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Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease

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Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease. / Dorr, Adrienne; Sahota, Bhupinder; Chinta, Lakshminarayan V. et al.
In: Brain, Vol. 135, No. 10, 01.10.2012, p. 3039-3050.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Dorr, A, Sahota, B, Chinta, LV, Brown, ME, Lai, AY, Ma, K, Hawkes, CA, McLaurin, J & Stefanovic, B 2012, 'Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease', Brain, vol. 135, no. 10, pp. 3039-3050. https://doi.org/10.1093/brain/aws243

APA

Dorr, A., Sahota, B., Chinta, L. V., Brown, M. E., Lai, A. Y., Ma, K., Hawkes, C. A., McLaurin, J., & Stefanovic, B. (2012). Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease. Brain, 135(10), 3039-3050. https://doi.org/10.1093/brain/aws243

Vancouver

Dorr A, Sahota B, Chinta LV, Brown ME, Lai AY, Ma K et al. Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease. Brain. 2012 Oct 1;135(10):3039-3050. doi: 10.1093/brain/aws243

Author

Dorr, Adrienne ; Sahota, Bhupinder ; Chinta, Lakshminarayan V. et al. / Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease. In: Brain. 2012 ; Vol. 135, No. 10. pp. 3039-3050.

Bibtex

@article{99172d600e154d7a982d041354368dbd,
title = "Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease",
abstract = "The majority of patients with Alzheimer's disease have cerebral amyloid angiopathy, thus showing deposition of amyloid-β peptides in the walls of leptomeningeal and cortical arterioles. These deposits are believed to result from impaired clearance of parenchymal amyloid-β peptides. In the current work, we examined the changes in cortical microvascular structure and function in situ in TgCRND8, a transgenic mouse model of Alzheimer's disease. In contrast to venules, cortical arterioles were shown to increase in tortuosity and decrease in calibre with amyloid-β peptide accumulation. These structural changes were accompanied by progressive functional compromise, reflected in higher dispersion of microvascular network transit times, elongation of the transit times, and impaired microvascular reactivity to hypercapnia in the transgenic mice. Moreover, inhibition of amyloid-β peptide oligomerization and fibrillization via post-weaning administration of scyllo-inositol, a naturally occurring stereoisomer of myo-inositol, rescued both structural and functional impairment of the cortical microvasculature in this Alzheimer's disease model. These results demonstrate that microvascular impairment is directly correlated with amyloid-β accumulation and highlight the importance of targeting cerebrovascular amyloid angiopathy clearance for effective diagnosis, monitoring of disease progression and treatment of Alzheimer's disease.",
keywords = "cerebral amyloid angiopathy, microvasculature, scyllo-inositol, two-photon fluorescence microscopy, vessel tortuosity",
author = "Adrienne Dorr and Bhupinder Sahota and Chinta, {Lakshminarayan V.} and Brown, {Mary E.} and Lai, {Aaron Y.} and Keran Ma and Hawkes, {Cheryl A.} and Joanne McLaurin and Bojana Stefanovic",
year = "2012",
month = oct,
day = "1",
doi = "10.1093/brain/aws243",
language = "English",
volume = "135",
pages = "3039--3050",
journal = "Brain",
issn = "0006-8950",
publisher = "Oxford University Press",
number = "10",

}

RIS

TY - JOUR

T1 - Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer's disease

AU - Dorr, Adrienne

AU - Sahota, Bhupinder

AU - Chinta, Lakshminarayan V.

AU - Brown, Mary E.

AU - Lai, Aaron Y.

AU - Ma, Keran

AU - Hawkes, Cheryl A.

AU - McLaurin, Joanne

AU - Stefanovic, Bojana

PY - 2012/10/1

Y1 - 2012/10/1

N2 - The majority of patients with Alzheimer's disease have cerebral amyloid angiopathy, thus showing deposition of amyloid-β peptides in the walls of leptomeningeal and cortical arterioles. These deposits are believed to result from impaired clearance of parenchymal amyloid-β peptides. In the current work, we examined the changes in cortical microvascular structure and function in situ in TgCRND8, a transgenic mouse model of Alzheimer's disease. In contrast to venules, cortical arterioles were shown to increase in tortuosity and decrease in calibre with amyloid-β peptide accumulation. These structural changes were accompanied by progressive functional compromise, reflected in higher dispersion of microvascular network transit times, elongation of the transit times, and impaired microvascular reactivity to hypercapnia in the transgenic mice. Moreover, inhibition of amyloid-β peptide oligomerization and fibrillization via post-weaning administration of scyllo-inositol, a naturally occurring stereoisomer of myo-inositol, rescued both structural and functional impairment of the cortical microvasculature in this Alzheimer's disease model. These results demonstrate that microvascular impairment is directly correlated with amyloid-β accumulation and highlight the importance of targeting cerebrovascular amyloid angiopathy clearance for effective diagnosis, monitoring of disease progression and treatment of Alzheimer's disease.

AB - The majority of patients with Alzheimer's disease have cerebral amyloid angiopathy, thus showing deposition of amyloid-β peptides in the walls of leptomeningeal and cortical arterioles. These deposits are believed to result from impaired clearance of parenchymal amyloid-β peptides. In the current work, we examined the changes in cortical microvascular structure and function in situ in TgCRND8, a transgenic mouse model of Alzheimer's disease. In contrast to venules, cortical arterioles were shown to increase in tortuosity and decrease in calibre with amyloid-β peptide accumulation. These structural changes were accompanied by progressive functional compromise, reflected in higher dispersion of microvascular network transit times, elongation of the transit times, and impaired microvascular reactivity to hypercapnia in the transgenic mice. Moreover, inhibition of amyloid-β peptide oligomerization and fibrillization via post-weaning administration of scyllo-inositol, a naturally occurring stereoisomer of myo-inositol, rescued both structural and functional impairment of the cortical microvasculature in this Alzheimer's disease model. These results demonstrate that microvascular impairment is directly correlated with amyloid-β accumulation and highlight the importance of targeting cerebrovascular amyloid angiopathy clearance for effective diagnosis, monitoring of disease progression and treatment of Alzheimer's disease.

KW - cerebral amyloid angiopathy

KW - microvasculature

KW - scyllo-inositol

KW - two-photon fluorescence microscopy

KW - vessel tortuosity

U2 - 10.1093/brain/aws243

DO - 10.1093/brain/aws243

M3 - Journal article

C2 - 23065792

AN - SCOPUS:84867722515

VL - 135

SP - 3039

EP - 3050

JO - Brain

JF - Brain

SN - 0006-8950

IS - 10

ER -