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首页> 外文期刊>Microvascular Research: An International Journal >Diet-induced obesity causes cerebral vessel remodeling and increases the damage caused by ischemic stroke.
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Diet-induced obesity causes cerebral vessel remodeling and increases the damage caused by ischemic stroke.

机译:饮食引起的肥胖会导致脑血管重构,并增加缺血性中风引起的损害。

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摘要

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.
机译:喂高脂(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。我们的目标是评估从儿童期开始的肥胖对成人心血管系统的影响。我们假设喂养高脂饮食的大鼠会出现更大的缺血性脑梗塞和大脑中动脉(MCA)重塑。给三周大的Sprague Dawley雄性大鼠喂食HF(肥胖)或对照饮食10周。 MCA闭塞(MCAO)可诱发脑缺血。通过压力肌电图和脑血管基质金属蛋白酶(MMP)活性评估MCA结构,并测量未经历MCAO的大鼠血管中的表达和胶原蛋白水平。肥胖大鼠的脑梗塞比对照组大(半球梗塞的46.0 +/- 2.1比28.0 +/- 7.5%,肥胖vs对照p <0.05)。肥胖大鼠的MCA的流明更小(232 +/- 7.2 vs 254 +/- 7.8 microm肥胖vs对照p <0.05)和较厚的壁(19.6 +/- 0.8 vs 17.8 +/- 0.9 microm肥胖vs对照p <0.05) ),且比对照组大鼠的MCA依从性差。肥胖大鼠血管中MMP-2活性和胶原I表达增加,MMP-13表达降低。这些结果表明,肥胖症从儿童期开始,就导致血管向内重构,并伴随着胶原蛋白沉积增加而使血管僵硬。 MCA结构的这些变化可能是MCAO后缺血性损伤增加的原因。

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