Alterations in the Renin-Angiotensin System in Experimental Septic Shock

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...

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Veröffentlicht in:Critical care explorations 2024-10, Vol.6 (10), p.e1163
Hauptverfasser: Garcia, Bruno, Ter Schiphorst, Benoit, Su, Fuhong, Picod, Adrien, Ikenna-Uba, Theo, Favory, Raphaël, Annoni, Filippo, Mebazaa, Alexandre, Vincent, Jean-Louis, Creteur, Jacques, Taccone, Fabio S, Herpain, Antoine
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Sprache:eng
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Zusammenfassung: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.
ISSN:2639-8028
2639-8028
DOI:10.1097/CCE.0000000000001163