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正常男性血液单核细胞中攻击、敌意和愤怒与脂多糖刺激的肿瘤坏死因子(TNF)-α之间的关系。

The relation of aggression, hostility, and anger to lipopolysaccharide-stimulated tumor necrosis factor (TNF)-alpha by blood monocytes from normal men.

作者信息

Suarez Edward C, Lewis James G, Kuhn Cynthia

机构信息

Department of Psychiatry and Behavioral Sciences, Box 3328, Duke University Medical Center, Durham, NC 27110, USA.

出版信息

Brain Behav Immun. 2002 Dec;16(6):675-84. doi: 10.1016/s0889-1591(02)00019-3.

Abstract

Aggression, hostility, and anger significantly predict morbidity and mortality from atherosclerotic cardiovascular disease (ACVD). ACVD is believed to be an inflammatory disease characterized by increased expression of a number of proinflammatory cytokines, such as tumor necrosis factor (TNF)-alpha. This study examined the relation of aggression, hostility, and anger to monocyte-associated TNF-alpha expression following lipopolysaccharide (LPS) stimulation. Participants were 62 healthy, non-smoking men (aged 18-45 years). Hostility, anger, verbal, and physical aggression were assessed using the Buss-Perry aggression questionnaire (BPAQ). LPS-stimulated TNF-alpha expression was determined using dual-color flow cytometry gating for CD14(+) cells. After controlling for age, race, education, and alcohol use, scores on the hostility (p=.013), physical aggression (p=.010), and verbal aggression (p=.034) subscales, and the total score (p=.007) on the BPAQ were positively associated with LPS-stimulated TNF-alpha expression. The results suggest that hostility and aggression are associated with an increased expression of TNF-alpha, a cytokine implicated in ACVD.

摘要

攻击性、敌意和愤怒是动脉粥样硬化性心血管疾病(ACVD)发病和死亡的重要预测因素。ACVD被认为是一种炎症性疾病,其特征是多种促炎细胞因子表达增加,如肿瘤坏死因子(TNF)-α。本研究探讨了攻击性、敌意和愤怒与脂多糖(LPS)刺激后单核细胞相关TNF-α表达之间的关系。研究对象为62名健康、不吸烟的男性(年龄18 - 45岁)。使用布斯-佩里攻击性问卷(BPAQ)评估敌意、愤怒、言语攻击和身体攻击。通过双色流式细胞术对CD14(+)细胞进行门控,测定LPS刺激后的TNF-α表达。在控制年龄、种族、教育程度和饮酒情况后,BPAQ的敌意分量表得分(p = 0.013)、身体攻击分量表得分(p = 0.010)、言语攻击分量表得分(p = 0.034)以及总分(p = 0.007)与LPS刺激后的TNF-α表达呈正相关。结果表明,敌意和攻击行为与TNF-α表达增加有关,TNF-α是一种与ACVD相关的细胞因子。

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