4.7 Article

Salidroside from Rhodiola rosea L. attenuates diabetic nephropathy in STZ induced diabetic rats via anti-oxidative stress, anti-inflammation, and inhibiting TGF-β1/Smad pathway

Journal

JOURNAL OF FUNCTIONAL FOODS
Volume 77, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jff.2020.104329

Keywords

Salidroside; Diabetes; Renal pathology; Fibrosis

Funding

  1. Natural Science Project of Shaanxi Science and Technology Department [2020JM-601]
  2. Key research project of Education Department of Shaanxi Province [20JY005]
  3. open project of Shaanxi Provincial Key Laboratory of Resource Biology [SLGPT2019KF03-06]
  4. Key Laboratory of Se-enriched Products Development and Quality Control, Ministry of Agriculture and Rural Affairs/National-Local Joint Engineering Laboratory of Se-enriched Food Development [Se-2020C05]

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Salidroside from Rhodiola rosea L. has beneficial effects on diabetic nephropathy in rats, including improving blood glucose, kidney pathology, oxidative defense system activity, and decreasing inflammatory cytokines. The main mechanisms are anti-inflammatory, anti-oxidative stress, and inhibition of the TGF-beta 1/Smad2/3 pathway. This suggests that salidroside could be a useful nutrient for treating DN and diabetes.
Salidroside from Rhodiola rosea L. has hypoglycemic effects, and has anti-osteoporosis effect in diabetic rats. Whether it has beneficial effects on diabetic nephropathy (DN) has not been fully reported. Here, a DN rat model was established by streptozotocin (STZ). Salidroside (10, and 20 mg kg(-1) d(-1)) were orally giving for eight weeks. The purity of salidroside was 99%. The results showed that eight weeks salidroside supplementation dosedependently decreased blood glucose, serum insulin, serum creatinine, blood urea nitrogen (BUN), as well as urinary albumin of DN rats, repaired the pathological changes of kidney tissue, the renal sclerosis and fibrosis in the kidney of DN rats were improved, and the activities of oxidative defense system associated enzyme such as superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX) were also improved. Serum inflammatory cytokines (including tumor necrosis factor-alpha, monocyte chemoattractant protein-1, interleukin-18, and interleukin-6) were decreased significantly in DN rats after eight weeks salidroside supplementation. Immunohistochemical results showed that fibrosis related proteins such as transforming growth factor-beta 1 (TGF-beta 1), phospho-Smad2 (p-Smad2), and phospho-Smad3 (p-Smad3) expression levels were decreased significantly in the kidney of salidroside treated group. Our results indicate that daily salidroside consumption could alleviate DN in rats, the main mechanisms are anti-inflammatory, anti-oxidative stress, and inhibition of the TGF-beta 1/Smad2/3 pathway. This study suggested that salidroside could be used as a nutrient against DN, as well as diabetes.

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