Experimental Laboratory of the Department of Intensive Care, Erasme University Hospital, Hôpitaux Universitaires de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Department of Intensive Care, Centre Hospitalier Universitaire de Lille, Lille, France.
Crit Care Explor. 2024 Oct 11;6(10):e1163. doi: 10.1097/CCE.0000000000001163. eCollection 2024 Oct.
To analyze dynamic changes in the renin-angiotensin system (RAS) during septic shock, focusing on angiotensin-converting enzyme (ACE) activity and the balance between angiotensin peptides, using a mass spectrometry method.
Experimental septic shock model induced by peritonitis in swine.
Experimental Laboratory, Department of Intensive Care, Erasme Hospital, Université Libre de Bruxelles.
Forty time points from eight mechanically ventilated pigs.
Septic shock was induced using intraperitoneal instillation of autologous feces, followed by standardized fluid resuscitation, norepinephrine infusion, antibiotic administration, and peritoneal lavage.
The induction of sepsis resulted in a significant increase in plasma renin activity and levels of angiotensin I and II, with a significant decrease in ACE activity observed from 4 hours post-resuscitation and a notable rise in the angiotensin I/angiotensin II ratio at 12 hours. Additionally, a shift toward the angiotensin-(1-7) axis was observed, evidenced by an increased angiotensin-(1-7)/angiotensin II ratio.
The study highlighted dynamic shifts in the RAS during septic shock, characterized by reduced circulating ACE activity, elevated angiotensin I/II ratio, and a shift toward the angiotensin-(1-7) axis. These findings suggest an adaptive response within the RAS, potentially offering new insights into sepsis management and therapeutic targets.
使用质谱法分析脓毒症休克期间肾素-血管紧张素系统(RAS)的动态变化,重点关注血管紧张素转换酶(ACE)活性和血管紧张素肽之间的平衡。
通过腹膜炎在猪中诱导实验性脓毒症休克模型。
布鲁塞尔自由大学伊拉斯谟医院重症监护部的实验实验室。
8 头机械通气猪的 40 个时间点。
通过腹腔内注入自体粪便诱导脓毒症,然后进行标准化液体复苏、去甲肾上腺素输注、抗生素治疗和腹腔灌洗。
脓毒症的诱导导致血浆肾素活性和血管紧张素 I 和 II 水平显著增加,从复苏后 4 小时开始观察到 ACE 活性显著下降,12 小时时血管紧张素 I/血管紧张素 II 比值明显升高。此外,观察到向血管紧张素-(1-7)轴转移,表现为血管紧张素-(1-7)/血管紧张素 II 比值增加。
该研究强调了脓毒症休克期间 RAS 的动态变化,表现为循环 ACE 活性降低、血管紧张素 I/II 比值升高以及向血管紧张素-(1-7)轴转移。这些发现表明 RAS 内存在适应性反应,可能为脓毒症的治疗提供新的见解和治疗靶点。