Mercury-induced excitotoxicity in presynaptic brain nerve terminals: modulatory effects of carbonaceous airborne particulate simulants.
Carbon dots, Nanodiamonds
Carbonaceous aerosol
Glutamate
Mercury neurotoxicity
Nerve terminals
Journal
Environmental science and pollution research international
ISSN: 1614-7499
Titre abrégé: Environ Sci Pollut Res Int
Pays: Germany
ID NLM: 9441769
Informations de publication
Date de publication:
12 Dec 2023
12 Dec 2023
Historique:
received:
30
06
2023
accepted:
30
11
2023
medline:
12
12
2023
pubmed:
12
12
2023
entrez:
12
12
2023
Statut:
aheadofprint
Résumé
Multipollutant approach is a breakthrough in up-to-date environmental quality and health risk estimation. Both mercury and carbonaceous air particulate are hazardous neurotoxicants. Here, the ability of carbonaceous air particulate simulants, i.e. carbon dots obtained by heating of organics, and nanodiamonds, to influence Hg
Identifiants
pubmed: 38085481
doi: 10.1007/s11356-023-31359-x
pii: 10.1007/s11356-023-31359-x
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : National Research Foundation of Ukraine
ID : 2021.01/0061
Informations de copyright
© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Références
Aschner M (2000) Methylmercury alters glutamate transport in astrocytes. Neurochem Int 37:199–206. https://doi.org/10.1016/S0197-0186(00)00023-1
doi: 10.1016/S0197-0186(00)00023-1
Baby R, Saifullah B, Hussein MZ (2019) Carbon nanomaterials for the treatment of heavy metal-contaminated water and environmental remediation. Nanoscale Res Lett 14:341. https://doi.org/10.1186/S11671-019-3167-8
doi: 10.1186/S11671-019-3167-8
Borisova T (2016) Permanent dynamic transporter-mediated turnover of glutamate across the plasma membrane of presynaptic nerve terminals: arguments in favor and against. Rev Neurosci 27:71–81. https://doi.org/10.1515/revneuro-2015-0023
doi: 10.1515/revneuro-2015-0023
Borisova T (2018) Nervous system injury in response to contact with environmental, engineered and planetary micro- and nano-sized particles. Front Physiol 9:728. https://doi.org/10.3389/fphys.2018.00728
doi: 10.3389/fphys.2018.00728
Borisova T (2019) Express assessment of neurotoxicity of particles of planetary and interstellar dust. npj Microgravity 5:2. https://doi.org/10.1038/s41526-019-0062-7
doi: 10.1038/s41526-019-0062-7
Borisova T, Borysov A (2016) Putative duality of presynaptic events. Rev Neurosci 27:377–383. https://doi.org/10.1515/revneuro-2015-0044
doi: 10.1515/revneuro-2015-0044
Borisova T, Komisarenko S (2021) Air pollution particulate matter as a potential carrier of SARS-CoV-2 to the nervous system and/or neurological symptom enhancer: arguments in favor. Environ Sci Pollut Res Int 28:40371–40377. https://doi.org/10.1007/S11356-020-11183-3
doi: 10.1007/S11356-020-11183-3
Borisova T, Krisanova N, Sivko R et al (2011) Presynaptic malfunction: the neurotoxic effects of cadmium and lead on the proton gradient of synaptic vesicles and glutamate transport. Neurochem Int 59:272–279. https://doi.org/10.1016/j.neuint.2011.05.014
doi: 10.1016/j.neuint.2011.05.014
Borisova T, Nazarova A, Dekaliuk M et al (2015) Neuromodulatory properties of fluorescent carbon dots: effect on exocytotic release, uptake and ambient level of glutamate and GABA in brain nerve terminals. Int J Biochem Cell Biol 59:203–215. https://doi.org/10.1016/j.biocel.2014.11.016
doi: 10.1016/j.biocel.2014.11.016
Borisova T, Borysov A, Pastukhov A, Krisanova N (2016) Dynamic gradient of glutamate across the membrane: glutamate/aspartate-induced changes in the ambient level of L-[(14)C]glutamate and D-[(3)H]aspartate in rat brain nerve terminals. Cell Mol Neurobiol 36:1229–1240. https://doi.org/10.1007/s10571-015-0321-4
doi: 10.1007/s10571-015-0321-4
Borisova T, Dekaliuk M, Pozdnyakova N et al (2017) Harmful impact on presynaptic glutamate and GABA transport by carbon dots synthesized from sulfur-containing carbohydrate precursor. Environ Sci Pollut Res 24:17688–17700. https://doi.org/10.1007/s11356-017-9414-6
doi: 10.1007/s11356-017-9414-6
Borisova T, Kucherenko D, Soldatkin O et al (2018) An amperometric glutamate biosensor for monitoring glutamate release from brain nerve terminals and in blood plasma. Anal Chim Acta 1022:113–123
doi: 10.1016/j.aca.2018.03.015
Borysov A, Tarasenko A, Krisanova N et al (2020) Plastic smoke aerosol: nano-sized particle distribution, absorption/fluorescent properties, dysregulation of oxidative processes and synaptic transmission in rat brain nerve terminals. Environ Pollut 263:114502. https://doi.org/10.1016/j.envpol.2020.114502
doi: 10.1016/j.envpol.2020.114502
Bradham KD, Green W, Hayes H et al (2016) Estimating relative bioavailability of soil lead in the mouse. J Toxicol Environ Heal - Part A Curr Issues 79:1179–1182. https://doi.org/10.1080/15287394.2016.1221789
doi: 10.1080/15287394.2016.1221789
Bridges CC, Zalups RK (2010) Transport of inorganic mercury and methylmercury in target tissues and organs. J Toxicol Environ Heal Part B 13:385–410. https://doi.org/10.1080/10937401003673750
doi: 10.1080/10937401003673750
Buzea C, Pacheco II, Robbie K (2007) Nanomaterials and nanoparticles: sources and toxicity. Biointerphases 2:MR17–MR71. https://doi.org/10.1116/1.2815690
doi: 10.1116/1.2815690
Chizhik AMAI, Stein S, Dekaliuk MO et al (2016) Super-resolution optical fluctuation bio-imaging with dual-color carbon nanodots. Nano Lett 16:237–242. https://doi.org/10.1021/acs.nanolett.5b03609
doi: 10.1021/acs.nanolett.5b03609
Chrysochoou C, Rutishauser C, Rauber-Lüthy C et al (2003) An 11-month-old boy with psychomotor regression and auto-aggressive behaviour. Eur J Pediatr 162:559–561. https://doi.org/10.1007/s00431-003-1239-2
doi: 10.1007/s00431-003-1239-2
Cotman CW (1974) Isolation of synaptosomal and synaptic plasma membrane fractions. Methods Enzymol 31:445–452
doi: 10.1016/0076-6879(74)31050-6
Deuschl G, Beghi E, Fazekas F et al (2020) The burden of neurological diseases in Europe: an analysis for the Global Burden of Disease Study 2017. Lancet Public Heal 5:e551–e567. https://doi.org/10.1016/S2468-2667(20)30190-0
doi: 10.1016/S2468-2667(20)30190-0
Diamond GL, Bradham KD, Brattin WJ et al (2016) Predicting oral relative bioavailability of arsenic in soil from in vitro bioaccessibility. J Toxicol Environ Heal - Part A Curr Issues 79:165–173. https://doi.org/10.1080/15287394.2015.1134038
doi: 10.1080/15287394.2015.1134038
Engin AB, Engin ED, Golokhvast K et al (2017) Glutamate-mediated effects of caffeine and interferon-γ on mercury-induced toxicity. Int J Mol Med 39:1215–1223. https://doi.org/10.3892/ijmm.2017.2937
doi: 10.3892/ijmm.2017.2937
Fine PM, Shen S, Sioutas C (2004) Inferring the sources of fine and ultrafine particulate matter at downwind receptor sites in the Los Angeles Basin using multiple continuous measurements. Special Issue of Aerosol Science and Technology on Findings from the Fine Particulate Matter S. Aerosol Sci Technol 38:182–195. https://doi.org/10.1080/02786820390229499
doi: 10.1080/02786820390229499
Fonfría E, Vilaró MT, Babot Z et al (2005) Mercury compounds disrupt neuronal glutamate transport in cultured mouse cerebellar granule cells. J Neurosci Res 79:545–553. https://doi.org/10.1002/jnr.20375
doi: 10.1002/jnr.20375
Ghosh S, Chizhik AMAI, Karedla N et al (2014) Photoluminescence of carbon nanodots: dipole emission centers and electron–phonon coupling. Nano Lett 14:5656–5661. https://doi.org/10.1021/nl502372x
doi: 10.1021/nl502372x
Györffy BA, Kun J, Török G et al (2018) Local apoptotic-like mechanisms underlie complementmediated synaptic pruning. Proc Natl Acad Sci U S A 115:6303–6308. https://doi.org/10.1073/pnas.1722613115
doi: 10.1073/pnas.1722613115
Hare MF, Atchison WD (1992) Comparative action of methylmercury and divalent inorganic mercury on nerve terminal and intraterminal mitochondrial membrane potentials. J Pharmacol Exp Ther 261:166–172
Holmes P, James KAF, Levy LS (2009) Is low-level environmental mercury exposure of concern to human health? Sci Total Environ 408:171–182
doi: 10.1016/j.scitotenv.2009.09.043
Islam N, Saikia BK (2020) Atmospheric particulate matter and potentially hazardous compounds around residential/road side soil in an urban area. Chemosphere 259:127453. https://doi.org/10.1016/J.CHEMOSPHERE.2020.127453
Islam N, Dihingia A, Manna P et al (2019) Environmental and toxicological assessment of nanodiamond-like materials derived from carbonaceous aerosols. Science of The Total Environment 679:209–220. https://doi.org/10.1016/J.SCITOTENV.2019.04.446
doi: 10.1016/J.SCITOTENV.2019.04.446
Islam N, Dihingia A, Khare P, Saikia BK (2020) Atmospheric particulate matters in an Indian urban area: health implications from potentially hazardous elements, cytotoxicity, and genotoxicity studies. J Hazard Mater 384:121472. https://doi.org/10.1016/J.JHAZMAT.2019.121472
Islam N, Saikia BK (2022) An overview on atmospheric carbonaceous particulate matter into carbon nanomaterials: a new approach for air pollution mitigation. Chemosphere 303:135027. https://doi.org/10.1016/J.CHEMOSPHERE.2022.135027
doi: 10.1016/J.CHEMOSPHERE.2022.135027
Jarrahi A, Ahluwalia M, Khodadadi H et al (2020) Neurological consequences of COVID-19: what have we learned and where do we go from here? J Neuroinflammation 17:286. https://doi.org/10.1186/s12974-020-01957-4
doi: 10.1186/s12974-020-01957-4
Kilkenny C, Browne W, Cuthill IC et al (2010) Animal research: reporting in vivo experiments: the ARRIVE guidelines. Br J Pharmacol 160:1577–1579. https://doi.org/10.1111/j.1476-5381.2010.00872.x
doi: 10.1111/j.1476-5381.2010.00872.x
Krisanova NV, Trikash IO, Borisova TA (2009) Synaptopathy under conditions of altered gravity: changes in synaptic vesicle fusion and glutamate release. Neurochem Int 55:724–731. https://doi.org/10.1016/J.NEUINT.2009.07.003
doi: 10.1016/J.NEUINT.2009.07.003
Krisanova N, Kasatkina L, Sivko R et al (2013) Neurotoxic potential of lunar and martian dust: influence on em, proton gradient, active transport, and binding of glutamate in rat brain nerve terminals. Astrobiology 13:679–692. https://doi.org/10.1089/ast.2012.0950
doi: 10.1089/ast.2012.0950
Landrigan PJ, Fuller R, Acosta NJRR et al (2018) The Lancet Commission on pollution and health. Lancet 391:462–512. https://doi.org/10.1016/S0140-6736(17)32345-0
doi: 10.1016/S0140-6736(17)32345-0
Larson E, Howlett B, Jagendorf A (1986) Artificial reductant enhancement of the Lowry method for protein determination. Anal Biochem 155:243–248. https://doi.org/10.1016/0003-2697(86)90432-X
doi: 10.1016/0003-2697(86)90432-X
Li Y, Zhang ZY, Yang HF et al (2018) Highly selective fluorescent carbon dots probe for mercury(II) based on thymine-mercury(II)-thymine structure. RSC Adv 8:3982–3988. https://doi.org/10.1039/c7ra11487g
doi: 10.1039/c7ra11487g
Long CM, Nascarella MA, Valberg PA (2013) Carbon black vs. black carbon and other airborne materials containing elemental carbon: physical and chemical distinctions. Environ Pollut 181:271–286. https://doi.org/10.1016/j.envpol.2013.06.009
doi: 10.1016/j.envpol.2013.06.009
McGrath J, Drummond G, McLachlan E et al (2010) Guidelines for reporting experiments involving animals: the ARRIVE guidelines. Br J Pharmacol 160:1573–1576. https://doi.org/10.1111/j.1476-5381.2010.00873.x
doi: 10.1111/j.1476-5381.2010.00873.x
Nicholls DG (1993) The glutamatergic nerve terminal. Eur J Biochem 212:613–631. https://doi.org/10.1111/j.1432-1033.1993.tb17700.x
doi: 10.1111/j.1432-1033.1993.tb17700.x
Nixdorff K, Borisova T, Komisarenko S, Dando M (2018) Dual-use nano-neurotechnology. Polit Life Sci 37:180–202. https://doi.org/10.1017/pls.2018.15
doi: 10.1017/pls.2018.15
Oberdörster G, Oberdörster E, Oberdörster J (2005) Nanotoxicology: an emerging discipline evolving from studies of ultrafine particles. Environ Health Perspect 113:823–839. https://doi.org/10.1289/ehp.7339
doi: 10.1289/ehp.7339
Obrist D, Kirk JL, Zhang L et al (2018) A review of global environmental mercury processes in response to human and natural perturbations: changes of emissions, climate, and land use. Ambio 47:116–140. https://doi.org/10.1007/s13280-017-1004-9
doi: 10.1007/s13280-017-1004-9
Orel VE, Shevchenko AD, Bogatyreva GP et al (2012) Magnetic characteristics and anticancer activity of a nanocomplex consisting of detonation nanodiamond and doxorubicin. J Superhard Mater 34:179–185. https://doi.org/10.3103/S1063457612030057
doi: 10.3103/S1063457612030057
Pastukhov A, Paliienko K, Pozdnyakova N et al (2023) Disposable facemask waste combustion emits neuroactive smoke particulate matter. Sci Rep 131(13):1–16. https://doi.org/10.1038/s41598-023-44972-0
doi: 10.1038/s41598-023-44972-0
Petr GT, Sun Y, Frederick NM et al (2015) Conditional deletion of the glutamate transporter GLT-1 reveals that astrocytic GLT-1 protects against fatal epilepsy while neuronal GLT-1 contributes significantly to glutamate uptake into synaptosomes. J Neurosci 35:5187–5201. https://doi.org/10.1523/JNEUROSCI.4255-14.2015
doi: 10.1523/JNEUROSCI.4255-14.2015
Pozdnyakova N, Dudarenko M, Yatsenko L et al (2014) Perinatal hypoxia: different effects of the inhibitors of GABA transporters GAT1 and GAT3 on the initial velocity of [3H]GABA uptake by cortical, hippocampal, and thalamic nerve terminals. Croat Med J 55:250–258. https://doi.org/10.3325/CMJ.2014.55.250
doi: 10.3325/CMJ.2014.55.250
Pozdnyakova N, Pastukhov A, Dudarenko M et al (2016) Neuroactivity of detonation nanodiamonds: dose-dependent changes in transporter-mediated uptake and ambient level of excitatory/inhibitory neurotransmitters in brain nerve terminals. J Nanobiotechnology 14:25. https://doi.org/10.1186/s12951-016-0176-y
doi: 10.1186/s12951-016-0176-y
Pozdnyakova N, Pastukhov A, Dudarenko M et al (2017) Enrichment of inorganic martian dust simulant with carbon component can provoke neurotoxicity. Microgravity Sci Technol. https://doi.org/10.1007/s12217-016-9533-6
doi: 10.1007/s12217-016-9533-6
Rabha S, Saikia BK (2020) An environmental evaluation of carbonaceous aerosols in PM10 at micro- and nano-scale levels reveals the formation of carbon nanodots. Chemosphere 244:125519. https://doi.org/10.1016/J.CHEMOSPHERE.2019.125519
Reichel D, Tripathi M, Perez JM (2019) Biological effects of nanoparticles on macrophage polarization in the tumor microenvironment. Nanotheranostics 3:66–88. https://doi.org/10.7150/ntno.30052
doi: 10.7150/ntno.30052
Saikia J, Narzary B, Roy S et al (2016) Nanominerals, fullerene aggregates, and hazardous elements in coal and coal combustion-generated aerosols: an environmental and toxicological assessment. Chemosphere 164:84–91. https://doi.org/10.1016/J.CHEMOSPHERE.2016.08.086
doi: 10.1016/J.CHEMOSPHERE.2016.08.086
Scheckel KG, Diamond GL, Burgess MF et al (2013) Amending soils with phosphate as means to mitigate soil lead hazard: a critical review of the state of the science. J Toxicol Environ Heal - Part B Crit Rev 16:337–380. https://doi.org/10.1080/10937404.2013.825216
doi: 10.1080/10937404.2013.825216
Shatursky OY, Demchenko AP, Panas I et al (2022) The ability of carbon nanoparticles to increase transmembrane current of cations coincides with impaired synaptic neurotransmission. Biochim Biophys Acta - Biomembr 1864:183817. https://doi.org/10.1016/J.BBAMEM.2021.183817
doi: 10.1016/J.BBAMEM.2021.183817
Shim YK, Lewin MD, Ruiz P et al (2017) Prevalence and associated demographic characteristics of exposure to multiple metals and their species in human populations: the United States NHANES, 2007–2012. J Toxicol Environ Heal - Part A Curr Issues 80:502–512. https://doi.org/10.1080/15287394.2017.1330581
doi: 10.1080/15287394.2017.1330581
Smith-Downey NV, Sunderland EM, Jacob DJ (2010) Anthropogenic impacts on global storage and emissions of mercury from terrestrial soils: Insights from a new global model. J Geophys Res 115:G03008. https://doi.org/10.1029/2009JG001124
doi: 10.1029/2009JG001124
Sudhof TC (2004) The synaptic vesicle cycle. Annu Rev Neurosci 27:509–547. https://doi.org/10.1146/annurev.neuro.26.041002.131412
doi: 10.1146/annurev.neuro.26.041002.131412
Tagne-Fotso R, Leroyer A, Howsam M et al (2016) Current sources of lead exposure and their relative contributions to the blood lead levels in the general adult population of Northern France: The IMEPOGE Study, 2008–2010. J Toxicol Environ Heal - Part A Curr Issues 79:245–265. https://doi.org/10.1080/15287394.2016.1149131
doi: 10.1080/15287394.2016.1149131
Tarasenko A, Pozdnyakova N, Paliienko K et al (2022) A comparative study of wood sawdust and plastic smoke particulate matter with a focus on spectroscopic, fluorescent, oxidative, and neuroactive properties. Environ Sci Pollut Res Int 29:38315–38330. https://doi.org/10.1007/s11356-022-18741-x
doi: 10.1007/s11356-022-18741-x
The Lancet Neurology (2021) Long COVID: understanding the neurological effects. Lancet Neurol 20:247. https://doi.org/10.1016/S1474-4422(21)00059-4
doi: 10.1016/S1474-4422(21)00059-4
Tranvik LJ (2018) New light on black carbon. Nature Geoscience 11:547–548. https://doi.org/10.1038/s41561-018-0181-x
doi: 10.1038/s41561-018-0181-x
Tuch T, Brand P, Wichmann HE, Heyder J (1997) Variation of particle number and mass concentration in various size ranges of ambient aerosols in Eastern Germany. Atmos Environ 31:4193–4197. https://doi.org/10.1016/S1352-2310(97)00260-4
doi: 10.1016/S1352-2310(97)00260-4
WHO (2011) Safety evaluation of certain contaminants in food Prepared by the seventy-second meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA). WHO food additives series 63
WHO (2012) Scientific Opinion on the risk for public health related to the presence of mercury and methylmercury in food. EFSA J 10(12):2985. https://doi.org/10.2903/j.efsa.2012.2985
doi: 10.2903/j.efsa.2012.2985
WHO (2016) Exposure to mercury: a major public health concern. Chem major Public Heal concern Geneva, WHO
WHO (2017) Mercury and health. Newsroom https://www.who.int/news-room/fact-sheets/detail/mercury-and-health
Xu F, Farkas S, Kortbeek S et al (2012) Mercury-induced toxicity of rat cortical neurons is mediated through N-methyl-D-aspartate receptors. Mol Brain 5:30. https://doi.org/10.1186/1756-6606-5-30
doi: 10.1186/1756-6606-5-30