Bonthu S, Heistad D D, Chappell D A, Lamping K G, Faraci F M
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242-1081, USA.
Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2333-40. doi: 10.1161/01.atv.17.11.2333.
We examined the vascular structure and endothelium-dependent relaxation in two genetic models of hypercholesterolemia: apolipoprotein E (apoE)-knockout mice and combined apoE/LDL receptor-double-knockout mice. Intimal area was increased markedly in proximal segments of thoracic aortas from apoE/LDL receptor-knockout mice [0.13 +/- 0.03 (mean +/- SE) mm2] compared with normal (C57BL/6J) mice (0.002 +/- 0.002 mm2, P < .05). Despite intimal thickening, the vascular lumen was not smaller in the aortas of apoE/LDL receptor-knockout mice (0.52 +/- 0.03 mm2) than in normal mice (0.50 +/- 0.03 mm2). In apoE-deficient mice, intimal thickening was minimal or absent, even though the concentration of plasma cholesterol was only modestly less than that in the double-knockout mouse (14.9 +/- 1.1 vs 18.0 +/- 1.2 mmol/L, respectively, P < .05). Relaxation of the aorta was examined in vitro in vascular rings precontracted with U46619. In normal mice, acetylcholine produced relaxation, which was markedly attenuated by the nitric oxide synthase inhibitor NG-nitro-L-arginine (100 microM). Relaxation to acetylcholine and the calcium ionophore A23187 was normal in apoE-deficient mice (in which lesions were minimal) but greatly impaired in the proximal segments of thoracic aortas of apoE/LDL receptor-deficient mice, which contained atherosclerotic lesions. Vasorelaxation to nitroprusside was similar in normal and apoE-knockout mice, with modest but statistically significant impairment in atherosclerotic segments of apoE/LDL receptor-knockout mice. In distal segments of the thoracic aorta of apoE/LDL receptor-deficient mice, atherosclerotic lesions were minimal or absent, and the endothelium-dependent relaxation to acetylcholine and calcium ionophore was normal. Thus, in apoE/LDL receptor-knockout mice (a genetic model of hyperlipidemia), there is vascular remodeling with preservation of the aortic lumen despite marked intimal thickening, with impairment of endothelium-dependent relaxation to receptor- and nonreceptor-mediated agonists. Atherosclerosis may be accelerated in the apoE/LDL receptor-double-knockout mouse compared with the apoE-knockout strain alone. We speculate that other factors, such as the absence of LDL receptors, may contribute to the differences in the extent of atherosclerosis in these two models of hyperlipidemia.
载脂蛋白E(apoE)基因敲除小鼠和apoE/LDL受体双基因敲除小鼠。与正常(C57BL/6J)小鼠(0.002±0.002mm²,P<.05)相比,apoE/LDL受体基因敲除小鼠胸主动脉近端段的内膜面积显著增加[0.13±0.03(均值±标准误)mm²]。尽管内膜增厚,但apoE/LDL受体基因敲除小鼠主动脉的血管腔(0.52±0.03mm²)并不比正常小鼠(0.50±0.03mm²)小。在apoE缺陷小鼠中,内膜增厚很轻微或没有,尽管其血浆胆固醇浓度仅略低于双基因敲除小鼠(分别为14.9±1.1和18.0±1.2mmol/L,P<.05)。用U46619预收缩血管环后,在体外检测主动脉的舒张功能。在正常小鼠中,乙酰胆碱可引起舒张,一氧化氮合酶抑制剂NG-硝基-L-精氨酸(100μM)可显著减弱这种舒张。在apoE缺陷小鼠(病变轻微)中,对乙酰胆碱和钙离子载体A23187的舒张反应正常,但在含有动脉粥样硬化病变的apoE/LDL受体缺陷小鼠胸主动脉近端段,这种舒张功能严重受损。正常小鼠和apoE基因敲除小鼠对硝普钠的血管舒张反应相似,而apoE/LDL受体基因敲除小鼠的动脉粥样硬化段有适度但具有统计学意义的舒张功能受损。在apoE/LDL受体缺陷小鼠胸主动脉远端段,动脉粥样硬化病变轻微或没有,对乙酰胆碱和钙离子载体的内皮依赖性舒张功能正常。因此,在apoE/LDL受体基因敲除小鼠(一种高脂血症的遗传模型)中,尽管内膜显著增厚,但仍存在血管重塑并保留了主动脉腔,对受体介导和非受体介导的激动剂的内皮依赖性舒张功能受损。与单独的apoE基因敲除品系相比,apoE/LDL受体双基因敲除小鼠的动脉粥样硬化可能进展更快。我们推测,其他因素,如缺乏LDL受体,可能导致这两种高脂血症模型中动脉粥样硬化程度的差异。