Open Access

AMPKα, hs-CRP and FcγR in diabetic nephropathy and drug intervention

  • Authors:
    • Ping Sun
    • Lei Lu
    • Jun Chen
    • Xiao Dan  Liu
    • Qing Zhang
    • Xu Wang
  • View Affiliations

  • Published online on: April 4, 2018     https://doi.org/10.3892/etm.2018.6034
  • Pages: 4659-4664
  • Copyright: © Sun et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

The aim of this study was to investigate the roles of AMP-activated protein kinase α subunit (AMPKα), hypersensitive C-reactive protein (hs-CRP) and Fcγ receptor (FcγR) in diabetic nephropathy and drug intervention effects. Sixty Sprague Dawley male rats were randomly divided into the control (n=30) and observation (n=30) groups. The model of type 2 diabetic nephropathy was established by high-fat and high-glucose diet and streptozotocin injection. The rats in the observation group were treated with baicalein and the rats in control group did not receive any drug intervention. The pathological changes of kidneys were observed by hematoxylin and eosin (H&E) staining. The expression of AMPKα mRNA in renal tissue was detected by reverse transcription-polymerase chain reaction (RT-PCR). The levels of hs-CRP and FcγR were measured by enzyme‑linked immunosorbent assay (ELISA) at 1, 4, 6 and 8 weeks after drug intervention and blood urea nitrogen (BUN) and the 24 h urinary micro-albumin (U-ALB) levels were compared at 1, 4, 6 and 8 weeks after intervention. After 8 weeks of drug intervention, the pathological changes of kidneys in the observation group were significantly lower than those in the control group (p<0.05), while the relative expression levels of AMPKα mRNA and protein in the control group were higher than those in the observation group (p<0.05). The levels of hs-CRP, BUN and 24 h U-ALB in the control group were significantly higher than those in the observation group at different time-points after drug intervention and the level of FcγR in the control group was significantly lower than that in the observation group (p<0.05). Baicalein may protect renal function by inhibiting the expression of AMPKα and inflammatory reaction, and can also decrease BUN and 24 h U-ALB levels and improve the pathological changes of the kidney.
View Figures
View References

Related Articles

Journal Cover

June-2018
Volume 15 Issue 6

Print ISSN: 1792-0981
Online ISSN:1792-1015

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Sun P, Lu L, Chen J, Liu X, Zhang Q and Wang X: AMPKα, hs-CRP and FcγR in diabetic nephropathy and drug intervention. Exp Ther Med 15: 4659-4664, 2018
APA
Sun, P., Lu, L., Chen, J., Liu, X., Zhang, Q., & Wang, X. (2018). AMPKα, hs-CRP and FcγR in diabetic nephropathy and drug intervention. Experimental and Therapeutic Medicine, 15, 4659-4664. https://doi.org/10.3892/etm.2018.6034
MLA
Sun, P., Lu, L., Chen, J., Liu, X., Zhang, Q., Wang, X."AMPKα, hs-CRP and FcγR in diabetic nephropathy and drug intervention". Experimental and Therapeutic Medicine 15.6 (2018): 4659-4664.
Chicago
Sun, P., Lu, L., Chen, J., Liu, X., Zhang, Q., Wang, X."AMPKα, hs-CRP and FcγR in diabetic nephropathy and drug intervention". Experimental and Therapeutic Medicine 15, no. 6 (2018): 4659-4664. https://doi.org/10.3892/etm.2018.6034