Modified Hu-Lu-Ba-Wan Alleviates Early-Stage Diabetic Kidney Disease via Inhibiting Interleukin-17A in Mice.
10.1007/s11655-024-3919-x
- Author:
Min-Min GONG
1
;
Meng-di ZHU
1
;
Wen-Bin WU
1
;
Hui DONG
1
;
Fan WU
2
;
Jing GONG
2
;
Fu-Er LU
3
,
4
Author Information
1. Institute of Integrated Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
2. Department of Integrated Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
3. Institute of Integrated Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. felutjh88@
4. com.
- Publication Type:Journal Article
- Keywords:
Chinese medicine;
Modified Hu-Lu-Ba-Wan;
diabetic kidney disease;
early fibrosis;
inflammation;
interleukin-17A
- MeSH:
Animals;
Diabetic Nephropathies/genetics*;
Interleukin-17/antagonists & inhibitors*;
Drugs, Chinese Herbal/therapeutic use*;
Male;
Kidney/ultrastructure*;
Podocytes/metabolism*;
Mice;
Albuminuria;
Lipid Metabolism/drug effects*;
Mice, Inbred C57BL
- From:
Chinese journal of integrative medicine
2025;31(6):506-517
- CountryChina
- Language:English
-
Abstract:
OBJECTIVE:To identify the underlying molecular mechanism of Modified Hu-Lu-Ba-Wan (MHW) in alleviating renal lesions in mice with diabetic kidney disease (DKD).
METHODS:The db/db mice were divided into model group and MHW group according to a random number table, while db/m mice were settled as the control group (n=8 per group). The control and model groups were gavaged daily with distilled water [10 mL/(kg·d)], and the MHW group was treated with MHW [17.8 g/(kg·d)] for 6 weeks. After MHW administration for 6 weeks, indicators associated with glucolipid metabolism and urinary albumin were tested. Podocytes were observed by transmission electron microscopy. Kidney transcriptomics was performed after confirming therapeutic effects of MHW on DKD mice. The relevant target of MHW' effect in DKD was further determined by enzyme-linked immunosorbent assay, Western blot analysis, immunohistochemistry, and immunofluorescence staining.
RESULTS:Compared with the model group, MHW improved glucose and lipid metabolism (P<0.05), and reduced lipid deposition in the kidney. Meanwhile, MHW reduced the excretion of urinary albumin (P<0.05) and ameliorated renal damage. Transcriptomic analysis revealed that the inflammation response, particularly the interleukin-17 (IL-17) signaling pathway, may be responsible for the effect of MHW on DKD. Furtherly, our results found that MHW inhibited IL-17A and alleviated early fibrosis in the diabetic kidney.
CONCLUSION:MHW ameliorated renal damage in DKD via inhibiting IL-17A, suggesting a potential strategy for DKD therapy.
