4.5 Article

Cellular and physiological mechanisms underlying blood flow regulation in the retina and choroid in health and disease

期刊

PROGRESS IN RETINAL AND EYE RESEARCH
卷 31, 期 5, 页码 377-406

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.preteyeres.2012.04.004

关键词

Blood flow; Retina; Choroid; Regulation; Functional hyperemia; Autoregulation; Pathology; Diabetic retinopathy; Microvasculature; Review

资金

  1. Fondation Leducq of France
  2. National Institutes of Health of the United States [EY004077]
  3. National Health and Medical Research Council of Australia [571100, 1005730]
  4. Rebecca L. Cooper Medical Research Foundation
  5. Brian M Kirby Foundation - Gift of Sight Initiative
  6. NSW Optometrist Registration Board - Best Practice Grant
  7. National Health and Medical Research Council of Australia [571100] Funding Source: NHMRC

向作者/读者索取更多资源

We review the cellular and physiological mechanisms responsible for the regulation of blood flow in the retina and choroid in health and disease. Due to the intrinsic light sensitivity of the retina and the direct visual accessibility of fundus blood vessels, the eye offers unique opportunities for the non-invasive investigation of mechanisms of blood flow regulation. The ability of the retinal vasculature to regulate its blood flow is contrasted with the far more restricted ability of the choroidal circulation to regulate its blood flow by virtue of the absence of glial cells, the markedly reduced pericyte ensheathment of the choroidal vasculature, and the lack of intermediate filaments in choroidal pericytes. We review the cellular and molecular components of the neurovascular unit in the retina and choroid, techniques for monitoring retinal and choroidal blood flow, responses of the retinal and choroidal circulation to light stimulation, the role of capillaries, astrocytes and pericytes in regulating blood flow, putative signaling mechanisms mediating neurovascular coupling in the retina, and changes that occur in the retinal and choroidal circulation during diabetic retinopathy, age-related macular degeneration, glaucoma, and Alzheimer's disease. We close by discussing issues that remain to be explored. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.

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