Natural polysaccharides as potential anti-fibrotic agents: A review of their progress

Life Sci. 2022 Nov 1:308:120953. doi: 10.1016/j.lfs.2022.120953. Epub 2022 Sep 11.

Abstract

Fibrosis, as a common disease which could be found in nearly all organs, is normally initiated by organic injury and eventually ended in cellular dysfunction and organ failure. Currently, effective and safe therapeutic strategies targeting fibrogenesis still in highly demand. Natural polysaccharides derived from natural resources possess promising anti-fibrosis potential, with no deleterious side effects. Based on the etiology and pathogenesis of fibrosis, this review summarizes the intervention effects and mechanisms of natural polysaccharides in the prevention and treatment of fibrosis. Natural polysaccharides are able to regulate each phase of the fibrogenic response, including primary injury to organs, activation of effector cells, the elaboration of extracellular matrix (ECM) and dynamic deposition. In addition, polysaccharides significantly reduce fibrosis levels in multiple organs including heart, lung, liver and kidney. The investigation of the pathogenesis of fibrosis indicates that mechanisms including the inhibition of TGF-β/Smad, NF-κB, HMGB1/TLR4, cAMP/PKA signaling pathways, MMPs/TIMPs system as well as microRNAs are promising therapeutic targets. Natural polysaccharides can target these mediators or pathways to alleviate fibrosis. The information reviewed here offer new insights into the understanding the protective role of natural polysaccharides against fibrosis, help design further experimental studies related to polysaccharides and fibrotic responses, and shed light on a potential treatment for fibrosis.

Keywords: Antifibrotic drug; Natural product; Polysaccharide; Therapy target; Tissue fibrosis.

Publication types

  • Review

MeSH terms

  • Antifibrotic Agents
  • Fibrosis
  • HMGB1 Protein*
  • Humans
  • MicroRNAs*
  • NF-kappa B
  • Polysaccharides / pharmacology
  • Polysaccharides / therapeutic use
  • Toll-Like Receptor 4
  • Transforming Growth Factor beta / metabolism

Substances

  • Antifibrotic Agents
  • HMGB1 Protein
  • MicroRNAs
  • NF-kappa B
  • Polysaccharides
  • Toll-Like Receptor 4
  • Transforming Growth Factor beta