首页> 美国卫生研究院文献>The Journals of Gerontology Series A: Biological Sciences and Medical Sciences >Aging Exacerbates Obesity-Induced Oxidative Stress and Inflammation in Perivascular Adipose Tissue in Mice: A Paracrine Mechanism Contributing to Vascular Redox Dysregulation and Inflammation
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Aging Exacerbates Obesity-Induced Oxidative Stress and Inflammation in Perivascular Adipose Tissue in Mice: A Paracrine Mechanism Contributing to Vascular Redox Dysregulation and Inflammation

机译:衰老加剧了肥胖引起的小鼠氧化应激和炎症的血管周围脂肪组织:旁分泌机制有助于血管氧化还原调节异常和炎症。

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摘要

Obesity in the elderly individuals is increasing at alarming rates and there is evidence suggesting that elderly individuals are more vulnerable to the deleterious cardiovascular effects of obesity than younger individuals. However, the specific mechanisms through which aging and obesity interact to promote the development of cardiovascular disease remain unclear. The present study was designed to test the hypothesis that aging exacerbates obesity-induced inflammation in perivascular adipose tissue, which contributes to increased vascular oxidative stress and inflammation in a paracrine manner. To test this hypothesis, we assessed changes in the secretome, reactive oxygen species production, and macrophage infiltration in periaortic adipose tissue of young (7 month old) and aged (24 month old) high-fat diet–fed obese C57BL/6 mice. High-fat diet–induced vascular reactive oxygen species generation significantly increased in aged mice, which was associated with exacerbation of endothelial dysfunction and vascular inflammation. In young animals, high-fat diet–induced obesity promoted oxidative stress in the perivascular adipose tissue, which was associated with a marked proinflammatory shift in the profile of secreted cytokines and chemokines. Aging exacerbated obesity-induced oxidative stress and inflammation and significantly increased macrophage infiltration in periaortic adipose tissue. Using cultured arteries isolated from young control mice, we found that inflammatory factors secreted from the perivascular fat tissue of obese aged mice promote significant prooxidative and proinflammatory phenotypic alterations in the vascular wall, mimicking the aging phenotype. Overall, our findings support an important role for localized perivascular adipose tissue inflammation in exacerbation of vascular oxidative stress and inflammation in aging, an effect that likely enhances the risk for development of cardiovascular diseases from obesity in the elderly individuals.
机译:老年人的肥胖症正在以惊人的速度增加,并且有证据表明,老年人比年轻人更容易遭受肥胖的有害心血管作用。但是,衰老和肥胖相互作用以促进心血管疾病发展的具体机制仍不清楚。本研究旨在测试以下假设:衰老加剧了肥胖引起的血管周围脂肪组织的炎症,从而以旁分泌方式增加了血管氧化应激和炎症。为了检验这一假设,我们评估了年轻(7个月大)和年龄大(24个月大)高脂饮食喂养的肥胖C57BL / 6小鼠的腹主动脉脂肪组织中的分泌组,活性氧产生和巨噬细胞浸润的变化。高脂饮食诱导的衰老小鼠血管活性氧的产生显着增加,这与内皮功能障碍和血管炎症的加剧有关。在幼小的动物中,高脂饮食诱导的肥胖会促进血管周围脂肪组织的氧化应激,这与分泌的细胞因子和趋化因子的特征明显的促炎性转变有关。衰老加剧了肥胖引起的氧化应激和炎症,并显着增加了腹主动脉脂肪组织中巨噬细胞的浸润。使用从年轻对照小鼠中分离出的培养动脉,我们发现肥胖老年小鼠的血管周脂肪组织分泌的炎性因子会促进血管壁的显着的促氧化和促炎表型改变,从而模仿衰老表型。总的来说,我们的发现支持局部血管周围脂肪组织炎症在加剧血管氧化应激和衰老中的炎症中起重要作用,这种作用可能会增加老年人肥胖引起心血管疾病的风险。

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