Villanueva J A, Devlin A M, Halsted C H
Department of Internal Medicine, University of California, Davis 95616, USA.
Alcohol Clin Exp Res. 2001 Mar;25(3):415-20.
Folate deficiency is common in alcoholic patients, in part due to abnormal transport across membranes relevant to folate homeostasis. The reduced folate carrier (RFC) transports monoglutamyl folates across tissue membranes and could be affected by chronic exposure to ethanol. The micropig model is suitable to study the effect of alcoholism on RFC and folate transport across membranes.
The membrane transport of [3H]-folic acid was measured by a vacuum filtration method in jejunal brush border (JBB), liver plasma membrane (LPM), and kidney brush border (KBB) membranes vesicles from micropigs fed control or 40% ethanol diets for 12 months. RFC transcripts were analyzed by reverse transcription polymerase chain reaction in jejunal mucosa, liver, and kidney from the same animals.
When we compared results from three relevant membranes in control animals, the transport of [3H]-folic acid was highest in LPM, 3-fold lower in KBB (p < 0.001), and 6-fold lower in JBB (p < 0.001). The concentration of RFC transcripts per total RNA was greatest in liver, followed by kidney and jejunum. The transport of [3H]-folic acid by JBB vesicles from chronic ethanol-fed animals exhibited 2-fold lower Km and Vmax (p < 0.05), whereas there was no ethanol effect on the Vmax of [3H]-folic acid transport by LPM or KBB. RFC transcript levels were 10-fold lower in jejunal mucosa from ethanol-fed animals than in control-fed animals (p < 0.005).
Although our findings demonstrate different RFC transcript amounts and transport efficiencies among tissues, the present studies suggest that chronic ethanol exposure decreases the intestinal absorption of folic acid by altering the expression of RFC and consequently its transport kinetics in JBB. These findings provide a mechanism for the clinical finding of reduced folic acid absorption in chronic alcoholics.
叶酸缺乏在酒精性患者中很常见,部分原因是与叶酸稳态相关的跨膜转运异常。还原型叶酸载体(RFC)将单谷氨酸叶酸转运穿过组织膜,可能会受到长期乙醇暴露的影响。微型猪模型适合研究酒精中毒对RFC和叶酸跨膜转运的影响。
通过真空过滤法,在喂食对照或40%乙醇饮食12个月的微型猪的空肠刷状缘(JBB)、肝细胞膜(LPM)和肾刷状缘(KBB)膜囊泡中测量[3H]-叶酸的膜转运。通过逆转录聚合酶链反应分析同一动物空肠黏膜、肝脏和肾脏中的RFC转录本。
当我们比较对照动物中三个相关膜的结果时,[3H]-叶酸在LPM中的转运最高,在KBB中低3倍(p<0.001),在JBB中低6倍(p<0.001)。每总RNA中RFC转录本的浓度在肝脏中最高,其次是肾脏和空肠。慢性乙醇喂养动物的JBB囊泡对[3H]-叶酸的转运表现出Km和Vmax降低2倍(p<0.05),而乙醇对LPM或KBB对[3H]-叶酸转运的Vmax没有影响。乙醇喂养动物空肠黏膜中的RFC转录水平比对照喂养动物低10倍(p<0.005)。
虽然我们的研究结果表明不同组织之间RFC转录本数量和转运效率存在差异,但目前的研究表明,长期乙醇暴露通过改变RFC的表达及其在JBB中的转运动力学,降低了叶酸的肠道吸收。这些发现为慢性酒精中毒患者叶酸吸收减少的临床发现提供了一种机制。