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饲喂共轭亚油酸可提高大鼠乳腺组织中共轭亚油酸的水平,并抑制癌前病变的发展。

Vaccenic acid feeding increases tissue levels of conjugated linoleic acid and suppresses development of premalignant lesions in rat mammary gland.

作者信息

Banni S, Angioni E, Murru E, Carta G, Melis M P, Bauman D, Dong Y, Ip C

机构信息

Dipartimento di Biologia Sperimentale, Sezione di Patologia Sperimentale, Universita degli Studi di Cagliari, Cittadella Universitaria, 09042 Monserrato, Cagliari, Italy.

出版信息

Nutr Cancer. 2001;41(1-2):91-7. doi: 10.1080/01635581.2001.9680617.

Abstract

The objective of this report was to determine whether vaccenic acid (t11-18:1) is converted efficiently to conjugated linoleic acid (c9,t11-18:2, CLA) in rats via the delta 9-desaturase reaction and, if so, whether vaccenic acid could substitute for CLA as an anticancer agent. In Study 1, rats were fed 1%, 2%, or 3% vaccenic acid in their diet, and tissue levels of CLA and CLA metabolites were determined in liver and mammary gland. In general, concentrations of CLA and CLA metabolites increased proportionately with an increase in vaccenic acid intake, at least up to the 2% dose level. Beyond this dose, there was clearly a plateauing effect. Thus vaccenic acid concentration increased from an undetectable level in the control to 78.5 nmol/mg lipid in the liver of rats fed a 2% vaccenic acid diet. This was accompanied by an increase in CLA from 2.3 to 33.6 nmol/mg lipid. These changes were also mirrored in the mammary gland, where increases in vaccenic acid (from 27.5 to 163.2 nmol/mg lipid) and CLA (from 17.8 to 108.9 nmol/mg lipid) were similarly observed. Vaccenic acid at 2% produced a CLA concentration in the mammary gland that was historically associated with a positive response in tumor inhibition based on our past experience. This provided the basis for selecting 2% vaccenic acid in Study 2, which was designed to evaluate its efficacy in blocking the development of premalignant lesions in the rat mammary gland. In this experiment, formation of histologically identifiable pathology due to intraductal proliferation of terminal end bud cells of mammary epithelium was used as the end point of analysis at 6 wk after carcinogen administration. Treatment with vaccenic acid reduced the total number of these premalignant lesions by approximately 50%. We hypothesize that the anticancer response to vaccenic acid is likely to be mediated by its endogenous conversion to CLA via delta 9-desaturase.

摘要

本报告的目的是确定反式vaccenic酸(t11-18:1)在大鼠体内是否能通过Δ9-去饱和酶反应有效地转化为共轭亚油酸(c9,t11-18:2,CLA),如果可以,vaccenic酸是否能替代CLA作为抗癌剂。在研究1中,给大鼠喂食含1%、2%或3% vaccenic酸的日粮,并测定肝脏和乳腺中CLA及其代谢产物的组织水平。一般来说,CLA及其代谢产物的浓度随着vaccenic酸摄入量的增加而成比例增加,至少在2%的剂量水平之前是这样。超过这个剂量,明显出现了平台效应。因此,vaccenic酸浓度从对照组中不可检测的水平增加到喂食2% vaccenic酸日粮的大鼠肝脏中的78.5 nmol/mg脂质。同时,CLA从2.3增加到33.6 nmol/mg脂质。这些变化在乳腺中也有体现,同样观察到vaccenic酸(从27.5增加到163.2 nmol/mg脂质)和CLA(从17.8增加到108.9 nmol/mg脂质)的增加。2%的vaccenic酸在乳腺中产生的CLA浓度,根据我们过去的经验,在历史上与肿瘤抑制的阳性反应相关。这为在研究2中选择2%的vaccenic酸提供了依据,该研究旨在评估其在阻断大鼠乳腺中癌前病变发展方面的功效。在这个实验中,以致癌物给药6周后乳腺上皮终末芽细胞导管内增殖导致的组织学可识别病理形成作为分析终点。用vaccenic酸处理使这些癌前病变的总数减少了约50%。我们假设对vaccenic酸的抗癌反应可能是通过其经Δ9-去饱和酶内源性转化为CLA来介导的。

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