Effect of N-(2-aminoethyl) ethanolamine on hypertrophic scarring changes in vitro: Finding novel anti-fibrotic therapies

Toxicol Appl Pharmacol. 2019 Jan 1:362:9-19. doi: 10.1016/j.taap.2018.09.026. Epub 2018 Sep 22.

Abstract

Hypertrophic scars (HS) limit movement, decrease quality of life, and remain a major impediment to rehabilitation from burns. However, no effective pharmacologic therapies for HS exist. Here we tested the in vitro anti-fibrotic effects of the novel chemical N-(2-aminoethyl) ethanolamine (AEEA) at non-toxic concentrations. Scanning electron microscopy showed that AEEA markedly altered the structure of the extracellular matrix (ECM) produced by primary dermal fibroblasts isolated from a HS of a burn patient (HTS). Compression atomic force microscopy revealed that AEEA stiffened the 3D nanostructure of ECM formed by HTS fibroblasts. Western blot analysis in three separate types of primary human dermal fibroblasts (including HTS) showed that AEEA exposure increased the extractability of type I collagen in a dose- and time-dependent fashion, while not increasing collagen synthesis. A comparison of the electrophoretic behavior of the same set of samples under native and denaturing conditions suggested that AEEA alters the 3D structure of type I collagen. The antagonization effect of AEEA to TGF-β1 on ECM formation was also observed. Furthermore, analyses of the anti-fibrotic effects of analogs of AEEA (with modified pharmacophores) suggest the existence of a chemical structure-activity relationship. Thus, AEEA and its analogs may inhibit HS development; further study and optimization of analogs may be a promising strategy for the discovery for effective HS therapies.

Keywords: Atomic Force Microscopy (AFM); Collagen; Drug Discovery; Scanning Electron Microscopy (SEM); Wound Healing.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cicatrix, Hypertrophic / drug therapy*
  • Cicatrix, Hypertrophic / metabolism
  • Collagen / metabolism
  • Ethanolamines / pharmacology*
  • Extracellular Matrix / drug effects
  • Fibroblasts / drug effects*
  • Fibroblasts / metabolism
  • Fibrosis
  • Humans
  • Structure-Activity Relationship
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Ethanolamines
  • TGFB1 protein, human
  • Transforming Growth Factor beta1
  • Collagen