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Deneysel Florozis Oluşturulmuş Ratların Böbrek Dokusunda C ve E Vitaminlerinin İnflamasyon Gen Ekspresyonu Üzerine Etkisi

Yıl 2021, , 199 - 208, 30.08.2021
https://doi.org/10.52976/vansaglik.872528

Öz

Amaç: İnflamasyon, florozis toksikasyon mekanizmalarının aydınlatılmasında önemli bir adımdır. Antioksidan C ve E vitaminlerinin, floroziste tedavi amacıyla uygulanmasının, inflamasyon gen ekspresyonları üzerine olası etkilerinin ortaya konulması amacıyla bu çalışma planlanmıştır.
Materyal ve Metod: Çalışmada 48 adet 200–250 g ağırlığında Wistar-Albino ırkı erkek rat kullanıldı. Kontrol(K), Mısır yağı(M), NaF(N), NaF+vitamin E(NVE), NaF+vitamin C(NVC), NaF+vitamin C+vitamin E(NVCE) olarak her biri 8 rattan oluşan 6 grup kullanıldı. 16 hafta NaF hayvanların içme sularına eklenerek 150 mg/kg olarak verildi. Vitamin E mısır yağında eritilerek verildiği için mısır yağı kontrol grubu oluşturuldu ve ratlara 0,2 ml/gün olarak mısır yağı verildi. Tedavi gruplarına 16 hafta NaF verildikten sonra 4 hafta vitamin C(100 mg/kg), vitamin E(300 mg/kg), vitamin C+vitamin E(100 mg/kg+300 mg/kg) oral olarak uygulandı. Deney sonunda tüm gruplarda rat böbrek dokusundan elde edilen RNA izolasyon ürünlerinde, inflamasyon markırlarından IL1-β, TNF-α genlerinin ekspresyonu real time-qPCR ile belirlendi. İnternal kontrol geni olarak beta-aktin (Actb) kullanıldı.
Bulgular: TNF-α ekspresyon seviyeleri, en yüksek NaF grubunda bulundu. Diğer tüm gruplarda önemli oranda düşüktü. IL-1 β gen ekspresyon düzeylerinin Mısır yağı ve NaF+vitamin C+E gruplarında en düşük bulundu. NaF ve NaF+vitamin C gruplarında en yüksek bulundu.
Sonuç: NaF ile deneysel oluşturulan floroziste artan florürün oluşturduğu olası böbrek hasarında tedavi amaçlı antioksidan vitamin uygulamasının inflamasyonu azalttığı görüldü. Vitamin C, vitamin E, vitamin C+vitamin E’nin inflamasyon markırları üzerinde kayda değer yararlı etkilerinin olduğu tespit edildi. NaF+vitamin C, NaF+vitamin E verilen gruplara kıyasla vitamin C+E kombinasyonunun inflamasyonu düşürmede daha etkili olduğu görüldü.

Destekleyen Kurum

Van Yüzüncü Yıl Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi

Proje Numarası

THD-2020-8852

Teşekkür

Van Yüzüncü Yıl Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimine teşekkürlerimizi sunarız.

Kaynakça

  • Agalakova NI, Nadei OV. Inorganic fluoride and functions of brain. Crit Rev Toxicol. 2020; 50(1): 28-46.
  • Ailani V, Gupta R C, Gupta SK, Gupta K. Oxidative stress in cases of chronic fluoride intoxication. Indian J Clin Biochem. 2009; 24(4): 426-9.
  • Blaylock RL. Fluoride neurotoxicity and excitotoxicity/microglial activation: critical need for more research. Fluoride. 2007; 40(1): 89–92.
  • Bustin, SA. (ed.) A-Z of Quantitative PCR. La Jolla, CA: International University Line; USA; 2004.
  • Chomczynski P, Mackey K. Substitution of chloroform by bromo-chloropropane in the single-step method of RNA isolation. Anal Biochem. 1995; 225(1): 163-4.
  • Efsa (European Food Safety Authority). Dietetic Products, Nutrition, Allergies Panel Scientific opinion on dietary reference values for fluoride. EFSA J. 2013;11:3332. doi:10.2903/j.efsa.2013.3332.
  • Guan ZZ, Xiao KQ, Zeng XY, Long YG, Cheng YH, Jiang SF ve ark. Changed cellular membrane lipid composition and lipid peroxidation of kidney in rats with chronic fluorosis. Arch Toxicol. 2000; 74(10): 602-8.
  • Guney M, Oral B, Take G, Giray SG, Mungan T. Effect of fluoride intoxication on endometrial apoptosis and lipid peroxidation in rats: role of vitamins E and C. Toxicology. 2007; 231(2-3): 215-23.
  • Izquierdo-Vega JA, Sánchez-Gutiérrez M, Del Razo LM. NADPH oxidase participates in the oxidative damage caused by fluoride in rat spermatozoa. Protective role of α-tocopherol. J Appl Toxicol. 2011; 31(6): 579-88.
  • Jetti R, Raghuveer CV, Mallikarjuna RC. Protective effect of ascorbic acid and Ginkgo biloba against learning and memory deficits caused by fluoride. Toxicol Ind Health. 2016; 32(1): 183-7.
  • Kumar N, Sood S, Arora B, Singh M, Beena, Roy PS. To Study the Effect of Vitamin D and E on Sodium-Fluoride-induced Toxicity in Reproductive Functions of Male Rabbits. Toxicol Int. 2012; 19(2): 182-7.
  • Liao Q, Zhang R, Wang X, Nian W, Ke L, Ouyang W ve ark. Effect of fluoride exposure on mRNA expression of Cav1.2 and calcium signal pathway apoptosis regulators in PC12 cells. Environ Toxicol Pharmacol. 2017; 54(1): 74–9.
  • Mcdowell LR, Williams SN, Hidiroglou N, Njerud CA, Hille GM, Ochoaf L ve ark. Vitamin E supplementation for the ruminant. Animal Feed Science Technology. 1996; 60(1): 273-96.
  • Miltonprabu S, Thangapandiyan S. Epigallocatechin gallate potentially attenuates Fluoride induced oxidative stress mediated cardiotoxicity and dyslipidemia in rats. J Trace Elem Med Biol. 2015; 29(1): 321-35.
  • Mittal M, Flora SJ. Vitamin E supplementation protects oxidative stress during arsenic and fluoride antagonism in male mice. Drug Chem Toxicol. 2007; 30(3): 263-81.
  • Peng W, Xu S, Zhang J, Zhang Y. Vitamin C Attenuates Sodium Fluoride-Induced Mitochondrial Oxidative Stress and Apoptosis via Sirt1-Sod2 Pathway in F9 Cells. Biol Trace Elem Res. 2019; 191(1): 189-98.
  • Qin SL, Deng J, Lou DD, Yu WF, Pei J, Guan ZZ. The decreased expression of mitofusin-1 and increased fission-1 together with alterations in mitochondrial morphology in the kidney of rats with chronic fluorosis may involve elevated oxidative stress. J Trace Elem Med Biol. 2015; 29(1): 263-8.
  • Quadri JA, Sarwar S, Pinky, Kar P, Singh S, Mallick SR ve ark. Fluoride induced tissue hypercalcemia, IL-17 mediated inflammation and apoptosis lead to cardiomyopathy: Ultrastructural and biochemical findings. Toxicology. 2018; 406-407(1): 44-57.
  • Raina R, Baba NA, Verma PK, Sultana M, Singh M. Hepatotoxicity Induced by Subchronic Exposure of Fluoride and Chlorpyrifos in Wistar Rats: Mitigating Effect of Ascorbic Acid. Biol Trace Elem Res. 2015; 166(2): 157-62.
  • Santoyo-Sanchez, MP, Del Carmen Silva-Lucero M, Arreola Mendoza L, Barbier OC. Effects of acute sodium fluoride exposure on kidney function, water homeostasis, and renal handling of calcium and inorganic phosphate. Biol Trace Elem Res. 2013; 152(3): 367-72.
  • Shao D, Zhang J, Tang L, Yu Q, Hu X, Ruan Q ve ark. Effects and Molecular Mechanism of L-Type Calcium Channel on Fluoride-Induced Kidney Injury. Biol Trace Elem Res. 2020; 197(1): 213-23.
  • Stawiarska-Pieta B, Paszczela A, Grucka-Mamczar E, Szaflarska-Stojko E, Birkner E. The effect of antioxidative vitamins A and E and coenzyme Q on the morphological picture of the lungs and pancreata of rats intoxicated with sodium fluoride. Food Chem Toxicol. 2009; 47(10): 2544-50.
  • Stawiarska-Pieta B, Bielec B, Birkner K, Birkner E. The influence of vitamin E and methionine on the activity of enzymes and the morphological picture of liver of rats intoxicated with sodium fluoride. Food Chem Toxicol. 2012; 50(3-4): 972-8.
  • Stolecka D, Blaszczyk U, Zalejska-Fiolka J, Romuk E, Owczarek A, Birkner E. The influence of methionine and vitamin E on oxidative stress in rats' liver exposed to sodium fluoride. Med Pr. 2018; 20;69(4): 403-12.
  • Strunecka A, Strunecky O. Chronic Fluoride Exposure and the Risk of Autism Spectrum Disorder. Int J Environ Res Public Health. 2019; 16(18): 3431. doi: 10.3390/ijerph16183431.
  • Tian Y, Xiao Y, Wang B, Sun C, Tang K, Sun F. Vitamin E and lycopene reduce coal burning fluorosis-induced spermatogenic cell apoptosis via oxidative stress-mediated JNK and ERK signaling pathways. Biosci Rep. 2018; 38(4): BSR20171003. doi: 10.1042/BSR20171003.
  • Varol E, Aksoy F, Icli A, Arslan A, Yuksel O, Ersoy IH ve ark. Increased plasma neopterin and hs-CRP levels in patients with endemic fluorosis. Bull Environ Contam Toxicol. 2012; 89(5): 931-6.
  • Verma RJ, Guna Sherlin DM. Sodium fluoride-induced hypoproteinemia and hypoglycemia in parental and F(1)-generation rats and amelioration by vitamins. Food Chem Toxicol. 2002; 40(12): 1781-8.
  • Verma RJ, Sherlin DM. Vitamin C ameliorates fluoride-induced embryotoxicity in pregnant rats. Hum Exp Toxicol. 2001; 20(12): 619-23.
  • Waugh DT, Godfrey M, Limeback H, Potter W. Black tea source, production, and consumption: Assessment of health risks of fluoride intake in New Zealand. J. Environ. Public Health. 2017;2017:5120504. doi: 10.1155/2017/5120504.
  • Xiong X, Liu J, He W, Xia T, He P, Chen X ve ark. Dose-effect relationship between drinking water fluoride levels and damage to liver and kidney functions in children. Environ Res. 2007; 103(1): 112-6.
  • Xue C, Chen X, Yang K. Antagonistic effects of selenium and zinc on fluoride-induced kidney injury. Health Research. 2000; 29(1): 21–3.
  • Yüksek V, Dede S, Taşpınar M, Çetin S. The effects of certain vitamins on apoptosis and dna damage in sodium fluoride (NaF) administered renal and osteoblast cell lines. Fluoride. 2017a; 50(3): 300–13.
  • Yüksek V, Çetin S, Usta A, Kömüroğlu AU, Dede S. Effect of some vitamins on antioxidant/prooxidant parameters in sodium fluoride (NaF)-treated cell line (hFOB 1.19). Turkish J Veter Res. 2017b; 1(1): 1-6.
  • Yüksek V, Çetin S, Usta A. The effect of vitamin E and selenium combination in repairing fluoride-induced DNA damage to NRK-52E cells. Mol Biol Rep. 2020; 47(10): 7761-70.

The Effect of Vitamins C and E on Inflammation Gene Expression in Experimental Fluorosis-Induced Rat Kidney Tissue

Yıl 2021, , 199 - 208, 30.08.2021
https://doi.org/10.52976/vansaglik.872528

Öz

Objectives: Inflammation is an important step in elucidating fluorosis toxicity mechanisms. This study was planned in order to reveal the possible effects of the application of antioxidant vitamins C and E for the treatment of fluorosis on inflammation gene expressions.
Material and Methods: In the study, 48 male Wistar-Albino rats weighing 200-250 g were used. Six groups of 8 rats each were used as control(K), Corn oil(M), NaF(N), NaF+vitamin E(NVE), NaF+vitamin C(NVC), NaF+vitamin C+vitamin E(NVCE). NaF was added to the drinking water of the animals for 16 weeks and given as 150 mg / kg. Since vitamin E was dissolved in corn oil, the corn oil control group was formed and Corn oil was given to rats 0.2 ml/day. After NaF was administration to treatment groups16 weeks, vitamin C (100mg/kg), vitamin E (300mg/kg), vitamin C+vitamin E (100 mg/kg+300mg/kg) were administered orally for 4 weeks. At the end of the experiment, the expression of inflammation markers IL1-β, TNF-α genes in RNA isolation products obtained from rat liver tissue in all groups were determined by real time-qPCR. Beta-actin (Actb) was used as the internal control gene.
Results: TNF-α expression levels were highest in NaF group. It was significantly lower in all other groups. IL-1 β gene expression levels were the lowest in Corn oil and NaF+vitamin C+E groups. It was found the highest in NaF and NaF+vitamin C groups.
Conclusion: In possible kidney damage caused by increased fluoride in the experimentally induced fluorosis with NaF, it was observed that the application of antioxidant vitamins for therapeutic purposes reduced inflammation. It was determined that vitamin C, vitamin E, vitamin C+vitamin E had significant beneficial effects on inflammation markers. It was observed that the combination of vitaminC+E was more effective in reducing inflammation compared to the groups given NaF+vitamin C and NaF+vitamin E.

Proje Numarası

THD-2020-8852

Kaynakça

  • Agalakova NI, Nadei OV. Inorganic fluoride and functions of brain. Crit Rev Toxicol. 2020; 50(1): 28-46.
  • Ailani V, Gupta R C, Gupta SK, Gupta K. Oxidative stress in cases of chronic fluoride intoxication. Indian J Clin Biochem. 2009; 24(4): 426-9.
  • Blaylock RL. Fluoride neurotoxicity and excitotoxicity/microglial activation: critical need for more research. Fluoride. 2007; 40(1): 89–92.
  • Bustin, SA. (ed.) A-Z of Quantitative PCR. La Jolla, CA: International University Line; USA; 2004.
  • Chomczynski P, Mackey K. Substitution of chloroform by bromo-chloropropane in the single-step method of RNA isolation. Anal Biochem. 1995; 225(1): 163-4.
  • Efsa (European Food Safety Authority). Dietetic Products, Nutrition, Allergies Panel Scientific opinion on dietary reference values for fluoride. EFSA J. 2013;11:3332. doi:10.2903/j.efsa.2013.3332.
  • Guan ZZ, Xiao KQ, Zeng XY, Long YG, Cheng YH, Jiang SF ve ark. Changed cellular membrane lipid composition and lipid peroxidation of kidney in rats with chronic fluorosis. Arch Toxicol. 2000; 74(10): 602-8.
  • Guney M, Oral B, Take G, Giray SG, Mungan T. Effect of fluoride intoxication on endometrial apoptosis and lipid peroxidation in rats: role of vitamins E and C. Toxicology. 2007; 231(2-3): 215-23.
  • Izquierdo-Vega JA, Sánchez-Gutiérrez M, Del Razo LM. NADPH oxidase participates in the oxidative damage caused by fluoride in rat spermatozoa. Protective role of α-tocopherol. J Appl Toxicol. 2011; 31(6): 579-88.
  • Jetti R, Raghuveer CV, Mallikarjuna RC. Protective effect of ascorbic acid and Ginkgo biloba against learning and memory deficits caused by fluoride. Toxicol Ind Health. 2016; 32(1): 183-7.
  • Kumar N, Sood S, Arora B, Singh M, Beena, Roy PS. To Study the Effect of Vitamin D and E on Sodium-Fluoride-induced Toxicity in Reproductive Functions of Male Rabbits. Toxicol Int. 2012; 19(2): 182-7.
  • Liao Q, Zhang R, Wang X, Nian W, Ke L, Ouyang W ve ark. Effect of fluoride exposure on mRNA expression of Cav1.2 and calcium signal pathway apoptosis regulators in PC12 cells. Environ Toxicol Pharmacol. 2017; 54(1): 74–9.
  • Mcdowell LR, Williams SN, Hidiroglou N, Njerud CA, Hille GM, Ochoaf L ve ark. Vitamin E supplementation for the ruminant. Animal Feed Science Technology. 1996; 60(1): 273-96.
  • Miltonprabu S, Thangapandiyan S. Epigallocatechin gallate potentially attenuates Fluoride induced oxidative stress mediated cardiotoxicity and dyslipidemia in rats. J Trace Elem Med Biol. 2015; 29(1): 321-35.
  • Mittal M, Flora SJ. Vitamin E supplementation protects oxidative stress during arsenic and fluoride antagonism in male mice. Drug Chem Toxicol. 2007; 30(3): 263-81.
  • Peng W, Xu S, Zhang J, Zhang Y. Vitamin C Attenuates Sodium Fluoride-Induced Mitochondrial Oxidative Stress and Apoptosis via Sirt1-Sod2 Pathway in F9 Cells. Biol Trace Elem Res. 2019; 191(1): 189-98.
  • Qin SL, Deng J, Lou DD, Yu WF, Pei J, Guan ZZ. The decreased expression of mitofusin-1 and increased fission-1 together with alterations in mitochondrial morphology in the kidney of rats with chronic fluorosis may involve elevated oxidative stress. J Trace Elem Med Biol. 2015; 29(1): 263-8.
  • Quadri JA, Sarwar S, Pinky, Kar P, Singh S, Mallick SR ve ark. Fluoride induced tissue hypercalcemia, IL-17 mediated inflammation and apoptosis lead to cardiomyopathy: Ultrastructural and biochemical findings. Toxicology. 2018; 406-407(1): 44-57.
  • Raina R, Baba NA, Verma PK, Sultana M, Singh M. Hepatotoxicity Induced by Subchronic Exposure of Fluoride and Chlorpyrifos in Wistar Rats: Mitigating Effect of Ascorbic Acid. Biol Trace Elem Res. 2015; 166(2): 157-62.
  • Santoyo-Sanchez, MP, Del Carmen Silva-Lucero M, Arreola Mendoza L, Barbier OC. Effects of acute sodium fluoride exposure on kidney function, water homeostasis, and renal handling of calcium and inorganic phosphate. Biol Trace Elem Res. 2013; 152(3): 367-72.
  • Shao D, Zhang J, Tang L, Yu Q, Hu X, Ruan Q ve ark. Effects and Molecular Mechanism of L-Type Calcium Channel on Fluoride-Induced Kidney Injury. Biol Trace Elem Res. 2020; 197(1): 213-23.
  • Stawiarska-Pieta B, Paszczela A, Grucka-Mamczar E, Szaflarska-Stojko E, Birkner E. The effect of antioxidative vitamins A and E and coenzyme Q on the morphological picture of the lungs and pancreata of rats intoxicated with sodium fluoride. Food Chem Toxicol. 2009; 47(10): 2544-50.
  • Stawiarska-Pieta B, Bielec B, Birkner K, Birkner E. The influence of vitamin E and methionine on the activity of enzymes and the morphological picture of liver of rats intoxicated with sodium fluoride. Food Chem Toxicol. 2012; 50(3-4): 972-8.
  • Stolecka D, Blaszczyk U, Zalejska-Fiolka J, Romuk E, Owczarek A, Birkner E. The influence of methionine and vitamin E on oxidative stress in rats' liver exposed to sodium fluoride. Med Pr. 2018; 20;69(4): 403-12.
  • Strunecka A, Strunecky O. Chronic Fluoride Exposure and the Risk of Autism Spectrum Disorder. Int J Environ Res Public Health. 2019; 16(18): 3431. doi: 10.3390/ijerph16183431.
  • Tian Y, Xiao Y, Wang B, Sun C, Tang K, Sun F. Vitamin E and lycopene reduce coal burning fluorosis-induced spermatogenic cell apoptosis via oxidative stress-mediated JNK and ERK signaling pathways. Biosci Rep. 2018; 38(4): BSR20171003. doi: 10.1042/BSR20171003.
  • Varol E, Aksoy F, Icli A, Arslan A, Yuksel O, Ersoy IH ve ark. Increased plasma neopterin and hs-CRP levels in patients with endemic fluorosis. Bull Environ Contam Toxicol. 2012; 89(5): 931-6.
  • Verma RJ, Guna Sherlin DM. Sodium fluoride-induced hypoproteinemia and hypoglycemia in parental and F(1)-generation rats and amelioration by vitamins. Food Chem Toxicol. 2002; 40(12): 1781-8.
  • Verma RJ, Sherlin DM. Vitamin C ameliorates fluoride-induced embryotoxicity in pregnant rats. Hum Exp Toxicol. 2001; 20(12): 619-23.
  • Waugh DT, Godfrey M, Limeback H, Potter W. Black tea source, production, and consumption: Assessment of health risks of fluoride intake in New Zealand. J. Environ. Public Health. 2017;2017:5120504. doi: 10.1155/2017/5120504.
  • Xiong X, Liu J, He W, Xia T, He P, Chen X ve ark. Dose-effect relationship between drinking water fluoride levels and damage to liver and kidney functions in children. Environ Res. 2007; 103(1): 112-6.
  • Xue C, Chen X, Yang K. Antagonistic effects of selenium and zinc on fluoride-induced kidney injury. Health Research. 2000; 29(1): 21–3.
  • Yüksek V, Dede S, Taşpınar M, Çetin S. The effects of certain vitamins on apoptosis and dna damage in sodium fluoride (NaF) administered renal and osteoblast cell lines. Fluoride. 2017a; 50(3): 300–13.
  • Yüksek V, Çetin S, Usta A, Kömüroğlu AU, Dede S. Effect of some vitamins on antioxidant/prooxidant parameters in sodium fluoride (NaF)-treated cell line (hFOB 1.19). Turkish J Veter Res. 2017b; 1(1): 1-6.
  • Yüksek V, Çetin S, Usta A. The effect of vitamin E and selenium combination in repairing fluoride-induced DNA damage to NRK-52E cells. Mol Biol Rep. 2020; 47(10): 7761-70.
Toplam 35 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Veteriner Cerrahi
Bölüm Orijinal Araştırma Makaleleri
Yazarlar

Ayşe Usta 0000-0002-5522-3469

Ahmet Cihat Öner 0000-0001-6614-4347

Veysel Yüksek 0000-0001-7432-4989

Semiha Dede 0000-0001-5744-6327

Sedat Çetin 0000-0002-6102-8571

Proje Numarası THD-2020-8852
Yayımlanma Tarihi 30 Ağustos 2021
Gönderilme Tarihi 3 Şubat 2021
Yayımlandığı Sayı Yıl 2021

Kaynak Göster

APA Usta, A., Öner, A. C., Yüksek, V., Dede, S., vd. (2021). Deneysel Florozis Oluşturulmuş Ratların Böbrek Dokusunda C ve E Vitaminlerinin İnflamasyon Gen Ekspresyonu Üzerine Etkisi. Van Sağlık Bilimleri Dergisi, 14(2), 199-208. https://doi.org/10.52976/vansaglik.872528

ISSN 

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