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Krogh 圆柱在视网膜发育、全视网膜灌注不足和糖尿病性视网膜病变中的作用。

Krogh cylinders in retinal development, panretinal hypoperfusion and diabetic retinopathy.

机构信息

Academic Department of Ophthalmology, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

出版信息

Acta Ophthalmol. 2010 Dec;88(8):817-35. doi: 10.1111/j.1755-3768.2009.01796.x.

Abstract

The volume of cells that a length of capillary supplies with O(2) is called a Krogh cylinder. This geometric 'tissue unit' was named after the Danish zoophysiologist and Nobel laureate August Krogh who made important discoveries in the fields of external and internal respiration in the first half of the last century. Krogh's ideas concerning tissue O(2) distribution can be extrapolated to retinal oxygenation by larger vessels (including arterioles, arteries and even veins) and by vessel groups within higher-order 'microvascular units' (including the choroid). During retinal development, for example, the difference in pO(2) levels within arteries and capillaries determines Krogh cylinders of different radius and establishes the periarterial capillary-free zone of His. The O(2) supply to the venous end of a tissue unit may be compromised during periods of reduced perfusion, increased O(2) consumption or hypoxaemia, resulting in an 'anoxic corner' of the Krogh cylinder. A funnel of hypometabolic (and therefore hypoxia-tolerant) cells will likely intervene between the necrotic cells and unaffected cells located closer to the O(2) source. Macular perivenular whitening heralds anoxic corners and/or hypoxic funnels owing to hypoperfusion within second-order microvascular units. In eyes with extensive retinal capillary closure from diabetes, Krogh cylinders surround the medium-sized arteries and veins that form arteriovenous shunts while traversing the midperipheral retina. These isolated tissue units incorporate an outer sheath of hypoxic cells within which vascular endothelial growth factor is upregulated. This 'angiogenic sheath' expands following retinal detachment; it corresponds to the hypoxia-tolerant funnel within capillary-based tissue units and to the cerebral penumbra after stroke.

摘要

毛细血管供应氧气的细胞体积称为克氏圆柱。这个几何“组织单位”是以丹麦生理学家和诺贝尔奖获得者奥古斯特·克劳斯(August Krogh)的名字命名的,他在上个世纪前半叶在外部和内部呼吸领域做出了重要发现。克劳斯关于组织氧分布的思想可以通过较大的血管(包括小动脉、动脉甚至静脉)和更高阶“微血管单位”内的血管群(包括脉络膜)外推到视网膜氧合。例如,在视网膜发育过程中,动脉和毛细血管内的 pO2 水平差异决定了不同半径的克氏圆柱,并建立了 His 的动脉周围无毛细血管区。在灌注减少、耗氧量增加或低氧血症期间,组织单位静脉端的氧供应可能会受到影响,导致克氏圆柱的“缺氧角”。一个低代谢(因此耐受缺氧)细胞的漏斗可能会介入坏死细胞和更靠近氧源的未受影响的细胞之间。黄斑周围静脉变白预示着由于二级微血管单位内灌注不足,出现缺氧角和/或缺氧漏斗。在糖尿病引起的广泛视网膜毛细血管闭塞的眼中,克氏圆柱围绕着形成动静脉分流的中等大小的动脉和静脉,穿过中周部视网膜。这些孤立的组织单位包含一个缺氧细胞的外鞘,其中血管内皮生长因子上调。这种“血管生成鞘”在视网膜脱离后扩张;它对应于基于毛细血管的组织单位内耐受缺氧的漏斗,以及中风后的大脑半影。

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