Literature DB >> 30993709

Scaling of cardiac morphology is interrupted by birth in the developing sheep Ovis aries.

Edward P Snelling1, Roger S Seymour2, Dino A Giussani3, Andrea Fuller1, Shane K Maloney1,4, Anthony P Farrell5,6, Duncan Mitchell1,4, Keith P George7, Edward M Dzialowski8, Sonnet S Jonker9, Tilaye Wube10.   

Abstract

Scaling of the heart across development can reveal the degree to which variation in cardiac morphology depends on body mass. In this study, we assessed the scaling of heart mass, left and right ventricular masses, and ventricular mass ratio, as a function of eviscerated body mass across fetal and postnatal development in Horro sheep Ovis aries (~50-fold body mass range; N = 21). Whole hearts were extracted from carcasses, cleaned, dissected into chambers and weighed. We found a biphasic relationship when heart mass was scaled against body mass, with a conspicuous 'breakpoint' around the time of birth, manifest not by a change in the scaling exponent (slope), but rather a jump in the elevation. Fetal heart mass (g) increased with eviscerated body mass (Mb , kg) according to the power equation 4.90 Mb 0.88 ± 0.26 (± 95% CI ) , whereas postnatal heart mass increased according to 10.0 Mb 0.88 ± 0.10 . While the fetal and postnatal scaling exponents are identical (0.88) and reveal a clear dependence of heart mass on body mass, only the postnatal exponent is significantly less than 1.0, indicating the postnatal heart becomes a smaller component of body mass as the body grows, which is a pattern found frequently with postnatal cardiac development among mammals. The rapid doubling in heart mass around the time of birth is independent of any increase in body mass and is consistent with the normalization of wall stress in response to abrupt changes in volume loading and pressure loading at parturition. We discuss variation in scaling patterns of heart mass across development among mammals, and suggest that the variation results from a complex interplay between hard-wired genetics and epigenetic influences.
© 2019 Anatomical Society.

Entities:  

Keywords:  allometry; biphasic; cardiac; fetal; morphogenesis; ontogeny

Mesh:

Year:  2019        PMID: 30993709      PMCID: PMC6579936          DOI: 10.1111/joa.12990

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  51 in total

1.  Chamber formation and morphogenesis in the developing mammalian heart.

Authors:  V M Christoffels; P E Habets; D Franco; M Campione; F de Jong; W H Lamers; Z Z Bao; S Palmer; C Biben; R P Harvey; A F Moorman
Journal:  Dev Biol       Date:  2000-07-15       Impact factor: 3.582

2.  Normal right and left ventricular mass development during early infancy.

Authors:  James J Joyce; Patricia I Dickson; Ning Qi; Julie E Noble; J Usha Raj; Barry G Baylen
Journal:  Am J Cardiol       Date:  2004-03-15       Impact factor: 2.778

3.  The influence of body size on measurements of overall cardiac function.

Authors:  Paul D Chantler; R E Clements; L Sharp; K P George; L-B Tan; D F Goldspink
Journal:  Am J Physiol Heart Circ Physiol       Date:  2005-06-17       Impact factor: 4.733

Review 4.  Development of the human heart.

Authors:  Marc Sylva; Maurice J B van den Hoff; Antoon F M Moorman
Journal:  Am J Med Genet A       Date:  2013-04-30       Impact factor: 2.802

5.  Effects of birth-related events on central blood flow patterns.

Authors:  D F Teitel; H S Iwamoto; A M Rudolph
Journal:  Pediatr Res       Date:  1987-11       Impact factor: 3.756

Review 6.  Factors affecting changes in the neonatal systemic circulation.

Authors:  M A Heymann; H S Iwamoto; A M Rudolph
Journal:  Annu Rev Physiol       Date:  1981       Impact factor: 19.318

7.  Biphasic Allometry of Cardiac Growth in the Developing Kangaroo Macropus fuliginosus.

Authors:  Edward P Snelling; David A Taggart; Shane K Maloney; Anthony P Farrell; Roger S Seymour
Journal:  Physiol Biochem Zool       Date:  2015-01-08       Impact factor: 2.247

8.  Left ventricular stroke volume in the fetal sheep is limited by extracardiac constraint and arterial pressure.

Authors:  D A Grant; J C Fauchère; K J Eede; J V Tyberg; A M Walker
Journal:  J Physiol       Date:  2001-08-15       Impact factor: 5.182

9.  Cardiac fibroblasts regulate myocardial proliferation through beta1 integrin signaling.

Authors:  Masaki Ieda; Takatoshi Tsuchihashi; Kathryn N Ivey; Robert S Ross; Ting-Ting Hong; Robin M Shaw; Deepak Srivastava
Journal:  Dev Cell       Date:  2009-02       Impact factor: 12.270

10.  Left and right ventricular myocardial morphometry in fetal, neonatal, and adult sheep.

Authors:  J J Smolich; A M Walker; G R Campbell; T M Adamson
Journal:  Am J Physiol       Date:  1989-07
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