Synthetic and Natural Vitamin C Modulation of Leaded Paint-Induced Nephrotoxicity of Automobile Painters in Ile-Ife, Nigeria.


Authors : Adesiyan OF; Kumuyi SA; Iyanda AA; Adesiyan AA; Akiibinu MO

Volume/Issue : Volume 9 - 2024, Issue 6 - June


Google Scholar : https://tinyurl.com/4snv5xwj

Scribd : https://tinyurl.com/33b8fknc

DOI : https://doi.org/10.38124/ijisrt/IJISRT24JUN1235

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Abstract : Introduction: Lead (Pb) occupational exposure in painters has been documented to be contacted via additives in paints due to its many important properties and vitamin C has been the most widely studied when it comes to Pb- induced oxidative stress.  Aim: This study aimed at the use of freshly squeezed orange-juice due to its accessibility in investigating the modulating role of synthetic and natural vitamin-C on leaded paint-induced nephrotoxicity of automobile painters.  Study Design and Methods: Sixty (60) male automobile painters were consecutively selected and divided equally into 2 groups. Vitamin-C and orange juice were administered daily to painters for 4 weeks at dosage levels of 200 and 184 mg/day respectively. Thirty (30) male non-painters constituted the control group. Orange juice vitamin-C content was assessed by titrimetric method and synthetic vitamin-C served as the standard drug. Renal biomarkers and reduced glutathione (GSH) were done by Colorimetry. Urine aminolevulinic acid (ALA) and Pb were assessed by ELISA technique and atomic absorption spectrophotometry respectively. Phytochemical screenings (quantitative/qualitative) and proximate analysis were done using standard methods. Data were analyzed using Pearson’s correlation coefficient and One-way Analysis of Variance (ANOVA) followed by Tukey’s post-hoc test for pairwise comparison. Statistical significance was p< 0.05.  Results: Baseline results at 0-week of orange juice administered group showed a significantly (P<0.05) higher serum Pb, urea and creatinine compared to non- painters. Also, their urine baseline results at 0-week showed a significantly (P<0.05) higher levels of ALA and GSH compared to non-painters. Orange juice administration at 4 weeks showed significant (P<0.05) reductions in concentrations of lead, urea, and creatinine in serum, decreased concentrations of GSH and ALA in urine but increased urine Pb compared to baseline. However, compared with baseline, after 4 weeks of vitamin-C supplementation, serum Pb, urine GSH, and urine ALA were significantly (P<0.05) reduced and urine Pb significantly (P<0.05) increased. A positive correlation was observed at 2-weeks of taking orange- juice between serum lead and urine ALA (r= 0.703) and GSH (r= 0.913) but 4-week positive correlation between urea and urine GSH (r= 1.000). A negative correlation was observed at 2-week of taking vitamin-C between serum creatinine and urine lead (r= -0.857) while 4-week a negative correlation was observed between urine GSH and urine lead (r= -0.743). Presence of tannin, phenol, saponin, alkaloid, and flavonoid was detected in orange juice.  Conclusion: Orange juice administration conferred significant amelioration to renal and lead toxicity biomarkers by 4 weeks. The presence of phytochemicals suggests why orange juice may be a viable alternative in amelioration of toxic effects of leaded paint among automobile painters.

Keywords : Orange Juice, Vitamin-C, Renal Markers, Lead Toxicity Biomarkers, Automobile Painters, Paints.

References :

  1. O’Connor, K, Neff, DM, Pitman, S.  Burnout in mental health professionals: A systematic review and meta-analysis of prevalence and determinants. Fur Psych.. 2018; 53: 74-99. PMID:29957371. doi:10.1016/j.eurpsy.2018.06.003.
  2. Olaifa, FE, Ayodele, IA.  Presence of hydrocarbon and heavy metals in some fish species in the Cross River, Nigeria.  Afr. J. Livest. Ext. 2004; 3: 90-95.
  3. Tong R, et al. .Source analysis and health risk-assessment of ambient volatile organic compounds in automobile manufacturing processes. Hum. Ecol. Risk Assess. 2018; 26(2):359–383.
  4. Gliozzo E, and Ionescu, C. Pigments-lead-based whites, reds, yellows and oranges and their alteration phases. J. Anthropol. Archaeol.2022; 14(1):1-66.
  5. Bhasin, T, Lamture, Y, Kumar, M, Dhamecha, R. . Unveiling the Health Ramifications of Lead Poisoning: A Narrative Review. Cureus. 2023; 15(10).Bierwagen G.P. (2016). Surface Coating. Encyclopedia Britannica; Chicago, IL, USA: 2016.
  6. Niemeier, RT, Maier, A, Reichard,  JF.  Rapid Review of Dermal Penetration and Absorption of Inorganic Lead Compounds for Occupational Risk Assessment. Ann. Work Expo. Health. 2022; 66(3):291-311.doi: 10.1093/annweh/wxab097. PMID: 35051994; PMCID: PMC8930439.
  7. Obeng-Gyasi, E.  Lead Exposure and Oxidative Stress-A Life Course Approach in U.S. Adults. Toxics. 2018;6:42. ttps://doi.org/10.3390/toxics6030042
  8. Hugo, MO, Gracilene, PD, Arielle, MS, Priscila, T L, Rosa, AZC, Vanessa, MA.  Occupational risk assessment of paint industry workers. Indian J. Occup. Environ. Med. 2011;15(2):52–58.
  9. Disalvo,  L.  Cassain,  V,  Fasano,  MV,  Zar,  G,  et  al.   Environmental  exposure  to  lead  and  oxidative  stress biomarkers among healthy children in La Plata, Argentina. Archivos Argentinos Pediatria, 2022; 120(3):174-179.
  10. IARC. Some organic solvents, resin monomers and related compounds, pigments and occupational exposures in paint manufacture and painting. IARC Monogr Eval Carcinog Risks Hum. 1989; 47:1-442.
  11. IARC.  Painting, firefighting, and shiftwork. IARC Monogr Eval Carcinog Risks Hum. 2010; 98:1-804.
  12. Shraideh, ZA, Badran, DA , Hunaiti, AA, Battah,  A.  Delta-Aminolevulinic Acid Dehydratase Inhibition and RBC Abnormalities in Relation to Blood Lead among Selected Jordanian Workers. Jordan J. Biol. Sci. 2019; 12(2): 237 – 241.
  13. Gęgotek, A, Skrzydlewska, E.  Ascorbic acid as antioxidant. Vitamins and Hormones. 2023; 121:247-270. doi: 10.1016/bs.vh.2022.10.008. Epub 2022 Nov 29. PMID: 36707136.
  14. Vera JC, Rivas, CI, Fischbarg, J,  Golde, DW. Mammalian facilitative hexose transporters mediate the transport of dehydroascorbic acid. Nat.1993;364:79-82.
  15. Macan, M, Andrijana, Gazivoda Kraljević, T, Raić-Malić, S. Therapeutic Perspective of Vitamin C and Its Derivatives. J. Antioxid. Act.2019; 8(8):247. https;//doi.org/10.3390/antiox8080247
  16. Linowiecka, K, Foksinski, M, Brożyna, AA.  Vitamin C Transporters and Their Implications in Carcinogenesis. J. Nutr. 2020; 12(12):3869. doi: 10.3390/nu12123869. PMID: 33352824; PMCID: PMC7765979.
  17. Chang, BJ, Jang, BJ, Son, TG, Cho, IH, Quan, FS, Choe, NH, Nahm, SS, Lee, JH.  Ascorbic acid ameliorates oxidative damage induced by maternal low level lead exposure in the hippocampus of rat pups during gestation and lactation. Food Chem. Toxicol. 2012; 52:104-108.
  18. Elgailani, IEH, Gad-Elkareem, MAM, Noh, EAA, Adam, OEA,  Alghamdi, AMA.  Comparism of Two Methods for The Determination of Vitamin C (Ascorbic acid) on Some Fruits. Am. J. Chem. 2017; 2(1):1-7
  19. Kaneko, JJ.  Clinical Biochemistry of Animal. 4th Edition. Academic Press Inc. Page 932;1999
  20. 20.Jaffe, M.  ‘Uber den Niedefschlag, weichenPikrinsare in normalemHarnerzeugtunderubereineneue Reaction des Kreatinins’, Zeitschrift fur physiologischeChemie.1886; 10(5):391-400.
  21. Kaplan, A.  The determination of urea, ammonia, and urease. Methods of Biochemical Analysis.1969; 17:311-324.
  22. Tomokuni K, Ichiba, M.  A simple method for colorimetric determination of urinary delta-aminolevulinic acid in workers exposed to lead. Sangyo Igaku. 1988; 30(1):52-53.
  23. Eyer, P, Podhradský, D.  Evaluation of the micromethod for determination of glutathione using enzymatic cycling and Ellman's reagent. Anal. Biochem. 1986; 153(1), 57-66.
  24. Oladimeji, AV, Valan, MF.  HPLC techniques for phytochemistry. Int. J. Chem. Sci. 2020; 8(6): 2590-2596.
  25. Banso, A, Adeyemo, S.  Phytochemical screening and antimalarial assessment of Abutilon mauritianum, Bacopa monnifera and Datura stramonium. Biokemistri. 2006; 18: 39–44.
  26. Stankovic, MS.  Total phenolic content, flavonoid concentration and antioxidant activity of Marrubium peregrinum L. extracts. Kragujevac  J.  Sci. 2011; 33; 63–72.
  27. Joshi, A, Bhobe, M, and Saatarkar, A. (2013).Phytochemical investigation of the roots of Grewia microcos. JOCPR; 5: 80–87.
  28. AOAC.   Official Methods of Analysis of AOAC International. Eighteenth ed. AOAC International; Gaithersburg, MD., USA; 2005
  29. Tiencheu, B, Nji, DN, Achidi, AU, Egbe, AC, Tenyang, N, Ngongang, EFT, Djikeng, FT, Fossi, BT.  Nutritional, sensory, physico-chemical, phytochemical, microbiological and shelf-life studies of natural fruit juice formulated from orange (Citrus sinensis), lemon (Citrus limon), Honey and Ginger (Zingiber officinale). Heliyon. 2021; 7(6): e07177. doi:10.1016/j.heliyon.2021.e07177.
  30. Khoshakhlagh, AH, Yazdanirad, S, Saberi, HR, and Liao, P-C.  Health risk assessment of exposure to various vapors and fumes in a factory of automobile manufacturing. Heliyon; 2023:9(8): e18583.
  31. Velaga, MK, Daughtry, LK, Jones, AC, Yallapragada, PR, Rajanna, S, Rajanna, B.  Attenuation of lead-induced oxidative stress in rat brain, liver, kidney and blood of male Wistar rats by Moringa oleifera seed powder. J. Environ. Pathol. Toxicol. Oncol. 2014; 33(4):323–337.
  32. La-Llave-Leon, O, Mendez-Hernandez, EM, Castellanos-Juarez, FX, Esquivel-Rodriguez, E, Vazquez-Alaniz, F, Sandoval-Carrillo, A, Garcia-Vargas, G, Duarte-Sustaita, J, Candelas-Rangel, JL,  Salas-Pacheco, JM.  Association between Blood Lead Levels and Delta-Aminolevulinic Acid Dehydratase in Pregnant Women. Int. J. Environ. Res. Public Health. 2017; 14(4):432. doi:10.3390/ijerph14040432.
  33. Sachdeva, C, Thakur, K, Sharma, A, Sharma, KK.  Lead: Tiny but Mighty Poison. Indian J. Clin. Biochem. 2018; 33(2):132-146. doi: 10.1007/s12291-017-0680-3. Epub 2017 Jul 18. PMID: 29651203; PMCID: PMC5891462.
  34. Flora, G, Gupta, D, Tiwari, A.  Toxicity of lead. A review with recent updates. Interdiscip. Toxicol. 2012; 5(2): 47-58. doi: 10.2478/v10102-0009-2.
  35. Awodele, O, Popoola, TD, Ogbudu, BS, Akinyede, A, Coker, HAB,  Akintonwa, A.  Occupational hazards and safety measures among the paint factory workers in Lagos, Nigeria. Saf. Health Work. 2014; 5(2):106-111. doi:10.1016/j.shaw.2014.02.001.
  36. Weiner, ID, Mitch, WE, Sands,  JM.  Urea and ammonia metabolism and the control of renal nitrogen excretion. CJASN.  2015; 10(8):1444-1458
  37. Ahmad, F, Liu, P.  (Ascorb)ing Pb Neurotoxicity in the Developing Brain.  J. Antioxid. Act. (Basel). 2020; 9(12):1311. Doi:0.3390/antiox9121311. PMID: 33371438; PMCID: PMC7767447.
  38. Perez, RR, Sousa, CA, Vankeersbilck, T, Machado, MD, Soares, EV.  Evaluation of the role of glutathione in the lead-induced toxicity in Saccharomyces cerevisiae. Curr. Microbiol. 2013; 67(3): 300-5. doi: 10.1007/s00284-013-0364-z
  39. Ani, PN.  Abel, HC. (2018). Nutrient, phytochemical, and anti-nutrient composition of Citrus maxima fruit juice and peel extract. Food Sci. Nutr. 2018 Open Access. Citation  https://doi.org/10.1002/.fns3.604.
  40. Escobedo-Avellaneda, Z, Gutiérrez-Uribe, J, Valdez-Fragoso,  A, Torres, J A,  Welti-Chanes, J.  Phytochemicals and antioxidant activity of juice, flavedo, albedo and comminuted orange. J. Funct. Foods. 2014; 6: 470-481. doi:10.1016/j.jff.2013.11.013
  41. Chanson-Rolle, A, Braesco, V, Chupin, J.  Bouillot, L.  Nutritional Composition of Orange Juice: A Comparative Study between French Commercial and Home-Made Juices. Food Nutr. Sci. 2016; 7: 252-261. doi: 10.4236/fns.2016.74027.
  42. Obasi, B C, Whong, C M Z, Ameh, JB.  Nutritional and sensory qualities of commercially and laboratory prepared orange juice. Afr. J. Food Sci. 2017; 11(7): 189-199.
  43. Bala, M, Bashar, JB.  Proximate and mineral elements composition of five locally consumed fruits in Kano State, Nigeria. Food Sci. and Nutr. 2018; 6(3):653-658.
  44. Nowak, D, Gośliński, M, Wojtowicz, E, Przygoński,  K.  Antioxidant Properties and Phenolic Compounds of Vitamin C-Rich Juices. Journal of Food Sciences. 2018; 83(8):2237-2246. doi: 10.1111/1750-3841.14284. Epub 2018 Jul 25. PMID: 30044505.
  45. Wan, H, Wu, J, Sun, P, Yang, Y.  Investigation of delta-aminolevulinic acid dehydratase polymorphism affecting hematopoietic, hepatic and renal toxicity from lead in Han subjects of southwestern China. Akadémiai Kiadó, BudapestActa Physiologica Hungarica 2014; 101(1):59–66. doi: 10.1556/APhysiol.101.2014.1.7
  46. Tariq, SA.  Role of ascorbic acid in scavenging free radicals and lead toxicity from biosystem. Mol. Biotechnol. 2007; 37: 62-65.
  47. Tandon, SK, Chatterjee, M, Bhargava, A, Shukla, V,  Bihari, V.   Lead poisoning in Indian silver refiners. Sci. Total Environ. 2001; 281(1-3): 177-182.
  48. Dosedel, M, Jirkovsky,  E, Macakova, K, Krcmova, LK, Javorska, L, Pourova, J, Pourova, J, Mercolini, L, Remiao, F, Novakova, L.  Mladenka, P.  Vitamin C- Sources, Physiological Role, Kinetics, Deficiency, Use, Toxicity, and Determination. Nutr. 2021; 13(2):615. doi: 10.3390/nu 13020615.
  49. Berkheiser, K.  Ten natural ways to increase your glutathione levels. 2008; https://www.healthline.com.
  50. Ghanwat, G, Patil, J, Kshirsagar, M, Sontakke, A,  Ayachit, RK.  Effect of Vitamin C Supplementation on Blood Lead Level, oxidative Stress and Antioxidant Status of Battery Manufacturing Workers of Western Maharashtra, India. J. Clin. Diagn. Res. 2016; 10(4): BC08-BC11. doi: 10.7860/JCDR/2016/15968.7528.
  51. Sakai, T.  Biomarkers of lead exposure. J. Ind. Health. 2000; 38: 127–142. doi: 10.2486/indhealth.38.127.
  52. Ahamed, M, Fareed, M, Kumar, A, Siddiqui, W,  Siddiqui, M.  Oxidative stress and neurological disorders in relation to blood lead levels in children. J. Redox Rep. 2008; 13: 117–122. doi: 10.1179/135100008X259213.
  53. Ahamed, M, Akhtar, MJ, Verma, S, Kumar, A, Siddiqui,  MK.  Environmental lead exposure as a risk for childhood aplastic anemia. J. Biosci. Trends. 2011; 5: 38–43. doi: 10.5582/bst.2011.v5.1.38.
  54. Chiba, M, Shinohara, A, Matsushita, K, Watanabe, H, Inaba, Y.  Indices of lead exposure in blood and urine of lead exposed workers and concentrations of major and trace elements and activities of superoxide dismutase, glutathione peroxidase and catalase in their blood. Tohoku J. Exp. Med. 1996; 178: 49-62.

Introduction: Lead (Pb) occupational exposure in painters has been documented to be contacted via additives in paints due to its many important properties and vitamin C has been the most widely studied when it comes to Pb- induced oxidative stress.  Aim: This study aimed at the use of freshly squeezed orange-juice due to its accessibility in investigating the modulating role of synthetic and natural vitamin-C on leaded paint-induced nephrotoxicity of automobile painters.  Study Design and Methods: Sixty (60) male automobile painters were consecutively selected and divided equally into 2 groups. Vitamin-C and orange juice were administered daily to painters for 4 weeks at dosage levels of 200 and 184 mg/day respectively. Thirty (30) male non-painters constituted the control group. Orange juice vitamin-C content was assessed by titrimetric method and synthetic vitamin-C served as the standard drug. Renal biomarkers and reduced glutathione (GSH) were done by Colorimetry. Urine aminolevulinic acid (ALA) and Pb were assessed by ELISA technique and atomic absorption spectrophotometry respectively. Phytochemical screenings (quantitative/qualitative) and proximate analysis were done using standard methods. Data were analyzed using Pearson’s correlation coefficient and One-way Analysis of Variance (ANOVA) followed by Tukey’s post-hoc test for pairwise comparison. Statistical significance was p< 0.05.  Results: Baseline results at 0-week of orange juice administered group showed a significantly (P<0.05) higher serum Pb, urea and creatinine compared to non- painters. Also, their urine baseline results at 0-week showed a significantly (P<0.05) higher levels of ALA and GSH compared to non-painters. Orange juice administration at 4 weeks showed significant (P<0.05) reductions in concentrations of lead, urea, and creatinine in serum, decreased concentrations of GSH and ALA in urine but increased urine Pb compared to baseline. However, compared with baseline, after 4 weeks of vitamin-C supplementation, serum Pb, urine GSH, and urine ALA were significantly (P<0.05) reduced and urine Pb significantly (P<0.05) increased. A positive correlation was observed at 2-weeks of taking orange- juice between serum lead and urine ALA (r= 0.703) and GSH (r= 0.913) but 4-week positive correlation between urea and urine GSH (r= 1.000). A negative correlation was observed at 2-week of taking vitamin-C between serum creatinine and urine lead (r= -0.857) while 4-week a negative correlation was observed between urine GSH and urine lead (r= -0.743). Presence of tannin, phenol, saponin, alkaloid, and flavonoid was detected in orange juice.  Conclusion: Orange juice administration conferred significant amelioration to renal and lead toxicity biomarkers by 4 weeks. The presence of phytochemicals suggests why orange juice may be a viable alternative in amelioration of toxic effects of leaded paint among automobile painters.

Keywords : Orange Juice, Vitamin-C, Renal Markers, Lead Toxicity Biomarkers, Automobile Painters, Paints.

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