Therapeutic Potential of Naja Naja Atra Venom in A Rat Model of Diabetic Nephropathy

被引:12
作者
Dai Gui Li [1 ]
He Jing Kang [1 ]
Xie Yan [1 ]
Han Rong [2 ,3 ]
Qin Zheng Hong [2 ,3 ]
Zhu Lu Jia [2 ,3 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Suzhou 215006, Jiangsu, Peoples R China
[2] Soochow Univ, Dept Pharmacol, Sch Med, Suzhou 215123, Jiangsu, Peoples R China
[3] Soochow Univ, Lab Aging & Nervous Dis, Sch Med, Suzhou 215123, Jiangsu, Peoples R China
关键词
Diabetic nephropathy; Naja naja atra venom; Renal function; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; CYSTATIN-C; SUPEROXIDE-DISMUTASE; LIPID-PEROXIDATION; ACTIVATION; EXPRESSION; MICE; OVEREXPRESSION; RECRUITMENT;
D O I
10.3967/0895-3988.2012.06.004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Objective To study the protective effects of naja naja atra venom (NNAV) in a rat model of diabetic nephropathy (DN). Methods The rat diabetes model was induced by intraperitoneal injection of streptozotocin (STZ). Thirty-two model rats were randomly divided into one DN group (n=8) and three treatment groups (n=8 each) that received NNAV at doses of 30, 90, or 270 mu g/(kg.day) via oral gavage, another eight rats as normal controls. After 12 weeks, all rats were sacrificed and the changes in serum and urine biological index levels were determined by colorimetric assay. Microalbumin (mALB), N-acetyl-beta- glucosaminidase (NAG) and cystatin C (CysC) concentrations were measured by ELISA. Renal tissues were sliced for pathological and immunohistochemical observations. Results Comparied with the DN group, serum glucose was decreased by 31.04%, total cholesterol 21.96%, triglyceride 23.78%, serum creatinine 19.83%, blood urea nitrogen 31.28%, urinary protein excretion 45.42%, mALB 10.42%, NAG 20.65%, CysC 19.57%, whereas albumin increased by 5.55%, high-density lipoprotein cholesterol 59.09%, creatinine clearance 19.05% in the treatment group by NNAV administration at dose of 90 mu g/(kg.day). NNAV also reduced the levels of malondialdehyde in serum (22.56%) and kidney tissue (9.79%), and increased superoxide dismutase concentration in serum (15%) and decreased it in renal tissue (8.85%). In addition, under light microscopy kidney structure was improved and glomerular hypertrophy decreased by 8.29%. As shown by immunohistochemistry, NNAV inhibited transforming growth factor-beta 1 by 6.70% and nuclear actor-kappa B by 5.15%. Conclusion NNAV improves biological indexes in DN, and it may exert renoprotective effects in rats with STZ-induced diabetes.
引用
收藏
页码:630 / 638
页数:9
相关论文
共 36 条
  • [1] Microvascular alterations in diabetic mice correlate with level of hyperglycemia
    Algenstaedt, P
    Schaefer, C
    Biermann, T
    Hamann, A
    Schwarzloh, B
    Greten, H
    Rüther, W
    Hansen-Algenstaedt, N
    [J]. DIABETES, 2003, 52 (02) : 542 - 549
  • [2] NF-κB in Renal Inflammation
    Belen Sanz, Ana
    Dolores Sanchez-Nino, Maria
    Mario Ramos, Adrian
    Antonio Moreno, Juan
    Santamaria, Beatriz
    Ruiz-Ortega, Marta
    Egido, Jesus
    Ortiz, Alberto
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2010, 21 (08): : 1254 - 1262
  • [3] 1,25-Dihydroxyvitamin D3 suppresses high glucose-induced angiotensinogen expression in kidney cells by blocking the NF-κB pathway
    Deb, Dilip K.
    Chen, Yunzi
    Zhang, Zhongyi
    Zhang, Yan
    Szeto, Frances L.
    Wong, Kari E.
    Kong, Juan
    Li, Yan Chun
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2009, 296 (05) : F1212 - F1218
  • [4] Elevated cystatin C concentration and progression to pre-diabetes
    Donahue, Richard P.
    Stranges, Saverio
    Rejman, Karol
    Rafalson, Lisa B.
    Dmochowski, Jacek
    Trevisan, Maurizio
    [J]. DIABETES CARE, 2007, 30 (07) : 1724 - 1729
  • [5] Effects of propolis on blood glucose, blood lipid and free radicals in rats with diabetes mellitus
    Fuliang, HU
    Hepburn, HR
    Xuan, HX
    Chen, ML
    Daya, S
    Radloff, SE
    [J]. PHARMACOLOGICAL RESEARCH, 2005, 51 (02) : 147 - 152
  • [6] Leukocyte recruitment and vascular injury in diabetic nephropathy
    Galkina, Elena
    Ley, Klaus
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (02): : 368 - 377
  • [7] The tubulointerstitium in progressive diabetic kidney disease: More than an aftermath of glomerular injury?
    Gilbert, RE
    Cooper, ME
    [J]. KIDNEY INTERNATIONAL, 1999, 56 (05) : 1627 - 1637
  • [8] Kapoor VK, 2010, INDIAN J EXP BIOL, V48, P228
  • [9] Kelly DJ, 2001, J AM SOC NEPHROL, V12, P2098, DOI 10.1681/ASN.V12102098
  • [10] Role of oxidative stress in advanced glycation end product-induced mesangial cell activation
    Lal, MA
    Brismar, H
    Eklöf, AC
    Aperia, A
    [J]. KIDNEY INTERNATIONAL, 2002, 61 (06) : 2006 - 2014