Elsevier

JACC: Cardiovascular Imaging

Volume 2, Issue 2, February 2009, Pages 187-198
JACC: Cardiovascular Imaging

Original Research
Molecular Imaging for Efficacy of Pharmacologic Intervention in Myocardial Remodeling

https://doi.org/10.1016/j.jcmg.2008.11.011Get rights and content
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Objectives

Using molecular imaging techniques, we examined interstitial alterations during postmyocardial infarction (MI) remodeling and assessed the efficacy of antiangiotensin and antimineralocorticoid intervention, alone and in combination.

Background

The antagonists of the renin-angiotensin-aldosterone axis restrict myocardial fibrosis and cardiac remodeling after MI and contribute to improved survival. Radionuclide imaging with technetium-99m–labeled Cy5.5 RGD imaging peptide (CRIP) targets myofibroblasts and indirectly allows monitoring of the extent of collagen deposition post-MI.

Methods

CRIP was intravenously administered for gamma imaging after 4 weeks of MI in 63 Swiss-Webster mice and in 6 unmanipulated mice. Of 63 animals, 50 were treated with captopril (C), losartan (L), spironolactone (S) alone, or in combination (CL, SC, SL, and SCL), 8 mice received no treatment. Echocardiography was performed for assessment of cardiac remodeling. Hearts were characterized histopathologically for the presence of myofibroblasts and thick and thin collagen fiber deposition.

Results

Acute MI size was similar in all groups. The quantitative CRIP percent injected dose per gram uptake was greatest in the infarct area of untreated control mice (2.30 ± 0.14%) and decreased significantly in animals treated with 1 agent (C, L, or S; 1.71 ± 0.35%; p = 0.0002). The addition of 2 (CL, SC, or SL 1.31 ± 0.40%; p < 0.0001) or 3 agents (SCL; 1.16 ± 0.26%; p < 0.0001) demonstrated further reduction in tracer uptake. The decrease in echocardiographic left ventricular function, strain and rotation parameters, as well as histologically verified deposition of thin collagen fibers, was significantly reduced in treatment groups and correlated with CRIP uptake.

Conclusions

Radiolabeled CRIP allows for the evaluation of the efficacy of neurohumoral antagonists after MI and reconfirms superiority of combination therapy. If proven clinically, molecular imaging of the myocardial healing process may help plan an optimal treatment for patients susceptible to heart failure.

Key Words

collagen
remodeling
radionuclide imaging
angiotensin receptors
angiotensin-converting enzyme
mineralocorticoids
heart failure

Abbreviations and Acronyms

ACE-I
angiotensin-converting enzyme inhibitor
ARB
angiotensin receptor blocker
ASMA
alpha smooth muscle actin
C
captopril
CRIP
Cy5.5-RGD imaging peptide
L
losartan
LV
left ventricular
MI
myocardial infarction
RGD
Arg-Gly-Asp.
S
spironolactone
SARA
selective aldosterone receptor antagonist
sCRIP
scrambled Cy5.5-RGD imaging peptide
99mTc
technetium-99m

Cited by (0)

Dr. van den Borne was partially supported by a grant from the Netherlands Heart Foundation (2006R013). Dr. Lovhaug is an employee of GE Healthcare, involved in tracer preparation for the imaging studies. Dr. Pitt is a consultant to Pfizer, Merck, Takeda, Astra Zeneca, Synvista, Novartis, and Nile therapeutics but has no conflicts directly with the project. H. William Strauss, MD, acted as Guest Editor for this paper.