Yang Hui-Ting, Chen Yue-Hwa, Chiu Wan-Chun, Huang Shih-Yi
School of Pharmaceutical Science, Taipei Medical University, Taiwan.
J Nutr Biochem. 2006 Jan;17(1):45-50. doi: 10.1016/j.jnutbio.2005.05.002. Epub 2005 May 31.
In this study, we attempted to evaluate changes in sulfur-containing amino acid (SCAA) metabolism after short-term high-dose alcohol ingestion. At the beginning of the study, six animals were sacrificed as the baseline group and then other animals in the experiment were consecutively gavaged with alcohol (30%, 3 g/kg) for 7 days. Animals (n=6 each) were subsequently sacrificed at the time points of Days 1 (Group E1), 3 (Group E3) and 7 (Group E7). Blood samples and selected tissues were collected at each time interval. SCAA, pyridoxal phosphate (PLP) and glutathione (GSH) levels were analyzed. Results showed that taurine levels of tissues (brain, liver, heart and kidneys) all declined after the ethanol intervention and continued to decrease in selected tissues except the brain during the experiment. Furthermore, the trends of plasma taurine and PLP contents were highly correlated (r=.98, P=.045). A similar utilization pattern of plasma taurine and PLP indicated that transsulfuration preferred taurine production to GSH synthesis. The trend of plasma taurine levels being positively correlated with PLP levels reveals that dramatic transsulfuration occurred to meet the urgent demand for taurine by brain cells. In conclusion, we reported that continual alcohol ingestion alters SCAA utilization, especially by depletion of taurine and hypotaurine and by elevation of S-adenosyl homocysteine in the selected organs.
在本研究中,我们试图评估短期高剂量摄入酒精后含硫氨基酸(SCAA)代谢的变化。在研究开始时,处死6只动物作为基线组,然后对实验中的其他动物连续7天灌胃酒精(30%,3 g/kg)。随后在第1天(E1组)、第3天(E3组)和第7天(E7组)的时间点处死动物(每组n = 6)。在每个时间间隔采集血样和选定的组织。分析了SCAA、磷酸吡哆醛(PLP)和谷胱甘肽(GSH)水平。结果显示,乙醇干预后组织(脑、肝、心和肾)中的牛磺酸水平均下降,且在实验过程中,除脑外的选定组织中牛磺酸水平持续降低。此外,血浆牛磺酸和PLP含量的变化趋势高度相关(r = 0.98,P = 0.045)。血浆牛磺酸和PLP的相似利用模式表明,转硫作用优先产生牛磺酸而非合成GSH。血浆牛磺酸水平与PLP水平呈正相关的趋势表明,发生了剧烈的转硫作用以满足脑细胞对牛磺酸的迫切需求。总之,我们报告持续摄入酒精会改变SCAA的利用,特别是通过消耗牛磺酸和次牛磺酸以及升高选定器官中的S-腺苷同型半胱氨酸来实现。