Acutely Inhibiting AQP4 With TGN-020 Improves Functional Outcome by Attenuating Edema and Peri-Infarct Astrogliosis After Cerebral Ischemia

Front Immunol. 2022 May 3:13:870029. doi: 10.3389/fimmu.2022.870029. eCollection 2022.

Abstract

Background: Ischemic stroke is one of the leading causes of human death and disability. Brain edema and peri-infarct astrocyte reactivity are crucial pathological changes, both involving aquaporin-4 (AQP4). Studies revealed that acute inhibition of AQP4 after stroke diminishes brain edema, however, its effect on peri-infarct astrocyte reactivity and the subacute outcome is unclear. And if diffusion-weighted imaging (DWI) could reflect the AQP4 expression patterns is uncertain.

Methods: Rats were subjected to middle cerebral artery occlusion (MCAO) and allocated randomly to TGN 020-treated and control groups. One day after stroke, brain swelling and lesion volumes of the rats were checked using T2-weighted imaging (T2-WI). Fourteen days after stroke, the rats successively underwent neurological examination, T2-WI and DWI with standard b-values and ultra-high b-values, apparent diffusion coefficient (ADC) was calculated correspondingly. Finally, the rats' brains were acquired and used for glial fibrillary acidic protein (GFAP) and AQP4 immunoreactive analysis.

Results: At 1 day after stroke, the TGN-020-treated animals exhibited reduced brain swelling and lesion volumes compared with those in the control group. At 14 days after stroke, the TGN-020-treated animals showed fewer neurological function deficits and smaller lesion volumes. In the peri-infarct region, the control group showed evident astrogliosis and AQP4 depolarization, which were reduced significantly in the TGN-020 group. In addition, the ultra-high b-values of ADC (ADCuh) in the peri-infarct region of the TGN-020 group was higher than that of the control group. Furthermore, correlation analysis revealed that peri-infarct AQP4 polarization correlated negatively with astrogliosis extent, and ADCuh correlated positively with AQP4 polarization.

Conclusion: We found that acutely inhibiting AQP4 using TGN-020 promoted neurological recovery by diminishing brain edema at the early stage and attenuating peri-infarct astrogliosis and AQP4 depolarization at the subacute stage after stroke. Moreover, ADCuh could reflect the AQP4 polarization.

Keywords: AQP4 polarization; astrogliosis; glymphatic system; ischemic stroke; ultra-high b-values diffusion weighted imaging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aquaporin 4 / biosynthesis
  • Brain Edema* / diagnostic imaging
  • Brain Edema* / metabolism
  • Brain Edema* / pathology
  • Brain Edema* / prevention & control
  • Brain Ischemia / diagnostic imaging
  • Brain Ischemia / drug therapy
  • Brain Ischemia / metabolism
  • Brain Ischemia / pathology
  • Gliosis* / diagnostic imaging
  • Gliosis* / metabolism
  • Gliosis* / pathology
  • Gliosis* / prevention & control
  • Infarction, Middle Cerebral Artery* / diagnostic imaging
  • Infarction, Middle Cerebral Artery* / drug therapy
  • Infarction, Middle Cerebral Artery* / metabolism
  • Infarction, Middle Cerebral Artery* / pathology
  • Magnetic Resonance Imaging
  • Niacinamide / analogs & derivatives
  • Niacinamide / therapeutic use
  • Rats
  • Stroke / diagnostic imaging
  • Stroke / drug therapy
  • Stroke / metabolism
  • Stroke / pathology
  • Thiadiazoles / therapeutic use

Substances

  • 2-(nicotinamide)-1,3,4-thiadiazole
  • Aqp4 protein, rat
  • Aquaporin 4
  • Thiadiazoles
  • Niacinamide