Chawla R K, Jones D P
Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322.
Biochim Biophys Acta. 1994 Jan 5;1199(1):45-51. doi: 10.1016/0304-4165(94)90094-9.
S-Adenosylmethionine (AdoMet) is an important biologic methylating agent for nucleic acids, phospholipids, biologic amines, and proteins. Previous studies indicated that hepatic AdoMet synthetase and hepatic levels of AdoMet are subnormal in patients with alcoholic cirrhosis. This abnormality limits the patients' capacity to convert phosphatidylethanolamine to phosphatidylcholine by way of phosphatidylethanolamine-N-methyltransferase (PEMT). Because alcoholic consumption appears to be associated with hepatic hypoxia, we previously measured AdoMet concentration in liver cells under acute hypoxia and found the level to be decreased substantially. In the present study, we determined whether a similar metabolic abnormality was also observed in rats maintained under physiologic hypoxia for 9 days and administered standard rat chow. The study showed that AdoMet levels in hypoxic rat (ave +/- SD) were significantly lower than those in the control (36.8 +/- 11.6 vs. 60.4 +/- 2.3 nmol/g liver; P < 0.05). Also significantly lower in the hypoxic group were the activities of AdoMet synthetase (0.60. +/- 0.07 vs. 0.97 +/- 0.20 U; P < 0.05) and PEMT (26.2 +/- 4.2 vs. 35.6 +/- 5.8 U; P < 0.02). The mRNA levels of AdoMet synthetase also declined in hypoxia indicating that hypoxia may modulate the gene expression of hepatic AdoMet synthetase. Thus, in vivo hypoxia may have an important effect on 1-carbon metabolism.
S-腺苷甲硫氨酸(AdoMet)是一种重要的生物甲基化剂,可作用于核酸、磷脂、生物胺和蛋白质。先前的研究表明,酒精性肝硬化患者的肝脏腺苷甲硫氨酸合成酶和肝脏中AdoMet水平低于正常水平。这种异常限制了患者通过磷脂酰乙醇胺-N-甲基转移酶(PEMT)将磷脂酰乙醇胺转化为磷脂酰胆碱的能力。由于饮酒似乎与肝脏缺氧有关,我们之前测量了急性缺氧条件下肝细胞中AdoMet的浓度,发现其水平大幅下降。在本研究中,我们确定在维持9天生理性缺氧并给予标准大鼠饲料的大鼠中是否也观察到类似的代谢异常。研究表明,缺氧大鼠的AdoMet水平(平均值±标准差)显著低于对照组(36.8±11.6对60.4±2.3 nmol/g肝脏;P<0.05)。缺氧组中腺苷甲硫氨酸合成酶的活性(0.60±0.07对0.97±0.20 U;P<0.05)和PEMT的活性(26.2±4.2对35.6±5.8 U;P<0.02)也显著降低。缺氧时腺苷甲硫氨酸合成酶的mRNA水平也下降,表明缺氧可能调节肝脏腺苷甲硫氨酸合成酶的基因表达。因此,体内缺氧可能对一碳代谢有重要影响。