Alterations in perivascular sympathetic and nitrergic innervation function induced by late pregnancy in rat mesenteric arteries

PLoS One. 2015 May 7;10(5):e0126017. doi: 10.1371/journal.pone.0126017. eCollection 2015.

Abstract

Background and purpose: We investigated whether pregnancy was associated with changed function in components of perivascular mesenteric innervation and the mechanism/s involved.

Experimental approach: We used superior mesenteric arteries from female Sprague-Dawley rats divided into two groups: control rats (in oestrous phase) and pregnant rats (20 days of pregnancy). Modifications in the vasoconstrictor response to electrical field stimulation (EFS) were analysed in the presence/absence of phentolamine (alpha-adrenoceptor antagonist) or L-NAME (nitric oxide synthase-NOS- non-specific inhibitor). Vasomotor responses to noradrenaline (NA), and to NO donor DEA-NO were studied, NA and NO release measured and neuronal NOS (nNOS) expression/activation analysed.

Key results: EFS induced a lower frequency-dependent contraction in pregnant than in control rats. Phentolamine decreased EFS-induced vasoconstriction in segments from both experimental groups, but to a greater extent in control rats. EFS-induced vasoconstriction was increased by L-NAME in arteries from both experimental groups. This increase was greater in segments from pregnant rats. Pregnancy decreased NA release while increasing NO release. nNOS expression was not modified but nNOS activation was increased by pregnancy. Pregnancy decreased NA-induced vasoconstriction response and did not modify DEA-NO-induced vasodilation response.

Conclusions and implications: Neural control of mesenteric vasomotor tone was altered by pregnancy. Diminished sympathetic and enhanced nitrergic components both contributed to the decreased vasoconstriction response to EFS during pregnancy. All these changes indicate the selective participation of sympathetic and nitrergic innervations in vascular adaptations produced during pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism
  • Animals
  • Female
  • Mesenteric Arteries / innervation*
  • Mesenteric Arteries / physiology*
  • Nitric Oxide / metabolism
  • Norepinephrine / metabolism
  • Potassium Chloride / metabolism
  • Pregnancy
  • Rats, Sprague-Dawley
  • Vasoconstriction
  • Vasodilation
  • Vasomotor System / physiology*

Substances

  • Nitric Oxide
  • Potassium Chloride
  • Acetylcholine
  • Norepinephrine

Grants and funding

This study was supported by Ministerio de Economía y Competitividad (SAF2012-38530), Red RIC (RD12/0042/0024), and Fundación MAPFRE. E. Sastre received a FPI-UAM fellowship. L. Caracuel received a fellowship from Alianza 4 Universidades Program.