Damage to the blood‑brain barrier and activation of neuroinflammation by focal cerebral ischemia under hyperglycemic condition

Int J Mol Med. 2021 Jul;48(1):142. doi: 10.3892/ijmm.2021.4975. Epub 2021 Jun 3.

Abstract

Hyperglycemia aggravates brain damage caused by cerebral ischemia/reperfusion (I/R) and increases the permeability of the blood‑brain barrier (BBB). However, there are relatively few studies on morphological changes of the BBB. The present study aimed to investigate the effect of hyperglycemia on BBB morphological changes following cerebral I/R injury. Streptozotocin‑induced hyperglycemic and citrate‑buffered saline‑injected normoglycemic rats were subjected to 30 min middle cerebral artery occlusion. Neurological deficits were evaluated. Brain infarct volume was assessed by 2,3,5‑triphenyltetrazolium chloride staining and BBB integrity was evaluated by Evans blue and IgG extravasation following 24 h reperfusion. Changes in tight junctions (TJ) and basement membrane (BM) proteins (claudin, occludin and zonula occludens‑1) were examined using immunohistochemistry and western blotting. Astrocytes, microglial cells and neutrophils were labeled with specific antibodies for immunohistochemistry after 1, 3 and 7 days of reperfusion. Hyperglycemia increased extravasations of Evan's blue and IgG and aggravated damage to TJ and BM proteins following I/R injury. Furthermore, hyperglycemia suppressed astrocyte activation and damaged astrocytic endfeet surrounding cerebral blood vessels following I/R. Hyperglycemia inhibited microglia activation and proliferation and increased neutrophil infiltration in the brain. It was concluded that hyperglycemia‑induced BBB leakage following I/R might be caused by damage to TJ and BM proteins and astrocytic endfeet. Furthermore, suppression of microglial cells and increased neutrophil infiltration to the brain may contribute to the detrimental effects of pre‑ischemic hyperglycemia on the outcome of cerebral ischemic stroke.

Keywords: blood‑brain barrier; cerebral ischemia; diabetes; hyperglycemia; neurovascular unit; reperfusion injury.

MeSH terms

  • Animals
  • Astrocytes / metabolism
  • Astrocytes / pathology
  • Basement Membrane* / metabolism
  • Basement Membrane* / pathology
  • Blood-Brain Barrier* / metabolism
  • Blood-Brain Barrier* / pathology
  • Brain Ischemia* / metabolism
  • Brain Ischemia* / pathology
  • Hyperglycemia* / metabolism
  • Hyperglycemia* / pathology
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Tight Junctions* / metabolism
  • Tight Junctions* / pathology

Grants and funding

The present study was supported by the National Natural Science Foundation of China (grant nos. 31960177 and 31780280) and the Natural Science Foundation of Ningxia (grant no. 2018AAC03092).