Aline D. Lima, Ning Hua, Raul C. Maranhão, James A. Hamilton. Evaluation of atherosclerotic lesions in cholesterol-fed mice during treatment with paclitaxel in lipid nanoparticles: a magnetic resonance imaging study[J]. The Journal of Biomedical Research, 2017, 31(2): 116-121. DOI: 10.7555/JBR.31.20160123
Citation:
Aline D. Lima, Ning Hua, Raul C. Maranhão, James A. Hamilton. Evaluation of atherosclerotic lesions in cholesterol-fed mice during treatment with paclitaxel in lipid nanoparticles: a magnetic resonance imaging study[J]. The Journal of Biomedical Research, 2017, 31(2): 116-121. DOI: 10.7555/JBR.31.20160123
Aline D. Lima, Ning Hua, Raul C. Maranhão, James A. Hamilton. Evaluation of atherosclerotic lesions in cholesterol-fed mice during treatment with paclitaxel in lipid nanoparticles: a magnetic resonance imaging study[J]. The Journal of Biomedical Research, 2017, 31(2): 116-121. DOI: 10.7555/JBR.31.20160123
Citation:
Aline D. Lima, Ning Hua, Raul C. Maranhão, James A. Hamilton. Evaluation of atherosclerotic lesions in cholesterol-fed mice during treatment with paclitaxel in lipid nanoparticles: a magnetic resonance imaging study[J]. The Journal of Biomedical Research, 2017, 31(2): 116-121. DOI: 10.7555/JBR.31.20160123
Evaluation of atherosclerotic lesions in cholesterol-fed mice during treatment with paclitaxel in lipid nanoparticles: a magnetic resonance imaging study
Laboratory of Metabolism and Lipids, Heart Institute of the Medical School Hospital, S?o Paulo, Brazil
2.
Department of Physiology and Biophysics, Boston University School of Medicine, Boston, MA 02118, USA
3.
Department of Physiology and Biophysics, Boston University School of Medicine, Boston, MA 02118, USA
Funds:
Research funding was provided by a grant from Boston University, United States, Funda??o de Amparo à Pesquisa do Estado de S?o Paulo (FAPESP), S?o Paulo, and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brasília, Brazil. Lima had a scholarship from Coordena??o de Aperfei?oamento de Pessoal de Nível Superior – CAPES and express her appreciation.
Cholesterol-core nanoparticles (LDE) have been shown to be recognized by low-density lipoprotein receptors (LDLR) after administration; therefore, LDE is an ideal vehicle to deliver drug with targeting property. Paclitaxel, when incorporated into LDE, promotes atherosclerosis regression with reduced drug toxicity in rabbits through LDLR. Here, we tested whether LDE paclitaxel could still be effective in reducing diet-induced atherosclerosis in a mouse model without LDLR. Nineteen LDLR knockout male mice were fed 1% cholesterol for 12 weeks. Then, 12 animals received 4-weekly intraperitoneal LDE-paclitaxel (4 mg/kg) while 7 controls received saline solution. On week 12 and 16, in vivo MRI of the aortic roots was performed. Aorta macroscopy was made after euthanasia. Reduction of atherosclerotic lesions was observed. LDE-paclitaxel treatment resulted in reduction of wall area (14%) and stenosis (22%) by MRI and 33% by macroscopy. Thus, LDE-paclitaxel may produce pharmacological effects through LDE uptake by mechanisms other than LDLR.
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