Renal Injury and Its Mechanisms in Lepr db/db Mice

YAN Ting-ting, XU Guang-cui, PENG Qiang, WU Wei-dong, YI Xian-wen, ZHAO Ying-zheng

Abstract

To study the mechanism of renal injury in Leprdb/db mice with the leptin receptor homozygous deficiency.  Methods  Ten male of 28-week-old Leprdb/+ mice with leptin receptor heterozygous deficiency were selected as control group and ten male Leprdb/db mice with leptin receptor homozygous deficiency were used in this study. After fasting for 8 hours, the body mass, fasting blood glucose (FBG) and glycosylated hemoglobulin (HbA1c) of the mice were measured. Blood of the mice was obtained from femoral artery before euthanasia. Serum creatinine (CRE), blood urea nitrogen (BUN), superoxide dismutase (SOD), glutathione (GSH) and malonaldehyde (MDA) were detected by corresponding kits, and serum interleukin-1β (IL-1β), monocyte chemotactic protein-1 (MCP-1) and tumor necrosis factor-α (TNF-α) were measured using enzyme-linked immunosorbent assay (ELISA) method. The kidney was taken for pathological observation. The expression levels of nuclear factor E2-related factor 2 (Nrf2) and nuclear factor kappa B (NF-κB) in renal were analyzed by Western blotting. The mitochondria of renal was isolated by the corresponding kit. Meanwhile, the expression level of lipoic acid synthase (LIAS) in renal mitochondria was measured by Western blotting.  Results  The body mass, FPG, HbA1c, CRE and BUN levels of the Leprdb/db mice were significantly increased in comparison with the Leprdb/+ mice (P<0.05). Compared with the Leprdb/+ mice, the Leprdb/db mice renal exhibited glomerular hypertrophy, thickened basement membrane and capillary wall, the mesangial matrix expansion and mesangial cell hyperplasia. Compared with the Leprdb/+ mice, the serum level of GSH in the Leprdb/db mice was decreased significantly (P<0.05). The levels of MDA and concentrations of MCP-1, IL-1β and TNF-α in serum of the Leprdb/db mice were higher than those of the Leprdb/+ mice (P<0.05). Compared with the Leprdb/+ mice, the expression of LIAS and Nrf2 protein in the Leprdb/db mice renal were decreased (P<0.05), while the expression of NF-κB protein was increased (P<0.05).  Conclusion  LIAS, Nrf2 and NF-κB might play significant roles through regulation of oxidative stress and inflammation in the renal injury of Leprdb/db mice.

 

Keywords: Leprdb/db mice, Renal injury, LIAS, Nrf2, NF-κB

 

Full Text:

PDF


References


NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in diabetes since 1980: a pooled analysis of 751 population-based studies with 4.4 million participants. Lancet (London, England). 2016. 387(10027): 1513-1530.

HOU X. LU J. WENG J, et al. Impact of waist circumference and body mass index on risk of eardiometabolie disorder and cardiovascular disease in Chinese adults: a national diabetes and metabolic disorders survey. PLoS One. 2013. 8(3): e57319(2018-06-l 1]. https://doi.org/10.1371/ journal.pone.0057319.

NAVARRO-GONZALEZ JF. MORA-FERNANDEZ C. The role of inflame- matory cyto-kines in diabetic nephropathy. J Am Soc Nephrol. 2008. 19(3): 433-442.

ELMARAKBY AA. SULLIVAN JC. Relationship between oxidative stress and inflammatory cytokines in diabetic nephropathy. Cardiovasc Ther. 2012. 30(l):49-59.

NAVARRO-GONZALEZ JF. MORA-FERNANDEZ С. MUROSD FM, et al. Inflammatory molecules and pathways in the pathogenesis of diabetic nephropathy. Nat Rev Nephrol. 2011. 7(6): 327-340.

SUH JH. WANG H. LIU RM. et al. (R)-alpha-lipoic acid reverses the age-related loss in tissues: evidence for increased cysteine requirement for GSH synthesis. Arch Biochem Biophys. 2004.42(3): 126-135.

LIU J. The effects and mechanisms of mitochondrial nutrient alpha-lipoic acid on improving age-associated mitochondrial and cognitive dysfunction: an overview. Neurochem Res, 2008. 33(1): 194-203.

PACKER L, KRAEMER K. RIMBACH G. Molecular aspects of lipoic acid in the prevention of diabetes complications. Nutrition. 2001. 17(10): 888-895.

AZUSHIMA K. GURLEY SB, COFFMAN TM. Modelling diabetic nephropathy in mice. Nat Rev Nephrol. 2018. 14(1): 48-56.

JIANG Z. LU W, ZENG Q. et al. High glucose-induced excessive reactive oxygen species promote apoptosis through mitochondrial damage in rat cartilage endplate cells. I Orthop Res. 2018(2018-06-11 J. https://doi.org/10.1002/jor.24016.

SAKAI N. WADA T. Revisiting inflammation in diabetic nephropathy: the role of the Nlrp3 inflammasome in glomerular resident cells. Kidney Int. 2015, 87(1): 12-14.

JEONG WS. JUN M, KONG AN. Nrf2: a potential molecular target for cancer chcmoprevcntion by natural compounds. Antioxid Redox Signal. 2006. 8(1-2): 99-106.

LV C. MAHARJAN S, VVrANG Q, et al. a-lipoic acid promotes neurological recovery after ischemic stroke by activating the Nrf2/HO-1 pathway to attenuate oxidative damage. Cell Physiol Biochem. 2017, 43(3): 12/3-128/.

ZHANG J. MCCULLOUGH PA. Lipoic acid in the prevention of acute kidney injur)'. Nephron. 2016. 134(3): 133-140.

TUTTLE KR. Linking metabolism and immunology: diabetic nephropathy is an inflammatory disease. J Am Soc Nephrol. 2005. 16(6): 1537-1538.

RASHID S. NAFEES S. S1DDIQ1 A, et al. Partial protection by 18p Glycrrhetinic acid against Cisplatin induced oxidative intestinal damage in wistar rats: possible role of NF-кВ and caspases. Pharmacol Rep. 2017. 69(5): 1007-1013.

ZHANG WJ, FREI B. Alpha-lipoic acid inhibits TNF-alpha-induced NF- kappaB activation and adhesion molecule expression in human aortic endothelial cells. FASEB J. 2001. 15(13): 2423-2432.


Refbacks

  • There are currently no refbacks.