The Lipid Research Laboratory, Technion Faculty of Medicine, The Rappaport Family Institute for Research in the Medical Sciences, Rambam Medical Center, Haifa 31096, Israel.
Atherosclerosis. 2010 Sep;212(1):86-92. doi: 10.1016/j.atherosclerosis.2010.04.039. Epub 2010 May 6.
To examine whether the beneficial effects of PJ consumption by mice on their macrophages are mediated via PJ-induced increment in serum paraoxonase 1 (PON1) activity and/or in macrophage PON2 expression.
We performed studies in peritoneal macrophages (MPM) from C57BL/6 control mice, or from PON1KO mice, or from PON2KO mice that consumed PJ (200 microg of gallic acid equivalents/mouse/day, for 1 month period). PJ consumption by C57BL/6 mice resulted in a significant increment, by 36% in serum PON1 catalytic activities, and upregulated MPM PON2 expression. In MPM from C57BL/6 or from PON1KO mice that consumed PJ, the extent of cell-mediated LDL oxidation was decreased by 22%, and that of cellular superoxide release by 20-26%. In contrast, PJ consumption by PON2KO mice resulted in a minimal inhibitory effect on macrophage oxidative stress by only 4-9%. Unlike PJ antioxidative effects in MPM, PJ anti-atherogenic effects on MPM cholesterol and triglyceride metabolism were similar in all mice groups that consumed PJ. After PJ consumption, cellular cholesterol content was decreased by 14-19%, and this could be attributed to a significant inhibition in MPM cholesterol biosynthesis rate by 20-32%, and/or to stimulation of HDL-mediated cholesterol efflux from the cells by 22-37%. Similarly, MPM triglyceride content and triglyceride biosynthesis rate were both significantly decreased after PJ consumption, by 16-27% and by 22-28%, respectively.
PJ consumption antioxidative properties on mouse macrophages, but not PJ beneficial effects on macrophage cholesterol and triglyceride metabolism, are mediated via PJ-induced stimulation of macrophage PON2 expression. Serum PON1 stimulation by PJ consumption, however, was not involved in PJ-induced effects on macrophages.
研究 PJ 对小鼠巨噬细胞的有益作用是否通过 PJ 诱导的血清对氧磷酶 1(PON1)活性增加和/或巨噬细胞 PON2 表达增加来介导。
我们在 C57BL/6 对照小鼠、PON1KO 小鼠或 PON2KO 小鼠的腹腔巨噬细胞(MPM)中进行了研究,这些小鼠在一个月的时间内每天消耗 PJ(200 微克没食子酸当量/只)。PJ 消耗使 C57BL/6 小鼠的血清 PON1 催化活性增加了 36%,并上调了 MPM PON2 表达。在消耗 PJ 的 C57BL/6 或 PON1KO 小鼠的 MPM 中,细胞介导的 LDL 氧化程度降低了 22%,细胞内超氧化物释放降低了 20-26%。相比之下,PJ 消耗对 PON2KO 小鼠的巨噬细胞氧化应激只有 4-9%的最小抑制作用。与 PJ 在 MPM 中的抗氧化作用不同,PJ 对 MPM 胆固醇和甘油三酯代谢的抗动脉粥样硬化作用在消耗 PJ 的所有小鼠组中都相似。PJ 消耗后,细胞内胆固醇含量降低了 14-19%,这归因于 MPM 胆固醇生物合成率显著降低 20-32%,和/或 HDL 介导的胆固醇从细胞内流出增加 22-37%。同样,PJ 消耗后 MPM 甘油三酯含量和甘油三酯生物合成率分别降低了 16-27%和 22-28%。
PJ 对小鼠巨噬细胞的抗氧化特性,而不是 PJ 对巨噬细胞胆固醇和甘油三酯代谢的有益作用,是通过 PJ 诱导的巨噬细胞 PON2 表达刺激介导的。然而,PJ 消耗对血清 PON1 的刺激与 PJ 对巨噬细胞的作用无关。