Profile of circulating vasoactive substances in hemorrhagic shock and their pharmacologic manipulation

B. A. Jakschik, G. R. Marshall, J. L. Kourik, P. Needleman

Research output: Contribution to journalArticlepeer-review

61 Scopus citations

Abstract

Hemorrhage in dogs (to 45-50 mm Hg) was associated with a 10 fold increase in plasma renin activity (PRA) which remained elevated throughout the time course of shock including the irreversible (decompensation) stage. The presence of angiotensin II (AII) in arterial blood was demonstrated by the bloodbathed organ technique and confirmed by blockade with specific AII antagonists (cysteine AII or isoleucine AII). The contribution of AII to systemic peripheral resistance during hemorrhage shock in dogs was established by administering AII antagonists which immediately cause a further fall in blood pressure. Plasma catecholamines (CA) steadily increased during hemorrhage and peaked during compensation (a 100 fold increase). The CA decreased progressively during decompensation. Prostaglandin (PG) E like material was observed in arterial blood for 15-60 min (after hemorrhage); the peak arterial concentration was 2.6 ng/ml blood. Indomethacin (i.v. before 80% of maximum bleedout): confirmed the presence of PGE, increased blood pressure and increased blood loss. Thus: peripheral resistance during hemorrhagic shock seems temporally correlated with blood CA levels (and not PRA), and the renin AII system contributes to the maintenance of vascular resistance and may markedly decrease perfusion of organs, such as kidney; the administration of the proper combination of specific antagonists of vasoconstrictor humoral substances may radically improve organ perfusion and could contribute to ultimate recovery from hemorrhagic shock.

Original languageEnglish
Pages (from-to)842-852
Number of pages11
JournalJournal of Clinical Investigation
Volume54
Issue number4
DOIs
StatePublished - 1974

Fingerprint Dive into the research topics of 'Profile of circulating vasoactive substances in hemorrhagic shock and their pharmacologic manipulation'. Together they form a unique fingerprint.

Cite this