Embryonic developmental oxygen preconditions cardiovascular functional response to acute hypoxic exposure and maximal β-adrenergic stimulation of anesthetized juvenile American alligators (Alligator mississippiensis)

J Exp Biol. 2019 Nov 8;222(Pt 21):jeb205419. doi: 10.1242/jeb.205419.

Abstract

The effects of the embryonic environment on juvenile phenotypes are widely recognized. We investigated the effect of embryonic hypoxia on the cardiovascular phenotype of 4-year-old American alligators (Alligator mississippiensis). We hypothesized that embryonic 10% O2 preconditions cardiac function, decreasing the reduction in cardiac contractility associated with acute 5% O2 exposure in juvenile alligators. Our findings indicate that dobutamine injections caused a 90% increase in systolic pressure in juveniles that were incubated in 21% and 10% O2, with the 10% O2 group responding with a greater rate of ventricular relaxation and greater left ventricle output compared with the 21% O2 group. Further, our findings indicate that juvenile alligators that experienced embryonic hypoxia have a faster rate of ventricular relaxation, greater left ventricle stroke volume and greater cardiac power following β-adrenergic stimulation, compared with juvenile alligators that did not experience embryonic hypoxia. When juveniles were exposed to 5% O2 for 20 min, normoxic-incubated juveniles had a 50% decline in left ventricle maximal rate of pressure development and maximal pressure; however, these parameters were unaffected and decreased less in the hypoxic-incubated juveniles. These data indicate that embryonic hypoxia in crocodilians alters the cardiovascular phenotype, changing the juvenile response to acute hypoxia and β-adrenergic stimulation.

Keywords: Crocodilian; Developmental programming; Hypoxia; Phenotypic plasticity; Reptile.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adrenergic beta-1 Receptor Agonists / pharmacology*
  • Alligators and Crocodiles / growth & development
  • Alligators and Crocodiles / metabolism*
  • Anaerobiosis
  • Animals
  • Cardiovascular System / drug effects
  • Cardiovascular System / physiopathology
  • Dobutamine / metabolism*
  • Embryo, Nonmammalian / drug effects
  • Embryo, Nonmammalian / metabolism
  • Embryonic Development
  • Oxygen / metabolism*
  • Receptors, Adrenergic, beta / metabolism*

Substances

  • Adrenergic beta-1 Receptor Agonists
  • Receptors, Adrenergic, beta
  • Dobutamine
  • Oxygen