Whole-body imaging of high-dose ionizing irradiation-induced tissue injuries using 99mTc-duramycin.

Steven E Johnson, Zhixin Li, Yu Liu, John E Moulder, Ming Zhao
Author Information
  1. Steven E Johnson: Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.

Abstract

High-dose ionizing irradiation can cause extensive injuries in susceptible tissues. A noninvasive imaging technique that detects a surrogate marker of apoptosis may help characterize the dynamics of radiation-induced tissue damage. The goal of this study was to prove the concept of imaging the temporal and spatial distribution of damage in susceptible tissues after high-dose radiation exposure, using (99m)Tc-duramycin as a phosphatidylethanolamine-binding radiopharmaceutical.
METHODS: Rats were subjected to 15 Gy of total-body irradiation with x-rays. Planar whole-body (99m)Tc-duramycin scanning (n = 4 per time point) was conducted at 24, 48, and 72 h using a clinical γ-camera. On the basis of findings from planar imaging, preclinical SPECT data were acquired on control rats and on irradiated rats at 6 and 24 h after irradiation (n = 4 per time point). Imaging data were validated by γ-counting and histology, using harvested tissues in parallel groups of animals (n = 4).
RESULTS: Prominent focal uptake was detected in the thymus as early as 6 h after irradiation, followed by a gradual decline in (99m)Tc-duramycin binding accompanied by extensive thymic atrophy. Early (6-24 h) radioactivity uptake in the gastrointestinal region was detected. Significant signal was seen in major bones in a slightly delayed fashion, at 24 h, which persisted for at least 2 d. This finding was paralleled by an elevation in signal intensity in the kidneys, spleen, and liver. The imaging results were consistent with ex vivo γ-counting results and histology. Relatively high levels of apoptosis were detected from histology in the thymus, guts, and bones, with the thymus undergoing substantial atrophy.
CONCLUSION: As a proof of principle, this study demonstrated a noninvasive imaging technique that allows characterization of the temporal and spatial dynamics of injuries in susceptible tissues during the acute phase after high-dose ionizing irradiation. Such an imaging capability will potentially be useful for global, whole-body, assessment of tissue damage after radiation exposure. These data, in turn, will contribute to our general knowledge of tissue susceptibility to ionizing irradiation, as well as the onset and progression of tissue injuries.

Keywords

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Grants

  1. S10 RR027540/NCRR NIH HHS
  2. S10 OD016398/NIH HHS
  3. 5U19AI067734/NIAID NIH HHS
  4. R01 HL102085/NHLBI NIH HHS
  5. U19 AI067734/NIAID NIH HHS
  6. 5R01HL102085/NHLBI NIH HHS

MeSH Term

Animals
Apoptosis
Bacteriocins
Feasibility Studies
Female
Imaging, Three-Dimensional
Multimodal Imaging
Organotechnetium Compounds
Positron-Emission Tomography
Radiation Dosage
Radiation Injuries, Experimental
Rats
Tomography, X-Ray Computed
Whole Body Imaging

Chemicals

Bacteriocins
Organotechnetium Compounds
technetium 99m HYNIC-duramycin

Word Cloud

Created with Highcharts 10.0.0imagingirradiationinjuriestissuehionizingtissuesusingsusceptibleapoptosisdamagehigh-doseradiation99mTc-duramycinn=424datahistologydetectedthymusextensivenoninvasivetechniquedynamicsstudytemporalspatialexposurewhole-bodypertimepointrats6γ-countinguptakeatrophysignalbonesresultswillHigh-dosecancausedetectssurrogatemarkermayhelpcharacterizeradiation-inducedgoalproveconceptdistributionphosphatidylethanolamine-bindingradiopharmaceuticalMETHODS:Ratssubjected15Gytotal-bodyx-raysPlanarscanningconducted4872clinicalγ-camerabasisfindingsplanarpreclinicalSPECTacquiredcontrolirradiatedImagingvalidatedharvestedparallelgroupsanimalsRESULTS:ProminentfocalearlyfollowedgradualdeclinebindingaccompaniedthymicEarly6-24radioactivitygastrointestinalregionSignificantseenmajorslightlydelayedfashionpersistedleast2dfindingparalleledelevationintensitykidneysspleenliverconsistentexvivoRelativelyhighlevelsgutsundergoingsubstantialCONCLUSION:proofprincipledemonstratedallowscharacterizationacutephasecapabilitypotentiallyusefulglobalassessmentturncontributegeneralknowledgesusceptibilitywellonsetprogressionWhole-bodyirradiation-induced99mTc-duramycin99mTc-Duramycinphosphatidylethanolamine

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