Remodeling of Wall Mechanics and the Myogenic Mechanism of Rat Intramural Coronary Arterioles in Response to a Short-Term Daily Exercise Program: Role of Endothelial Factors

J Vasc Res. 2018;55(2):87-97. doi: 10.1159/000486571. Epub 2018 Feb 14.

Abstract

Purpose: Exercise elicits early adaptation of coronary vessels enabling the coronary circulation to respond adequately to higher flow demands. We hypothesized that short-term daily exercise induces biomechanical and functional remodeling of the coronary resistance arteries related to pressure.

Methods: Male rats were subjected to a progressively increasing 4-week treadmill exercise program (over 60 min/day, 1 mph in the final step). In vitro pressure-diameter measurements were performed on coronary segments (119 ± 5 μm in diameter at 50 mm Hg) with microarteriography. The magnitude of the myogenic response and contribution of endogenous nitric oxide and prostanoid production to the wall mechanics and pressure-diameter relationship were assessed.

Results: Arterioles isolated from exercised ani mals - compared to the sedentary group - had thicker walls, increased distensibility, and a decreased elastic modulus as a result of reduced wall stress in the low pressure range. The arterioles of exercised rats exhibited a more powerful myogenic response and less endogenous vasoconstrictor prostanoid modulation at higher pressures, while vasodilator nitric oxide modulation of diameter was augmented at low pressures (< 60 mm Hg).

Conclusions: A short-term daily exercise program induces remodeling of rat intramural coronary arterioles, likely resulting in a greater range of coronary autoregulatory function (constrictor and dilator reserves) and more effective protection against great changes in intraluminal pressure, contributing thereby to the optimization of coronary blood flow during exercise.

Keywords: Contractility; Coronary arterioles; Daily exercise; Elasticity; Endothelium; Remodeling; Vascular.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Arterioles / metabolism
  • Arterioles / physiology*
  • Biomechanical Phenomena
  • Coronary Circulation*
  • Coronary Vessels / metabolism
  • Coronary Vessels / physiology*
  • Elastic Modulus
  • Hemodynamics*
  • Male
  • Nitric Oxide / metabolism
  • Physical Conditioning, Animal / methods*
  • Prostaglandins / metabolism
  • Rats, Wistar
  • Time Factors
  • Vascular Remodeling*
  • Vascular Stiffness
  • Vasoconstriction
  • Vasodilation

Substances

  • Prostaglandins
  • Nitric Oxide