mTOR/ULK1 signaling axis mediated ultrashort wave regulation of autophagy to alleviate diabetic kidney disease

Adv Clin Exp Med. 2023 Nov;32(11):1265-1277. doi: 10.17219/acem/161733.

Abstract

Background: Diabetic kidney disease (DKD) is closely related to autophagy and inflammation. The mTOR/unc-51 like autophagy activating kinase 1 (ULK1) signaling axis is involved in the regulation of autophagy. Ultrashort wave (USW) therapy has been extensively studied in inflammatory diseases. However, the therapeutic effect of USW on DKD and the role of the mTOR/ULK1 signaling axis in USW interventions remain uncertain.

Objectives: This study aimed to explore the therapeutic effects of USW on DKD rats and the role of the mTOR/ULK1 signaling axis in USW interventions.

Material and methods: A DKD rat model was established using a high-fat diet (HFD)/sugar diet and streptozocin (STZ) induction. The optimal duration of USW intervention was determined using different USW treatments. The levels of metabolism, inflammation and fibrosis associated with kidney injury in rats were measured. Western blot analysis was performed on the related indexes of autophagy and the mTOR/ULK1 signaling axis.

Results: In DKD rats, microalbuminuria (MAU), glucose (GLU), creatinine (CRE), and blood urea nitrogen (BUN) levels decreased after the USW intervention. Levels of interleukin (IL)-1β, inducible nitric oxide synthase (iNOS), immunoglobulin M (IgM), immunoglobulin G (IgG), IL-18, tumor necrosis factor alpha (TNF-α), and IL-6 decreased in the USW group compared to the model group. The IL-10 and arginase (Arg-1) levels were increased in the USW group. The content of fibrosis-related indexes (vascular endothelial growth factor (VEGF), fibronectin (FN), type IV collagen, and type I collagen) decreased in the urine of the DKD rats. After USW treatment, LC3B and Beclin1 levels increased, while the level of p62 decreased. The levels of nephrin, podocin and synaptopodin increased. Ultrashort wave could reduce p-mTOR/mTOR ratios and increase ULK1 expression. After the overexpression of ULK1, the levels of LC3B and Beclin1 were higher in the overexpression (oe)-ULK1 group than in the oe-negative control (NC) group, while the level of p62 decreased. After mTOR activation, LC3B and ULK1 expression decreased, while CRE, BUN, MAU, and GLU levels increased.

Conclusions: Ultrashort wave alleviated kidney injury induced by the HFD/sugar diet and STZ. The USW intervention reversed the decreased autophagy levels in the DKD rats. The mTOR/ULK1 signaling axis mediated USW to promote autophagy.

Keywords: autophagy; diabetic kidney disease (DKD); inflammation; mTOR/ULK1 signaling axis; ultrashort wave (USW).

MeSH terms

  • Animals
  • Autophagy
  • Autophagy-Related Protein-1 Homolog / metabolism
  • Beclin-1 / pharmacology
  • Diabetes Mellitus*
  • Diabetic Nephropathies* / etiology
  • Diabetic Nephropathies* / prevention & control
  • Fibrosis
  • Inflammation
  • Rats
  • Sugars / pharmacology
  • TOR Serine-Threonine Kinases / metabolism
  • Vascular Endothelial Growth Factor A

Substances

  • Beclin-1
  • Vascular Endothelial Growth Factor A
  • TOR Serine-Threonine Kinases
  • Sugars
  • mTOR protein, rat
  • ULK1 protein, rat
  • Autophagy-Related Protein-1 Homolog