4.5 Article

Cerebral small vessel endothelial structural changes predate hypertension in stroke-prone spontaneously hypertensive rats: a blinded, controlled immunohistochemical study of 5- to 21-week-old rats

Journal

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
Volume 37, Issue 7, Pages 711-726

Publisher

WILEY
DOI: 10.1111/j.1365-2990.2011.01170.x

Keywords

blood-brain barrier; immunohistochemistry; salt loading; SHRSP; small vessel disease

Funding

  1. Medical Research Council
  2. Scottish Funding Council
  3. British Heart Foundation Chair [CH98001, RG/07/005]
  4. European Union [LSHG_CT 2005-019015]
  5. Chief Scientist Office [CZB/4/517] Funding Source: researchfish
  6. Medical Research Council [G0700704B] Funding Source: researchfish

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Aims: The spontaneously hypertensive stroke-prone rat (SHRSP) is a potential animal model of human lacunar stroke, but there is little information on SHRSP small vessel pathology, especially in young rats. We investigated the structural changes that occur in cortical and subcortical vessels and adjacent tissue in SHRSP before, during and after the onset of hypertension. Methods: We examined brains from SHRSP and Wistar Kyoto rats (WKY) at 5, 16 and 21 weeks of age. Structural changes in small arterioles and adjacent tissue were studied using antibodies to investigate different components of the neurovascular unit. We quantified staining in three standard regions, at two coronal levels. Results: Immunostaining for claudin-5, a marker of endothelial tight junctions, was reduced in SHRSP at all ages compared to age-matched WKY controls. Smooth muscle actin, glial fibrillary acidic protein and ionized calcium-binding adaptor molecule 1 were increased in SHRSP vs. WKY by 16 weeks. Additionally, 21-week-old WKY and SHRSP rats fed a high-salt diet showed differences in claudin-5, glial fibrillary acidic protein and matrix metalloproteinase 9 staining compared to those fed a normal diet. Conclusion: Endothelial tight junction alterations of SHRSP rats from the earliest ages point towards increased susceptibility to blood-brain barrier dysfunction and stroke, which is exacerbated by salt loading. Salt loading may also damage the neurovascular unit in WKY controls.

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