazard and health benefi ts in biomedicine. Part
Fibre Toxicol. 2020; 17: 53. DOI: https://doi.
org/10.1186/s12989-020-00372-0
46. Galloway T.S. Micro-and nano-plastics and human health. In: Marine
Anthropogenic Litter. 1st ed. Cham: Springer, 2015: 343–66. DOI:
https://doi.org/10.1007/978-3-319-16510-3_13
47. Deng Y.F., Zhang Y., Lemos B., Ren H.Q. Tissue accumulation of microplastics
in mice and biomarker responses suggest widespread health risks of exposure. Sci
Rep. 2017; 7: 46687. DOI: https://doi. org/10.1038/srep46687
48. Yong C.Q.Y., Valiyaveetill S., Tang B.L. Toxicity of microplastics and
nanoplastics in mammalian systems. Int J Environ Res Public Health. 2020; 17:
E1509. DOI: https://doi.org/10.3390/ij erph17051509
49. Carr K.E., Smyth S.H., McCullough M.T., Morris J.F., Moyes S.M. Morphological
aspects of interactions between microparticles and mammalian cells: intestinal
uptake and onward movement. Prog Histochem Cytochem. 2012; 46: 185–252.
DOI: https://doi.org/10.1016/j. proghi.2011.11.001
50. Campanale C., Massarelli C., Savino I., Locaputo V., Uricchio V.F.A. Detailed
review study on potential eff ects of microplastics and additives of concern on
human health. Int J Environ Res Public Health. 2020; 17 (4): 1212. DOI:
https://doi.org/10.3390/ij erph17041212 PMID: 32069998.
51. Mckechnie J.L., Blish C.A. The innate immune system: fi ghting on the front lines
or fanning the fl ames of COVID-19? Cell Host Microbe.
2020; 27: 863–9. DOI: https://doi.org/10.1016/j.chom.2020.05.009
52. Zhang G.F., Luo W.H., Yang W.J., Li S., Li D.J., Zeng Y.Q., et al. The importance
of IL-1 family cytokines in nanoimmunosafety and Nanotoxicology. Wiley
Interdiscip Rev Nanomed Nanobiotechnol. 2022; 14 (6): e1850. DOI:
https://doi.org/10.1002/wnan.1850
53. Boraschi D., Italiani P. Innate immune memory: time for adopting a correct
terminology. Front Immunol. 2018; 9: 799. DOI: https://doi. org/10.3389/fi
mmu.2018.00799
54. Limonta G., Mancia A., Benkhalqui A., Bertolucci C., Abelli L., Fossi M.C., et al.
Microplastics induce transcriptional changes, immune response and behavioral
alterations in adult zebrafi sh. Sci Rep. 2019; 9: 15775. DOI:
https://doi.org/10.1038/s41598-019-52292-5
55. Merkley S.D., Moss H.C., Goodfellow S.M., Ling C.L., Meyer-Hagen J.L.,
Weaver J., et al. Polystyrene microplastics induce an immunemetabolic active state
in macrophages. Cell Biol Toxicol. 2021; 38 (1): 31–41. DOI:
https://doi.org/10.1007/s10565-021-09616-x
56. Zou W., Xia M., Jiang K., Cao Z., Zhang X., Hu X. Photo-oxidative degradation
mitigated the developmental toxicity of polyamide microplastics to zebrafi sh
larvae by modulating macrophage-triggered proinfl ammatory responses and
apoptosis. Environ Sci Technol. 2020; 54 (21): 13 888–98. DOI:
https://doi.org/10.1021/acs.est.0c05399
57. Yunna C., Mengru H., Lei W., Weidong C. Macrophage M1/M2 polarization. Eur
J Pharmacol. 2020; 877: 173090. DOI: https://doi.
org/10.1016/j.ejphar.2020.173090
58. Zhao L., Shi W., Hu F., Song X., Cheng Z., Zhou J. Prolonged oral ingestion of
microplastics induced infl ammation in the liver tissues of C57BL/6J mice through
polarization of macrophages and increased infi ltration of natural killer cells.
Ecotoxicol Environ Saf. 2021; 227: 112882. DOI:
https://doi.org/10.1016/j.ecoenv.2021. 112882
59. Huangfu N., Zheng W., Xu Z., Wang S., Wang Y., Cheng J., et al. RBM4 regulates
M1 macrophages polarization through targeting STAT1-mediated glycolysis. Int
Immunopharmacol. 2020; 83: 106432.
DOI: https://doi.org/10.1016/j.intimp.2020.106432
60. Hayyan M., Hashim M.A., AlNashef I.M. Superoxide ion: generation and chemical
implications. Chem Rev. 2016; 116: 3029–85. DOI: https://doi.org/
10.1021/acs.chemrev.5b00407
61. Bedard K., Krause K.H. The NOX family of ROS-generating NADPH oxidases:
physiology and pathophysiology. Physiol Rev. 2007; 87: 245–313. DOI:
https://doi.org/10.1152/physrev.00044.2005
62. Gong T., Liu L., Jiang W., Zhou R. DAMP-sensing receptors in sterile infl
ammation and infl ammatory diseases. Nat Rev Immunol. 2020; 20: 95–112. DOI:
https://doi.org/10.1038/s41577-019-0215-7
63. Li S., Shi M., Wang Y., Xiao Y., Cai D., Xiao F. Keap1-Nrf2 pathway up-
regulation via hydrogen sulfi de mitigates polystyrene microplastics induced-
hepatotoxic eff ects. J Hazard Mater. 2021; 402: 123933. DOI:
https://doi.org/10.1016/j.jhazmat.2020.123933
64. Li S., Wang Q., Yu H., Yang L., Sun Y., Xu N., et al. Polystyrene microplastics
induce blood-testis barrier disruption regulated by the MAPKNrf2 signaling
pathway in rats. Environ Sci Pollut Res Int. 2021; 28: 47 921–31. DOI:
https://doi.org/10.1007/s11356-021-13911-9
65. Liu S., Li H., Wang J., Wu B., Guo X. Polystyrene microplastics aggravate infl
ammatory damage in mice with intestinal immune imbalance.
Sci Total Environ. 2022; 833: 155198. DOI: https://doi.org/10.1016/j.
scitotenv.2022.155198
66. Li B., Ding Y., Cheng X., Sheng D., Xu Z., Rong Q., et al. Polyethylene
microplastics aff ect the distribution of gut microbiota and infl ammation
development in mice. Chemosphere. 2020; 244: 125492. DOI: https://
doi.org/10.1016/j.chemosphere.2019.125492
67. Lu L, Wan Z, Luo T., Fu Z., Jin Y. Polystyrene microplastics induce gut microbiota
dysbiosis and hepatic lipid metabolism disorder in mice. Sci Total Environ. 2018;
631–632: 449–58. DOI: https://doi.org/10.1016/ j.scitotenv.2018.03.051
68. Jin Y., Lu L., Tu W., Luo T., Fu Z. Impacts of polystyrene microplastic on the gut
barrier, microbiota and metabolism of mice. Sci Total Environ. 2019; 649: 308–