College of Nursing and Health Innovation, Arizona State University, Tempe, AZ 85287-4501, USA.
Horm Metab Res. 2011 Jun;43(7):470-6. doi: 10.1055/s-0031-1273763. Epub 2011 Mar 29.
Rats fed a high fat diet develop increased adiposity and oxidative stress leading to impaired vasodilation. The purpose of the present study was to examine the effects of high fat-induced increases in adiposity and oxidative stress on vasoconstrictor reactivity of isolated mesenteric arteries. We hypothesized that rats with more adiposity would develop oxidative stress-potentiated increases in iNOS-derived nitric oxide leading to diminished vasoconstriction. Male Sprague-Dawley rats were fed either a control (Chow) or high fat diet for 6 weeks. The roles of oxidative stress and iNOS in the impaired vasoconstrictor responses to endothelin-1 were characterized in small mesenteric arteries. Rats fed the HFD developed significantly more adiposity compared to Chow rats. Plasma levels of nitric oxide and the inflammatory factor tumor necrosis factor α were significantly higher in high fat fed rats compared to Chow rats (nitric oxide: 95.36±19.3 vs. 38.96±6.7 μM; tumor necrosis factor α: 598±111.4 vs. 292±71.8 pg/ml, respectively). Despite exhibiting elevated systolic blood pressure compared to Chow rats (153.5±2.4 vs. 137.5±2.7 mm Hg), endothelin-1 mediated vasoconstriction was impaired in isolated mesenteric arteries from high fat fed rats but was normalized by individual or combined inhibition of nitric oxide synthase, iNOS, or oxidative stress. Therefore, oxidative stress and iNOS are involved in the attenuation of endothelin-1 mediated vasoconstriction observed in isolated mesenteric arteries from high fat fed rats.
高脂饮食喂养的大鼠会增加脂肪堆积和氧化应激,导致血管舒张功能受损。本研究旨在探讨高脂饮食引起的脂肪堆积和氧化应激增加对离体肠系膜动脉收缩反应性的影响。我们假设,脂肪堆积较多的大鼠会产生氧化应激增强的诱导型一氧化氮合酶(iNOS)衍生的一氧化氮增加,导致血管收缩减弱。雄性 Sprague-Dawley 大鼠分别用对照(Chow)或高脂饮食喂养 6 周。在小肠系膜动脉中,研究了氧化应激和 iNOS 在血管紧张素-1 引起的血管收缩反应受损中的作用。与 Chow 组大鼠相比,高脂饮食喂养的大鼠明显增加了脂肪堆积。与 Chow 组相比,高脂饮食喂养大鼠的血浆一氧化氮和炎症因子肿瘤坏死因子-α水平显著升高(一氧化氮:95.36±19.3 比 38.96±6.7μM;肿瘤坏死因子-α:598±111.4 比 292±71.8pg/ml)。尽管与 Chow 组相比,高脂饮食喂养大鼠的收缩压升高(153.5±2.4 比 137.5±2.7mmHg),但离体肠系膜动脉对内皮素-1 介导的血管收缩反应受损,但经单独或联合抑制一氧化氮合酶、iNOS 或氧化应激可恢复正常。因此,氧化应激和 iNOS 参与了高脂饮食喂养大鼠离体肠系膜动脉中观察到的内皮素-1 介导的血管收缩减弱。