Inhibition of Cochlear HMGB1 Expression Attenuates Oxidative Stress and Inflammation in an Experimental Murine Model of Noise-Induced Hearing Loss

Cells. 2021 Apr 5;10(4):810. doi: 10.3390/cells10040810.

Abstract

Noise-induced hearing loss (NIHL) is a common inner ear disease but has complex pathological mechanisms, one of which is increased oxidative stress in the cochlea. The high-mobility group box 1 (HMGB1) protein acts as an inflammatory mediator and shows different activities with redox modifications linked to the generation of reactive oxygen species (ROS). We aimed to investigate whether manipulation of cochlear HMGB1 during noise exposure could prevent noise-induced oxidative stress and hearing loss. Sixty CBA/CaJ mice were divided into two groups. An intraperitoneal injection of anti-HMGB1 antibodies was administered to the experimental group; the control group was injected with saline. Thirty minutes later, all mice were subjected to white noise exposure. Subsequent cochlear damage, including auditory threshold shifts, hair cell loss, expression of cochlear HMGB1, and free radical activity, was then evaluated. The levels of HMGB1 and 4-hydroxynonenal (4-HNE), as respective markers of reactive nitrogen species (RNS) and ROS formation, showed slight increases on post-exposure day 1 and achieved their highest levels on post-exposure day 4. After noise exposure, the antibody-treated mice showed markedly less ROS formation and lower expression of NADPH oxidase 4 (NOX4), nitrotyrosine, inducible nitric oxide synthase (iNOS), and intercellular adhesion molecule-1 (ICAM-1) than the saline-treated control mice. A significant amelioration was also observed in the threshold shifts of the auditory brainstem response and the loss of outer hair cells in the antibody-treated versus the saline-treated mice. Our results suggest that inhibition of HMGB1 by neutralization with anti-HMGB1 antibodies prior to noise exposure effectively attenuated oxidative stress and subsequent inflammation. This procedure could therefore have potential as a therapy for NIHL.

Keywords: NADPH oxidase (NOX); cochlea; high-mobility group box 1 (HMGB1); inflammation; noise-induced hearing loss (NIHL); oxidative stress; reactive nitrogen species (RNS); reactive oxygen species (ROS).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / metabolism
  • Animals
  • Antibodies, Neutralizing / pharmacology
  • Cells, Cultured
  • Cochlea / metabolism*
  • Cochlea / pathology*
  • Disease Models, Animal
  • HMGB1 Protein / metabolism*
  • Hair Cells, Auditory / drug effects
  • Hair Cells, Auditory / pathology
  • Hearing Loss, Noise-Induced / metabolism*
  • Hearing Loss, Noise-Induced / pathology*
  • Inflammation / pathology*
  • Mice
  • Mice, Inbred CBA
  • NADPH Oxidase 4 / metabolism
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism
  • Oxidative Stress*
  • Protective Agents / pharmacology
  • Reactive Oxygen Species / metabolism
  • Recombinant Proteins / metabolism
  • Up-Regulation / genetics

Substances

  • Aldehydes
  • Antibodies, Neutralizing
  • HMGB1 Protein
  • Protective Agents
  • Reactive Oxygen Species
  • Recombinant Proteins
  • Nitric Oxide Synthase Type II
  • NADPH Oxidase 4
  • 4-hydroxy-2-nonenal