Lespedeza davurica (Lax.) Schindl. extract protects against cytokine-induced β-cell damage and streptozotocin-induced diabetes.
Bhesh Raj SharmaDong Young RhyuPublished in: BioMed research international (2015)
Lespedeza has been used for the management of diabetes in folklore medicine. The purpose of this study is to investigate the protective effects of the methanol extract of Lespedeza davurica (LD) on cytokine-induced β-cell damage and streptozotocin- (STZ-) induced diabetes. RINm5F cells were treated with interleukin- (IL-) 1β and interferon- (IFN-) γ to induce pancreatic β-cell damage. The exposure of LD extract significantly decreased cell death, nitric oxide (NO) production, nitric oxide synthase (iNOS) expression, and nucleus factor-kappa B (NF-κB) p65 activation. Antidiabetic effects of LD extract were observed by oral glucose tolerance test (OGTT) in normal rats and by checking the biochemical, physiological, and histopathological parameters in STZ-induced diabetic rats. In OGTT, glucose clearance levels improved by oral treatment of LD extract. The water intake, urine volume, blood glucose, and serum TG, TC, TBARS, and DPP-IV levels were significantly decreased, and liver glycogen content was significantly increased by treatment of LD extract (250 mg/kg BW) in STZ-induced diabetic rats. Also, insulin immunoreactivity of the pancreases was increased in LD extract administrated rats compared with diabetic control rats. These results indicate that LD extract may protect pancreatic β-cell damage and regulate the blood glucose in STZ-induced diabetic rats.
Keyphrases
- diabetic rats
- oxidative stress
- induced apoptosis
- blood glucose
- nitric oxide
- type diabetes
- glycemic control
- cell death
- single cell
- cardiovascular disease
- nitric oxide synthase
- cell therapy
- stem cells
- immune response
- signaling pathway
- skeletal muscle
- inflammatory response
- weight loss
- drug induced
- mesenchymal stem cells
- adipose tissue
- combination therapy
- cell proliferation
- long non coding rna
- toll like receptor
- bone marrow
- replacement therapy
- carbon dioxide
- endoplasmic reticulum stress
- weight gain