Biosynthetic growth hormone increases the collagen deposition rate in rat aorta and heart

1995 ◽  
Vol 132 (2) ◽  
pp. 195-199 ◽  
Author(s):  
A Brüel ◽  
H Oxlund

Brüel A, Oxlund H. Biosynthetic growth hormone increases the collagen deposition rate in rat aorta and heart. Eur J Endocrinol 1995;132:195–9. ISSN 0804–4643 Disorders of the cardiovascular system often are associated with alterations in the metabolism of the collagens of these tissues. A method for in vivo determination of collagen deposition rate in small tissue samples is delineated and used for assessment of the effect of biosynthetic growth hormone (GH) injections on the collagen deposition rate in rat aorta and cardiac musculature. Rats were injected with GH, and the controls with saline, twice daily for 7 days. The in vivo collagen deposition rate was measured by injecting iv a large dose of [3H]-proline with a flooding dose of "cold" proline, followed by determination of the production of [3H]-hydroxyproline during a 4-h labelling period. Extractable collagens that were not bound in the tissue and therefore do not contribute mechanical strength to it were removed from the samples. 3H-Labelled- and "cold" amino acids were assessed by reversed-phase HPLC combined with simultaneous flow scintillation detection on the same sample. In the control group the deposition per hour was 0.13 ± 0.02% (mean ± sem) in aortic intima media and 0.72 ± 0.09% in cardiac left ventricular musculature. Growth hormone induced a threefold increase (p < 0.001 and p < 0.01, respectively) in the collagen deposition rate: 0.45 ± 0.06% in aortic intima media and 2.43 ± 0.45% in cardiac left ventricular musculature. The method described enables a rapid and sensitive determination of collagen deposition per hour in small tissue samples from experimental animals. The collagen deposition rate of cardiac musculature is fivefold higher compared with that of aortic intima media. Biosynthetic GH induces a threefold increase in the collagen deposition rate of these tissues. Hans Oxlund, Department of Connective Tissue Biology, Institute of Anatomy, University of Aarhus, DK-8000 Aarhus C, Denmark

Circulation ◽  
1968 ◽  
Vol 37 (4) ◽  
pp. 489-508 ◽  
Author(s):  
PAUL G. HUGENHOLTZ ◽  
HENRY R. WAGNER ◽  
HAROLD SANDLER

1994 ◽  
Vol 24 (1) ◽  
pp. 247-253 ◽  
Author(s):  
John P. Fisher ◽  
Carrie A. Wolfberg ◽  
Joseph S. Mikan ◽  
Francis J. Kiernan ◽  
Daniel B. Fram ◽  
...  

1997 ◽  
Vol 272 (2) ◽  
pp. H1047-H1052 ◽  
Author(s):  
B. D. Hoit ◽  
Z. U. Khan ◽  
C. M. Pawloski-Dahm ◽  
R. A. Walsh

Although targeted alterations of the mouse genome are used increasingly to identify the mechanisms underlying cardiac function, the methods used to study the phenotypic expression of these alterations in vivo are limited. To derive a relatively noninvasive, load-independent measure of left ventricular (LV) contractility in mice, we cannulated the femoral artery and performed two-dimensional directed M-mode echo studies in 28 anesthetized FVB/N mice, using a 9-MHz transducer. Loading conditions were altered by intraarterial methoxamine (3-12 microg/g), and LV shortening fraction was determined at several steady states, both before and after myocardial contractility was altered by either 4 microg/g intraperitoneal dobutamine (n = 16) or 1-2 microg/g verapamil (n = 12). The relation between LV systolic meridional stress and fractional shortening derived from pooled baseline data was inverse and linear [r = 0.80, slope = -0.19, intercept = 48%, standard error of estimate (SEE) = 5.5%, P < 0.001]. Dobutamine produced a parallel upward shift of the relation (r = 0.87, slope = -0.21, intercept = 61%, SEE = 4.5%, P < 0.001), and verapamil produced a downward shift of the relation (r = 0.48, slope = -0.05, intercept = 24%, SEE = 3.7%, P < 0.05). At matched levels of end-systolic stress, dobutamine increased and verapamil decreased the LV shortening fraction. We conclude that 1) inverse stress-shortening relations can be assessed noninvasively in mice; and 2) these relations are sensitive to alterations in inotropic state, independent of loading conditions.


Bone ◽  
1996 ◽  
Vol 19 (3) ◽  
pp. 157 ◽  
Author(s):  
H. Oxlund ◽  
C. Ejersted ◽  
T.T. Andreassen

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