Puerarin ameliorates retinal ganglion cell damage induced by retinal ischemia/reperfusion through inhibiting the activation of TLR4/NLRP3 inflammasome

Life Sci. 2020 Sep 1:256:117935. doi: 10.1016/j.lfs.2020.117935. Epub 2020 Jun 9.

Abstract

Aims: Retinal ischemia/reperfusion (I/R) injury is common in the development of ophthalmic diseases and potentially causes blindness. In present study, the aim is to investigate the possible protective effects of puerarin on retinal I/R.

Main methods: Retinal I/R injury was conducted on the left eyes of male Sprague Dawley rats, which were subsequently received treatment with puerarin. After administration, retinal I/R-induced apoptosis, oxidative stress and inflammatory responses were detected. Meanwhile, we purified retinal ganglion cells (RGCs) from 7-day-old rats. After subjected RGCs to oxygen and glucose deprivation/reoxygenation (OGD/R), apoptosis and TLR4/NLRP3 inflammasome activation in RGCs were detected.

Key findings: Puerarin prominently suppressed apoptosis, alleviated oxidative stress and suppressed TLR4/NLRP3 inflammasome activation in rats with retinal I/R injury. Consistent with our in vivo study, we found puerarin ameliorated retinal I/R injury through suppressing apoptosis and TLR4/NLRP3 inflammasome activation in RGCs.

Significance: Our findings reveal that puerarin plays a protective role against retinal I/R injury by alleviating RGC damage, and is beneficial for the treatment of I/R injury-caused ophthalmic diseases.

Keywords: Puerarin; Retinal ganglion cells; Retinal ischemia/reperfusion; TLR4/NLRP3 inflammasome.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Humans
  • Inflammasomes / metabolism
  • Isoflavones / pharmacology*
  • Male
  • Models, Animal
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism
  • Oxidative Stress / drug effects
  • Rats, Sprague-Dawley
  • Reperfusion Injury / drug therapy*
  • Retina / metabolism
  • Retinal Diseases / drug therapy*
  • Retinal Ganglion Cells / metabolism*
  • Signal Transduction
  • Toll-Like Receptor 4 / metabolism

Substances

  • Inflammasomes
  • Isoflavones
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Toll-Like Receptor 4
  • puerarin