Hajdu M A, Heistad D D, Siems J E, Baumbach G L
Department of Pathology, University of Iowa College of Medicine, Iowa City 52242.
Circ Res. 1990 Jun;66(6):1747-54. doi: 10.1161/01.res.66.6.1747.
The purpose of this study was to examine effects of aging on the mechanics and composition of cerebral arterioles. We measured pressure (servo-null) and diameter in pial arterioles in anesthetized adult (9-12 months old) and aged (24-27 months old) Fischer 344 rats. After deactivation of smooth muscle with EDTA, diameter of pial arterioles at 70 mm Hg pial arteriolar pressure was less in aged than in adult rats (67 +/- 4 vs. 81 +/- 4 microns [mean +/- SEM], p less than 0.05). The stress-strain relation and the slope of tangential elastic modulus versus stress (6.8 +/- 0.6 vs. 5.3 +/- 0.3, p less than 0.05) indicated that distensibility of pial arterioles was reduced in aged rats. Cross-sectional area of the vessel wall, measured histologically, was less in aged than adult rats (1,239 +/- 91 vs. 1,832 +/- 180 microns2, p less than 0.05). Point counting stereology was used to quantitate smooth muscle, elastin, collagen, and basement membrane in the arteriolar wall. Cross-sectional areas of smooth muscle and elastin were significantly less in aged than adult rats (744 +/- 57 vs. 1,291 +/- 119 microns2 for smooth muscle, 52 +/- 6 vs. 113 +/- 15 microns2 for elastin; p less than 0.05), whereas cross-sectional areas of collagen and basement membrane were not significantly different in aged and adult rats (4 +/- 1 vs. 3 +/- 1 microns2 for collagen, 236 +/- 17 vs. 258 +/- 31 microns2 for basement membrane). The ratio of nondistensible (collagen and basement membrane) to distensible (smooth muscle and elastin) components was greater in aged than adult rats (0.30 +/- 0.01 vs. 0.18 +/- 0.01, p less than 0.05). Thus, we conclude that, during aging, cerebral arterioles undergo atrophy, distensibility of cerebral arterioles is reduced, and the relative proportion of distensible elements, elastin and smooth muscle, is reduced in the arteriolar wall.
本研究的目的是探讨衰老对脑小动脉力学性能和组成的影响。我们测量了麻醉状态下成年(9 - 12个月大)和老年(24 - 27个月大)的Fischer 344大鼠软脑膜小动脉的压力(伺服零位法)和直径。在用乙二胺四乙酸(EDTA)使平滑肌失活后,在软脑膜小动脉压力为70 mmHg时,老年大鼠软脑膜小动脉的直径小于成年大鼠(67±4 vs. 81±4微米[平均值±标准误],p < 0.05)。应力 - 应变关系以及切向弹性模量与应力的斜率(6.8±0.6 vs. 5.3±0.3,p < 0.05)表明老年大鼠软脑膜小动脉的扩张性降低。通过组织学测量的血管壁横截面积,老年大鼠小于成年大鼠(1239±91 vs. 1832±l80平方微米,p < 0.05)。采用点计数体视学方法对小动脉壁中的平滑肌、弹性蛋白、胶原蛋白和基底膜进行定量分析。老年大鼠平滑肌和弹性蛋白的横截面积显著小于成年大鼠(平滑肌:744±57 vs. 1291±119平方微米;弹性蛋白:52±6 vs. 113±15平方微米;p < 0.05),而老年大鼠和成年大鼠胶原蛋白和基底膜的横截面积无显著差异(胶原蛋白:4±1 vs. 3±1平方微米;基底膜:236±17 vs. 258±31平方微米)。老年大鼠中不可扩张成分(胶原蛋白和基底膜)与可扩张成分(平滑肌和弹性蛋白)的比例大于成年大鼠(0.30±0.01 vs. 0.18±0.01,p < 0.05)。因此,我们得出结论,在衰老过程中,脑小动脉会发生萎缩,脑小动脉的扩张性降低,并且小动脉壁中可扩张成分弹性蛋白和平滑肌的相对比例减少。