1989
DOI: 10.1016/0006-8993(89)90842-1
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Dorsal-ventral gradient in vulnerability of CA1 hippocampus to ischemia: a combined histological and electrophysiological study

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Cited by 57 publications
(25 citation statements)
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“…Similar to guinea pigs, in humans, there is a possibility that, at least in a reduced population of individuals, the ventralmost portion of the hippocampus and the related parahippocampal regions are supplied by a single arterial branch with little compensatory anastomotic circuits available. Our results are in agreement with the reported vulnerability of the hippocampus to transient global ischemia (Pulsinelli et al, 1982;Ashton et al, 1989;Sieber et al, 1995). It has been demonstrated in animal models of transient bilateral carotid occlusion or fourvessel occlusion that, in rats and in other mammals, the hippocampus always is injured by ischemia (Pulsinelli et al, 1982;Sieber et al, 1995).…”
Section: Discussionsupporting
confidence: 94%
“…Similar to guinea pigs, in humans, there is a possibility that, at least in a reduced population of individuals, the ventralmost portion of the hippocampus and the related parahippocampal regions are supplied by a single arterial branch with little compensatory anastomotic circuits available. Our results are in agreement with the reported vulnerability of the hippocampus to transient global ischemia (Pulsinelli et al, 1982;Ashton et al, 1989;Sieber et al, 1995). It has been demonstrated in animal models of transient bilateral carotid occlusion or fourvessel occlusion that, in rats and in other mammals, the hippocampus always is injured by ischemia (Pulsinelli et al, 1982;Sieber et al, 1995).…”
Section: Discussionsupporting
confidence: 94%
“…These hippocampal regions have been related to AD, vascular disease and ageing. HC could therefore play a role in neurodegenerative, vascular and age-related hippocampal disease [11, 12]. A possible relation to AD, however, appears less likely because even though HC was frequently found in patients with AD, Wegiel et al reported that only 4% of patients with Down syndrome showed VFC while 96% were affected by AD, opposing a common pathological mechanism [2].…”
Section: Discussionmentioning
confidence: 99%
“…2a). Over the hippocampal long axis, posterior CA1 is differentially affected by vascular disease 59 . Although a systematic investigation of age-related dentate gyrus alterations over the hippocampal long axis has not yet been completed, a recent study suggests that age-related pattern separation defects occur in relatively posterior aspects 58 .…”
Section: Hippocampal Regional Vulnerabilitymentioning
confidence: 99%