Oleuropein Supplementation Ameliorates Long-Course Diabetic Nephropathy and Diabetic Cardiomyopathy Induced by Advanced Stage of Type 2 Diabetes in db / db Mice.
Shujuan ZhengRuixuan GengJingya GuoSeong-Gook KangKunlun HuangTao TongPublished in: Nutrients (2024)
Previous studies have reported the therapeutic effects of oleuropein (OP) consumption on the early stage of diabetic nephropathy and diabetic cardiomyopathy. However, the efficacy of OP on the long-course of these diabetes complications has not been investigated. Therefore, in this study, to investigate the relieving effects of OP intake on these diseases, and to explore the underlying mechanisms, db / db mice (17-week-old) were orally administrated with OP (200 mg/kg bodyweight) for 15 weeks. We found that OP reduced expansion of the glomerular mesangial matrix, renal inflammation, renal fibrosis, and renal apoptosis. Meanwhile, OP treatment exerted cardiac anti-fibrotic, anti-inflammatory, and anti-apoptosis effects. Notably, transcriptomic and bioinformatic analyses indicated 290 and 267 differentially expressed genes in the kidney and heart replying to OP treatment, respectively. For long-course diabetic nephropathy, OP supplementation significantly upregulated the cyclic guanosine monophosphate-dependent protein kinase (cGMP-PKG) signaling pathway. For long-course diabetic cardiomyopathy, p53 and cellular senescence signaling pathways were significantly downregulated in response to OP supplementation. Furthermore, OP treatment could significantly upregulate the transcriptional expression of the ATPase Na + /K + transporting subunit alpha 3, which was enriched in the cGMP-PKG signaling pathway. In contrast, OP treatment could significantly downregulate the transcriptional expressions of cyclin-dependent kinase 1, G two S phase expressed protein 1, and cyclin B2, which were enriched in p53 and cellular senescence signal pathways; these genes were confirmed by qPCR validation. Overall, our findings demonstrate that OP ameliorated long-course diabetic nephropathy and cardiomyopathy in db / db mice and highlight the potential benefits of OP as a functional dietary supplement in diabetes complications treatment.
Keyphrases
- diabetic nephropathy
- signaling pathway
- early stage
- protein kinase
- type diabetes
- heart failure
- oxidative stress
- cardiovascular disease
- gene expression
- endothelial cells
- magnetic resonance
- nitric oxide
- squamous cell carcinoma
- cell cycle
- computed tomography
- magnetic resonance imaging
- systemic sclerosis
- poor prognosis
- left ventricular
- epithelial mesenchymal transition
- randomized controlled trial
- physical activity
- atrial fibrillation
- genome wide
- adipose tissue
- skeletal muscle
- stress induced
- long non coding rna
- induced apoptosis
- high resolution
- risk assessment
- weight loss
- replacement therapy
- idiopathic pulmonary fibrosis
- atomic force microscopy
- wound healing
- liver fibrosis
- human health
- bioinformatics analysis
- contrast enhanced