Quantification of bleomycin-induced murine lung damage in vivo with micro-computed tomography

被引:28
作者
Cavanaugh, Dawn
Travis, Elizabeth L.
Price, Roger E.
Gladish, Gregory
White, R. Allen
Wang, Min
Cody, Dianna D.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Biostat & Appl Math, Houston, TX 77030 USA
关键词
noninvasive small animal imaging; micro-CT; cone-beam CT; in vivo; lung damage quantification;
D O I
10.1016/j.acra.2006.08.011
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 [临床医学]; 100207 [影像医学与核医学]; 1009 [特种医学];
摘要
Rationale and Objectives. We explored noninvasive, in vivo cone-beam microcomputed tomography (micro-CT) to visualize and quantify fibrotic and inflammatory damage over the entire lung volume of mice. Materials and Methods. We used bleomycin to induce pulmonary damage in vivo and compared the results from micro-CT with histologic measurements. Ten C5713L/6 mice were given 5 U/kg bleomycin intratracheally. Seven surviving mice were scanned with micro-CT before administration of bleomycin, and again before sacrifice. The resulting images were analyzed for lung volume measurements. After the final scan, all lungs were examined histologically and pulmonary damage was quantified. Damaged lung tissue regions were matched between micro-CT images and histologic sections for each mouse. Results. The percent lung damage calculated from micro-CT and histology were correlated (r(2) = 0.49, r = 0.64 with P = 0.12), and the means of their respective distributions were not different (P > 0.05). Conclusion. This study shows that micro-CT is a promising alternative to predicting lung damage caused by bleomycin. CT image volumes of the thorax allow for global tissue sampling, which may be useful when following nonuniform lung damage that can occur from intratracheal administration of bleomycin.
引用
收藏
页码:1505 / 1512
页数:8
相关论文
共 18 条
[1]
Micro-CT with respiratory and cardiac gating [J].
Badea, C ;
Hedlund, LW ;
Johnson, GA .
MEDICAL PHYSICS, 2004, 31 (12) :3324-3329
[2]
Cavanaugh Dawn, 2004, Mol Imaging, V3, P55, DOI 10.1162/153535004773861723
[3]
HAAS CD, 1976, CANCER, V38, P8, DOI 10.1002/1097-0142(197607)38:1<8::AID-CNCR2820380103>3.0.CO
[4]
2-4
[5]
Haston CK, 1996, CANCER RES, V56, P2596
[6]
Limitations of clinical and biological histology [J].
Hillman, H .
MEDICAL HYPOTHESES, 2000, 54 (04) :553-564
[7]
High resolution computed tomography and MRI for monitoring lung tumor growth in mice undergoing radioimmunotherapy: Correlation with histology [J].
Kennel, SJ ;
Davis, IA ;
Branning, J ;
Pan, HJ ;
Kabalka, GW ;
Paulus, MJ .
MEDICAL PHYSICS, 2000, 27 (05) :1101-1107
[8]
BLEOMYCIN - A PHARMACOLOGICAL TOOL IN THE STUDY OF THE PATHOGENESIS OF INTERSTITIAL PULMONARY FIBROSIS [J].
LAZO, JS ;
HOYT, DG ;
SEBTI, SM ;
PITT, BR .
PHARMACOLOGY & THERAPEUTICS, 1990, 47 (03) :347-358
[9]
INTRATRACHEAL VERSUS INTRAVENOUS ADMINISTRATION OF BLEOMYCIN IN MICE - ACUTE EFFECTS [J].
LINDENSCHMIDT, RC ;
TRYKA, AF ;
GODFREY, GA ;
FROME, EL ;
WITSCHI, H .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1986, 85 (01) :69-77
[10]
INJURY TO THE LUNG FROM CANCER-THERAPY - CLINICAL SYNDROMES, MEASURABLE END-POINTS, AND POTENTIAL SCORING SYSTEMS [J].
MCDONALD, S ;
RUBIN, P ;
PHILLIPS, TL ;
MARKS, LB .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1995, 31 (05) :1187-1203