Cytokine profile of human septic shock serum inducing cardiomyocyte contractile dysfunction

被引:35
作者
Joulin, O.
Petillot, P.
Labalette, M.
Lancel, S.
Neviere, R.
机构
[1] Fac Med Lille, CHRU Lille, Dept Anesthesie Reanimat DAR 2, F-59045 Lille, France
[2] Fac Med Lille, CHRU Lille, Serv Immunol, F-59045 Lille, France
[3] Univ Lille, IMPRT IFR 114, Dept Physiol, Lille, France
[4] Univ Lille, IMPRT IFR 114, EA 2689, Lille, France
关键词
heart dysfunction; tumor necrosis factor; interleukin; sepsis; cell shortening;
D O I
10.33549/physiolres.930946
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This study was designed to measure nitrite/nitrate and cytokine levels of serum obtained from septic shock patients and to describe potential depressant effects of human septic serum on rat cardiomyocytes. Serum was prepared from 10 non-septic patients and 10 patients with documented septic shock. Adult rat ventricular myocytes were exposed to 20 % serum in the medium. Cardiomyocyte contractility was assessed by measuring shortening fraction and shortening velocity. Serum levels of nitrite/nitrate, a marker of nitric oxide final metabolites, and cytokines (tumor necrosis factor (TNF)-alpha interleukin (IL) 1 beta, 6, 10, 8 and 12p70) were measured. Compared with serum from non-septic patients, serum of septic shock patients induced rapid reduction of the extent and velocity of shortening in isolated cardiomyocytes. Nitrite/nitrate, TNF-alpha, IL-1 beta and IL-12p70 concentrations of tested serum for cardiomyocyte studies were not increased in septic serum compared with controls. In contrast, septic serum that induced a depression of in vitro contractility, had increased levels of IL-6, IL-8 and IL-10. We can conclude that the depression of in vitro contractility induced by septic serum is not directly dependent on elevated levels of nitric oxide metabolites, TNF-alpha or IL-1 beta. Our results support the view that other cytokines, including IL-6, IL-8 and IL-10, are potent circulating mediators of myocardial depression in cardiomyocytes.
引用
收藏
页码:291 / 297
页数:7
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