Sex-Mediated Response to the Beta-Blocker Landiolol in Sepsis: An Experimental, Randomized Study

Crit Care Med. 2018 Jul;46(7):e684-e691. doi: 10.1097/CCM.0000000000003146.

Abstract

Objectives: To investigate any gender effect of the beta-1 adrenergic blocker, landiolol, on cardiac performance and energy metabolism in septic rats, and to explore the expression of genes and proteins involved in this process.

Design: Randomized animal study.

Setting: University research laboratory.

Subjects: Male and female Wistar rats.

Interventions: One hour after cecal ligation and puncture, male and female rats were randomly allocated to the following groups: sham male, cecal ligation and puncture male, cecal ligation and puncture + landiolol male, sham female, cecal ligation and puncture female, and cecal ligation and puncture + landiolol female. Cardiac MRI was carried out 18 hours after cecal ligation and puncture to assess in vivo cardiac function. Ex vivo cardiac function measurement and P magnetic resonance spectroscopy were subsequently performed using an isovolumic isolated heart preparation. Finally, we assessed cardiac gene and protein expression.

Measurements and main results: In males, landiolol increased indexed stroke volume by reversing the indexed end-diastolic volume reduction without affecting left ventricle ejection fraction. In females, landiolol did not increase indexed stroke volume and indexed end-diastolic volume but decreased left ventricle ejection fraction. Landiolol had no effect on ex vivo cardiac function and on high-energy phosphate compounds. The effect of landiolol on the gene expression of natriuretic peptide receptor 3 and on protein expression of phosphorylated-AKT:AKT ratio and endothelial nitric oxide synthase was different in males and females.

Conclusions: Landiolol improved the in vivo cardiac performance of septic male rats while deleterious effects were reported in females. Expression of natriuretic peptide receptor 3, phosphorylated-AKT:AKT, and endothelial nitric oxide synthase are signaling pathways to investigate to better understand the sex differences in sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / therapeutic use*
  • Animals
  • Female
  • Heart / diagnostic imaging
  • Heart / drug effects
  • Heart / physiopathology
  • Magnetic Resonance Imaging
  • Male
  • Morpholines / therapeutic use*
  • Rats
  • Rats, Wistar
  • Sepsis / drug therapy*
  • Sex Factors
  • Stroke Volume / drug effects
  • Treatment Outcome
  • Urea / analogs & derivatives*
  • Urea / therapeutic use
  • Ventricular Function, Left / drug effects

Substances

  • Adrenergic beta-Antagonists
  • Morpholines
  • landiolol
  • Urea