Abstract
References
- Das AP, Sukla LB, Pradhan N, Nayak S. Manganese biomining: A review. Bioresour Technol 2011; 102: 7381–7.
- O’Neal SL, Zheng W. Manganese Toxicity Upon Overexposure: a Decade in Review Vol. 2, Current environmental health reports. Springer; 2015. p. 315–28.
- Zhaojun W, Lin W, Zhenyong W, Jian W, Ran L. Effects of manganese deficiency on serum hormones and biochemical markers of bone metabolism in chicks. J Bone Miner Metab 2013; 31: 285–92.
- Aguirre JD, Culotta VC. Battles with iron: Manganese in oxidative stress protection. J Biol Chem 2012; 287: 13541–8.
- Balachandran RC, Mukhopadhyay S, McBride D, Veevers J, Harrison FE, Aschner M, et al. Brain manganese and the balance between essential roles and neurotoxicity. J Biol Chem 2020; 295: 6312–29.
- Martinez-Finley EJ, Gavin CE, Aschner M, Gunter TE. Manganese neurotoxicity and the role of reactive oxygen species. Free Radic Biol Med 2013; 62: 65–75.
- Guilarte TR. Manganese neurotoxicity: New perspectives from behavioral, neuroimaging, and neuropathological studies in humans and non-human primates. Front Aging Neurosci 2013; 5: 1–10.
- Yamada M, Ohno S, Okayasu I, et al. Chronic manganese poisoning: A neuropathological study with determination of manganese distribution in the brain. Acta Neuropathol 1986; 70: 273–8.
- Benedetto A, Au C, Avila DS, Milatovic D, Aschner M. Extracellular dopamine potentiates Mn-induced oxidative stress, lifespan reduction, and dopaminergic neurodegeneration in a BLI-3-dependent manner in caenorhabditis elegans. PLoS Genet 2010; 6.
- Dobson AW, Weber S, Dorman DC, Lash LK, Erikson KM, Aschner M. Oxidative stress is induced in the rat brain following repeated inhalation exposure to manganese sulfate. Biol Trace Elem Res 2003; 93: 113–25.
- Mantovani A, Garlanda C, Doni A, Bottazzi B. Pentraxins in innate immunity: From C-reactive protein to the long pentraxin PTX3. J Clin Immunol 2008; 28: 1–13.
- Padeh S, Farzam N, Chayen G, Gerstein M, Berkun Y. Pentraxin 3 is a marker of early joint inflammation in patients with juvenile idiopathic arthritis. Immunol Res 2013; 56: 444–50.
- Uysal S, Yılmaz FM, Karatoprak K, Artüz F, Cumbul NU. The levels of serum pentraxin3, CRP, fetuin-A, and insulin in patients with psoriasis. Eur Rev Med Pharmacol Sci 2014 ;18: 3453-8.
- Karakas MF, Buyukkaya E, Kurt M, et al. Serum pentraxin 3 levels are associated with the complexity and severity of coronary artery disease in patients with stable angina pectoris. J Investig Med 2013; 61: 278–85.
- Lech M, Römmele C, Gröbmayr R, et al. Endogenous and exogenous pentraxin-3 limits postischemic acute and chronic kidney injury. Kidney Int 2013; 83: 647–61.
- Turksoy VA, Tutkun L, Iritas SB, Gunduzoz M, Deniz S. The effects of occupational lead exposure on selected inflammatory biomarkers. Arh Hig Rada Toksikol 2019; 70: 36–41.
- Ovayolu A, Turksoy VA, Gun I, Karaman E, Dogan I, Turgut A. Analyses of maternal plasma cadmium, lead, and vanadium levels in the diagnosis and severity of late-onset preeclampsia: a prospective and comparative study. J Matern Fetal Neonatal Med 2021; 1-8.
- Onat T, Caltekin MD, Turksoy VA, et al. The relationship between heavy metal exposure, trace element level, and monocyte to HDL cholesterol ratio with gestational diabetes mellitus. Biol Trace Elem Res 2021; 199: 1306–15.
- Ovayolu A, Bostancıeri N, Güler S, Doğan İ, Türksoy A, Kolusarı A. Preterm erken membran rüptürü ile komplike olan gebeliklerde seçilen eser elementler ve ağır metallerin maternal serum seviyeleri. Jinekoloji-Obstetrik ve Neonatoloji Tıp Derg 2021; 762–9.
- Turan E, Turksoy VA. Selenium, zinc, and copper status in euthyroid nodular goiter: a cross-sectional study. Int J Prev Med 2021; 12: 46.
- Yüksel B, Kayaalti Z, Söylemezoglu T, Türksoy VA. GFAAS Determination of Arsenic Levels in Biological Samples of Workers Occupationally Exposed to Metals: An Application in Analytical Toxicology. Atomic Spectroscopy 2015; 36: 171-6.
- Yüksel B, Kayaalti Z, Kaya-Akyüzlü D, Tekin D, Söylemezoglu T. Assessment of lead levels in maternal blood samples by graphite furnace atomic absorption spectrometry and influence of maternal blood lead on newborns. At Spectrosc 2016; 37: 114–9.
- O’Neal SL, Lee JW, Zheng W, Cannon JR. Subacute manganese exposure in rats is a neurochemical model of early manganese toxicity. Neurotoxicology 2014; 44: 303–13.
- Vorhees C V., Graham DL, Amos-Kroohs RM, et al. Effects of developmental manganese, stress, and the combination of both on monoamines, growth, and corticosterone. Toxicol Reports 2014; 1: 1046–61.
- Kim J, Pajarillo E, Rizor A, et al. LRRK2 kinase plays a critical role in manganese-induced inflammation and apoptosis in microglia. PLoS One 2019; 14.
- Bellusci M, La Barbera A, Padella F, et al. Biodistribution and acute toxicity of a nanofluid containing manganese iron oxide nanoparticles produced by a mechanochemical process. Int J Nanomedicine 2014 Apr 17; 9: 1919–29.
- Sánchez-González C, López-Chaves C, Gómez-Aracena J, Galindo P, Aranda P, Llopis J. Association of plasma manganese levels with chronic renal failure. J Trace Elem Med Biol 2015; 31: 78–84.
- Rajkovic I, Wong R, Lemarchand E, Tinker R, Allan SM, Pinteaux E. Pentraxin 3 regulates neutrophil infiltration to the brain during neuroinflammation. AMRC Open Res 2019; 1: 10.
The association between PTX3 and serum manganese levels of welders in comparison with controls: An application of anti-inflammatory biomarker
Abstract
Aim: The purpose of this study; it is to compare serum PTX3 levels of manganese-exposed welders with non-exposed people in order to evaluate the nature of manganese-induced inflammatory response.
Material and Method: 51 of whom were exposed to manganese and 52 of whom were volunteers working in the same workplace, were evaluated in the study. PTX-3 levels were analyzed in the serum samples with ELISA. Mn levels were analyzed in whole blood samples in ICP-MS.
Results: The mean values of manganese and Pentraxin-3 of the control group were found to be statistically significantly lower than those of the exposure group, respectively, for Mn levels: 5.04±2.32 µg/L and 11.54±3.09 µg/L; for PTX-3 36.96±24.20 ng/mL and 48.29±27.13 ng/mL; p<0.05).
Conclusion: In this study, the relationship between manganese levels and PTX-3 was shown for the first time in this hypothetical observational study.
Keywords
References
- Das AP, Sukla LB, Pradhan N, Nayak S. Manganese biomining: A review. Bioresour Technol 2011; 102: 7381–7.
- O’Neal SL, Zheng W. Manganese Toxicity Upon Overexposure: a Decade in Review Vol. 2, Current environmental health reports. Springer; 2015. p. 315–28.
- Zhaojun W, Lin W, Zhenyong W, Jian W, Ran L. Effects of manganese deficiency on serum hormones and biochemical markers of bone metabolism in chicks. J Bone Miner Metab 2013; 31: 285–92.
- Aguirre JD, Culotta VC. Battles with iron: Manganese in oxidative stress protection. J Biol Chem 2012; 287: 13541–8.
- Balachandran RC, Mukhopadhyay S, McBride D, Veevers J, Harrison FE, Aschner M, et al. Brain manganese and the balance between essential roles and neurotoxicity. J Biol Chem 2020; 295: 6312–29.
- Martinez-Finley EJ, Gavin CE, Aschner M, Gunter TE. Manganese neurotoxicity and the role of reactive oxygen species. Free Radic Biol Med 2013; 62: 65–75.
- Guilarte TR. Manganese neurotoxicity: New perspectives from behavioral, neuroimaging, and neuropathological studies in humans and non-human primates. Front Aging Neurosci 2013; 5: 1–10.
- Yamada M, Ohno S, Okayasu I, et al. Chronic manganese poisoning: A neuropathological study with determination of manganese distribution in the brain. Acta Neuropathol 1986; 70: 273–8.
- Benedetto A, Au C, Avila DS, Milatovic D, Aschner M. Extracellular dopamine potentiates Mn-induced oxidative stress, lifespan reduction, and dopaminergic neurodegeneration in a BLI-3-dependent manner in caenorhabditis elegans. PLoS Genet 2010; 6.
- Dobson AW, Weber S, Dorman DC, Lash LK, Erikson KM, Aschner M. Oxidative stress is induced in the rat brain following repeated inhalation exposure to manganese sulfate. Biol Trace Elem Res 2003; 93: 113–25.
- Mantovani A, Garlanda C, Doni A, Bottazzi B. Pentraxins in innate immunity: From C-reactive protein to the long pentraxin PTX3. J Clin Immunol 2008; 28: 1–13.
- Padeh S, Farzam N, Chayen G, Gerstein M, Berkun Y. Pentraxin 3 is a marker of early joint inflammation in patients with juvenile idiopathic arthritis. Immunol Res 2013; 56: 444–50.
- Uysal S, Yılmaz FM, Karatoprak K, Artüz F, Cumbul NU. The levels of serum pentraxin3, CRP, fetuin-A, and insulin in patients with psoriasis. Eur Rev Med Pharmacol Sci 2014 ;18: 3453-8.
- Karakas MF, Buyukkaya E, Kurt M, et al. Serum pentraxin 3 levels are associated with the complexity and severity of coronary artery disease in patients with stable angina pectoris. J Investig Med 2013; 61: 278–85.
- Lech M, Römmele C, Gröbmayr R, et al. Endogenous and exogenous pentraxin-3 limits postischemic acute and chronic kidney injury. Kidney Int 2013; 83: 647–61.
- Turksoy VA, Tutkun L, Iritas SB, Gunduzoz M, Deniz S. The effects of occupational lead exposure on selected inflammatory biomarkers. Arh Hig Rada Toksikol 2019; 70: 36–41.
- Ovayolu A, Turksoy VA, Gun I, Karaman E, Dogan I, Turgut A. Analyses of maternal plasma cadmium, lead, and vanadium levels in the diagnosis and severity of late-onset preeclampsia: a prospective and comparative study. J Matern Fetal Neonatal Med 2021; 1-8.
- Onat T, Caltekin MD, Turksoy VA, et al. The relationship between heavy metal exposure, trace element level, and monocyte to HDL cholesterol ratio with gestational diabetes mellitus. Biol Trace Elem Res 2021; 199: 1306–15.
- Ovayolu A, Bostancıeri N, Güler S, Doğan İ, Türksoy A, Kolusarı A. Preterm erken membran rüptürü ile komplike olan gebeliklerde seçilen eser elementler ve ağır metallerin maternal serum seviyeleri. Jinekoloji-Obstetrik ve Neonatoloji Tıp Derg 2021; 762–9.
- Turan E, Turksoy VA. Selenium, zinc, and copper status in euthyroid nodular goiter: a cross-sectional study. Int J Prev Med 2021; 12: 46.
- Yüksel B, Kayaalti Z, Söylemezoglu T, Türksoy VA. GFAAS Determination of Arsenic Levels in Biological Samples of Workers Occupationally Exposed to Metals: An Application in Analytical Toxicology. Atomic Spectroscopy 2015; 36: 171-6.
- Yüksel B, Kayaalti Z, Kaya-Akyüzlü D, Tekin D, Söylemezoglu T. Assessment of lead levels in maternal blood samples by graphite furnace atomic absorption spectrometry and influence of maternal blood lead on newborns. At Spectrosc 2016; 37: 114–9.
- O’Neal SL, Lee JW, Zheng W, Cannon JR. Subacute manganese exposure in rats is a neurochemical model of early manganese toxicity. Neurotoxicology 2014; 44: 303–13.
- Vorhees C V., Graham DL, Amos-Kroohs RM, et al. Effects of developmental manganese, stress, and the combination of both on monoamines, growth, and corticosterone. Toxicol Reports 2014; 1: 1046–61.
- Kim J, Pajarillo E, Rizor A, et al. LRRK2 kinase plays a critical role in manganese-induced inflammation and apoptosis in microglia. PLoS One 2019; 14.
- Bellusci M, La Barbera A, Padella F, et al. Biodistribution and acute toxicity of a nanofluid containing manganese iron oxide nanoparticles produced by a mechanochemical process. Int J Nanomedicine 2014 Apr 17; 9: 1919–29.
- Sánchez-González C, López-Chaves C, Gómez-Aracena J, Galindo P, Aranda P, Llopis J. Association of plasma manganese levels with chronic renal failure. J Trace Elem Med Biol 2015; 31: 78–84.
- Rajkovic I, Wong R, Lemarchand E, Tinker R, Allan SM, Pinteaux E. Pentraxin 3 regulates neutrophil infiltration to the brain during neuroinflammation. AMRC Open Res 2019; 1: 10.
Details
| Primary Language | English |
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| Subjects | Health Care Administration |
| Journal Section | Original Article |
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| Publication Date | July 15, 2021 |
| Published in Issue | Year 2021 Volume: 4 Issue: 4 |
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