open access

Vol 80, No 4 (2021)
Original article
Submitted: 2020-10-08
Accepted: 2020-10-19
Published online: 2020-10-30
Get Citation

Protective effect of resveratrol on acrylamide-induced renal impairment

M. M. Nasralla, S. M. Zaki12, R. A. Attia1
·
Pubmed: 33169356
·
Folia Morphol 2021;80(4):985-993.
Affiliations
  1. Faculty of Medicine, Cairo University, Cairo, Egypt
  2. Fakeeh College for Medical Sciences, Jeddah, Saudi Arabia

open access

Vol 80, No 4 (2021)
ORIGINAL ARTICLES
Submitted: 2020-10-08
Accepted: 2020-10-19
Published online: 2020-10-30

Abstract

Background: Acrylamide (ACR) has a wide range of uses. It possesses a renal impairment effect. The work aimed to study the possible protecting role of resveratrol (RVS) over the ACR-mediated renal impairment in rats. The suggested underlying mechanisms participating in such protection were investigated.
Materials and methods: Thirty Sprague-Dawley adult albino rats were divided into three groups: control, ACR, and RVS. After 4 weeks, the kidney was removed and prepared for histological, immunohistochemical, and biochemical studies. The activity of tissue oxidative (malondialdehyde [MDA]) and anti-oxidative (glutathione [GSH]) markers were assessed.
Results: Acrylamide induced glomerular renal affection in the form of shrinkage and distortion of the glomeruli with wrinkling of their basement membranes and widening of the urinary spaces. Degenerative tubular changes were markedly present in the proximal convoluted tubules. The necrotic tubular cells exhibited cytoplasmic vacuolation with desquamated epithelial cells within the tubular lumen. ACR increases the deposition of collagen fibres in the basement membrane of the glomerular capillaries and induced thickening of the basement membranes of the renal corpuscles and renal tubules. The administration of RVS affords high protection to the kidney. The glomeruli and renal tubules were nearly normal. The content of collagen fibres and the periodic acid Schiff reaction of the basement membrane of the renal tubules were 70% and 19% lower linked to the ACR group. The creatinine and urea levels decreased by 51% and 47%. RVS induced such a protective role through its antioxidant effect as the MDA level decreased by 45%, while the GSH level increased by 83% compared with the ACR group.
Conclusions: Acrylamide causes structural and functional disorders of the kidney. It induces kidney damage through oxidative stress and apoptosis. With the use of RVS, normal kidney architecture was preserved with little structural changes. Adding, functional kidney test became normal. RVS exerts its protective effect through its anti-apoptotic and antioxidant features.

Abstract

Background: Acrylamide (ACR) has a wide range of uses. It possesses a renal impairment effect. The work aimed to study the possible protecting role of resveratrol (RVS) over the ACR-mediated renal impairment in rats. The suggested underlying mechanisms participating in such protection were investigated.
Materials and methods: Thirty Sprague-Dawley adult albino rats were divided into three groups: control, ACR, and RVS. After 4 weeks, the kidney was removed and prepared for histological, immunohistochemical, and biochemical studies. The activity of tissue oxidative (malondialdehyde [MDA]) and anti-oxidative (glutathione [GSH]) markers were assessed.
Results: Acrylamide induced glomerular renal affection in the form of shrinkage and distortion of the glomeruli with wrinkling of their basement membranes and widening of the urinary spaces. Degenerative tubular changes were markedly present in the proximal convoluted tubules. The necrotic tubular cells exhibited cytoplasmic vacuolation with desquamated epithelial cells within the tubular lumen. ACR increases the deposition of collagen fibres in the basement membrane of the glomerular capillaries and induced thickening of the basement membranes of the renal corpuscles and renal tubules. The administration of RVS affords high protection to the kidney. The glomeruli and renal tubules were nearly normal. The content of collagen fibres and the periodic acid Schiff reaction of the basement membrane of the renal tubules were 70% and 19% lower linked to the ACR group. The creatinine and urea levels decreased by 51% and 47%. RVS induced such a protective role through its antioxidant effect as the MDA level decreased by 45%, while the GSH level increased by 83% compared with the ACR group.
Conclusions: Acrylamide causes structural and functional disorders of the kidney. It induces kidney damage through oxidative stress and apoptosis. With the use of RVS, normal kidney architecture was preserved with little structural changes. Adding, functional kidney test became normal. RVS exerts its protective effect through its anti-apoptotic and antioxidant features.

Get Citation

Keywords

resveratrol, acrylamide, kidney

About this article
Title

Protective effect of resveratrol on acrylamide-induced renal impairment

Journal

Folia Morphologica

Issue

Vol 80, No 4 (2021)

Article type

Original article

Pages

985-993

Published online

2020-10-30

Page views

6587

Article views/downloads

985

DOI

10.5603/FM.a2020.0133

Pubmed

33169356

Bibliographic record

Folia Morphol 2021;80(4):985-993.

Keywords

resveratrol
acrylamide
kidney

Authors

M. M. Nasralla
S. M. Zaki
R. A. Attia

References (32)
  1. Abdel-Daim MM, Abd Eldaim MA, Hassan AGA. Trigonella foenum-graecum ameliorates acrylamide-induced toxicity in rats: Roles of oxidative stress, proinflammatory cytokines, and DNA damage. Biochem Cell Biol. 2015; 93(3): 192–198.
  2. Baskar G, Aiswarya R. Overview on mitigation of acrylamide in starchy fried and baked foods. J Sci Food Agric. 2018; 98(12): 4385–4394.
  3. Birben E, Sahiner UM, Sackesen C, et al. Oxidative stress and antioxidant defense. World Allergy Organ J. 2012; 5(1): 9–19.
  4. Buege J, Aust S. [30] Microsomal lipid peroxidation. Methods Enzymol. 1978: 302–310.
  5. Carere A. Genotoxicity and carcinogenicity of acrylamide: a critical review. Ann Ist Super Sanita. 2006; 42(2): 144–155.
  6. Crowley C, Gillham B, Thorn MB. A direct enzymic method for the determination of reduced glutathione in blood and other tissues. Biochem Med. 1975; 13(3): 287–292.
  7. Dearfield KL, Abernathy CO, Ottley MS, et al. Acrylamide: its metabolism, developmental and reproductive effects, genotoxicity, and carcinogenicity. Mutat Res. 1988; 195(1): 45–77.
  8. Dudka J, Gieroba R, Korga A, et al. Different effects of resveratrol on dose-related Doxorubicin-induced heart and liver toxicity. Evid Based Complement Alternat Med. 2012; 2012: 606183.
  9. Ghorbel I, Elwej A, Fendri N, et al. Olive oil abrogates acrylamide induced nephrotoxicity by modulating biochemical and histological changes in rats. Ren Fail. 2017; 39(1): 236–245.
  10. Gülçin İ. Antioxidant activity of food constituents: an overview. Arch Toxicol. 2012; 86(3): 345–391.
  11. Halliwell B, Gutteridge JM. Free radicals and antioxidant protection: mechanisms and significance in toxicology and disease. Hum Toxicol. 1988; 7(1): 7–13.
  12. Kjuus H, Hansteen IL, Ryberg D, et al. Chromosome aberrations in tunnel workers exposed to acrylamide and N-methylolacrylamide. Scand J Work Environ Health. 2005; 31(4): 300–306.
  13. Kurt A, Tumkaya L, Turut H, et al. Protective effects of infliximab on lung injury induced by methotrexate. Arch Bronconeumol. 2015; 51(11): 551–557.
  14. Liu Y. Epithelial to mesenchymal transition in renal fibrogenesis: pathologic significance, molecular mechanism, and therapeutic intervention. J Am Soc Nephrol. 2004; 15(1): 1–12.
  15. McCance KL, Huether SE. Pathophysiology: the biologic basis for disease in adults and children. 7th ed. . Elsevier, St. Louis, Missouri 2014.
  16. McCord JM. Human disease, free radicals, and the oxidant/antioxidant balance. Clin Biochem. 1993; 26(5): 351–357.
  17. Nangaku M. Chronic hypoxia and tubulointerstitial injury: a final common pathway to end-stage renal failure. J Am Soc Nephrol. 2005; 17(1): 17–25.
  18. Qiao Y, Gao Ke, Wang Y, et al. Resveratrol ameliorates diabetic nephropathy in rats through negative regulation of the p38 MAPK/TGF-β1 pathway. Exp Ther Med. 2017; 13(6): 3223–3230.
  19. Rajeh NA, Al-Dhaheri NM. Antioxidant effect of vitamin E and 5-aminosalicylic acid on acrylamide induced kidney injury in rats. Saudi Med J. 2017; 38(2): 132–137.
  20. Ramos-Vara JA, Kiupel M, Baszler T, et al. Suggested guidelines for immunohistochemical techniques in veterinary diagnostic laboratories. J Vet Diagn Invest. 2008; 20(4): 393–413.
  21. Rašić D, Micek V, Klarić MS, et al. Oxidative stress as a mechanism of combined OTA and CTN toxicity in rat plasma, liver and kidney. Hum Exp Toxicol. 2019; 38(4): 434–445.
  22. Semla M, Goc Z, Martiniaková M, et al. Acrylamide: a common food toxin related to physiological functions and health. Physiol Res. 2017; 66(2): 205–217.
  23. Sengul E, Gelen V, Yildirim S, et al. The effects of selenium in acrylamide-induced nephrotoxicity in rats: roles of oxidative stress, inflammation, apoptosis, and DNA damage. Biol Trace Elem Res. 2021; 199(1): 173–184.
  24. Suvarna SK, Layton C, Bancroft JD. Bancroft's theory and practice of histological techniques. 8th ed. Elsevier, Oxford 2019.
  25. Tareke E, Rydberg P, Karlsson P, et al. Acrylamide: a cooking carcinogen? Chem Res Toxicol. 2000; 13(6): 517–522.
  26. Terao J. Dietary flavonoids as antioxidants. Forum of Nutr. 2009: 87–94.
  27. Tirapelli LF, Barione DF, Trazzi BFM, et al. Comparison of two models for evaluation histopathology of experimental renal ischemia. Transplant Proc. 2009; 41(10): 4083–4087.
  28. Totani N, Yawata M, Ojiri Y, et al. Effects of trace acrylamide intake in Wistar rats. J Oleo Sci. 2007; 56(9): 501–506.
  29. Tsujimoto Y. Role of Bcl-2 family proteins in apoptosis: apoptosomes or mitochondria? Genes Cells. 1998; 3(11): 697–707.
  30. Xia N, Daiber A, Förstermann U, et al. Antioxidant effects of resveratrol in the cardiovascular system. Br J Pharmacol. 2017; 174(12): 1633–1646.
  31. Zhang Y. Study on reduction of acrylamide in fried bread sticks by addition of antioxidant of bamboo leaves and extract of green tea. Asia Pac J Clin Nutr. 2007; 16(Suppl 1): 131–136.
  32. Zhang L, Yang J, Eastwood GM, et al. Extended daily dialysis versus continuous renal replacement therapy for acute kidney injury: a meta-analysis. Am J Kidney Dis. 2015; 66(2): 322–330.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp. z o.o., Grupa Via Medica, Świętokrzyska 73, 80–180 Gdańsk, Poland

tel.: +48 58 320 94 94, faks: +48 58 320 94 60, e-mail: viamedica@viamedica.pl