血浆晚期糖基化终产物和可溶性糖基化受体作为人类颈动脉粥样硬化斑块中甾醇含量的指标

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
R. Pinto, G. Ferreira, G. Silvestre, M. Santana, V. Nunes, Lucas Ledesma, P. R. Pinto, S. D. de Assis, U. Machado, E. D. da Silva, M. Passarelli
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Lipids from plaques were extracted and sterols (oxysterols, cholesterol, desmosterol, lathosterol, sitosterol, and campesterol) were determined by using gas chromatography/mass spectrometry. Plasma total AGEs and pentosidine were measured by using fluorimetry and sRAGE by using ELISA. In symptomatic subjects´ atherosclerotic plaques, an increased amount of cholesterol (3x) and oxysterols [7 α-hydroxycholesterol (1.4x); 7 β−hydroxycholesterol (1.2x); 25-hydroxycholesterol (1.3x); 24-hydroxycholesterol (2.7x), and 27-hydroxycholesterol, (1.15x)], with exception to 7 ketocholesterol, were found in comparison to asymptomatic individuals. Plasma total AGEs and pentosidine significantly and positively correlated to sterols accumulated in the atherosclerotic lesion, including cholesterol, desmosterol, campesterol, sitosterol, and oxysterols. 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引用次数: 5

摘要

晚期糖基化终产物(AGEs)与心血管疾病(CVD)独立相关,有利于巨噬细胞泡沫细胞中胆固醇和氧化甾醇的积累。可溶性RAGE(sRAGE)损害细胞AGE信号传导,减轻AGE在动脉粥样硬化形成中的有害影响。在接受颈动脉内膜切除术的受试者中,评估了血浆AGEs和sRAGE与动脉粥样硬化斑块中胆固醇含量、胆固醇合成和吸收标志物以及氧化甾醇之间的关系。从有症状(n=23)和无症状受试者(n=40)中获得血浆和颈动脉斑块。从斑块中提取脂质,并通过使用气相色谱/质谱法测定甾醇(氧化甾醇、胆固醇、连糖甾醇、泡沫甾醇、谷甾醇和樟脑甾醇)。用荧光法测定血浆总AGEs和戊聚糖,用ELISA法测定sRAGE。在有症状的受试者的动脉粥样硬化斑块中,与无症状的个体相比,发现胆固醇(3x)和氧化固醇[7α-羟基胆固醇(1.4x);7β-羟胆固醇(1.2x);25羟基胆固醇(1.3x);24羟基胆固醇(2.7x)和27羟基胆固醇(1.15x)]的含量增加,但7酮胆固醇除外。血浆总AGEs和戊糖苷与动脉粥样硬化病变中积累的固醇显著正相关,包括胆固醇、桥甾醇、樟脑甾醇、谷甾醇和氧化固醇。另一方面,sRAGE与血浆中的总AGEs和戊糖苷呈负相关,与动脉粥样硬化病变中的主要氧化甾醇、胆固醇以及胆固醇合成和吸收标志物呈负相关。在多元回归分析中,观察到sRAGE与24-羟基胆固醇和桥骨醇之间存在显著的负相关,戊糖苷与24-羟胆固醇、27-羟基胆固醇、和樟脑醇之间存在正相关。总之,AGEs和sRAGE的血浆浓度是预测有症状和无症状个体动脉粥样硬化病变中甾醇积累的工具,有助于预防和改善急性心血管并发症的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma advanced glycation end products and soluble receptor for advanced glycation end products as indicators of sterol content in human carotid atherosclerotic plaques
Advanced glycation end products (AGEs) are independently related to cardiovascular disease (CVD) and favor cholesterol and oxysterol accumulation in macrophage foam cells. Soluble RAGE (sRAGE) impairs cellular AGE signaling alleviating the deleterious effects of AGE in atherogenesis. The association between plasma AGEs and sRAGE with the content of cholesterol, markers of cholesterol synthesis and absorption, and oxysterols in atherosclerotic plaques was evaluated in subjects undergoing carotid endarterectomy. Plasma and carotid plaques were obtained from symptomatic (n = 23) and asymptomatic subjects (n = 40). Lipids from plaques were extracted and sterols (oxysterols, cholesterol, desmosterol, lathosterol, sitosterol, and campesterol) were determined by using gas chromatography/mass spectrometry. Plasma total AGEs and pentosidine were measured by using fluorimetry and sRAGE by using ELISA. In symptomatic subjects´ atherosclerotic plaques, an increased amount of cholesterol (3x) and oxysterols [7 α-hydroxycholesterol (1.4x); 7 β−hydroxycholesterol (1.2x); 25-hydroxycholesterol (1.3x); 24-hydroxycholesterol (2.7x), and 27-hydroxycholesterol, (1.15x)], with exception to 7 ketocholesterol, were found in comparison to asymptomatic individuals. Plasma total AGEs and pentosidine significantly and positively correlated to sterols accumulated in the atherosclerotic lesion, including cholesterol, desmosterol, campesterol, sitosterol, and oxysterols. On the other hand, sRAGE inversely correlated to total AGEs and pentosidine in plasma, and with major species of oxysterols, cholesterol, and markers of cholesterol synthesis and absorption in the atherosclerotic lesion. In multiple regression analyses, it was observed a significant inverse correlation between sRAGE and 24-hydroxycholesterol and desmosterol, and a positive significant correlation between pentosidine and 24-hydroxycholesterol, 27-hydroxycholesterol, and campesterol. In conclusion, the plasma concentration of AGEs and sRAGE is a tool to predict the accumulation of sterols in atherosclerotic lesions in symptomatic and asymptomatic individuals, helping to prevent and improve the management of acute cardiovascular complications.
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来源期刊
Diabetes & Vascular Disease Research
Diabetes & Vascular Disease Research ENDOCRINOLOGY & METABOLISM-PERIPHERAL VASCULAR DISEASE
CiteScore
4.40
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: Diabetes & Vascular Disease Research is the first international peer-reviewed journal to unite diabetes and vascular disease in a single title. The journal publishes original papers, research letters and reviews. This journal is a member of the Committee on Publication Ethics (COPE)
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