Oxytocin's role on the cardiorespiratory activity of endotoxemic rats

Respir Physiol Neurobiol. 2017 Feb:236:19-22. doi: 10.1016/j.resp.2016.10.008. Epub 2016 Oct 29.

Abstract

Background: Recent findings concerning oxytocin indicate its anti-inflammatory, cardioprotective and parasympathetic modulating properties. In this study, we investigated the effects of systemically applied oxytocin on the cardiorespiratory activity in a rodent model of moderate endotoxemia.

Methods: Telemetrically recorded electrocardiogram (ECGs) from animals which received lipopolysaccharide (LPS); oxytocin (Ox); lipopolysaccharide+oxytocin (LPS+Ox), or vehicle (V) were analyzed using the ECG-derived respiration (EDR) technique to estimate the respiratory rate. The mean R-R interval and the spectral parameters of heart rate variability (HRV), such as the natural logarithm of the high frequency (lnHF) and low frequency (lnLF) components were also estimated up to 24h after treatment.

Results: The endotoxemic animals (LPS) showed an elevated respiratory rate as well as a reduced mean R-R interval, lnHF and lnLF components compared to controls (V) from +5 to +12h after the treatment. The administration of oxytocin significantly attenuated the hyperventilation produced by the LPS-induced endotoxemia (LPS+Ox) and restored the values of the mean R-R interval and such spectral parameters at different time points.

Conclusions: Our results support the existence of a link among the respiratory, cardiovascular, and immune systems in which oxytocin seems to act as a potential cardioprotective peptide by favoring cardiac cholinergic autonomic coupling. As a result, oxytocin diminished animal's endotoxemic tachypnea and restored the cardiorespiratory interactions, which was indicated by the spectral components of HRV.

Keywords: Anti-inflammatory cholinergic pathway; ECG-derived respiration; HRV; LPS; Oxytocin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure / drug effects
  • Blood Pressure / physiology*
  • Disease Models, Animal
  • Electrocardiography
  • Endotoxemia / chemically induced
  • Endotoxemia / drug therapy*
  • Endotoxemia / physiopathology*
  • Heart Rate / drug effects
  • Heart Rate / physiology*
  • Lipopolysaccharides / toxicity
  • Male
  • Oxytocin / pharmacology
  • Oxytocin / therapeutic use*
  • Rats
  • Respiratory Rate / drug effects
  • Respiratory Rate / physiology*

Substances

  • Lipopolysaccharides
  • Oxytocin