Literature DB >> 1858917

Effect of chronic verapamil treatment on ventricular function and growth in chick embryos.

E B Clark1, N Hu, D R Turner, J E Litter, J Hansen.   

Abstract

Adjustment of myocardial mass to work load is a fundamental characteristic of the heart. We studied the effect of verapamil, a calcium channel blocker, on growth and function of chick embryonic ventricle. We treated stage 18 chick embryos with verapamil delivered to the extraembryonic vascular bed by a miniosmotic pump and compared them with saline-treated control and untreated embryos. At stages 24, 27, and 29, we measured ventricular pressure and dP/dt by a servo-null system, dorsal aortic stroke volume and dV/dt by pulsed-Doppler, and ventricular and embryo wet weights. Mean myocyte profile area was measured by digital planimetry technique, and cell growth response by DNA and protein assay. Verapamil treatment decreased ventricular pressure in experimental (P less than 0.05) compared with saline control and normal embryos; at stage 27, 1.59 +/- 0.21 vs. 2.17 +/- 0.05 and 2.35 +/- 0.08 (SE) mmHg, respectively. Mean dorsal aortic blood flow decreased in experimental (P less than 0.05) vs. control and normal embryos; at stage 27, 0.98 +/- 0.07 vs. 1.54 +/- 0.10 and 1.56 +/- 0.07 mm3/s, respectively. Stroke volume remained the same in all experimental, normal, and control embryos except at stage 29. Ventricular weight decreased in experimental (P less than 0.05) vs. control and normal embryos; at stage 27, 1.09 +/- 0.07 vs. 1.51 +/- 0.08 and 1.54 +/- 0.11 mg, respectively. Embryo weights, myocyte size, and cytoplasmic fractional volume were similar in all groups. Morphology of ventricles was normal. DNA was lower in experimental (P less than 0.05) compared with control and normal embryos.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1858917     DOI: 10.1152/ajpheart.1991.261.1.H166

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  6 in total

1.  Embryotoxic effects of L-691,121, a class III antiarrhythmic agent, in rats.

Authors:  Y Ban; R Konishi; K Kawana; T Nakatsuka; T Fujii; J M Manson
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

2.  Cyclic strain induces proliferation of cultured embryonic heart cells.

Authors:  C E Miller; K J Donlon; L Toia; C L Wong; P R Chess
Journal:  In Vitro Cell Dev Biol Anim       Date:  2000 Nov-Dec       Impact factor: 2.416

3.  Stress and strain adaptation in load-dependent remodeling of the embryonic left ventricle.

Authors:  Christine M Buffinton; Daniela Faas; David Sedmera
Journal:  Biomech Model Mechanobiol       Date:  2012-12-20

4.  A new method for measuring deformation of folding surfaces during morphogenesis.

Authors:  Benjamen A Filas; Andrew K Knutsen; Philip V Bayly; Larry A Taber
Journal:  J Biomech Eng       Date:  2008-12       Impact factor: 2.097

Review 5.  Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects.

Authors:  William J Kowalski; Kerem Pekkan; Joseph P Tinney; Bradley B Keller
Journal:  Front Physiol       Date:  2014-10-21       Impact factor: 4.566

Review 6.  Validating the Paradigm That Biomechanical Forces Regulate Embryonic Cardiovascular Morphogenesis and Are Fundamental in the Etiology of Congenital Heart Disease.

Authors:  Bradley B Keller; William J Kowalski; Joseph P Tinney; Kimimasa Tobita; Norman Hu
Journal:  J Cardiovasc Dev Dis       Date:  2020-06-12
  6 in total

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