4.5 Article

Hyperelastic remodeling in the intrauterine growth restricted (IUGR) carotid artery in the near-term fetus

Journal

JOURNAL OF BIOMECHANICS
Volume 46, Issue 5, Pages 956-963

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jbiomech.2012.12.013

Keywords

Fetal programming; Extracellular matrix; Vascular remodeling; Collagen; Mechanics

Funding

  1. American Heart Association
  2. Sigma Xi grants in aid
  3. NIH [1K08HD060688-1, 1K25HL094749-1, IR01DK088139-01A1]
  4. Center for Women's Health Research
  5. University of Colorado Junior Faculty Research Development Award

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A constitutive model for a fiber reinforced hyperelastic material was applied to understand arterial fiber remodeling in a sheep model of Intrauterine Growth Restriction (IUGR). IUGR is associated altered hemodynamics characterized by increased resistance to blood flow in the placenta and elevated fetal arterial pressure and pulsatility. The constitutive model describes the collagen contribution to the mechanics within the arterial wall in both control and IUGR carotid artery through defining the material modulus and the orientation of the microstructure. A sheep model of placental insufficiency induced IUGR (PI-IUGR) was created by exposure of the pregnant ewe to elevated ambient temperatures. Experimental data was collected using pressure-diameter measurements to measure passive compliance in control and PI-IUGR carotid arteries. The constitutive model was optimized to fit the experimental data predicting the material parameters. Specifically, the collagen fiber predicted angle (gamma) in the control artery was 49.9 degrees from the circumferential axis while the PI-IUGR was 16.6 degrees with a 23.5% increase in fiber orientation (kappa). Quantitative assessment of collagen fiber orientation in secondary harmonic generation images confirmed the shift in orientation between the two groups. Together these suggest vascular remodeling of the ECM fiber orientation plays a major role in arterial stiffening in the PI-IUGR near-term fetal sheep. Published by Elsevier Ltd.

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