Groeneveld M E, van der Reijden J J, Tangelder G J, Westin L C, Renwarin L, Musters R J P, Wisselink W, Yeung K K
Department of Vascular Surgery, ICaR-VU, VU University Medical Center (VUmc), Amsterdam, The Netherlands; Department of Physiology, ICaR-VU, VU University Medical Center (VUmc), Amsterdam, The Netherlands.
Department of Radiology, Deventer Ziekenhuis, Deventer, The Netherlands.
Eur J Vasc Endovasc Surg. 2017 Sep;54(3):331-339. doi: 10.1016/j.ejvs.2017.06.003. Epub 2017 Jul 14.
Extensive reactive oxygen and nitrogen species (also reactive species) production is a mechanism involved in abdominal aortic aneurysm (AAA) development. White blood cells (WBCs) are a known source of reactive species. Their production may be decreased by statins, thereby reducing the AAA growth rate. Reactive species production in circulating WBCs of AAA patients and the effect of statins on their production was investigated.
This observational study investigated reactive species production in vivo and ex vivo in circulating WBCs of AAA patients, using venous blood from patients prior to elective AAA repair (n = 34; 18 statin users) and from healthy volunteers (n = 10). Reactive species production was quantified in circulating WBCs using immunofluorescence microscopy: nitrotyrosine (footprint of peroxynitrite, a potent reactive nitrogen species) in snap frozen blood smears; mitochondrial superoxide and cytoplasmic hydrogen peroxide (both reactive oxygen species) by live cell imaging. Neutrophils, lymphocytes, and monocytes were examined individually.
In AAA patients using statins, the median nitrotyrosine level in neutrophils was 646 (range 422-2059), in lymphocytes 125 (range 74-343), and in monocytes 586 (range 291-663). Median levels in AAA patients not using statins were for neutrophils 928 (range 552-2095, p = .03), lymphocytes 156 (101-273, NS), and for monocytes 536 (range 535-1635, NS). The statin dose tended to correlate negatively with nitrotyrosine in neutrophils (R -0.32, p = .06). The median levels in controls were lower for neutrophils 466 (range 340-820, p < .01) and for monocytes 191 (range 102-386, p = .03), but similar for lymphocytes 99 (range 82-246) when compared to the AAA patients. There were no differences in mitochondrial superoxide and cytoplasmic hydrogen peroxide between statin and non-statin users within AAA patients.
It was found that the peroxynitrite footprint in circulating neutrophils and monocytes of AAA patients is higher than in controls. AAA patients treated with statins had a lower peroxynitrite footprint in neutrophils than non-statin users.
大量活性氧和活性氮(也称反应性物种)的产生是腹主动脉瘤(AAA)发展过程中的一种机制。白细胞(WBCs)是已知的反应性物种来源。他汀类药物可能会降低其产生,从而降低AAA的生长速度。本研究调查了AAA患者循环白细胞中反应性物种的产生情况以及他汀类药物对其产生的影响。
本观察性研究使用择期AAA修复术前患者(n = 34;18名他汀类药物使用者)和健康志愿者(n = 10)的静脉血,对AAA患者循环白细胞中反应性物种的体内和体外产生情况进行了研究。使用免疫荧光显微镜对循环白细胞中反应性物种的产生进行定量:在速冻血涂片上检测硝基酪氨酸(过氧亚硝酸盐的印记,一种强效的反应性氮物种);通过活细胞成像检测线粒体超氧化物和细胞质过氧化氢(均为反应性氧物种)。分别对中性粒细胞、淋巴细胞和单核细胞进行检测。
在使用他汀类药物的AAA患者中,中性粒细胞中硝基酪氨酸的中位数水平为646(范围422 - 2059),淋巴细胞中为125(范围74 - 343),单核细胞中为586(范围291 - 663)。未使用他汀类药物的AAA患者中,中性粒细胞的中位数水平为928(范围552 - 2095,p = 0.03),淋巴细胞为156(101 - 273,无统计学意义),单核细胞为536(范围535 - 1635,无统计学意义)。他汀类药物剂量与中性粒细胞中的硝基酪氨酸呈负相关趋势(R - 0.32,p = 0.06)。与AAA患者相比,对照组中性粒细胞的中位数水平较低,为466(范围340 - 820,p < 0.01),单核细胞为191(范围102 - 386,p = 0.03),但淋巴细胞的中位数水平相似,为99(范围82 - 246)。在AAA患者中,使用他汀类药物和未使用他汀类药物的患者之间,线粒体超氧化物和细胞质过氧化氢没有差异。
研究发现,AAA患者循环中性粒细胞和单核细胞中的过氧亚硝酸盐印记高于对照组。接受他汀类药物治疗的AAA患者中性粒细胞中的过氧亚硝酸盐印记低于未使用他汀类药物的患者。