Research Article
BibTex RIS Cite

PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ

Year 2020, Volume: 30 Issue: 4, 5711 - 578, 15.10.2020
https://doi.org/10.17567/ataunidfd.783461

Abstract

Amaç: Bu çalışmanın amacı prenatal dönemden itibaren değişik konsantrasyonlarda sistemik fluora (F) maruz kalan sıçanlarda; F’nin, böbrek dokuları üzerindeki toksik etkilerinin incelenmesi ve meydana gelen histopatolojik değişikliklerin araştırılmasıdır.
Gereç ve yöntem: Bu çalışmada, daha önceden prenatal dönemden itibaren içme suyu ile 0, 30 ve 100 ppm F dozları verilen ve 1., 3. ile 5. aylarda sakrifiye edilen sıçanlara ait böbrek dokuları kullanılmıştır. Histolojik değerlendirme için hematoksilen ve eozin (H&E), immünohistokimyasal inceleme için ise TUNEL yöntemi ile boyama yapılarak, tubulus ve glomerulus bölgelerinde meydana gelen apoptozis değerlendirilmiştir.
Bulgular: 100 ppm F gruplarında tespit edilen apoptotik hücre sayısı, kontrol grubu ve 30 ppm F grubununa kıyasla anlamlı derecede yüksek bulunmuştur. Ayrıca hem tubulus hem de glomerulus bölgelerinde, tüm sıçanlarda böbrek dokularının 5. ay apoptozis değerlerinin, 1. ve 3. ay değerlerinden anlamlı şekilde olduğu tespit edilmiştir. Böbrek dokularında yapılan histolojik incelemelerde ise içme suyundaki F miktarının artması ile tübüler dilatasyon, glomeruluslarda atrofi ve nekroz alanları, vasküler konjesyon ve hemorajik kanama odakları gözlemlenmiştir.
Sonuç: Yüksek F konsantrasyonunda sıçan böbrek dokularında apoptoziste artış ve belirgin bir yıkım gözlenmiştir.
Anahtar sözcükler: fluor, böbrek, TUNEL, apoptozis

Investigation of apoptosis in renal tissues of rats exposed from prenatal period to systemic fluoride
ABSTRACT
Aim: The aim of this study was to evaluate fluoride (F) induced toxic effects and histopathological changes on renal tissues of rats exposed to different concentrations of fluoride pre and postnatally.
Material and Methods: Kidneys of the rats that had received 0, 30 and 100 ppm F in drinking water starting from the prenatal period and sacrificed at first, third and fifth months were used in this study. Renal tissues were sectioned and stained with hematoxylin and eosin (H&E) for histological analysis and with TUNEL technique for immunohistochemical evaluations of apoptosis in glomerular and tubular sections.
Results: In the 100 ppm F group, the number of glomerular and tubular apoptotic cells were significantly higher than control and 30 ppm F groups. In all groups, higher apoptosis was detected in the 5th month than the 1st and 3rd months in glomerular and tubular sections and the differences were statistically significant. The transverse section of kidney of the 5th month rat group showed tubular dilatations, glomerular atrophies and necrosis areas, vascular congestions and hemorrhagic regions.
Conclusion: High F doses administered in drinking water caused severe apoptosis and a marked destruction in rat kidney tissues.
Key Words: fluoride, kidney, TUNEL, apoptosis

References

  • 1. Whitford GM. The physiological and toxicological characteristics of fluoride. J Dent Res 1990;69:539-44.
  • 2. Fejerskov O, Ekstrand J. Burt BA. Fluoride in Dentistry. 2nd. ed. Munksgraad, Copenhagen;Boisen Print:1996.
  • 3. Fawell J, Bailey K, Chilton J, Dahi E, Fewtrell L, Magara Y. Fluoride in drinking water. London; IWA Publishing: 2006. p.346-352.
  • 4. Agalakova IN, Gusev GP. Molecular Mechanisms of Cytotoxicity and Apoptosis Induced by Inorganic Fluoride. ISRN Cell Biology 2012:1-16.
  • 5. Doull J, Boekelheide K, Farishian BG, Isaacson RL, Klotz JB, Kumar JV. Fluoride in drinking water: A scientific review of EPA’s standards. Washington, DC. Fluoride 2006;80:74–80.
  • 6. WHO (World Health Organization). Guidelines for drinking water quality. 3th ed, Geneva;2008.p.221-459.
  • 7. Whitford GM. Effects of plasma fluoride and dietary calcium concentrations on GI absorption and secretion of fluoride in the rat. Calcif Tissue Int 1994;54: 421–425.
  • 8. Den Besten PK. Dental fluorosis: its use as a biomarker. Adv Dent Res 1994;8(1): 105–110.
  • 9. Michel-Crosato E, Biazevic MG, Crosato E. (2005). Relationship between dental fluorosis and quality of life: a population based study. Braz Oral Res 2005; 19(2): 150-155.
  • 10. Aoba T, Fejerskov O. Dental fluorosis: chemistry and biology. Crit Rev Oral Biol Med 2002;13(2):155-170.
  • 11. Pendrys DG. (2000). Risk of enamel fluorosis in nonfluoridated and optimally fluoridated populations: considerations for the dental professional. J Am Dent Assoc 2000;131(6):746-55.
  • 12. Bartlett JD, Dwyer SE, Beniash E, Skobe Z, Payne-Ferreira TL. (2005) Fluorosis: a new model and new insights. J Dent Res 2005;84(9):832-6.
  • 13. Lantz O, Jouvin MH, DeVernejoul MC, Druet P. Fluoride-Induced Chronic Renal Failure. Am J Kidney Dis 1987;10: 136–139.
  • 14. Villa A, Anabalon M, Zohouri V, Maguire A, Franco AM, Rugg-Gunn A. Relationships between fluoride intake, urinary fluoride excretion and fluoride retention in children and adults: an analysis of available data. Caries Res 2010;44:60–68.
  • 15. Reggabi M. Renal functions in residents of endemic fluorosis in southern Algeria. Fluoride 1984;17:35-41.
  • 16. Wimalawansa, Sunil J. "Molecular and cellular toxicity of fluoride in mystery, tubulointerstitial chronic kidney disease: A systematic review." Reviews in Environmental Science and Bio/Technology 2020;19(1):117-147.
  • 17. Wang, H. W., Zhu, S. Q., Liu, J., Miao, C. Y., Zhang, Y., & Zhou, B. H. (2020). Fluoride-induced renal dysfunction via respiratory chain complex abnormal expression and fusion elevation in mice. Chemosphere 2020;238:124607.
  • 18. Singh PP, Barjatiya MK, Dhing S, Bhatnagar R, Kothari S, Dhar V. Evidence Suggesting that High Intake of Fluoride Provokes Nephrolithiasis in Tribal Populations. Urol Res 2001;29(4):238-244.
  • 19. Ameisen J S. The origin of programmed cell death. Science 1996; 272:1278.
  • 20. Bellamy CO, Malcomson RD, Harrison DJ, Wyllie AH. Cell death in health and disease: the biology and regulation of apoptosis. Cancer Biology 1995; 6:3-16.
  • 21. Cummings MC, Winterford CM, Walker NI. Apoptosis. Am J Surg Pathol 1997;21: 88-101.
  • 22. Güner Ş, Bozkurt S, Haznedaroğlu E, Mentes A. Dental Fluorosis and Catalase Immunoreactivity of the Brain Tissues in Rats Exposed to High Fluoride Pre and Postnatally. Biological Trace Element Research. 2016;174:150-157.
  • 23. Li XL The research progress of oxidative stress on non phrenology damage in fluorosis. Med Inform 2010;23:347–348.
  • 24. Anarudha CD, Kanno S, Hirano S. Fluoride induces apoptosis by caspase-3 activation in human leukemia HL-60 cells. Arch Toxicol 2000;74:226–230.
  • 25. Khadar Basha S. ve K. Jayantha Rao. Sodium Fluoride Induced Histopathological Changes In Liver And Kidney Of Albino Mice. Acta Chim. Pharm. Indica 2014;4(1): 58-62.
  • 26. Shashi A, Singh JP, Thapar SP. Toxic Effects Of Fluoride On Rabbit Kidney. Fluoride 2002;35:138-50.
  • 27. Karaöz E, Gülle, Mumcu EF, Gökçimen A, Öncü M. The Structural Changes In Second Generation At The Rats Kidney And Liver Tissues Which Have Experimentally Acquired Chronic Fluorosis. Turk Klin Med Sci 2003;23:129-134.
  • 28. Kobayashi CAN, Leite AL, Silva TL, Santos LD, Nogueira FCS, Oliveira RC, Palma MS, Domont GB, Buzalaf MAR. Proteomic analysis of kidney in rats chronically exposed to fluoride. Chemico-Biological Interactions 2009 24;180(2):305-311.
  • 29. Quadri JA, Sarwar S, Sinha A, Kalaivani M, Dinda AK, Bagga A, Shariff A. Fluoride-associated ultrastructural changes and apoptosis in human renal tubule:a pilot study. Human & experimental toxicology 2018;37(11): 1199-1206.
  • 30. Murao H, Sakagami N, Iguchi T, Murakami T, Suketa Y. Sodium fluoride increase intracellular calcium in rat renal epithelial cell line NRK-52E. Biol Pharm Bull 2000;23:581–584.
  • 31. Chlubek D, Grucka-Mamczar E, Birkner E, Polaniak R, Stawiarska-Pieta B, H Duliban H. Activity of pancreatic antioxidative enzymes and malondialdehyde concentrations in rats with hyperglycemia caused by fluoride intoxication, J. Trace Elem. Med. Biol 2003;17(1):57-60.
  • 32. Kubota K, Lee DH, Tsuchiya M, Young CS, Everett ET, Martinez-Mier EA, Snead ML, Nguyen L, Urano F, Bartlett JD. Fluoride induces endoplasmic reticulum stress in ameloblasts responsible for dental enamel formation. J Biol Chem 2005;280(3):23194–23202.
  • 33. Li XL. The research progress of oxidative stress on non phrenology damage in fluorosis. Med Inform 2010;23:347–348.
  • 34. Yu RA, Xia T, Wang AG, Chen XG. Effects Of Selenium And Zinc On Renal Oxidative Stress And Apoptosis Induced By Fluoride In Rats. Biomedical And Environmental Sciences 2006;19: 439-444.
  • 35. Zhan X, Wang M, Xu ZR, Hangzhou JL. Toxic Effects Of Fluoride On Kidney Function And Histological Structure In Young Pigs Research Report Fluoride 2000;39(1):22–26
  • 36. Karube H., G. Nishitai, K. Inageda, H. Kurosu, M. Matsuoka. NaF activates MAPKs and induces apoptosis in odontoblast-like cells, J Dent Res. 2009;88 461–465.
  • 37. Flora SJ, Mittal M, Mishra D. Co-exposure to arsenic and fluoride on oxidative stress, glutathione linked enzymes, biogenic amines and DNA damage in mouse brain, J. Neurol. Sci. 2009;285:198–205.
  • 38. Mohammadi S, Movahedin M, Mowla SJ. Up-regulation of CatSper genes family by selenium, Reprod. Biol. Endocrinol. 2009;81:539–544.
  • 39. Song Y, Wang J, Xu H, Du Z, Zhang G, Selim HA, Li G, Wang Q, Gao Z. Fluorosis caused cellular apoptosis and oxidative stress of rat kidneys. Chemical Research in Chinese Universities 2013;29(2): 263-269.
Year 2020, Volume: 30 Issue: 4, 5711 - 578, 15.10.2020
https://doi.org/10.17567/ataunidfd.783461

Abstract

References

  • 1. Whitford GM. The physiological and toxicological characteristics of fluoride. J Dent Res 1990;69:539-44.
  • 2. Fejerskov O, Ekstrand J. Burt BA. Fluoride in Dentistry. 2nd. ed. Munksgraad, Copenhagen;Boisen Print:1996.
  • 3. Fawell J, Bailey K, Chilton J, Dahi E, Fewtrell L, Magara Y. Fluoride in drinking water. London; IWA Publishing: 2006. p.346-352.
  • 4. Agalakova IN, Gusev GP. Molecular Mechanisms of Cytotoxicity and Apoptosis Induced by Inorganic Fluoride. ISRN Cell Biology 2012:1-16.
  • 5. Doull J, Boekelheide K, Farishian BG, Isaacson RL, Klotz JB, Kumar JV. Fluoride in drinking water: A scientific review of EPA’s standards. Washington, DC. Fluoride 2006;80:74–80.
  • 6. WHO (World Health Organization). Guidelines for drinking water quality. 3th ed, Geneva;2008.p.221-459.
  • 7. Whitford GM. Effects of plasma fluoride and dietary calcium concentrations on GI absorption and secretion of fluoride in the rat. Calcif Tissue Int 1994;54: 421–425.
  • 8. Den Besten PK. Dental fluorosis: its use as a biomarker. Adv Dent Res 1994;8(1): 105–110.
  • 9. Michel-Crosato E, Biazevic MG, Crosato E. (2005). Relationship between dental fluorosis and quality of life: a population based study. Braz Oral Res 2005; 19(2): 150-155.
  • 10. Aoba T, Fejerskov O. Dental fluorosis: chemistry and biology. Crit Rev Oral Biol Med 2002;13(2):155-170.
  • 11. Pendrys DG. (2000). Risk of enamel fluorosis in nonfluoridated and optimally fluoridated populations: considerations for the dental professional. J Am Dent Assoc 2000;131(6):746-55.
  • 12. Bartlett JD, Dwyer SE, Beniash E, Skobe Z, Payne-Ferreira TL. (2005) Fluorosis: a new model and new insights. J Dent Res 2005;84(9):832-6.
  • 13. Lantz O, Jouvin MH, DeVernejoul MC, Druet P. Fluoride-Induced Chronic Renal Failure. Am J Kidney Dis 1987;10: 136–139.
  • 14. Villa A, Anabalon M, Zohouri V, Maguire A, Franco AM, Rugg-Gunn A. Relationships between fluoride intake, urinary fluoride excretion and fluoride retention in children and adults: an analysis of available data. Caries Res 2010;44:60–68.
  • 15. Reggabi M. Renal functions in residents of endemic fluorosis in southern Algeria. Fluoride 1984;17:35-41.
  • 16. Wimalawansa, Sunil J. "Molecular and cellular toxicity of fluoride in mystery, tubulointerstitial chronic kidney disease: A systematic review." Reviews in Environmental Science and Bio/Technology 2020;19(1):117-147.
  • 17. Wang, H. W., Zhu, S. Q., Liu, J., Miao, C. Y., Zhang, Y., & Zhou, B. H. (2020). Fluoride-induced renal dysfunction via respiratory chain complex abnormal expression and fusion elevation in mice. Chemosphere 2020;238:124607.
  • 18. Singh PP, Barjatiya MK, Dhing S, Bhatnagar R, Kothari S, Dhar V. Evidence Suggesting that High Intake of Fluoride Provokes Nephrolithiasis in Tribal Populations. Urol Res 2001;29(4):238-244.
  • 19. Ameisen J S. The origin of programmed cell death. Science 1996; 272:1278.
  • 20. Bellamy CO, Malcomson RD, Harrison DJ, Wyllie AH. Cell death in health and disease: the biology and regulation of apoptosis. Cancer Biology 1995; 6:3-16.
  • 21. Cummings MC, Winterford CM, Walker NI. Apoptosis. Am J Surg Pathol 1997;21: 88-101.
  • 22. Güner Ş, Bozkurt S, Haznedaroğlu E, Mentes A. Dental Fluorosis and Catalase Immunoreactivity of the Brain Tissues in Rats Exposed to High Fluoride Pre and Postnatally. Biological Trace Element Research. 2016;174:150-157.
  • 23. Li XL The research progress of oxidative stress on non phrenology damage in fluorosis. Med Inform 2010;23:347–348.
  • 24. Anarudha CD, Kanno S, Hirano S. Fluoride induces apoptosis by caspase-3 activation in human leukemia HL-60 cells. Arch Toxicol 2000;74:226–230.
  • 25. Khadar Basha S. ve K. Jayantha Rao. Sodium Fluoride Induced Histopathological Changes In Liver And Kidney Of Albino Mice. Acta Chim. Pharm. Indica 2014;4(1): 58-62.
  • 26. Shashi A, Singh JP, Thapar SP. Toxic Effects Of Fluoride On Rabbit Kidney. Fluoride 2002;35:138-50.
  • 27. Karaöz E, Gülle, Mumcu EF, Gökçimen A, Öncü M. The Structural Changes In Second Generation At The Rats Kidney And Liver Tissues Which Have Experimentally Acquired Chronic Fluorosis. Turk Klin Med Sci 2003;23:129-134.
  • 28. Kobayashi CAN, Leite AL, Silva TL, Santos LD, Nogueira FCS, Oliveira RC, Palma MS, Domont GB, Buzalaf MAR. Proteomic analysis of kidney in rats chronically exposed to fluoride. Chemico-Biological Interactions 2009 24;180(2):305-311.
  • 29. Quadri JA, Sarwar S, Sinha A, Kalaivani M, Dinda AK, Bagga A, Shariff A. Fluoride-associated ultrastructural changes and apoptosis in human renal tubule:a pilot study. Human & experimental toxicology 2018;37(11): 1199-1206.
  • 30. Murao H, Sakagami N, Iguchi T, Murakami T, Suketa Y. Sodium fluoride increase intracellular calcium in rat renal epithelial cell line NRK-52E. Biol Pharm Bull 2000;23:581–584.
  • 31. Chlubek D, Grucka-Mamczar E, Birkner E, Polaniak R, Stawiarska-Pieta B, H Duliban H. Activity of pancreatic antioxidative enzymes and malondialdehyde concentrations in rats with hyperglycemia caused by fluoride intoxication, J. Trace Elem. Med. Biol 2003;17(1):57-60.
  • 32. Kubota K, Lee DH, Tsuchiya M, Young CS, Everett ET, Martinez-Mier EA, Snead ML, Nguyen L, Urano F, Bartlett JD. Fluoride induces endoplasmic reticulum stress in ameloblasts responsible for dental enamel formation. J Biol Chem 2005;280(3):23194–23202.
  • 33. Li XL. The research progress of oxidative stress on non phrenology damage in fluorosis. Med Inform 2010;23:347–348.
  • 34. Yu RA, Xia T, Wang AG, Chen XG. Effects Of Selenium And Zinc On Renal Oxidative Stress And Apoptosis Induced By Fluoride In Rats. Biomedical And Environmental Sciences 2006;19: 439-444.
  • 35. Zhan X, Wang M, Xu ZR, Hangzhou JL. Toxic Effects Of Fluoride On Kidney Function And Histological Structure In Young Pigs Research Report Fluoride 2000;39(1):22–26
  • 36. Karube H., G. Nishitai, K. Inageda, H. Kurosu, M. Matsuoka. NaF activates MAPKs and induces apoptosis in odontoblast-like cells, J Dent Res. 2009;88 461–465.
  • 37. Flora SJ, Mittal M, Mishra D. Co-exposure to arsenic and fluoride on oxidative stress, glutathione linked enzymes, biogenic amines and DNA damage in mouse brain, J. Neurol. Sci. 2009;285:198–205.
  • 38. Mohammadi S, Movahedin M, Mowla SJ. Up-regulation of CatSper genes family by selenium, Reprod. Biol. Endocrinol. 2009;81:539–544.
  • 39. Song Y, Wang J, Xu H, Du Z, Zhang G, Selim HA, Li G, Wang Q, Gao Z. Fluorosis caused cellular apoptosis and oxidative stress of rat kidneys. Chemical Research in Chinese Universities 2013;29(2): 263-269.
There are 39 citations in total.

Details

Primary Language Turkish
Subjects Dentistry
Journal Section Araştırma Makalesi
Authors

Serhat Karaca This is me 0000-0003-1588-1480

Şirin Güner Onur This is me 0000-0002-6890-3500

İlker Tinay This is me 0000-0001-6768-9373

Süheyla Uyar Bozkurt This is me 0000-0002-5947-947X

Ali – Orcid Number: Menteş This is me 0000-0002-2778-6803

Publication Date October 15, 2020
Published in Issue Year 2020 Volume: 30 Issue: 4

Cite

APA Karaca, S., Güner Onur, Ş., Tinay, İ., Uyar Bozkurt, S., et al. (2020). PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ. Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi, 30(4), 5711-578. https://doi.org/10.17567/ataunidfd.783461
AMA Karaca S, Güner Onur Ş, Tinay İ, Uyar Bozkurt S, Menteş A–ON. PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ. Ata Diş Hek Fak Derg. October 2020;30(4):5711-578. doi:10.17567/ataunidfd.783461
Chicago Karaca, Serhat, Şirin Güner Onur, İlker Tinay, Süheyla Uyar Bozkurt, and Ali – Orcid Number: Menteş. “PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ”. Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi 30, no. 4 (October 2020): 5711-578. https://doi.org/10.17567/ataunidfd.783461.
EndNote Karaca S, Güner Onur Ş, Tinay İ, Uyar Bozkurt S, Menteş A–ON (October 1, 2020) PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ. Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi 30 4 5711–578.
IEEE S. Karaca, Ş. Güner Onur, İ. Tinay, S. Uyar Bozkurt, and A. –. O. N. Menteş, “PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ”, Ata Diş Hek Fak Derg, vol. 30, no. 4, pp. 5711–578, 2020, doi: 10.17567/ataunidfd.783461.
ISNAD Karaca, Serhat et al. “PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ”. Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi 30/4 (October 2020), 5711-578. https://doi.org/10.17567/ataunidfd.783461.
JAMA Karaca S, Güner Onur Ş, Tinay İ, Uyar Bozkurt S, Menteş A–ON. PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ. Ata Diş Hek Fak Derg. 2020;30:5711–578.
MLA Karaca, Serhat et al. “PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ”. Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi, vol. 30, no. 4, 2020, pp. 5711-578, doi:10.17567/ataunidfd.783461.
Vancouver Karaca S, Güner Onur Ş, Tinay İ, Uyar Bozkurt S, Menteş A–ON. PRENATAL DÖNEMDEN İTİBAREN SİSTEMİK FLUOR VERİLEN SIÇANLARIN BÖBREK DOKULARINDA GÖRÜLEN APOPTOZİSİN İNCELENMESİ. Ata Diş Hek Fak Derg. 2020;30(4):5711-578.

Bu eser Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır. Tıklayınız.