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  • ISSN 1674-8301
  • CN 32-1810/R
Volume 31 Issue 2
Feb.  2017
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Article Contents
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

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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.

More Information
  • Received Date: September 26, 2016
  • Revised Date: October 11, 2016
  • 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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    1. Perera B, Wu Y, Nguyen NT, et al. Advances in drug delivery to atherosclerosis: Investigating the efficiency of different nanomaterials employed for different type of drugs. Mater Today Bio, 2023, 22: 100767. DOI:10.1016/j.mtbio.2023.100767
    2. Lu Y, Cui X, Zhang L, et al. The Functional Role of Lipoproteins in Atherosclerosis: Novel Directions for Diagnosis and Targeting Therapy. Aging Dis, 2022, 13(2): 491-520. DOI:10.14336/AD.2021.0929
    3. Di L, Maiseyeu A. Low-density lipoprotein nanomedicines: mechanisms of targeting, biology, and theranostic potential. Drug Deliv, 2021, 28(1): 408-421. DOI:10.1080/10717544.2021.1886199
    4. Härdtner C, Kornemann J, Krebs K, et al. Inhibition of macrophage proliferation dominates plaque regression in response to cholesterol lowering. Basic Res Cardiol, 2020, 115(6): 78. DOI:10.1007/s00395-020-00838-4
    5. Bedin A, Maranhão RC, Tavares ER, et al. Nanotechnology for the treatment of deep endometriosis: uptake of lipid core nanoparticles by LDL receptors in endometriotic foci. Clinics (Sao Paulo), 2019, 74: e989. DOI:10.6061/clinics/2019/e989

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