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Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice

  • Authors:
    • Jianzhen Lv
    • Wen Xiong
    • Tiantian Lei
    • Hailian Wang
    • Minghan Sun
    • Erwei Hao
    • Zhiping Wang
    • Xiaoqi Huang
    • Shaoping Deng
    • Jiagang Deng
    • Yi Wang
  • View Affiliations / Copyright

    Affiliations: Guangxi Key Laboratory of Efficacy Study on Chinese Materia Medica, Guangxi University of Chinese Medicine, Nanning, Guangxi 530200, P.R. China, Department of Ultrasound, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, Sichuan 610072, P.R. China, Department of Pharmacy, Medical School of University of Electronic Science and Technology of China, Chengdu, Sichuan 610054, P.R. China, Institute of Organ Transplantation, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, Sichuan 610072, P.R. China, Department of Gynecology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, Sichuan 610072, P.R. China, Affiliated Hospital of Guangxi Traditional Chinese Medical University, Nanning, Guangxi 530001, P.R. China, Department of Pharmacy, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, Sichuan 610072, P.R. China
    Copyright: © Lv et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 8171-8179
    |
    Published online on: September 25, 2017
       https://doi.org/10.3892/mmr.2017.7609
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Abstract

Previous studies have demonstrated that regulatory T cells (Tregs) are pivotal in the regulation of T cell‑mediated immune responses in atherosclerosis, a chronic autoimmune‑like disease. In the authors' previous studies, it was demonstrated that amygdalin ameliorated atherosclerosis by the regulation of Tregs in apolipoprotein E‑deficient (ApoE‑/‑) mice. Therefore, the aim of the present study was to investigate the therapeutic effect of amygdalin on low‑density lipoprotein (LDL) receptor deficient (LDLR‑/‑) mice, and to examine its immune regulatory function by the stimulation of Tregs. To establish an atherosclerosis mouse model, the LDLR‑/‑ mice were fed a high fat and high cholesterol diet then the total plasma cholesterol, triglyceride, LDL and chemokines levels were measured by an ELISA. Following sacrificing the mice, the upper sections of the aorta were stained by hematoxylin and eosin, and Oil red O to assess the plaque area. Then western blotting and reverse transcription polymerase chain reactions were performed to analysis the expression levels of cluster of differentiation 68, monocyte chemoattractant protein‑1, matrix metalloproteinase (MMP)‑2, MMP‑9 and forkhead box P3 (Foxp3). To further confirm the activation of FOXP3 by amygdalin, lentiviruses carrying Foxp3 shRNA were injected into the mice, and the serum cytokines levels were measured by ELISA. Following feeding of the mice with a high‑fat/high‑cholesterol diet, the LDLR‑/‑ mice demonstrated comparatively higher levels of triglyceride, total cholesterol and LDL, compared with levels in the amygdalin‑treated mice. By comparing the vessel area, lumen area, plaque area, and percentage aortic plaque coverage, the effects of amygdalin on pre‑existing lesions were assessed. In addition, the levels of CD68, monocyte chemoattractant protein‑1, MMP‑2 and MMP‑9 were analyzed, and analysis of the expression of interleukin (IL)‑1β, IL‑6 and tumor necrosis factor (TNF)‑α indicated that the mice treated with amygdalin had decreased expression of pro‑inflammatory cytokines. The mRNA and protein levels of Foxp3 were also quantified, and the mice treated with amygdalin demonstrated an increased number of Tregs. The knockdown of Foxp3mRNA resulted in the increased secretion of IL‑1β, IL‑6 and TNF‑α. Therefore, the data indicated that amygdalin regulated the formation of atherosclerosis and stabilized the plaque by suppressing inflammatory responses and promoting the immune‑modulation function of Tregs. Taken together, the results demonstrated the therapeutic effect of amygdalin on atherosclerosis.
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Copy and paste a formatted citation
Spandidos Publications style
Lv J, Xiong W, Lei T, Wang H, Sun M, Hao E, Wang Z, Huang X, Deng S, Deng J, Deng J, et al: Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice. Mol Med Rep 16: 8171-8179, 2017.
APA
Lv, J., Xiong, W., Lei, T., Wang, H., Sun, M., Hao, E. ... Wang, Y. (2017). Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice. Molecular Medicine Reports, 16, 8171-8179. https://doi.org/10.3892/mmr.2017.7609
MLA
Lv, J., Xiong, W., Lei, T., Wang, H., Sun, M., Hao, E., Wang, Z., Huang, X., Deng, S., Deng, J., Wang, Y."Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice". Molecular Medicine Reports 16.6 (2017): 8171-8179.
Chicago
Lv, J., Xiong, W., Lei, T., Wang, H., Sun, M., Hao, E., Wang, Z., Huang, X., Deng, S., Deng, J., Wang, Y."Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice". Molecular Medicine Reports 16, no. 6 (2017): 8171-8179. https://doi.org/10.3892/mmr.2017.7609
Copy and paste a formatted citation
x
Spandidos Publications style
Lv J, Xiong W, Lei T, Wang H, Sun M, Hao E, Wang Z, Huang X, Deng S, Deng J, Deng J, et al: Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice. Mol Med Rep 16: 8171-8179, 2017.
APA
Lv, J., Xiong, W., Lei, T., Wang, H., Sun, M., Hao, E. ... Wang, Y. (2017). Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice. Molecular Medicine Reports, 16, 8171-8179. https://doi.org/10.3892/mmr.2017.7609
MLA
Lv, J., Xiong, W., Lei, T., Wang, H., Sun, M., Hao, E., Wang, Z., Huang, X., Deng, S., Deng, J., Wang, Y."Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice". Molecular Medicine Reports 16.6 (2017): 8171-8179.
Chicago
Lv, J., Xiong, W., Lei, T., Wang, H., Sun, M., Hao, E., Wang, Z., Huang, X., Deng, S., Deng, J., Wang, Y."Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice". Molecular Medicine Reports 16, no. 6 (2017): 8171-8179. https://doi.org/10.3892/mmr.2017.7609
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