A Scanning Electron Microscopy Study of The Renal Glomeruli and Tubules in Adult Albino Rats Following Oral Administration of Sodium Fluoride, And the Possible Protective and Curative Role of Plant Leaf Extract Boerhaavia Diffusa L
DOI:
https://doi.org/10.69980/ajpr.v28i5.299Keywords:
Albino rats, Boerhaavia diffusa L., Scanning electron microscopy, Sodium fluorideAbstract
This study used microdissection methods, such as scanning electron microscopy, to clarify the morphological alterations in the kidneys of albino rats treated with sodium fluoride. Eight groups of six rats each were randomly selected from a total of forty-eight animals. Rats in Control I were given deionized water orally. For 40 days, rats in the first and second groups received daily doses of 300 and 600 mg NaF/kg bw, respectively. For 20 days, 500 mg/kg b.w./day of Boerhaavia diffusa L. leaf extract was given orally to Control II rats. After receiving a 20-day pretreatment of 500 mg/kg bw/day of Boerhaavia diffusa L. leaf extract, groups third and fourth were subjected to 40 days of exposure to 300 and 600 mg NaF/kg bw/ /day. Groups fifth and sixth were exposed firstly to 300 and 600 mg NaF/ kg bw /day and then post-treated with leaf extract of Boerhaavia diffusa L. for 20 days. Scanning electron microscopy was used to examine the morphological characteristics of the rat kidneys treated with sodium fluoride. The features included the shortening of the podocyte processes, cytoplasmic blebs, hypertrophy, atrophy, knob-like projections at the end of the podocytes, shrinkage of the cell body, extreme deprivation of erythrocytes, and collagen fibers. It might be said that sodium fluoride negatively impacted the kidney's morphological structure. The renal damage changes may be lessened by administering Boerhaavia diffusa L. leaf extract both before and after treatment.
References
1. Alhusaini, A.M., Faddah, L.M., El Orabi, N.F. and , I.H. 2018. Role of some natural antioxidants in the modulation of some proteins expressions against sodium fluoride-induced renal injury. Biomed Research International , 5614803. https://doi.org/10.1155/2018/5614803
2. Asselman, M., Verhulst, A., De Bore, M. and Verkoelen, C. 2003. Calcium oxalate crystal adherence to hyaluronan, osteopontin and CD44-expressing injured/regenerating tubular epithelial cells in rat kidneys. Journal of American Society of Nephrology, 14 (12): 3155–3166.
3. Babaei, Z., Hussein, F., Kianbakht, S. and Changaei, P. 2017. Malva sylvestris L. protects from fluoride nephrotoxicity in rat. Journal of Medicinal plants, 16 (61): 21-32.
4. Bernstein, J., Evan, A.P., and Gardner K.D. 1987. Epithelial hyperplasia in human polycystic kidney diseases its role in pathogenesis and risk of neoplasia. American Journal of Pathology, 129 (1): 92-101.
5. Blattmann, A., Denk, L., Strehe, R., Castrop, H., and Minuth, W.W. 2008. The formation of pores in the basal lamina of regenerated renal tubules.
6. Boa, I.S.F., Porto, M.L., Porerira, A.C,H., Romos, J.P.L., Scherer, R., Oliviera, J.P., Nogueira, B.V., Meyrelles, S.S., Vasquez E.C.and Endringer D.C. and Pereira T.M.C. 2015. Resin from variola oleifera protects against radio contrast induced nephropathy in mice. Public Library of Science, 10 (12): 1-15.
7. Chaudhary, G. and Dantu P.K. 2011. Morphological, phytochemical and pharmacological studies on Boerhaavia diffusa L. Journal of Medicinal Plant Research, 5 (11): 2125-2130.
8. Castelino, D., Parida, A., Chogtu, B., Fathima, A., & Rao, K. G. M. 2025. A preclinical study on effect of betanin on sodium fluoride induced hepatorenal toxicity in Wistar rats. Journal of Complementary and Integrative Medicine. https://doi.org/10.1515/jcim-2024-0262
9. Davies, O. and Azeez, 2018. Modulatory effects of gallic acid on sodium fluoride induced nephrotoxicity in the wistar rats. Journal of Pharmacognosy and Phytochemistry, 72 (2) : 1561-70.
10. Enestrom, S., Druid, H. and Rammer, L. 1988. Fibrin deposition in the kidney in post-ischaemic renal kidney. British Journal of Experimental Pathology, 69: 387-394.
11. Forbes, J.M. and Thorburn, D.R., 2018. Mitochondrial dysfunction in diabetic kidney disease. Natures Reveiw Nephrology, 14 (5): 291-312.
12. Gupta, A., Puri, V., Sharma, R. and Puri S., 2012. Folic acid induces acute renal failure by enhancing renal prooxidant state. Experimental Toxicologic Pathology Journal, 64 (3): 225-232.
13. Hafez M.S. 2011. The effect of pentoxifylline in a rat model of renal ischemic reperfusion injury, light, transmission, and scanning electron microscopical study. The Egyptian Journal of Histology, 35: 148-158.
14. Hollenberg, M. J. and Erickson, A.M. 1973. The scanning electron microscope: Potential usefulness to biologists. A review. Journal of Histochemistry and Cytochemisty, 21(2):109-130. doi:10.1177/21.2.109
15. Hostetter, T.H., Olson, J.L., Renkke, H.G., Venkatachalan, M.A., and Brenner, B.M. 2001. Hyperfiltration in remnant nephrons: A potentially adverse response to renal ablation. Journal of American Society of Nephrology, 12: 1315-1325.
16. Khan, S., Johnson, J., Peck, J. and Cornelius, A. 2002. Expression of osteopontin in rat kidneys: Induction during ethyleneglycol induced calcium oxalate nephrolithiasis. Journal of Urology, 168 (3):1173-1181.
17. Khattab, F.K.E. 1994. Ultrastructure studies on the effect of organophosphorus insecticide dimethoate on the kidney cortex of rat. Egyptian Journal of Histology, 17 (2): 441-448.
18. Kondo, Y., Kubosawa, H., Akikusa, B. and Sugano, I. 1986.A scanning electron microscopic study of crescentic Masugi nephritis in the rabbit. Virchow Archiv, 50: 345-353.
19. Kaur, J. 2022. The in-vivo effect of sodium fluoride on the activities of renal enzymes in the brush border membrane of rat kidney is mitigated by supplementing with leaf extract of Boerhaavia diffusa L. European Chemical Bulletin, 11 (6), 891–900.
20. Makino, H. and Ota, Z., 1989. Three dimensional architecture of the mesangial matrix comparison of the intact and acellular glomerulus. Japanese Journal of Nephrology, 31 (10): 1039-1045.
21. Menon, M. and Resnick M. 2002.Urinary lithiasis: etiology, diagnosis, and medical management In: Patrick C. Walsh E. Darracott Vaughan Alan J. Wein Alan B. Retik E. Darracott Vaughn Jr Campbell’s Urology, 8th ed Saunders: pp. 3229-3292.
22. Mohamaden, W., Wang, H., Guan, H. and Li, J. 2013. Effect of potassium oxalate on liver function and kidney tissue of dogs. Archives of Biological Science, 65 (4):1363-1370.
23. Mohamed, N.A. and Saleh, S.M. 2010. Effect of pre and postnatal exposure to lead acetate on the kidney of male albino rat: A light and electron microscopic study. Egyptian Journal of Histology, 33 (2): 365-379.
24. Narendhirakannan, R.T., Subramanian, S. and Kandaswamy, M. 2006.Bio-chemical evaluation of antidiabetogenic properties of some commonly used Indian plants on streptozotocin induced diabetes in experimental rats. Clinical Experimental Pharmacology and Physiology, 33:1150-1157.
25. Oken, D.E. 1983.Theoretical analysis of pathogenetic mechanisms in experimental acute renal failure. Kidney International, 24:16-26.
26. Padmini, M.P. and Kumar, J.V. 2013. An experimental study of biochemical and histopathological study on gentamycin induced renal failure in albino rat and the effectiveness of punarnava (Boerhaavia diffusa) on reversal of renal damage. Journal of Medical and Dental Sciences, 9 (6): 17-21.
27. Pillai, B.S., Pawar, S.S., Shahzad, A., Patil, S.B. and Pillewar, D.D. 2017. Fluoride intoxication and possible changes in trace elements of kidney and thigh muscles in rats. International Journal of Innovative Research and Advanced Studies, 4 (3): 153-156.
28. Racusen, L.C., Solez, K. and Whelton, A. 1982. Glomerular podocyte changes and increased permeability to protein in early post-ischemic acute renal failure. In Acute Renal Failure. ed. H.E. Eliahou. London: John Libbey, pp. 215-218.
29. Schepers, M., VanBallegooijen, E., Bangma, S. and Verkoelen, C. 2005. Crystals cause acute necrotic cell death in renal proximal tubule cells, but not in collecting tubule cells. Kidney International. 68 (4):1543–1553.
30. Tan, P.P., Zhou, B.H., Zhao, W.P., Jia, L.S., Liu, J. and Wang, H.W., 2018. Mitochondria mediated pathway regulates C2C12 cell apoptosis induced by fluoride. Biological Trace Element Research, 185 (2): 440-447.
31. Tian, X., Xie, J., Chen, X., Dong, N., Feng, J., Gao, Y., Tian, F., Zhang, W., Qui, Y., Niu, R., Ren, X. and Yan, X. 2020. Deregulation of autophagy is involved in nephrotoxicity of arsenite and fluoride exposure during gestation to puberty in rat offspring. Archives of Toxicology, 94: 749-760.
32. Tsuji, K., Painescu, T. G., Suleiman, H., Xie, D., Mamuya, F.A., Miner, J.H. and Lu, H.A.J. 2017. Recharacterization of the glomerulopathy in CD2AP deficient mice by high resolution helium ion scanning microscopy. Scientific Reports, 7 (8321): 1-13.
33. Wagner, M.C., Rhodes, G., Wang, E., Pruthi, V., Arif, E., Saleem, M.A., Wean, S.E., Garg, P., Verma, R., Holzman, L.B., Gattone, V., Molitoris, B.A. and Nihalani, D. 2008. Ischemic injury to kidney induces glomerular podocyte effacement and dissociation of slit diaphragm proteins Neph 1 and Zo-1. The Journal of Biological Chemistry, 283 (51): 35579-35589.
34. Wang, E.H., Yu, Z.L., Ping, G.F. and Zhai, D.S.2020. Grape seed procyanadin extract attenuate sodium fluoride induced oxidative damage and apoptosis in rat kidneys. Biomedical and Environmental Sciences, 33 (6): 454-457.
35. Xu, W., Ge, Y., Liu, Z. and Gang, R. 2015. Glycogen synthase kinase 3β orchestrates microtubule remodeling in compensatory glomerular adaptation to podocyte depletion. The Journal of Biological Chemistry, 290 (3): 1348-1363.
36. Zaghloul, D.A.M., 2009. A histological study on the effect of lead acetate on the developing metanephros in rabbit. Egyptian Journal of Anatomy, 32 (2): 73-87.
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