Experimental models for nephropathy

被引:53
作者
Balakumar, Pitchai [1 ]
Chakkarwar, Vishal Arvind
Kumar, Vijay [2 ]
Jain, Akash
Reddy, Jayarami
Singh, Majeet
机构
[1] Inst Pharmaceut Sci & Drug Res, ISF Coll Pharm, Cardiovasc Pharmacol Div, Moga 142001, India
[2] Lovely Profess Univ, Dept Pharm, Jalandhar, India
关键词
animal models; nephropathy; signalling mechanisms;
D O I
10.1177/1470320308098343
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Nephropathy is a leading cause of morbidity and mortality and its prevalence is Continuously increasing in industrialised nations. Nephropathy is characterised to varying degrees by nodular glomerulosclcrosis, glomerular basement membrane thickness and mesangial expansion, leading to a decline in glomerular filtration rate, persistent elevated albuminuria, elevated arterial blood pressure and fluid retention. Hyperglycaemia, hyperlipidaemia and hypertension are considered to be the major risk factors implicated in the progression of nephropathy. Various signalling systems, such as vasoconstrictor peptides, inflammatory mediators, growth factors and adhesion molecules, are involved in the pathogenesis of nephropathy. At present, no promising therapy is available to treat patients with nephropathy due to lack Of understanding of signalling culprits involved in the pathogenesis of 1-nephropathy. Animal models are being developed to better understand the disease pathogenesis and develop drugs for nephropathy. In the present review, we have discussed various animal models for nephropathy, which may open vistas for developing new drugs to treat nephropathy.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 65 条
  • [1] Al-Qattan K., 2008, EUR J CLIN NUTR META, V3, pe62, DOI DOI 10.1016/J.ECLNM.2007.12.001
  • [2] Balakumar P., 2007, J PHARM TOXICOL, V2, P437
  • [3] Pharmacological interventions to prevent vascular endothelial dysfunction: Future directions
    Balakumar, Pitchai
    Koladiya, Rajeshkumar U.
    Ramasamy, Subbiah
    Rathinavel, Andiappan
    Singh, Manjeet
    [J]. JOURNAL OF HEALTH SCIENCE, 2008, 54 (01) : 1 - 16
  • [4] Potential target sites to modulate vascular endothelial dysfunction: Current perspectives and future directions
    Balakumar, Pitchai
    Kaur, Tajpreet
    Singh, Manjeet
    [J]. TOXICOLOGY, 2008, 245 (1-2) : 49 - 64
  • [5] Expression of renal transforming growth factor-β and its receptors in a rat model of chronic cyclosporine-induced nephropathy
    Bing, P.
    Maode, L.
    Li, F.
    Sheng, H.
    [J]. TRANSPLANTATION PROCEEDINGS, 2006, 38 (07) : 2176 - 2179
  • [6] Nitric oxide dynamics and endothelial dysfunction in type II model of genetic diabetes
    Bitar, MS
    Wahid, S
    Mustafa, S
    Al-Saleh, E
    Dhaunsi, GS
    Al-Mulla, F
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 511 (01) : 53 - 64
  • [7] Diabetic nephropathy in the elderly
    Blickle, J. F.
    Doucet, J.
    Krummel, T.
    Hannedouche, T.
    [J]. DIABETES & METABOLISM, 2007, 33 : S40 - S55
  • [8] Pravastatin modulates early diabetic nephropathy in an experimental model of diabetic renal disease
    Casey, RG
    Joyce, M
    Roche-Nagle, G
    Chen, G
    Bouchier-Hayes, D
    [J]. JOURNAL OF SURGICAL RESEARCH, 2005, 123 (02) : 176 - 181
  • [9] Macrophages in streptozotocin-induced diabetic nephropathy: potential role in renal fibrosis
    Chow, FY
    Nikolic-Paterson, DJ
    Atkins, RC
    Tesch, GH
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2004, 19 (12) : 2987 - 2996
  • [10] Dosimetry considerations in the enhanced sensitivity of male Wistar rats to chronic ethylene glycol-induced nephrotoxicity
    Corley, R. A.
    Wilson, D. M.
    Hard, G. C.
    Stebbins, K. E.
    Bartels, M. J.
    Soelberg, J. J.
    Dryzga, M. D.
    Gingell, R.
    McMartin, K. E.
    Snellings, W. M.
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2008, 228 (02) : 165 - 178