Dergiler / Medicine Science / 2018 / Cilt: 7 - Sayı: 4

The effect of manganese exposure on erythropoietic and reproductive system parameters

Sayfa
817–820
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Consequently, although Mn is a trace element, it was concluded that, in high levels,it might reduce the testosterone synthesis with direct toxic effect on the testicle in the long-term exposures leading.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:The aim of this study is determining the effect of manganese (Mn) exposure on erythropoietic and reproductive system.
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Temel Bulgular & Veri:A study group consisting of 51 non-smoking welders older than 18 years old with Mn exposure, who visited Ankara Occupational and Environmental Diseases Hospital, and a control group consisting of 79 healthy office employees without Mn exposure, were chosen as study group.
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Sonuç & Katkı:Consequently, although Mn is a trace element, it was concluded that, in high levels,it might reduce the testosterone synthesis with direct toxic effect on the testicle in the long-term exposures leading.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

The aim of this study is determining the effect of manganese (Mn) exposure on erythropoietic and reproductive system. A study group consisting of 51 non-smoking welders older than 18 years old with Mn exposure, who visited Ankara Occupational and Environmental Diseases Hospital, and a control group consisting of 79 healthy office employees without Mn exposure, were chosen as study group. Blood Mn level, total testosterone (TT), freetestosterone (FT), alanine aminotransferase (ALT), aspartate aminotransferase(AST), thyroid stimulant hormone (TSH), triiodothyronine (T3), thyroxine (T4), uric acid, creatinine, complete blood count (CBC), prolactin, follicle stimulating hormone (FSH), luteinizing hormone (LH) levels were analysed along with the demographic data of the patient. The study and control groups consisting of a total of 130 persons were all male, 39.2% (n=51) of which represented the study group with manganese exposure and 60.8% (n=79) of which represented the healthy control group. A significant difference was identified statistically between Mn (t= 4,501, p= 0,000), FT (t= -6.959, p=0.000), TT (t= -2.835, p=0.005) values of those with and without manganese exposure. AST and ALT levels were not found significant although they were higher in the exposed group. When the values are examined according to uric acid, creatinine, TSH, T3, T4and complete blood count, it was observed that the values of exposure group and control group were almost identical. Although FHS, LH and PRL values were high in the study group, the differences were not found significant. Consequently, although Mn is a trace element, it was concluded that, in high levels,it might reduce the testosterone synthesis with direct toxic effect on the testicle in the long-term exposures leading.

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Bu Makaleye Atıf Yap

İRİTAS, S. B., TUTKUN, L., GÜNDÜZÖZ, M., DENİZ, S., TÜRKSOY, V. A. (2018). The effect of manganese exposure on erythropoietic and reproductive system parameters. Medicine Science, Cilt: 7 - Sayı: 4, 817–820. https://ajindex.com/articles/277635

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Kaynakça (11)

  1. Saric M. Manganese. Handbook on the toxicology of metals, vol. II: Specific metals. New York: Elsevier Science Publishing Co. 1986; p. 354-86. Santamaria AB. Manganese exposure, essentiality & toxicity. Indian J Med Res. 2008;128:484-500. U.S. Centers for Disease Control (ATSDR). “Toxicological Profile for Manganese” Registry. 2012. Available at: https://www.atsdr.cdc.gov/ toxprofiles/tp151.pdf Barceloux. DG. Manganese. J Toxicol Clin Toxicol. 1999;37:293-307. Institute of Medicine (US) Panel on Micronutrients. Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. Washington (DC): National Academies Press (US); 2001.
  2. Davis, CD, Greger, JL. Longitudinal changes of manganese-dependent superoxide dismutase and other indexes of manganese and iron status in women. Am J Clin Nutr. 1992;55,747-52.
  3. Rabin O, Hegedus L, Bourre JM, et al. Rapid brain uptake of manganese (II) across the blood–brain barrier. J Neurochem. 1993;61:509-17.
  4. Santamaria AB, Sulsky SI. Risk Assessment of an essential element: manganese. J Toxicol Environ Health A. 2010;73:128-55.
  5. Adedara IA, Subair TI, Ego VC, et al. Chemoprotective role of quercetin in manganese-induced toxicity along the brain-pituitary-testicular axis in rats. Chem-Biol Interact. 2017;263:88-98.
  6. Alessio L, Apostoli P, Ferioli A. et al. Interference of manganese on neuroendocrinal system in exposed workers. Preliminary report. Biol Trace Elem Res. 1989;21:249-53.
  7. Huang YL, Tseng WC Lin TH. In vitro effects of metal ions (Fe2+, Mn2+, Pb2+) on sperm motility and lipid peroxidation in human semen. J. Toxicol. Environ. Health A. 2001;62:259-67.
  8. Bowler RM, Roels HA, Nakagawa S, et al. Dose-effect relations between manganese exposure and neurological, neuropsychological and pulmonary function in confined space bridge welders. Occup Environ Med. 2007;64:16777. Wirth JJ, Rossano MG, Daly DC, et al. Ambient Manganese Exposure is Negatively Associated with Human Sperm Motility and Concentration. Epidemiology. 2007;18:270-3.
  9. Kim EA, Cheong HK, Joo KD, et al. Effect of manganese exposure on the neuroendocrine system in welders. Neurotoxicology. 2007;28:263-9.
  10. Crossgrove J, Zheng W. Manganese toxicity upon overexposure. NMR Biomed. 2004;17:544–53.
  11. Jain M, Kalsi AK, Srivastava A, Gupta YK, et al. High serum estradiol and Heavy Metals Responsible for Human Spermiation Defect-A Pilot Study. J Clin Diagn Res. 2016;10:09-13. Pahune PP,