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强力霉素对弹性蛋白酶诱导的大鼠腹主动脉瘤模型中动脉瘤退变的抑制作用:主动脉弹性蛋白的保留与92kD明胶酶产生的抑制相关

Doxycycline inhibition of aneurysmal degeneration in an elastase-induced rat model of abdominal aortic aneurysm: preservation of aortic elastin associated with suppressed production of 92 kD gelatinase.

作者信息

Petrinec D, Liao S, Holmes D R, Reilly J M, Parks W C, Thompson R W

机构信息

Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

J Vasc Surg. 1996 Feb;23(2):336-46. doi: 10.1016/s0741-5214(96)70279-3.

Abstract

PURPOSE

Increased local production of matrix metalloproteinases (MMPs) is a potential mechanism underlying structural protein degradation in abdominal aortic aneurysms (AAA). With an elastase-induced rodent model of AAA, we determined whether pharmacologic treatment with an MMP-inhibiting tetracycline might limit the development of experimental AAA in vivo.

METHODS

Forty-eight Wistar rats underwent a 2-hour perfusion of the abdominal aorta with 50 U porcine pancreatic elastase and were then treated with either subcutaneous doxycycline (25 mg/day; n=24) or saline solution vehicle (n=24). Aortic diameter was measured before and after elastase perfusion was performed and before the rats were killed at 0, 2, 7, or 14 days, and AAAs were defined as an increase in aortic diameter to at least twice that before perfusion. At death the aortic tissues were either perfusion-fixed for histologic evaluation or extracted for substrate zymographic evaluation.

RESULTS

Aortic diameter was not different between groups at 0 or 2 days, but it was significantly less in animals treated with doxycycline at both 7 and 14 days (mean+/-SEM, p<0.01). After day 2 the incidence of AAA was reduced from 83% (10 of 12 rats treated with saline solution) to 8% (1 of 12 animals treated with doxycycline). By histologic assessment doxycycline prevented the structural deterioration of aortic elastin without decreasing the influx of inflammatory cells. Increased aortic wall production of 92 kD gelatinase observed in a saline solution-treated control group was markedly suppressed in animals treated with doxycycline.

CONCLUSIONS

Treatment with an MMP-inhibiting tetracycline inhibits the development of experimental AAA in vivo. This inhibition may be due to selective blockade of elastolytic MMP expression in infiltrating inflammatory cells. Additional experiments, however, are necessitated to fully delineate this process.

摘要

目的

基质金属蛋白酶(MMPs)局部产生增加是腹主动脉瘤(AAA)结构蛋白降解的潜在机制。利用弹性蛋白酶诱导的AAA啮齿动物模型,我们确定用MMP抑制性四环素进行药物治疗是否可能限制实验性AAA在体内的发展。

方法

48只Wistar大鼠接受了50 U猪胰弹性蛋白酶对腹主动脉的2小时灌注,然后分别用皮下强力霉素(25 mg/天;n = 24)或生理盐水载体(n = 24)进行治疗。在弹性蛋白酶灌注前后以及在0、2、7或14天处死大鼠之前测量主动脉直径,AAA定义为主动脉直径增加至灌注前的至少两倍。处死时,主动脉组织要么进行灌注固定以进行组织学评估,要么提取以进行底物酶谱评估。

结果

在0天或2天时,两组之间的主动脉直径没有差异,但在7天和14天时,用强力霉素治疗的动物的主动脉直径明显更小(平均值±标准误,p < 0.01)。第2天后,AAA的发生率从83%(用生理盐水治疗的12只大鼠中的10只)降至8%(用强力霉素治疗的12只动物中的1只)。通过组织学评估,强力霉素可防止主动脉弹性蛋白的结构恶化,而不会减少炎症细胞的流入。在生理盐水治疗的对照组中观察到的主动脉壁92 kD明胶酶产生增加在强力霉素治疗的动物中受到明显抑制。

结论

用MMP抑制性四环素治疗可抑制实验性AAA在体内的发展。这种抑制可能是由于对浸润性炎症细胞中弹性溶解MMP表达的选择性阻断。然而,需要进一步的实验来全面描述这一过程。

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