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Imaging of αvβ3 integrin expression in experimental myocardial ischemia with [68Ga]NODAGA-RGD positron emission tomography

Kuivanen A; Saukko P; Halonen P; Teuho J; Tarkia M; Saraste A; Käkelä M; Metsälä O; Pietilä M; Tolvanen T; Grönman M; Knuuti J; Kiviniemi T; Savunen T; Ylä-Herttuala S; Roivainen A

Imaging of αvβ3 integrin expression in experimental myocardial ischemia with [68Ga]NODAGA-RGD positron emission tomography

Kuivanen A
Saukko P
Halonen P
Teuho J
Tarkia M
Saraste A
Käkelä M
Metsälä O
Pietilä M
Tolvanen T
Grönman M
Knuuti J
Kiviniemi T
Savunen T
Ylä-Herttuala S
Roivainen A
Katso/Avaa
Publisher's version (1.900Mb)
Lataukset: 

doi:10.1186/s12967-017-1245-1
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042716949
Tiivistelmä

BACKGROUND:

Radiolabeled RGD peptides detect αvβ3 integrin expression associated with angiogenesis and extracellular matrix remodeling after myocardial infarction. We studied whether cardiac positron emission tomography (PET) with [68Ga]NODAGA-RGD detects increased αvβ3 integrin expression after induction of flow-limiting coronary stenosis in pigs, and whether αvβ3 integrin is expressed in viable ischemic or injured myocardium.

METHODS:

We studied 8 Finnish landrace pigs 13 ± 4 days after percutaneous implantation of a bottleneck stent in the proximal left anterior descending coronary artery. Antithrombotic therapy was used to prevent stent occlusion. Myocardial uptake of [68Ga]NODAGA-RGD (290 ± 31 MBq) was evaluated by a 62 min dynamic PET scan. The ischemic area was defined as the regional perfusion abnormality during adenosine-induced stress by [15O]water PET. Guided by triphenyltetrazolium chloride staining, tissue samples from viable and injured myocardial areas were obtained for autoradiography and histology.

RESULTS:

Stent implantation resulted in a partly reversible myocardial perfusion abnormality. Compared with remote myocardium, [68Ga]NODAGA-RGD PET showed increased tracer uptake in the ischemic area (ischemic-to-remote ratio 1.3 ± 0.20, p = 0.0034). Tissue samples from the injured areas, but not from the viable ischemic areas, showed higher [68Ga]NODAGA-RGD uptake than the remote non-ischemic myocardium. Uptake of [68Ga]NODAGA-RGD correlated with immunohistochemical detection of αvβ3 integrin that was expressed in the injured myocardial areas.

CONCLUSIONS:

Cardiac [68Ga]NODAGA-RGD PET demonstrates increased myocardial αvβ3 integrin expression after induction of flow-limiting coronary stenosis in pigs. Localization of [68Ga]NODAGA-RGD uptake indicates that it reflects αvβ3 integrin expression associated with repair of recent myocardial injury.

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