Cordycepin attenuates traumatic brain injury-induced impairments of blood-brain barrier integrity in rats

Brain Res Bull. 2016 Oct:127:171-176. doi: 10.1016/j.brainresbull.2016.09.010. Epub 2016 Sep 16.

Abstract

Loss of blood-brain barrier (BBB) integrity is a downstream event caused by traumatic brain injury (TBI). BBB integrity is affected by certain physiological conditions, including inflammation and oxidative stress. Cordycepin is a susbtance with anti-inflammatory and anti-oxidative effects. Therefore, it is necessary to investigate whether cordycepin affects TBI-induced impairments of BBB integrity. Using TBI rats as the in vivo model and applying multiple techniques, including stroke severity evaluation, Evans blue assessment, quantitative real-time PCR, Western blotting and ELISA, we investigated the dose-dependent protective effects of cordycepin on the TBI-induced impairments of BBB integrity. Cordycepin treatment attenuated the TBI-induced impairments in a dose-dependent manner, and played a role in protecting BBB integrity. Cordycepin was able to alleviate TBI-induced loss of tight junction proteins zonula occludens protein-1 (ZO-1) and occludin, which are important for BBB integrity. Moreover, cordycepin suppressed pro-inflammatory factors, including IL-1β, iNOS, MPO and MMP-9, and promoted anti-inflammation-associated factors arginase 1 and IL-10. Furthermore, cordycepin inhibited NADPH oxidase (NOX) expression and activity following TBI, probably through NOX1, but not NOX2 and NOX4. Cordycepin has protective effects against brain damages induced by TBI. The protection of cordycepin on BBB integrity was probably achieved through recovery of tight junction proteins, inhibition of local inflammation, and prevention of NOX activity.

Keywords: Anti-inflammatory; Anti-oxidative; Blood-brain barrier integrity; Cordycepin; Neuroprotective; Traumatic brain injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / drug effects*
  • Blood-Brain Barrier / metabolism
  • Blood-Brain Barrier / pathology
  • Brain Injuries, Traumatic / drug therapy*
  • Brain Injuries, Traumatic / metabolism
  • Brain Injuries, Traumatic / pathology
  • Deoxyadenosines / pharmacology*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Interleukin-10 / metabolism
  • Interleukin-1beta / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • NADPH Oxidases / antagonists & inhibitors
  • NADPH Oxidases / metabolism
  • Neuroprotective Agents / pharmacology*
  • Nitric Oxide Synthase Type II / metabolism
  • Occludin / metabolism
  • Rats, Sprague-Dawley
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Deoxyadenosines
  • IL1B protein, rat
  • Interleukin-1beta
  • Neuroprotective Agents
  • Occludin
  • Ocln protein, rat
  • Tjp1 protein, rat
  • Zonula Occludens-1 Protein
  • Interleukin-10
  • Nitric Oxide Synthase Type II
  • Nos2 protein, rat
  • NADPH Oxidases
  • Matrix Metalloproteinase 9
  • Mmp9 protein, rat
  • cordycepin