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A major inducer of anticarcinogenic protective enzymes from broccoli: isolation and elucidation of structure.

机译:西兰花抗癌保护酶的主要诱因:结构的分离和阐明。

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摘要

Consumption of vegetables, especially crucifers, reduces the risk of developing cancer. Although the mechanisms of this protection are unclear, feeding of vegetables induces enzymes of xenobiotic metabolism and thereby accelerates the metabolic disposal of xenobiotics. Induction of phase II detoxication enzymes, such as quinone reductase [NAD(P)H:(quinone-acceptor) oxidoreductase, EC 1.6.99.2] and glutathione S-transferases (EC 2.5.1.18) in rodent tissues affords protection against carcinogens and other toxic electrophiles. To determine whether enzyme induction is responsible for the protective properties of vegetables in humans requires isolation of enzyme inducers from these sources. By monitoring quinone reductase induction in cultured murine hepatoma cells as the biological assay, we have isolated and identified (-)-1-isothiocyanato-(4R)-(methylsulfinyl)butane [CH3-SO-(CH2)4-NCS, sulforaphane] as a major and very potent phase II enzyme inducer in SAGA broccoli (Brassica oleracea italica). Sulforaphane is a monofunctional inducer, like other anticarcinogenic isothiocyanates, and induces phase II enzymes selectively without the induction of aryl hydrocarbon receptor-dependent cytochromes P-450 (phase I enzymes). To elucidate the structural features responsible for the high inducer potency of sulforaphane, we synthesized racemic sulforaphane and analogues differing in the oxidation state of sulfur and the number of methylene groups: CH3-SOm-(CH2)n-NCS, where m = 0, 1, or 2 and n = 3, 4, or 5, and measured their inducer potencies in murine hepatoma cells. Sulforaphane is the most potent inducer, and the presence of oxygen on sulfur enhances potency. Sulforaphane and its sulfide and sulfone analogues induced both quinone reductase and glutathione transferase activities in several mouse tissues. The induction of detoxication enzymes by sulforaphane may be a significant component of the anticarcinogenic action of broccoli.
机译:食用蔬菜,尤其是十字花科植物,可以降低患癌的风险。尽管这种保护的机制尚不清楚,但蔬菜的进食会诱导异种生物代谢的酶,从而加速异种生物的代谢处理。在啮齿动物组织中诱导阶段II的解毒酶,例如醌还原酶[NAD(P)H :(醌-受体)氧化还原酶,EC 1.6.99.2]和谷胱甘肽S-转移酶(EC 2.5.1.18)可以防止致癌物和其他有毒的亲电试剂。为了确定酶诱导是否对人类蔬菜的保护性能负责,需要从这些来源中分离酶诱导剂。通过监测培养的鼠肝癌细胞中醌还原酶的诱导,作为生物学检测方法,我们分离并鉴定了(-)-1-异硫氰酸根-(4R)-(甲基亚磺酰基)丁烷[CH3-SO-(CH2)4-NCS,萝卜硫烷]作为SAGA西兰花(Brassica oleracea italica)中主要且非常有效的II期酶诱导剂。萝卜硫烷是一种单功能诱导剂,与其他抗癌异硫氰酸酯一样,可选择性诱导II期酶,而无需诱导芳基烃受体依赖性细胞色素P-450(I期酶)。为了阐明负责萝卜硫烷的高诱导剂效能的结构特征,我们合成了外消旋的萝卜硫烷和类似物,其硫原子的氧化态和亚甲基数量不同:CH3-SOm-(CH2)n-NCS,其中m = 0, 1或2,n = 3、4或5,并测量它们在鼠肝癌细胞中的诱导力。萝卜硫烷是最有效的诱导剂,硫上氧的存在会增强药效。萝卜硫烷及其硫化物和砜类似物在几种小鼠组织中均诱导了醌还原酶和谷胱甘肽转移酶的活性。萝卜硫烷对脱毒酶的诱导可能是西兰花抗癌作用的重要组成部分。

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