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镁缺乏会抑制大鼠体内血液中谷胱甘肽的生物合成以及肿瘤生长。

Magnesium deficiency inhibits biosynthesis of blood glutathione and tumor growth in the rat.

作者信息

Mills B J, Lindeman R D, Lang C A

出版信息

Proc Soc Exp Biol Med. 1986 Mar;181(3):326-32. doi: 10.3181/00379727-181-42260.

Abstract

Previously we found that blood glutathione (GSH) levels increase in response to tumor growth in the rat and that this increase is not prevented with zinc deficiency. We also found that zinc deficiency which inhibited tumor growth did not prevent this increase in blood GSH. Therefore, the objectives of this study were to determine the effects of another nutritional modification, namely magnesium deficiency, on blood GSH status and on tumor growth. Magnesium was selected because it is an obligatory cofactor in GSH synthesis and in all biosynthetic reactions involving ATP. To this end, magnesium- and zinc-deficient rats with and without tumors were compared to pair-fed control rats with and without tumors. After 32 days of depletion, the rats were killed, and blood samples were analyzed for nonprotein sulfhydryls (SH) and specifically for GSH. The key finding was that in magnesium-deficient rats with or without tumors, blood GSH levels were low and SH levels were normal indicating a decrease in GSH biosynthesis. In contrast, zinc deficiency affected SH and GSH in parallel. Thus, these two deficiencies must act by different mechanisms. The zinc data verified our earlier results obtained with a different tumor type and rat strain, for blood GSH levels increased in tumor-bearing rats fed control diets, and zinc deficiency did not prevent this increase. Depletion of magnesium or zinc was equally effective in inhibiting tumor growth. These results provide in vivo evidence of a magnesium requirement for GSH biosynthesis in rat erythrocytes. Further, the results suggest that magnesium deficiency may inhibit tumor growth by limiting GSH synthesis from SH precursors.

摘要

此前我们发现,大鼠体内谷胱甘肽(GSH)水平会随着肿瘤生长而升高,且锌缺乏并不能阻止这种升高。我们还发现,抑制肿瘤生长的锌缺乏并未阻止血液中GSH的这种升高。因此,本研究的目的是确定另一种营养改变,即镁缺乏,对血液GSH状态和肿瘤生长的影响。选择镁是因为它是GSH合成以及所有涉及ATP的生物合成反应中必需的辅助因子。为此,将有肿瘤和无肿瘤的缺镁和缺锌大鼠与有肿瘤和无肿瘤的配对喂养对照大鼠进行比较。在消耗32天后,处死大鼠,并分析血液样本中的非蛋白巯基(SH),特别是GSH。关键发现是,无论有无肿瘤,缺镁大鼠的血液GSH水平都很低,而SH水平正常,这表明GSH生物合成减少。相比之下,锌缺乏对SH和GSH的影响是平行的。因此,这两种缺乏症的作用机制肯定不同。锌的数据证实了我们早期用不同肿瘤类型和大鼠品系获得的结果,因为在喂食对照饮食的荷瘤大鼠中血液GSH水平升高,而锌缺乏并不能阻止这种升高。镁或锌的消耗在抑制肿瘤生长方面同样有效。这些结果为大鼠红细胞中GSH生物合成对镁的需求提供了体内证据。此外,结果表明镁缺乏可能通过限制从SH前体合成GSH来抑制肿瘤生长。

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