Thyroid hormone manipulation influences development of cardiovascular regulation in embryonic Pekin duck, Anas platyrhynchos domestica

J Comp Physiol B. 2018 Sep;188(5):843-853. doi: 10.1007/s00360-018-1166-1. Epub 2018 Jun 8.

Abstract

Thyroid hormones are key regulators of avian metabolism and may play a significant role in development at hatching. To better understand the role of thyroid hormones in avian development, we examined autonomic control of heart rate and blood pressure while manipulating thyroid hormone levels in the late stage embryonic Pekin duck (Anas platyrhynchos domestica). Thyroid hormone levels were manipulated on day 24 of a 28-day incubation period with the thyroperoxidase inhibitor methimazole (MMI), triiodothyronine (T3), or saline. On day 25 of incubation, autonomic tone on cardiovascular function was studied by injections of cholinergic and adrenergic receptor antagonists. Embryos from all treatment groups expressed a cholinergic and β-adrenergic tone on heart rate at this age. Cholinergic blockade with atropine produced a larger change in heart rate in the hyperthyroid animals compared with euthyroid animals. In response to β-adrenergic blockade, hyperthyroid conditions produced a larger decrease in heart rate compared with euthyroid animals, with no change in mean arterial blood pressure. In response to α-adrenergic blockade, mean arterial blood pressure decreased in the euthyroid animals and more developed hyperthyroid animals. Collectively, the data indicate that elevated levels of T3 can influence maturation of cholinergic and adrenergic receptor-mediated cardiovascular regulation in developing Pekin ducks near the end of incubation.

Keywords: Adrenergic tone; Autonomic control; Cholinergic tone; Development; Heart rate; Thyroid hormone.

Publication types

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

MeSH terms

  • Animals
  • Antithyroid Agents / pharmacology*
  • Arterial Pressure / drug effects
  • Ducks / embryology*
  • Ducks / physiology*
  • Embryo, Nonmammalian / drug effects
  • Embryo, Nonmammalian / physiology
  • Embryonic Development / drug effects
  • Heart Rate / drug effects
  • Methimazole / pharmacology*
  • Triiodothyronine / blood
  • Triiodothyronine / pharmacology*

Substances

  • Antithyroid Agents
  • Triiodothyronine
  • Methimazole