Mitochondrial N-formyl peptides induce cardiovascular collapse and sepsis-like syndrome

Camilla Ferreira Wenceslau, Cameron G. McCarthy, Theodora Szasz, Styliani Goulopoulou, R. Clinton Webb

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Fifty percent of trauma patients who present sepsis-like syndrome do not have bacterial infections. This condition is known as systemic inflammatory response syndrome (SIRS). A unifying factor of SIRS and sepsis is cardiovascular collapse. Trauma and severe blood loss cause the release of endogenous molecules known as damage-associated molecular patterns. Mitochondrial N-formyl peptides (F-MIT) are damage-associated molecular patterns that share similarities with bacterial N-formylated peptides and are potent immune system activators. The goal of this study was to investigate whether F-MIT trigger SIRS, including hypotension and vascular collapse via formyl peptide receptor (FPR) activation. We evaluated cardiovascular parameters in Wistar rats treated with FPR or histamine receptor antagonists and inhibitors of the nitric oxide pathway before and after F-MIT infusion. F-MIT, but not nonformylated peptides or mitochondrial DNA, induced severe hypotension via FPR activation and nitric oxide and histamine release. Moreover, F-MIT infusion induced hyperthermia, blood clotting, and increased vascular permeability. To evaluate the role of leukocytes in F-MIT-induced hypotension, neutrophil, basophil, or mast cells were depleted. Depletion of basophils, but not neutrophils or mast cells, abolished F-MIT-induced hypotension. Rats that underwent hemorrhagic shock increased plasma levels of mitochondrial formylated proteins associated with lung damage and antagonism of FPR ameliorated hemorrhagic shock-induced lung injury. Finally, F-MIT induced vasodilatation in isolated resistance arteries via FPR activation; however, F-MIT impaired endothelium-dependent relaxation in the presence of blood. These data suggest that F-MIT may be the link among trauma, SIRS, and cardiovascular collapse.

Original languageEnglish
Pages (from-to)768-777
Number of pages10
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume308
Issue number7
DOIs
StatePublished - 1 Jan 2015

Fingerprint

Formyl Peptide Receptor
Systemic Inflammatory Response Syndrome
Controlled Hypotension
Peptides
Hemorrhagic Shock
Basophils
Mast Cells
Wounds and Injuries
Nitric Oxide
Neutrophils
N-Formylmethionine Leucyl-Phenylalanine
Histamine Receptors
Induced Hyperthermia
Histamine Release
Histamine Antagonists
Mitochondrial Proteins
Adult Respiratory Distress Syndrome
Capillary Permeability
Lung Injury
Blood Coagulation

Keywords

  • Cardiovascular collapse
  • Mitochondrial N-formyl peptides
  • Sepsis-like syndrome

Cite this

Wenceslau, Camilla Ferreira ; McCarthy, Cameron G. ; Szasz, Theodora ; Goulopoulou, Styliani ; Clinton Webb, R. / Mitochondrial N-formyl peptides induce cardiovascular collapse and sepsis-like syndrome. In: American Journal of Physiology - Heart and Circulatory Physiology. 2015 ; Vol. 308, No. 7. pp. 768-777.
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Mitochondrial N-formyl peptides induce cardiovascular collapse and sepsis-like syndrome. / Wenceslau, Camilla Ferreira; McCarthy, Cameron G.; Szasz, Theodora; Goulopoulou, Styliani; Clinton Webb, R.

In: American Journal of Physiology - Heart and Circulatory Physiology, Vol. 308, No. 7, 01.01.2015, p. 768-777.

Research output: Contribution to journalArticle

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T1 - Mitochondrial N-formyl peptides induce cardiovascular collapse and sepsis-like syndrome

AU - Wenceslau, Camilla Ferreira

AU - McCarthy, Cameron G.

AU - Szasz, Theodora

AU - Goulopoulou, Styliani

AU - Clinton Webb, R.

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