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Placental ischemia in pregnant rats impairs cerebral blood flow autoregulation and increases blood-brain barrier permeability

  • Junie P. Warrington
    ,
  • ,
  • Sydney R. Murphy
    ,
  • Richard J. Roman
    ,
  • Heather A. Drummond
    ,
  • Joey P. Granger
*Corresponding author for this work
  • University of Mississippi
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Cerebrovascular events contribute to ~40% of preeclampsia/eclampsia-related deaths, and neurological symptoms are common among preeclamptic patients. We previously reported that placental ischemia, induced by reducing uteroplacental perfusion pressure, leads to impaired myogenic reactivity and cerebral edema in the pregnant rat. Whether the impaired myogenic reactivity is associated with altered cerebral blood flow (CBF) autoregulation and the edema is due to altered blood-brain barrier (BBB) permeability remains unclear. Therefore, we tested the hypothesis that placental ischemia leads to impaired CBF autoregulation and a disruption of the BBB. CBF autoregulation, measured in vivo by laser Doppler flowmetry, was significantly impaired in placental ischemic rats. Brain water content was increased in the anterior cerebrum of placental ischemic rats and BBB permeability, assayed using the Evans blue extravasation method, was increased in the anterior cerebrum. The expression of the tight junction proteins: claudin-1 was increased in the posterior cerebrum, while zonula occludens-1, and occludin, were not significantly altered in either the anterior or posterior cerebrum. These results are consistent with the hypothesis that placental ischemia mediates anterior cerebral edema through impaired CBF autoregulation and associated increased transmission of pressure to small vessels that increases BBB permeability leading to cerebral edema.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e12134

Journal (Volume, Issue Number)

Physiological reports (Volume 2, Issue 8)

Publication milestones

  • Published - 2014

Publication status

Published - 2014

Publication IDs

  • Scopus: 85002579742

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Funding Details

Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health under Award Number P20GM104357, the National Heart, Lung, and Blood Institute of the National Institutes of Health under Award Number P01HL051971, the National Heart, Lung, and Blood Institute of the National Institutes of Health under Award Number R01HL108618, HL36279 and American Heart Association grant AHA 13POST16240000. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or the American Heart Association.