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终生摄入膳食鱼油会改变Walker 256荷瘤大鼠的巨噬细胞反应。

Lifelong exposure to dietary fish oil alters macrophage responses in Walker 256 tumor-bearing rats.

作者信息

Bonatto Sandro J R, Folador Alessandra, Aikawa Júlia, Yamazaki Ricardo K, Pizatto Nathalia, Oliveira Heloisa H P, Vecchi Rodrigo, Curi Rui, Calder Philip C, Fernandes Luiz C

机构信息

Department of Physiology, Biological Sciences Building, Federal University of Paraná, 81540-990 Curitiba-PR, Brazil.

出版信息

Cell Immunol. 2004 Sep-Oct;231(1-2):56-62. doi: 10.1016/j.cellimm.2004.12.001. Epub 2005 Jan 20.

Abstract

Supplementation of the diet with fish oil (FO) decreases growth of the Walker 256 tumor and decreases the cachexia associated with tumor-bearing. The mechanisms by which FO inhibits tumor growth and cachexia are unknown. Macrophages are very important in host defence against tumors since they produce several anti-tumor agents which in turn have been shown to be modified by dietary FO, but rarely in the setting of tumor bearing and never in relation to lifelong exposure. In this study, we compared the effects of supplementation of the diet of pregnant and lactating rats and subsequent supplementation of the offspring with coconut fat or FO on macrophage activities involved in anti-tumor defence. FO supplementation was able to induce an increase in phagocytosis, in O2-, H2O2, nitric oxide, and TNF-alpha production by macrophages and in lysosomal volume in non-tumor-bearing rats. However, phagocytosis, production of O2- and H2O2 and lysosomal volume were not affected by the FO diet when rats were bearing tumors, although nitric oxide production was higher in these animals. It appears that tumor bearing activates the innate immune system and that dietary FO has little effect on innate immunity in the presence of Walker 256 tumors. Thus, it is still unclear how FO decreases the growth of Walker 256 tumors and the associated cachexia.

摘要

在饮食中补充鱼油(FO)可抑制Walker 256肿瘤的生长,并减轻与荷瘤相关的恶病质。FO抑制肿瘤生长和恶病质的机制尚不清楚。巨噬细胞在宿主抗肿瘤防御中非常重要,因为它们能产生多种抗肿瘤因子,而这些因子又已被证明会受到饮食中FO的影响,但在荷瘤情况下这种影响很少见,在终身接触FO的情况下则从未有过相关研究。在本研究中,我们比较了在怀孕和哺乳期大鼠的饮食中补充FO,以及随后在其后代的饮食中补充椰子油或FO对参与抗肿瘤防御的巨噬细胞活性的影响。在未荷瘤大鼠中,补充FO能够诱导巨噬细胞的吞噬作用增强,超氧阴离子(O2-)、过氧化氢(H2O2)、一氧化氮和肿瘤坏死因子-α(TNF-α)的产生增加,以及溶酶体体积增大。然而,在荷瘤大鼠中,尽管这些动物的一氧化氮产生量较高,但FO饮食对吞噬作用、O2-和H2O2的产生以及溶酶体体积没有影响。看来荷瘤激活了先天免疫系统,并且在存在Walker 256肿瘤的情况下,饮食中的FO对先天免疫几乎没有影响。因此,FO如何降低Walker 256肿瘤的生长以及相关的恶病质仍不清楚。

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