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长期、急性抑制半胱氨酰白三烯以减少硅胶植入物周围的包膜挛缩。

Prolonged, acute suppression of cysteinyl leukotriene to reduce capsular contracture around silicone implants.

作者信息

Kim Byung Hwi, Park Min, Park Hyo Jin, Lee Seung Ho, Choi Sung Yoon, Park Chun Gwon, Han Su Min, Heo Chan Yeong, Choy Young Bin

机构信息

Department of Biomedical Engineering, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.

Interdisciplinary Program in Bioengineering, College of Engineering, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

Acta Biomater. 2017 Mar 15;51:209-219. doi: 10.1016/j.actbio.2017.01.033. Epub 2017 Jan 10.

Abstract

UNLABELLED

We hypothesize that periodically early, local suppression of cysteinyl leukotrienes (CysLTs), which are potent inflammatory mediators, can reduce the fibrotic capsular contracture around silicone implants. We tested this hypothesis with the silicone implants enabled with the sustained release of montelukast, a CysLT receptor antagonist, for 3 and 15days. In this work, we inserted each of the distinct implants into the pocket of the subpanniculus carnosus plane of living rats and performed histological and immunofluorescent (IF) analyses of the tissues biopsied at predetermined periods for 12weeks after implant insertion. The implants with montelukast exhibited significantly reduced polymorphonuclear leukocytes (i.e., PMNs), implying a concurrent reduction of CysLT. This effect was more prominent after long-term local montelukast exposure. Thus, fewer fibroblasts were recruited, thereby reducing transforming growth factor (TGF)-β and myofibroblasts in the tissue around the implant. Therefore, the fibrotic capsule formation, which was assessed using the capsule thickness and collagen density, decreased along with the myofibroblasts. Additionally, the tissue biopsied at the experimental end point exhibited significantly decreased mechanical stiffness.

STATEMENT OF SIGNIFICANCE

Capsular contracture is troublesome, making the tissues hardened around the silicone implant. This causes serious pain and discomfort to the patients, often leading to secondary surgery for implant replacement. To resolve this, we suggest a strategy of long-term, local suppression of cysteinyl leukotriene, an important mediator present during inflammation. For this, we propose a silicone implant abled to release a drug, montelukast, in a sustained manner. We tested our drug-release implant in living animals, which exhibited a significant decrease in capsule formation compared with the intact silicone implant. Therefore, we conclude that the sustained release of montelukast at the local insertion site represents a promising way to reduce capsular contracture around silicone implants.

摘要

未标记

我们假设,定期在早期对作为强效炎症介质的半胱氨酰白三烯(CysLTs)进行局部抑制,可减少硅胶植入物周围的纤维化包膜挛缩。我们使用能够持续释放半胱氨酰白三烯受体拮抗剂孟鲁司特3天和15天的硅胶植入物来验证这一假设。在这项研究中,我们将每种不同的植入物植入活大鼠的皮下肌肉平面囊袋中,并在植入后12周的预定时间对活检组织进行组织学和免疫荧光(IF)分析。含有孟鲁司特的植入物显示多形核白细胞(即PMN)显著减少,这意味着CysLT同时减少。长期局部暴露于孟鲁司特后,这种效果更为显著。因此,募集的成纤维细胞减少,从而减少了植入物周围组织中的转化生长因子(TGF)-β和肌成纤维细胞。因此,使用包膜厚度和胶原密度评估的纤维化包膜形成随着肌成纤维细胞的减少而降低。此外,在实验终点活检的组织显示机械硬度显著降低。

意义声明

包膜挛缩很麻烦,会使硅胶植入物周围的组织变硬。这给患者带来严重的疼痛和不适,常常导致进行植入物置换的二次手术。为了解决这个问题,我们提出一种长期局部抑制半胱氨酰白三烯的策略,半胱氨酰白三烯是炎症期间存在的一种重要介质。为此,我们提出一种能够持续释放药物孟鲁司特的硅胶植入物。我们在活体动物中测试了我们的药物释放植入物,与完整的硅胶植入物相比,其包膜形成显著减少。因此,我们得出结论,在局部植入部位持续释放孟鲁司特是减少硅胶植入物周围包膜挛缩的一种有前景的方法。

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