Division of Vascular and Endovascular Surgery Department of Visceral, Thoracic and Vascular Surgery University Hospital and Medical Faculty Carl Gustav Carus Technische Universität Dresden Dresden Germany.
Department of Physiology Medical Faculty Carl Gustav Carus Dresden Technische Universität Dresden Dresden Germany.
J Am Heart Assoc. 2021 Oct 19;10(20):e022747. doi: 10.1161/JAHA.121.022747. Epub 2021 Oct 8.
Background Rupture of abdominal aortic aneurysm (rAAA) is associated with high case fatality rates, and risk of rupture increases with the AAA diameter. Heme oxygenase-1 (gene , protein HO-1) is a stress-induced protein and induction has protective effects in the vessel wall. mice are more susceptible to angiotensin II-induced AAA formation, but the regulation in human nonruptured and ruptured AAA is only poorly understood. Our hypothesis proposed that HO-1 is reduced in AAA and lowering is inversely associated with the AAA diameter. Methods and Results AAA walls from patients undergoing elective open repair (eAAA) or surgery because of rupture (rAAA) were analyzed for aortic /HO-1 expression by quantitative real-time polymerase chain reaction and Western blot. Aortas from patients with aortic occlusive disease served as controls. /HO-1 expression was 1.1- to 7.6-fold upregulated in eAAA and rAAA. HO-1 expression was 3-fold higher in eAAA specimen with a diameter >84.4 mm, whereas HO-1 was not different in rAAA. Other variables that are known for associations with AAA and HO-1 induction were tested. In eAAA, HO-1 expression was negatively correlated with aortic collagen content and oxidative stress parameters HO release, oxidized proteins, and thiobarbituric acid reactive substances. Serum HO-1 concentrations were analyzed in patients with eAAA, and maximum values were found in an aortic diameter of 55 to 70 mm with no further increase >70 mm, compared with <55 mm. Conclusions Aortic HO-1 expression was increased in eAAA and rAAA. HO-1 increased with the severity of disease but was additionally connected to less oxidative stress and vasoprotective mechanisms.
背景
腹主动脉瘤破裂(rAAA)与高病死率相关,AAA 直径越大,破裂风险越高。血红素加氧酶-1(基因、蛋白 HO-1)是一种应激诱导蛋白,在血管壁中具有保护作用。HO-1 敲除小鼠更容易发生血管紧张素 II 诱导的 AAA 形成,但人类未破裂和破裂的 AAA 中的调控机制知之甚少。我们的假设是 HO-1 在 AAA 中减少,且降低与 AAA 直径呈负相关。
方法和结果
通过定量实时聚合酶链反应和 Western blot 分析接受择期开放修复(eAAA)或因破裂而手术(rAAA)的患者 AAA 壁中的主动脉 /HO-1 表达。将主动脉闭塞性疾病患者的主动脉作为对照。/HO-1 表达在 eAAA 和 rAAA 中上调了 1.1 到 7.6 倍。直径>84.4mm 的 eAAA 标本中 HO-1 表达增加了 3 倍,而 rAAA 中的 HO-1 则没有差异。还测试了与 AAA 和 HO-1 诱导相关的其他变量。在 eAAA 中,HO-1 表达与主动脉胶原含量和氧化应激参数 HO 释放、氧化蛋白和硫代巴比妥酸反应物质呈负相关。分析了 eAAA 患者的血清 HO-1 浓度,最大浓度出现在 55 至 70mm 的主动脉直径,而>70mm 时不再增加,与<55mm 时相比。
结论
eAAA 和 rAAA 中的主动脉 HO-1 表达增加。HO-1 随着疾病的严重程度而增加,但与较低的氧化应激和血管保护机制相关。