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Sterological analysis of podocyte mitochondria in adriamycin nephropathy rats
Vol 1, Issue 1, 2020
VIEWS - 1735 (Abstract)
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Abstract
Objective: To disclose the relationship between mitochondrial morphology, density and pro-teinuria in adriamycin nephropathy rats. Method: Thirty Sprague Dawley rats of clean grade were divided into adriamycin group and control group. In adriamycin nephropathy group, rats were given adriamycin at dosage of 0.7 mg /100 g body weight by tail vein injection. The control rats received equal volume of sa-line. At 2 weeks (control group = 3, adriamycin group = 3) , 4 weeks (control = 3, adriamycin group =6) and 6 weeks (control = 8, adriamycin group = 7) after adriamycin injection, the rats were sacrificed and kidneys were harvested for preparation of ultra-thin sections. Electron microscopy was performed, and podocyte mitochondrial morphology was observed. Sterological analysis was performed on morphology and density of mitochondria in podocytes. Results: 4 weeks after adriamycin injection, the rats developed proteinuria until 6 weeks. Mitochondria in the podocytes from control rats showed ellipsoid shape. Differ-ent shaped and sized mitochondria were observed in podocytes of the adriamycin nephropathy rats. No sig-nificant statistical difference was revealed in the mitochondrial area, circumference, form factor and aspect ratio between adriamycin and control groups. Before development of proteinuria, the mitochondrial density increased significantly at 2 weeks after adriamycin injection compared with that in control rats (0.17±0.00 vs. 0.14±0.01, t = 6.173, P < 0.01). Meanwhile, the surface density of mitochondria showed an increasing trend (0.78±0.03 vs. 0.71±0.04, t =-2.526, P = 0.065). 6 weeks after adriamycin injection, the surface density of mitochondria decreased significantly compared with that in the control rats (0.71±0.11 vs. 0.87±0.12, P = 0.02) , the density of mitochondria did not change significantly. Conclusions Dysmorphic mitochondria are involved in the development of proteinuria in adriamycin ne-phropathy. The increase of mitochondrial density is an early event in the development of proteinuria. De-crease of mitochondria surface density is involved in podocyte injury and development of adriamycin ne-phropathy rats.
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References
1. Guan Na, Ding Jie, Yang Jiyun, et al. Chinical charac-teristics and prognosis analysis of children with idiopathic nephrotic syndrome with different responses to steroid therapy from a single center in 20 years[J]. Chinese Journal of Applied Clinical Pediatric, 2014, 29 (17) : 1291-1295. (in Chinese)
2. Deng Jianghong, Ding Jie, Guan Na, et al. Morphomet-ric analysis of of glomerular foot process in puromycin aminonucleoside nephropathy in rat[J]. Chinese Journal of Sterology and Image Analysis, 2003, 8 (1) : 9-15. (in Chinese)
3. Tharaux P L, Huber T B. How many ways can a podo-cyte die? [J]. Seminars in Nephrology, 2012 , 32(4) : 394-404.
4. Hotta O, Inoue C N, Miyabayashi S, et al. Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial trna Leu (UUR) gene mutation [J]. Kidney International, 2001, 59(4) : 1236-1243.
5. Guan Na. Progress in diagnosis and treatment of mito-chondrial nephropathy[J]. Chinese Journal of Pediatric, 2014, 52(7) : 503-505. (in Chinese)
6. Xie Kewei, Gu Leyi. Mitochondria injury and glomerular dis-ease[J]. Chiese Journal of Integrated Traditional and West-ern Nephrology, 2013, 14(3) : 360-362. (in Chinese)
7. He Weichun, Yang Junwei. The study progression of mi-tochondria and podocyte[J]. Chinese Journal of Neph-rology, 2007, 23(1) : 61-63. (in Chinese)
8. Zhu C, Xuan X, Che R, et al. Dysfunction of the PGC-1 α-mitochondria axis confers adriamycin-in-duced podocyte injury[J]. American Journal of Physiology-Renal Physiology, 2014, 306(12) : 1410-1417.
9. GüCer S, Talim B, Asan E, et al. Focal segmental glomer-ulosclerosis associated with mitochondrial cytopathy: report of two cases with special emphasis on podocytes [J]. Pedi-atric Developmnetal Pathology, 2005, 8(6) : 710-717.
10. Yang Zhengwei. The basic tools for the study of quantita-tive morphology of biological tissue: The utility of stereo-logical method[M]. Beijing: Science Press, 2012. (in Chinese)
11. Imasawa T, Rossignol R. Podocyte energy metabolism and glomerular diseases[J]. The International Journal of Biochemistry and Cell, 2013, 45(9) : 2109-2118.
12. Dinour D,mini S, Polak-Charcon S, et al. Progressive nephropathy associated with mitochondrial trna gene mu-tation[J]. Clinical Nephrology, 2004, 62(2) : 149-154.
13. Barisoni L, Madaio M P, Eraso M, et al. The kd/kd mouse is a model of collapsing glomerulopathy [J]. Jour-nal of the American Society of Nephrology, 2005, 16 (10) : 2847-2851.
14. Markowitz G S, Appel G B, Fine P L, et al. Collapsing focal segmental glomerulosclerosis following treatment with high-dose pamidronate[J]. Journal of the American Society Nephrology, 2001, 12(6) : 1164-1172.
15. Coimbra T M, Janssen U, Grne H J, et al. Early events leading to renal injury in obese Zucker (fatty) rats with type II diabetes[J]. Kidney International, 2000, 57(1) : 167-182.
16. Mannella C A, Lederer W J, Jafri M S. The connection between inner membrane topology and mitochondrial function[J]. Journal of Molecular and Cellular Cardi-olgy, 2013, 62: 51-57
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Prof. Wei-Yen Hsu
National Chung Cheng University, Taiwan