Skip to main content
Top
Published in: Cardiovascular Toxicology 6/2018

01-12-2018

Application of a Simple Quantitative Assessment of Atherosclerotic Lesions in Freshly Isolated Aortas from Rabbits

Authors: Li-Jun Zhao, Ying Xiao, Xia Meng, Ning Wang, Y. James Kang

Published in: Cardiovascular Toxicology | Issue 6/2018

Login to get access

Abstract

Rabbits are widely used for the study of atherosclerosis; however, the lack of a unified and quantitative analysis of atheroma limits data interpretation and comparisons between laboratories. In this study, we applied a simple quantitative method, referred to as the oil red O (ORO) dye-eluting method, for analysis of atherosclerotic plaques in freshly isolated aortas. It employs ORO staining of the plaques followed by elution of the dye that is subjected to quantitative measurement. Atherosclerosis was induced in rabbits by feeding a 1% (w/w) high cholesterol diet for 4 or 12 weeks. Thoracic aortas were isolated and sufficiently stained by ORO. These dyes were easily and completely extracted by 100% ethanol and quantified by spectrophotometric measurement at 510 nm. A series of cross-sectional slices at 100-µm intervals were counterstained by elastic van Gieson. It was found that there was a highly positive correlation between the dye concentration and the amount of plaque tissue, determined as volume of plaques (regression coefficient r2: 0.8792, p < 0.001). The color equivalence of the dye content was expressed as µg/mm2 of intimal aorta area to allow direct comparisons among aortas. The color equivalences of ORO content in rabbits fed 12 weeks were almost 5.0 times higher than those fed 4 weeks. Thus, this ORO dye-eluting method is useful for quantification of atherosclerotic plaques in aortas in rabbits, as well as other animal models.
Literature
1.
go back to reference Fan, J., Kitajima, S., Watanabe, T., Xu, J., Zhang, J., Liu, E., & Chen, Y. E. (2015). Rabbit models for the study of human atherosclerosis: from pathophysiological mechanisms to translational medicine. Pharmacology & Therapeutics, 146, 104–119.CrossRef Fan, J., Kitajima, S., Watanabe, T., Xu, J., Zhang, J., Liu, E., & Chen, Y. E. (2015). Rabbit models for the study of human atherosclerosis: from pathophysiological mechanisms to translational medicine. Pharmacology & Therapeutics, 146, 104–119.CrossRef
2.
go back to reference Steinberg, D. (2004). Thematic review series: the pathogenesis of atherosclerosis. An interpretive history of the cholesterol controversy: part I. Journal of Lipid Research, 45, 1583–1593.CrossRefPubMed Steinberg, D. (2004). Thematic review series: the pathogenesis of atherosclerosis. An interpretive history of the cholesterol controversy: part I. Journal of Lipid Research, 45, 1583–1593.CrossRefPubMed
3.
go back to reference Hansson, G. K., Seifert, P. S., Olsson, G., & Bondjers, G. (1991). Immunohistochemical detection of macrophages and T lymphocytes in atherosclerotic lesions of cholesterol-fed rabbits. Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 11, 745–750.CrossRef Hansson, G. K., Seifert, P. S., Olsson, G., & Bondjers, G. (1991). Immunohistochemical detection of macrophages and T lymphocytes in atherosclerotic lesions of cholesterol-fed rabbits. Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 11, 745–750.CrossRef
4.
go back to reference Hong, M. K., Vossoughi, J., Mintz, G. S., Kauffman, R. D., Hoyt, R. F. Jr., Cornhill, J. F., … Hoeg, J. M. (1997). Altered compliance and residual strain precede angiographically detectable early atherosclerosis in low-density lipoprotein receptor deficiency. Arteriosclerosis, Thrombosis, and Vascular Biology, 17, 2209–2217.CrossRefPubMed Hong, M. K., Vossoughi, J., Mintz, G. S., Kauffman, R. D., Hoyt, R. F. Jr., Cornhill, J. F., … Hoeg, J. M. (1997). Altered compliance and residual strain precede angiographically detectable early atherosclerosis in low-density lipoprotein receptor deficiency. Arteriosclerosis, Thrombosis, and Vascular Biology, 17, 2209–2217.CrossRefPubMed
5.
go back to reference Wang, Y., Bai, L., Lin, Y., Chen, Y., Guan, H., Zhu, N., … Liu, E. (2015). Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits. Lipids in Health and Disease, 14, 82.CrossRefPubMedPubMedCentral Wang, Y., Bai, L., Lin, Y., Chen, Y., Guan, H., Zhu, N., … Liu, E. (2015). Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits. Lipids in Health and Disease, 14, 82.CrossRefPubMedPubMedCentral
6.
go back to reference Bentzon, J. F., Otsuka, F., Virmani, R., & Falk, E. (2014). Mechanisms of plaque formation and rupture. Circulation Research, 114, 1852–1866.CrossRefPubMed Bentzon, J. F., Otsuka, F., Virmani, R., & Falk, E. (2014). Mechanisms of plaque formation and rupture. Circulation Research, 114, 1852–1866.CrossRefPubMed
7.
go back to reference Paigen, B., Morrow, A., Holmes, P. A., Mitchell, D., & Williams, R. A. (1987). Quantitative assessment of atherosclerotic lesions in mice. Atherosclerosis, 68, 231–240.CrossRefPubMed Paigen, B., Morrow, A., Holmes, P. A., Mitchell, D., & Williams, R. A. (1987). Quantitative assessment of atherosclerotic lesions in mice. Atherosclerosis, 68, 231–240.CrossRefPubMed
8.
go back to reference Lin, Y., Bai, L., Chen, Y., Zhu, N., Bai, Y., Li, Q., … Liu, E. (2015). Practical assessment of the quantification of atherosclerotic lesions in apoE(−)/(−) mice. Molecular Medicine Reports, 12, 5298–5306.CrossRefPubMed Lin, Y., Bai, L., Chen, Y., Zhu, N., Bai, Y., Li, Q., … Liu, E. (2015). Practical assessment of the quantification of atherosclerotic lesions in apoE(−)/(−) mice. Molecular Medicine Reports, 12, 5298–5306.CrossRefPubMed
9.
go back to reference Weber, C., & Noels, H. (2011). Atherosclerosis: current pathogenesis and therapeutic options. Nature Medicine, 17, 1410–1422.CrossRefPubMed Weber, C., & Noels, H. (2011). Atherosclerosis: current pathogenesis and therapeutic options. Nature Medicine, 17, 1410–1422.CrossRefPubMed
10.
go back to reference Littie, R. D. (1944). Various oil soluble dyes as fat stains in the supersaturated isopropanol technic. Stain Technology, 19, 55–58.CrossRef Littie, R. D. (1944). Various oil soluble dyes as fat stains in the supersaturated isopropanol technic. Stain Technology, 19, 55–58.CrossRef
11.
go back to reference Zhang, C., Zheng, H., Yu, Q., Yang, P., Li, Y., Cheng, F., … Liu, E. (2010). A practical method for quantifying atherosclerotic lesions in rabbits. Journal of Comparative Pathology, 142, 122–128.CrossRefPubMed Zhang, C., Zheng, H., Yu, Q., Yang, P., Li, Y., Cheng, F., … Liu, E. (2010). A practical method for quantifying atherosclerotic lesions in rabbits. Journal of Comparative Pathology, 142, 122–128.CrossRefPubMed
12.
go back to reference Nunnari, J. J., Zand, T., Joris, I., & Majno, G. (1989). Quantitation of oil red O staining of the aorta in hypercholesterolemic rats. Experimental and Molecular Pathology, 51, 1–8.CrossRefPubMed Nunnari, J. J., Zand, T., Joris, I., & Majno, G. (1989). Quantitation of oil red O staining of the aorta in hypercholesterolemic rats. Experimental and Molecular Pathology, 51, 1–8.CrossRefPubMed
13.
go back to reference Beattie, J. H., Duthie, S. J., Kwun, I. S., Ha, T. Y., & Gordon, M. J. (2009). Rapid quantification of aortic lesions in apoE(−/−) mice. Journal of Vascular Research, 46, 347–352.CrossRefPubMed Beattie, J. H., Duthie, S. J., Kwun, I. S., Ha, T. Y., & Gordon, M. J. (2009). Rapid quantification of aortic lesions in apoE(−/−) mice. Journal of Vascular Research, 46, 347–352.CrossRefPubMed
14.
go back to reference Rutherford, C., Martin, W., Carrier, M., Anggard, E. E., & Ferns, G. A. (1997). Endogenously elicited antibodies to platelet derived growth factor-BB and platelet cytosolic protein inhibit aortic lesion development in the cholesterol-fed rabbit. International Journal of Experimental Pathology, 78, 21–32.CrossRefPubMedPubMedCentral Rutherford, C., Martin, W., Carrier, M., Anggard, E. E., & Ferns, G. A. (1997). Endogenously elicited antibodies to platelet derived growth factor-BB and platelet cytosolic protein inhibit aortic lesion development in the cholesterol-fed rabbit. International Journal of Experimental Pathology, 78, 21–32.CrossRefPubMedPubMedCentral
15.
go back to reference Yu, Q., Li, Y., Wang, Y., Zhao, S., Yang, P., Chen, Y., Fan, J., & Liu, E. (2012). C-reactive protein levels are associated with the progression of atherosclerotic lesions in rabbits. Histology and Histopathology, 27, 529–535.PubMed Yu, Q., Li, Y., Wang, Y., Zhao, S., Yang, P., Chen, Y., Fan, J., & Liu, E. (2012). C-reactive protein levels are associated with the progression of atherosclerotic lesions in rabbits. Histology and Histopathology, 27, 529–535.PubMed
16.
go back to reference Otto, C. M., Kuusisto, J., Reichenbach, D. D., Gown, A. M., & O’Brien, K. D. (1994). Characterization of the early lesion of ‘degenerative’ valvular aortic stenosis. Histological and immunohistochemical studies. Circulation, 90, 844–853.CrossRefPubMed Otto, C. M., Kuusisto, J., Reichenbach, D. D., Gown, A. M., & O’Brien, K. D. (1994). Characterization of the early lesion of ‘degenerative’ valvular aortic stenosis. Histological and immunohistochemical studies. Circulation, 90, 844–853.CrossRefPubMed
17.
go back to reference Xie, C., Ma, B., Wang, N., & Wan, L. (2017). Comparison of serological assessments in the diagnosis of liver fibrosis in bile duct ligation mice. Experimental Biology and Medicine, 242, 1398–1404.CrossRefPubMedPubMedCentral Xie, C., Ma, B., Wang, N., & Wan, L. (2017). Comparison of serological assessments in the diagnosis of liver fibrosis in bile duct ligation mice. Experimental Biology and Medicine, 242, 1398–1404.CrossRefPubMedPubMedCentral
18.
go back to reference Xiao, Y., Nie, X., Han, P., Fu, H., & Kang, J., Y (2016). Decreased copper concentrations but increased lysyl oxidase activity in ischemic hearts of rhesus monkeys. Metallomics: Integrated Biometal Science, 8, 973–980.CrossRef Xiao, Y., Nie, X., Han, P., Fu, H., & Kang, J., Y (2016). Decreased copper concentrations but increased lysyl oxidase activity in ischemic hearts of rhesus monkeys. Metallomics: Integrated Biometal Science, 8, 973–980.CrossRef
19.
go back to reference Koike, T., Kitajima, S., Yu, Y., Nishijima, K., Zhang, J., Ozaki, Y., … Fan, J. (2009). Human C-reactive protein does not promote atherosclerosis in transgenic rabbits. Circulation, 120, 2088–2094.CrossRefPubMedPubMedCentral Koike, T., Kitajima, S., Yu, Y., Nishijima, K., Zhang, J., Ozaki, Y., … Fan, J. (2009). Human C-reactive protein does not promote atherosclerosis in transgenic rabbits. Circulation, 120, 2088–2094.CrossRefPubMedPubMedCentral
20.
go back to reference Gao, B., Li, L., Zhu, P., Zhang, M., Hou, L., Sun, Y., … Gu, Y. (2015). Chronic administration of methamphetamine promotes atherosclerosis formation in ApoE−/− knockout mice fed normal diet. Atherosclerosis, 243, 268–277.CrossRefPubMed Gao, B., Li, L., Zhu, P., Zhang, M., Hou, L., Sun, Y., … Gu, Y. (2015). Chronic administration of methamphetamine promotes atherosclerosis formation in ApoE−/− knockout mice fed normal diet. Atherosclerosis, 243, 268–277.CrossRefPubMed
21.
go back to reference Hu, J. H., Touch, P., Zhang, J., Wei, H., Liu, S., Lund, I. K., Hoyer-Hansen, G., & Dichek, D. A. (2015). Reduction of mouse atherosclerosis by urokinase inhibition or with a limited-spectrum matrix metalloproteinase inhibitor. Cardiovascular Research, 105, 372–382.CrossRefPubMedPubMedCentral Hu, J. H., Touch, P., Zhang, J., Wei, H., Liu, S., Lund, I. K., Hoyer-Hansen, G., & Dichek, D. A. (2015). Reduction of mouse atherosclerosis by urokinase inhibition or with a limited-spectrum matrix metalloproteinase inhibitor. Cardiovascular Research, 105, 372–382.CrossRefPubMedPubMedCentral
22.
go back to reference Kamkar, M., Wei, L., Gaudet, C., Bugden, M., Petryk, J., Duan, Y., … Ruddy, T. D. (2016). Evaluation of Apoptosis with 99mTc-rhAnnexin V-128 and inflammation with 18F-FDG in a low-dose irradiation model of atherosclerosis in apolipoprotein E-deficient mice. Journal of Nuclear Medicine, 57, 1784–1791.CrossRefPubMed Kamkar, M., Wei, L., Gaudet, C., Bugden, M., Petryk, J., Duan, Y., … Ruddy, T. D. (2016). Evaluation of Apoptosis with 99mTc-rhAnnexin V-128 and inflammation with 18F-FDG in a low-dose irradiation model of atherosclerosis in apolipoprotein E-deficient mice. Journal of Nuclear Medicine, 57, 1784–1791.CrossRefPubMed
Metadata
Title
Application of a Simple Quantitative Assessment of Atherosclerotic Lesions in Freshly Isolated Aortas from Rabbits
Authors
Li-Jun Zhao
Ying Xiao
Xia Meng
Ning Wang
Y. James Kang
Publication date
01-12-2018
Publisher
Springer US
Published in
Cardiovascular Toxicology / Issue 6/2018
Print ISSN: 1530-7905
Electronic ISSN: 1559-0259
DOI
https://doi.org/10.1007/s12012-018-9465-z

Other articles of this Issue 6/2018

Cardiovascular Toxicology 6/2018 Go to the issue