4.7 Article

Paeoniflorin Ameliorates BiPN by Reducing IL6 Levels and Regulating PARKIN-Mediated Mitochondrial Autophagy

Journal

DRUG DESIGN DEVELOPMENT AND THERAPY
Volume 16, Issue -, Pages 2241-2259

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/DDDT.S369111

Keywords

multiple myeloma; paeoniflorin; peripheral neuropathy; mitochondria; autophagy

Funding

  1. National Natural Science Foundation of China [82074348]
  2. Taishan Scholar Project [tsqn201812145]
  3. Key Technology Research and Development Program of Shandong [2019GSF108162]
  4. Natural Science Foundation of Shandong Province [ZR2020MH388]

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This study confirmed the therapeutic effect of paeoniflorin on Bortezomib-induced peripheral neuropathy (BiPN) by reducing IL6 levels and regulating PARKIN-mediated mitochondrial autophagy and mitochondrial damage.
Background: Bortezomib-induced peripheral neuropathy (BiPN) is a common complication of multiple myeloma (MM) treatment that seriously affects the quality of life of patients. The purpose of the present study was to explore the therapeutic effect of paeoniflorin on BiPN and its possible mechanism.Methods: ELISA was used to measure the level of interleukin-6 (IL6) in the plasma of MM patients, and bioinformatics analysis was used to predict the mechanism underlying the effect of paeoniflorin on peripheral neuropathy. Cell and animal models of BiPN were constructed to evaluate mitochondrial function by measuring cell viability and mitochondrial quality and labeling mitochondria with MitoTracker Green. Nerve injury in mice with BiPN was assessed by behavioral tests, evaluation of motor nerve conduction velocity, hematoxylin-eosin (HE) staining, electron microscopy and analysis of the levels of reactive oxygen species (ROS). Western blotting and immunohistochemistry (IHC) were used to assess the expression of autophagy-related proteins.Results: In MM patients, IL6 levels were positively correlated with the degree of PN. The results of bioinformatics analysis suggested that paeoniflorin ameliorated PN by altering inflammation levels and mitochondrial autophagy. Paeoniflorin increased PC12 cell viability and mitochondrial autophagy levels, alleviated mitochondrial damage, and reduced IL6 levels. In addition, paeoniflorin effectively improved the behavior of mice with BiPN, relieved sciatic nerve injury in mice, increased the expression of LC3II/I, beclin-1, and Parkin in sciatic nerve cells, and increased the expression of LC3B and Parkin in the nerve tissue.Conclusion: The present study confirmed that paeoniflorin significantly ameliorated peripheral neuropathy (PN) caused by bortezo-mib, possibly by reducing IL6 levels to regulate PARKIN-mediated mitochondrial autophagy and mitochondrial damage.

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