Impaired function of cerebral parenchymal arterioles in experimental preeclampsia.

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  • Author(s): Johnson AC;Johnson AC; Cipolla MJ; Cipolla MJ; Cipolla MJ; Cipolla MJ
  • Source:
    Microvascular research [Microvasc Res] 2018 Sep; Vol. 119, pp. 64-72. Date of Electronic Publication: 2018 Apr 26.
  • Publication Type:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: Academic Press Country of Publication: United States NLM ID: 0165035 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-9319 (Electronic) Linking ISSN: 00262862 NLM ISO Abbreviation: Microvasc Res Subsets: MEDLINE
    • Publication Information:
      Original Publication: New York, Academic Press.
    • Subject Terms:
    • Abstract:
      Preeclampsia (PE), a dangerous hypertensive complication of pregnancy, is associated with widespread maternal vascular dysfunction. However, the effect of PE on the cerebral vasculature that can lead to stroke and cognitive decline is not well understood. We hypothesized that function of cortical parenchymal arterioles (PAs) would be impaired during PE. Using a high cholesterol diet to induce experimental PE in rats (ePE), we studied the function and structure of isolated and pressurized PAs supplying frontoparietal white matter (WM) tracts and cortex and compared to normal pregnant (Preg) and nonpregnant (Nonpreg) Sprague Dawley rats (n = 8/group). Myogenic reactivity and tone were similar between groups; however, constriction to intermediate-conductance calcium-activated potassium (IK) channel inhibition was diminished and dilation to inward-rectifying K + (K IR ) channel activation was impaired in PAs from ePE rats, suggesting altered ion channel function. Conducted vasodilation was significantly delayed in response to 12 mM KCl, but not 10 μM adenosine, in PAs from ePE rats versus Preg and Nonpreg rats (940 ± 300 ms vs. 70 ± 50 ms and 370 ± 90 ms; p < 0.05). Overall, dysfunction of PAs supplying frontoparietal WM and gray matter was present in ePE. If persistent these changes could potentiate neuronal injury that over time could contribute to WM lesions and early-onset cognitive decline.
      (Copyright © 2018 Elsevier Inc. All rights reserved.)
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    • Grant Information:
      R01 NS045940 United States NS NINDS NIH HHS; R01 NS108455 United States NS NINDS NIH HHS
    • Contributed Indexing:
      Keywords: Cerebral arterioles; Cerebrovascular dysfunction; Conducted vasodilation; Preeclampsia; Pregnancy
    • Accession Number:
      0 (Biomarkers)
      0 (Inflammation Mediators)
      0 (Intermediate-Conductance Calcium-Activated Potassium Channels)
      0 (Potassium Channels, Inwardly Rectifying)
    • Publication Date:
      Date Created: 20180430 Date Completed: 20190128 Latest Revision: 20240827
    • Publication Date:
      20240827
    • Accession Number:
      PMC6005767
    • Accession Number:
      10.1016/j.mvr.2018.04.007
    • Accession Number:
      29705580