Anti-abortive effect of quercetin and bornyl acetate on macrophages and IL-10 in uterus of mice
Author(s) -
Tao Zhao,
Dan Wang,
Shi Wan yu,
Zhong Hui
Publication year - 2011
Publication title -
african journal of biotechnology
Language(s) - English
Resource type - Journals
ISSN - 1684-5315
DOI - 10.5897/ajb11.939
Subject(s) - quercetin , lipopolysaccharide , uterus , embryo , fetus , chemistry , resorption , gestation , in utero , andrology , macrophage , endocrinology , medicine , pregnancy , biology , biochemistry , in vitro , microbiology and biotechnology , genetics , antioxidant
The objective of this work was to investigate the significance of macrophages and IL-10 in uterus in early embryo loss (or resorption), and to elucidate the anti-abortive effect and the immunological modulation of maternal-fetal interface with quercetin and bornyl Acetate. Lipopolysaccharide (LPS) (0.10 ig/mouse) was injected via the tail vein in order to induce abortion in 7-day-gestation mice which received quercetin and bornyl acetate at days 4 to 7 of gestation. Levels of IL-10 in uterus supernatant were measured using enzyme-linked immuno-absorbent assay (ELISA), and uterine macrophages of each group (n=10) were detected by immunohistochemistry. The levels of IL-10 declined significantly in uterus with LPS treatment. The amount of macrophages in the uterus of LPS-induced abortion mice was much higher than that of the control mice. When quercetin and bornyl acetate were used to prevent LPS-induced abortion, the effect of quercetin combined with bornyl acetate on anti-LPS-induced abortion was more significant, and the IL-10 content was close to normal and the amount of macrophages was decreased to 16.199 ± 0.802, which was significantly different from that of LPSinduced abortion group. The decrease of IL-10 and the increase of macrophage number in the LPStreated mice uterus were associated with the embryo loss, and quercetin and bornyl acetate has the anti-abortive effect through modulation of maternal-fetal interface immunity balance. Key words : Embryo resorption, lipopolysaccharide, macrophages, IL-10, mice.
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