Unknown

Dataset Information

0

Maslinic acid activates renal AMPK/SIRT1 signaling pathway and protects against diabetic nephropathy in mice.


ABSTRACT:

Background

Diabetic nephropathy has been a devastating complication. Clinically, there is an urgent need for nephroprotective agents to delay the onset of diabetic nephropathy and ameliorate its symptoms. Maslinic acid is a pentacyclic triterpene acid with protective effect on multiple organs against oxidative stress and inflammation. In this research, we hypothesized that maslinic acid protects renal function against diabetic nephropathy.

Methods

C57BL/6 J male mice administrated with 50 mg/kg of Streptozocin (STZ) daily were used to establish diabetic mouse model (blood glucose levels > 300 mg/dL). Urinary levels of albumin, total proteins, and creatinine were analyzed by an automatic analyzer. H&E staining was used to evaluate renal damage. qRT-PCR and ELISA were performed to investigate the inflammation and oxidative stress in renal tissues. Western blot was used to assess the activation of AMPK signaling.

Results

Maslinic acid treatment alleviated the loss of body weight and blood glucose in diabetic mice. Renal structure and function were protected by maslinic acid in diabetic mice. 20 mg/kg maslinic acid treatment for 8 weeks significantly alleviated the oxidative stress and inflammation in the kidney of diabetic rats. Maslinic acid treatment activated the renal AMPK/SIRT1 signaling pathway.

Conclusion

Maslinic acid ameliorates diabetic nephropathy and activates the renal AMPK/SIRT1 signaling pathway.

SUBMITTER: Gao H 

PROVIDER: S-EPMC8767743 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC11294604 | biostudies-literature
| S-EPMC6902708 | biostudies-literature
| S-EPMC8064124 | biostudies-literature
| S-EPMC9038418 | biostudies-literature
| S-EPMC7845558 | biostudies-literature
| S-EPMC8120163 | biostudies-literature
| S-EPMC5833650 | biostudies-literature
| S-EPMC8109052 | biostudies-literature
| S-EPMC6515701 | biostudies-literature
| S-EPMC5248989 | biostudies-literature