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围手术期硫化氢治疗可改善血管重塑并减轻静脉移植物疾病。

Periprocedural Hydrogen Sulfide Therapy Improves Vascular Remodeling and Attenuates Vein Graft Disease.

机构信息

Department of Surgery and the Heart and Vascular Center Brigham & Women's Hospital Harvard Medical School Boston MA.

Department of Molecular Metabolism Harvard T.H. Chan School of Public Health Boston MA.

出版信息

J Am Heart Assoc. 2020 Nov 17;9(22):e016391. doi: 10.1161/JAHA.120.016391. Epub 2020 Nov 4.

DOI:10.1161/JAHA.120.016391
PMID:33146045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7763704/
Abstract

Background Failure rates after revascularization surgery remain high, both in vein grafts (VG) and arterial interventions. One promising approach to improve outcomes is endogenous upregulation of the gaseous transmitter-molecule hydrogen sulfide, via short-term dietary restriction. However, strict patient compliance stands as a potential translational barrier in the vascular surgery patient population. Here we present a new therapeutic approach, via a locally applicable gel containing the hydrogen sulfide releasing prodrug (GYY), to both mitigate graft failure and improve arterial remodeling. Methods and Results All experiments were performed on C57BL/6 (male, 12 weeks old) mice. VG surgery was performed by grafting a donor-mouse cava vein into the right common carotid artery of a recipient via an end-to-end anastomosis. In separate experiments arterial intimal hyperplasia was assayed via a right common carotid artery focal stenosis model. All mice were harvested at postoperative day 28 and artery/graft was processed for histology. Efficacy of hydrogen sulfide was first tested via GYY supplementation of drinking water either 1 week before VG surgery (pre-GYY) or starting immediately postoperatively (post-GYY). Pre-GYY mice had a 36.5% decrease in intimal/media+adventitia area ratio compared with controls. GYY in a 40% Pluronic gel (or vehicle) locally applied to the graft/artery had decreased intimal/media area ratios (right common carotid artery) and improved vessel diameters. GYY-geltreated VG had larger diameters at both postoperative days 14 and 28, and a 56.7% reduction in intimal/media+adventitia area ratios. Intimal vascular smooth muscle cell migration was decreased 30.6% after GYY gel treatment, which was reproduced in vitro. Conclusions Local gel-based treatment with the hydrogen sulfide-donor GYY stands as a translatable therapy to improve VG durability and arterial remodeling after injury.

摘要

背景

血管再通手术后,静脉移植物(VG)和动脉介入治疗的失败率仍然很高。一种有前途的方法是通过短期饮食限制来提高内源性气体递质分子硫化氢的表达水平。然而,严格的患者依从性是血管外科患者群体中潜在的转化障碍。在这里,我们提出了一种新的治疗方法,通过局部应用含有硫化氢释放前体药物(GYY)的凝胶,来减轻移植物失败和改善动脉重塑。

方法和结果

所有实验均在 C57BL/6(雄性,12 周龄)小鼠中进行。VG 手术通过将供体小鼠腔静脉通过端端吻合术移植到受体右侧颈总动脉中来完成。在单独的实验中,通过右侧颈总动脉局灶性狭窄模型来测定动脉内膜增生。所有小鼠均在术后第 28 天处死,对动脉/移植物进行组织学处理。首先通过在 VG 手术前 1 周(术前 GYY)或术后立即开始在饮用水中添加 GYY 来测试硫化氢的疗效。术前 GYY 组小鼠的内膜/中膜+外膜面积比与对照组相比降低了 36.5%。局部应用于移植物/动脉的 40% Pluronic 凝胶(或载体)中的 GYY 降低了内膜/中膜面积比(右侧颈总动脉)并改善了血管直径。术后第 14 天和第 28 天,GYY 凝胶处理的 VG 直径更大,内膜/中膜+外膜面积比降低了 56.7%。GYY 凝胶处理后,内膜血管平滑肌细胞迁移减少了 30.6%,这在体外得到了重现。

结论

基于氢硫化物供体 GYY 的局部凝胶治疗是一种可转化的治疗方法,可提高 VG 的耐久性和损伤后动脉重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/6b93f85b7321/JAH3-9-e016391-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/41f94cd99624/JAH3-9-e016391-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/ff38918327c7/JAH3-9-e016391-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/027bfc6fe72b/JAH3-9-e016391-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/13b19175e80e/JAH3-9-e016391-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/84c7385a89a6/JAH3-9-e016391-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/6b93f85b7321/JAH3-9-e016391-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/41f94cd99624/JAH3-9-e016391-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/ff38918327c7/JAH3-9-e016391-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/027bfc6fe72b/JAH3-9-e016391-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/13b19175e80e/JAH3-9-e016391-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/84c7385a89a6/JAH3-9-e016391-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a0/7763704/6b93f85b7321/JAH3-9-e016391-g006.jpg

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