Chronic Diseases and Translational Medicine (Jun 2018)

Novel findings in relation to multiple anti-atherosclerotic effects of XueZhiKang in humans

  • Rui-Xia Xu,
  • Yan Zhang,
  • Yuan-Lin Guo,
  • Chun-Yan Ma,
  • Yu-Hong Yao,
  • Sha Li,
  • Xiao-Lin Li,
  • Ping Qing,
  • Ying Gao,
  • Na-Qiong Wu,
  • Cheng-Gang Zhu,
  • Geng Liu,
  • Qian Dong,
  • Jing Sun,
  • Jian-Jun Li

Journal volume & issue
Vol. 4, no. 2
pp. 117 – 126

Abstract

Read online

Background: Previous studies have clearly demonstrated that XueZhiKang (XZK), an extract of cholestin, can decrease low-density lipoprotein cholesterol (LDL-C) and cardiovascular events. However, the mechanism of the effects of XZK on atherosclerosis (AS) in humans has been reported less frequently. In the present study, we investigated the impact of XZK on lipoprotein subfractions, oxidized LDL (oxLDL), and interleukin-6 (IL-6). Methods: From October 2015 to July 2016, 40 subjects were enrolled in this study. Of them, 20 subjects with dyslipidemia received XZK 1200 mg/day for 8 weeks (XZK group); 20 additional healthy subjects who did not receive therapy acted as controls. The plasma lipoprotein subfractions, oxLDL, and IL-6 were examined at baseline and again at 8 weeks. Results: Data showed that XZK could significantly decrease not only plasma LDL-C levels (87.26 ± 24.45 vs. 123.34 ± 23.99, P < 0.001), total cholesterol (4.14 ± 0.87 vs. 5.08 ± 1.03, P < 0.001), triglycerides (0.95 ± 0.38 vs. 1.55 ± 0.61, P < 0.05), and apolipoprotein B (1.70 ± 0.35 vs. 1.81 ± 0.72, P < 0.05), but also oxLDL (36.36 ± 5.31 vs. 49.20 ± 15.01, P < 0.05) and IL-6 (8.50 ± 7.40 vs. 10.40 ± 9.49, P < 0.05). At the same time, XZK reduced the concentration of small LDL-C (1.78 ± 2.17 vs. 6.33 ± 7.78, P < 0.05) and the percentage of the small LDL subfraction (1.09 ± 1.12 vs. 3.07 ± 3.09, P < 0.05). Conclusions: Treatment with 1200 mg/day XZK for 8 weeks significantly decreased the atherogenic small LDL subfraction and reduced oxidative stress and inflammatory markers, in addition to affecting the lipid profile, suggesting multiple beneficial effects in coronary artery disease. Keywords: XueZhiKang, Hyperlipidemia, Low-density lipoprotein cholesterol subfraction, Oxidized LDL, Interleukin-6