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饮食诱导的肥胖会导致脑血管重塑,并增加缺血性中风造成的损伤。

Diet-induced obesity causes cerebral vessel remodeling and increases the damage caused by ischemic stroke.

作者信息

Deutsch Christian, Portik-Dobos Vera, Smith Anita D, Ergul Adviye, Dorrance Anne M

机构信息

Department of Physiology, Medical College of Georgia, Augusta, GA, USA.

出版信息

Microvasc Res. 2009 Jun;78(1):100-6. doi: 10.1016/j.mvr.2009.04.004. Epub 2009 Apr 15.

Abstract

Hypertension, elevated fasting blood glucose and plasma insulin develop in rats fed a high fat (HF) diet. Our goal was to assess the effects of obesity, beginning in childhood, on the adult cardiovascular system. We hypothesized that rats fed a HF diet would have larger ischemic cerebral infarcts and middle cerebral artery (MCA) remodeling. Three-week-old male Sprague Dawley rats were fed a HF (obese) or control diet for 10 weeks. Cerebral ischemia was induced by MCA occlusion (MCAO). MCA structure was assessed by pressure myography and cerebral vessel matrix metalloproteinase (MMP) activity and expression and collagen levels were measured in vessels from rats that did not undergo MCAO. The cerebral infarct was greater in the obese rats than the control (46.0+/-2.1 vs 28.0+/-7.5% of the hemisphere infarcted, obese vs control p<0.05). The MCAs from obese rats had smaller lumens (232+/-7.2 vs 254+/-7.8 microm obese vs control p<0.05) and thicker walls (19.6+/-0.8 vs 17.8+/-0.9 microm obese vs control p<0.05) and were less compliant than MCAs from control rats. MMP-2 activity and collagen I expression were increased in vessels from obese rats and MMP-13 expression was reduced. These results suggest that obesity, beginning in childhood, causes inward vessel remodeling with a concomitant increase in vessel stiffness due to increased collagen deposition. These changes in MCA structure may be responsible for the increase in the ischemic damage after MCAO.

摘要

喂食高脂(HF)饮食的大鼠会出现高血压、空腹血糖升高和血浆胰岛素升高的情况。我们的目标是评估始于童年期的肥胖对成年心血管系统的影响。我们假设喂食HF饮食的大鼠会有更大的缺血性脑梗死和大脑中动脉(MCA)重塑。将3周龄雄性Sprague Dawley大鼠喂食HF(肥胖)或对照饮食10周。通过大脑中动脉闭塞(MCAO)诱导脑缺血。通过压力肌动描记法评估MCA结构,并测量未接受MCAO的大鼠血管中的脑血管基质金属蛋白酶(MMP)活性、表达及胶原蛋白水平。肥胖大鼠的脑梗死面积大于对照组(梗死半球的46.0±2.1%对28.0±7.5%,肥胖组对对照组,p<0.05)。肥胖大鼠的MCA管腔较小(232±7.2对254±7.8微米,肥胖组对对照组,p<0.05),管壁较厚(19.6±0.8对17.8±0.9微米,肥胖组对对照组,p<0.05),且与对照组大鼠的MCA相比顺应性更低。肥胖大鼠血管中的MMP-2活性和I型胶原蛋白表达增加,而MMP-13表达降低。这些结果表明,始于童年期的肥胖会导致血管向内重塑,并因胶原蛋白沉积增加而伴随血管僵硬度增加。MCA结构的这些变化可能是MCAO后缺血损伤增加的原因。

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