کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5947191 1172366 2012 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Inhibition of neointimal hyperplasia in the rat carotid artery injury model by a HMGB1 inhibitor
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کاردیولوژی و پزشکی قلب و عروق
پیش نمایش صفحه اول مقاله
Inhibition of neointimal hyperplasia in the rat carotid artery injury model by a HMGB1 inhibitor
چکیده انگلیسی

ObjectiveHigh mobility group box 1 protein (HMGB1) is expressed in atherosclerotic lesions. However, its role in vascular system is unknown. In this study, we explore whether the inhibition of HMGB1 attenuates neointimal formation in animal models.Methods and resultsExperiments were performed with VSMCs from thoracic aorta of SD rats in vitro, and a rat carotid artery balloon injury model in vivo. HMGB1 levels were increased after stimulation of angiotensin II (Ang II) and 10% serum in cultured VSMCs. HMGB1 inhibitor (glycyrrhizin) significantly inhibited the proliferation and migration of Ang II-treated VSMCs, which was accompanied with decreased oxidative stress and inflammation. The underlying mechanisms were related with the promotion of antioxidant systems activity and deactivation of p38 MAPK/NF-κB signaling pathway, respectively. Furthermore, inhibition of HMGB1 blunted Notch signaling pathway during VSMCs phenotypic transition, and correspondingly restored VSMCs differentiated phenotype under 10% serum stimulation. In vivo study, HMGB1 expression was elevated after artery injury. Meanwhile, glycyrrhizin treatment suppressed HMGB1 expression, which was accompanied with blunted inflammation and oxidative stress after 7 days of balloon injury. Moreover, the area of neointimal to media area ratio was significantly decreased in glycyrrhizin group compared with injury group at 14 days after balloon injury.ConclusionsInhibition of HMGB1 activity attenuated VSMCs activation and neointimal formation after carotid injury. Therefore, blockage of HMGB1 might represent a novel therapeutic strategy for vascular injury.

► The role of HMGB1 is vascular system is still unclear. ► Inhibition of HMGB1 activity attenuated VSMCs activation and neointimal formation. ► Blockage of HMGB1 might represent a novel therapeutic strategy for vascular injury.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Atherosclerosis - Volume 224, Issue 2, October 2012, Pages 332-339
نویسندگان
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