Skip to main content

Advertisement

Log in

Effects of panax notoginoside on the nephropathy in rats with type 1 diabetes mellitus

  • Original Article
  • Published:
Chinese Journal of Integrative Medicine Aims and scope Submit manuscript

Abstract

Objective

To explore the effects and underlying mechanisms of Panax notoginoside (PNS) on the nephropathy in rats with type 1 diabetes.

Methods

A murine model of diabetic nephropathy was set up by an intravenous injection of streptozotocin (STZ). Wistar rats were randomly divided into 5 groups: the control group, the diabetic group (DM), the group treated with low-dosage PNS (PNS-L), the group treated with high-dosage PNS (PNS-H) and the group treated with catopril. Rats in the PNS-L and PNS-H groups were given different dosages of PNS while rats in the catopril group were given catopril through gastrogavage every day for the next four consecutive weeks. Serum creatinine (Cr) levels, endogenous creatinine clearance rate (CCr), and 24-h urinary microalbumin (UAlb) were examined and calculated. Meanwhile, immunohistochemistry was applied to determine the expression of vascular endothelial growth factor (VEGF) and bone morphogenetic protein-7 (BMP-7) in the kidney tissue.

Results

The levels of Cr, Ccr, and UAlb were all elevated significantly in the DM group (P<0.01). The expression of VEGF protein was increased but BMP-7 protein was decreased in the kidney tissue (P<0.01). However, the above items decreased in the PNS-L, PNS-H and catopril groups compared with the DM group (P<0.05, P<0.01). In the PNS-L, PNS-H and catopril groups, the expression of VEGF protein was decreased but BMP-7 protein was increased in the kidney tissue (P<0.05, P<0.01).

Conclusion

PNS shows protective effects on the kidney in type 1 diabetic rats at the early stage. The protective mechanism might be closely related to its role of inhibiting the expression of VEGF protein and enhancing the expression of BMP-7 protein in the kidney.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Kreisberg JI, Ayo SH. The glomerular mesangium in diabetes mellitus. Kidney Int 1993;43:109–113.

    Article  PubMed  CAS  Google Scholar 

  2. Gilbert RE, Cooper ME. The tubulointerstitium in progressive diabetic kidney disease: more than an aftermath of glomerular injury? Kidney Int 1999;56:1627–1637.

    Article  PubMed  CAS  Google Scholar 

  3. Chen S, Ziyadeh FN. Vascular endothelial growth factor and diabetic nephropathy. Curr Diabete Rep 2008;8:470–476.

    Article  Google Scholar 

  4. Zhang Y, Zhang Q. Bone morphogentic protein-7 and gremlin: new emerging therapeutic targets for diabetic nephropathy. Biochem Biophys Res Commun 2009;383:1–3.

    Article  PubMed  CAS  Google Scholar 

  5. Gao HL, Liu FY, Xia ZL. Theoretical study and application of experimental diabetic animal models. Chin J Rehabil (Chin) 2005;9:210–212.

    Google Scholar 

  6. Cooper ME, Vranes D, Youssef S, Stacker SA, Cox AJ, Rizkalla B, et al. Increased renal expression of vascular endothelial growth factor (VEGF) and its receptor VEGFR-2 in experimental diabetes. Diabetes 1999;48:2229–2239.

    Article  PubMed  CAS  Google Scholar 

  7. De Vriese AS, Tilton RG, Elger M, Stephan CC, Kriz W, Lameire NH. Antibodies against vascular endothelial growth factor improve early renal dysfunction in experimental diabetes. J Am Soc Nephrol 2001;12:993–1000.

    PubMed  Google Scholar 

  8. Flyvbjerg A, Dagnaes-Hansen F, de Vriese AS, Schrijvers. BF, Tilton RG, Rasch R. Amelioration of long term renal changes in obese type 2 diabetic mice by a neutralizing vascular endothelial growth factor antibody. Diabetes 2002;51:3090–3094.

    Article  PubMed  CAS  Google Scholar 

  9. Wang S, Chen Q, Simon TC, Strebeck F, Chaudhary L, Morrissey J, et al. Bone morphogenic protein-7 (BMP-7), a novel therapy for diabetic nephropathy. Kidney Int 2003;63:2037–2049.

    Article  PubMed  CAS  Google Scholar 

  10. Wang S, de Caestecker M, Kopp J, Mitu G, Lapage J, Hirschberg R. Renal bone morphogenetic protein-7 protects against diabetic nephropathy. J Am Soc Nephrol 2006;17:2504–2512.

    Article  PubMed  CAS  Google Scholar 

  11. Dong XL, Niu SY, Xu HB, Han MY. Effects of hyperbaric oxygenation associated with Panax notoginseng saponins therapy on hemorrhology indexes in patients with ischemic cerebrovascular disease. Chin J Rehabil (Chin) 2005;9:6–7.

    Google Scholar 

  12. Guo M, Liu HY, Chen XW. The mechanisms of progression of renal interstitial fibrosis and the therapeutic effects of Panax notoginoside. Chin J Integr Tradit West Nephrol (Chin) 2007;8:175–178.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hui Dong  (董 慧).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tu, Qn., Dong, H. & Lu, Fe. Effects of panax notoginoside on the nephropathy in rats with type 1 diabetes mellitus. Chin. J. Integr. Med. 17, 612–615 (2011). https://doi.org/10.1007/s11655-011-0825-9

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11655-011-0825-9

Keywords

Navigation