Diabetic Nephropathy: Pathogenesis to Cure

被引:16
作者
Kushwaha, Kriti [1 ]
Kabra, Uma [2 ]
Dubey, Rupal [1 ,3 ]
Gupta, Jeena [1 ,4 ]
机构
[1] Lovely Profess Univ, Sch Bioengn & Biosci, Dept Biochem, Phagwara 144411, Punjab, India
[2] Parul Univ, Parul Inst Pharm, Dept Pharmaceut Chem, Vadodara 391760, Gujarat, India
[3] Lovely Profess Univ LPU, Sch Pharmaceut Sci, Dept Med Lab Sci, Jalandhar Delhi GT Rd, Phagwara 144411, Punjab, India
[4] Lovely Profess Univ LPU, Sch Bioengn & Biosci, Dept Biochem, Jalandhar Delhi GT Rd, Phagwara 144411, Punjab, India
关键词
Diabetic nephropathy; urinary albumin excretion; microalbuminuria; macroalbuminuria; renal damage; pathogenesis; GLYCATION END-PRODUCTS; NECROSIS-FACTOR-ALPHA; BLOOD-PRESSURE; RENAL HYPERTROPHY; JAPANESE PATIENTS; SODIUM RETENTION; THERAPY PREVENTS; KIDNEY INJURY; TNF-ALPHA; INFLAMMASOME;
D O I
10.2174/1389450123666220820110801
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetic nephropathy (DN) is a leading cause of end-stage renal disorder (ESRD). It is defined as the increase in urinary albumin excretion (UAE) when no other renal disease is present. DN is categorized into microalbuminuria and macroalbuminuria. Factors like high blood pressure, high blood sugar levels, genetics, oxidative stress, hemodynamic and metabolic changes affect DN. Hyperglycemia causes renal damage through activating protein kinase C (PKC), producing advanced end glycation products (AGEs) and reactive oxygen species (ROS). Growth factors, chemokines, cell adhesion molecules, inflammatory cytokines are found to be elevated in the renal tissues of the diabetic patient. Many different and new diagnostic methods and treatment options are available due to the increase in research efforts and progression in medical science. However, until now, no permanent cure is available. This article aims to explore the mechanism, diagnosis, and therapeutic strategies in current use for increasing the understanding of DN.
引用
收藏
页码:1418 / 1429
页数:12
相关论文
共 119 条
  • [31] IL-6 signaling in diabetic nephropathy: From pathophysiology to therapeutic perspectives
    Feigerlova, Eva
    Battaglia-Hsu, Shyue-Fang
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2017, 37 : 57 - 65
  • [32] SGLT2 Inhibitors and the Diabetic Kidney
    Fioretto, Paola
    Zambon, Alberto
    Rossato, Marco
    Busetto, Luca
    Vettor, Roberto
    [J]. DIABETES CARE, 2016, 39 : S165 - S171
  • [33] The breakdown of pre-existing advanced glycation end products is associated with reduced renal fibrosis in experimental diabetes
    Forbes, JM
    Thallas, V
    Thomas, MC
    Founds, HW
    Burns, WC
    Jerums, G
    Cooper, ME
    [J]. FASEB JOURNAL, 2003, 17 (10) : 1762 - +
  • [34] Effect of lipid reduction on the progression of renal disease: A meta-analysis
    Fried, LF
    Orchard, TJ
    Kasiske, BL
    [J]. KIDNEY INTERNATIONAL, 2001, 59 (01) : 260 - 269
  • [35] Predictors of diabetic nephropathy
    Gaballa, Mahmoud R.
    Farag, Youssef M. K.
    [J]. CENTRAL EUROPEAN JOURNAL OF MEDICINE, 2013, 8 (03): : 287 - 296
  • [36] NADPH oxidases in the kidney
    Gill, Pritmohinder S.
    Wilcox, Christopher S.
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 2006, 8 (9-10) : 1597 - 1607
  • [37] Grundy Scott M, 2004, J Am Coll Cardiol, V44, P720, DOI 10.1016/j.jacc.2004.07.001
  • [38] Reactive oxygen species amplify glucose signalling in renal cells cultured under high glucose and in diabetic kidney
    Ha, H
    Lee, HB
    [J]. NEPHROLOGY, 2005, 10 : S7 - S10
  • [39] DEXAMETHASONE AND PENTOXIFYLLINE INHIBIT ENDOTOXIN-INDUCED CACHECTIN TUMOR-NECROSIS-FACTOR SYNTHESIS AT SEPARATE POINTS IN THE SIGNALING PATHWAY
    HAN, J
    THOMPSON, P
    BEUTLER, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (01) : 391 - 394
  • [40] Reactive oxygen species promote tubular injury in diabetic nephropathy: The role of the mitochondrial ros-txnip-nlrp3 biological axis
    Han, Yachun
    Xu, Xiaoxuan
    Tang, Chengyuan
    Gao, Peng
    Chen, Xianghui
    Xiong, Xiaofen
    Yang, Ming
    Yang, Shikun
    Zhu, Xuejing
    Yuan, Shuguang
    Liu, Fuyou
    Xiao, Li
    Kanwa, Yashpal S.
    Sun, Lin
    [J]. REDOX BIOLOGY, 2018, 16 : 32 - 46