Literature DB >> 27586835

A structure-function analysis of the left ventricle.

Edward P Snelling1, Roger S Seymour2, J E F Green3, Leith C R Meyer4, Andrea Fuller4, Anna Haw5, Duncan Mitchell6, Anthony P Farrell7, Mary-Ann Costello8, Adian Izwan9, Margaret Badenhorst10, Shane K Maloney6.   

Abstract

This study presents a structure-function analysis of the mammalian left ventricle and examines the performance of the cardiac capillary network, mitochondria, and myofibrils at rest and during simulated heavy exercise. Left ventricular external mechanical work rate was calculated from cardiac output and systemic mean arterial blood pressure in resting sheep (Ovis aries; n = 4) and goats (Capra hircus; n = 4) under mild sedation, followed by perfusion-fixation of the left ventricle and quantification of the cardiac capillary-tissue geometry and cardiomyocyte ultrastructure. The investigation was then extended to heavy exercise by increasing cardiac work according to published hemodynamics of sheep and goats performing sustained treadmill exercise. Left ventricular work rate averaged 0.017 W/cm3 of tissue at rest and was estimated to increase to ∼0.060 W/cm3 during heavy exercise. According to an oxygen transport model we applied to the left ventricular tissue, we predicted that oxygen consumption increases from 195 nmol O2·s-1·cm-3 of tissue at rest to ∼600 nmol O2·s-1·cm-3 during heavy exercise, which is within 90% of the oxygen demand rate and consistent with work remaining predominantly aerobic. Mitochondria represent 21-22% of cardiomyocyte volume and consume oxygen at a rate of 1,150 nmol O2·s-1·cm-3 of mitochondria at rest and ∼3,600 nmol O2·s-1·cm-3 during heavy exercise, which is within 80% of maximum in vitro rates and consistent with mitochondria operating near their functional limits. Myofibrils represent 65-66% of cardiomyocyte volume, and according to a Laplacian model of the left ventricular chamber, generate peak fiber tensions in the range of 50 to 70 kPa at rest and during heavy exercise, which is less than maximum tension of isolated cardiac tissue (120-140 kPa) and is explained by an apparent reserve capacity for tension development built into the left ventricle.
Copyright © 2016 the American Physiological Society.

Entities:  

Keywords:  capillary; heart; mitochondria; myofibril; work

Mesh:

Substances:

Year:  2016        PMID: 27586835      PMCID: PMC5142313          DOI: 10.1152/japplphysiol.00435.2016

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  67 in total

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2.  Cardiac work and efficiency.

Authors:  N Westerhof
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Review 3.  Angiogenesis in skeletal and cardiac muscle.

Authors:  O Hudlicka; M Brown; S Egginton
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5.  The postnatal development of the human cardiac ventricles.

Authors:  E N KEEN
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8.  Sarcomere dynamics in intact cardiac muscle.

Authors:  G H Pollack; J W Krueger
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Authors:  H Hoppeler; E R Weibel
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  4 in total

1.  Ameliorating the adverse cardiorespiratory effects of chemical immobilization by inducing general anaesthesia in sheep and goats: implications for physiological studies of large wild mammals.

Authors:  Adian Izwan; Edward P Snelling; Roger S Seymour; Leith C R Meyer; Andrea Fuller; Anna Haw; Duncan Mitchell; Anthony P Farrell; Mary-Ann Costello; Shane K Maloney
Journal:  J Comp Physiol B       Date:  2018-09-19       Impact factor: 2.200

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