丙氨酸和谷氨酰胺联合给药对长期饮酒引起的肝再生抑制的影响。

T Tanaka, M Imano, T Yamashita, T Monna, S Nishiguchi, T Kuroki, S Otani, K Maezono, K Mawatari
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引用次数: 0

摘要

我们研究了丙氨酸和谷氨酰胺混合物对酒精引起的肝再生的抑制作用,在开始给药6周后,大鼠接受部分肝切除术。给予酒精的大鼠部分肝切除术后24小时DNA合成受到抑制,但丙氨酸和谷氨酰胺治疗部分阻止了这种抑制。为了确定这种作用的机制,研究了多胺代谢。酒精或丙氨酸加谷氨酰胺对鸟氨酸脱羧酶的活性没有影响,鸟氨酸脱羧酶是多胺代谢的限速酶。在肝脏中,三种多胺中只有精胺的浓度有显著变化。在长期服用酒精期间,它会下降,而用丙氨酸和谷氨酰胺治疗可以防止这种下降。酒精使亚精胺乙酰化产物N(1)-乙酰亚精胺水平升高,而丙氨酸和谷氨酰胺使其升高幅度明显降低。肝脏亚精胺/精胺N(1)-乙酰转移酶是多胺乙酰化的关键酶,经长期酒精诱导后,丙氨酸加谷氨酰胺抑制了这种诱导作用。结果表明,丙氨酸和谷氨酰胺可以通过维持精胺水平和抑制精胺乙酰化来预防酒精引起的肝脏再生抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of combined alanine and glutamine administration on the inhibition of liver regeneration caused by long-term administration of alcohol.

We studied the effect of administration of a mixture of alanine and glutamine on the inhibition of liver regeneration caused by alcohol in rats undergoing partial hepatectomy 6 weeks after the start of alcohol administration. DNA synthesis was inhibited 24 hr after partial hepatectomy in rats given alcohol, but treatment with alanine and glutamine partially prevented this inhibition. To identify the mechanism of this effect, polyamine metabolism was studied. Administration of alcohol or alanine plus glutamine had no effect on the activity of ornithine decarboxylase, a rate-limiting enzyme of polyamine metabolism. In the liver, of the three polyamines, only the spermine concentration changed significantly. It decreased during long-term administration of alcohol, and this decrease was prevented by treatment with alanine and glutamine. The level of N(1)-acetylspermidine, the acetylated product of spermidine, was increased by alcohol, and its elevation was significantly less when alanine and glutamine were given. Hepatic spermidine/spermine N(1)-acetyltransferase, the key enzyme of polyamine acetylation, was induced by long-term administration of alcohol, and this induction was suppressed by alanine plus glutamine. The results suggest that treatment with alanine and glutamine can help to prevent the inhibition of liver regeneration caused by alcohol by maintaining the spermine level and suppressing the acetylation of spermidine.

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