Ammon H V, Tapper E J, Komorowski R A, Charaf U K, Loeffler R F, Lewand D, Walter L G
Am J Physiol. 1985 Apr;248(4 Pt 1):G485-93. doi: 10.1152/ajpgi.1985.248.4.G485.
To determine how sulfation alters the biological properties of dihydroxy bile acids, we compared the effects of 3-sulfodeoxycholate (SDC) and deoxycholate (DC) in the rat and rabbit intestine. While 5 mM DC induced water and electrolyte secretion and inhibited glucose absorption in the rat, SDC enhanced jejunal and ileal water and solute absorption. SDC had no effect in the rabbit ileum. In the rat jejunum DC caused mucosal injury and enhanced mucosal permeability while SDC had no effect. In vitro in the rabbit ileum, 10 mM SDC enhanced net sodium flux and decreased net residual flux, while 0.5 mM DC reduced net sodium flux and induced Cl- secretion. Both bile acids increased short-circuit current and potential difference and decreased tissue conductance. During reversed-phase, high-performance liquid chromatography SDC was more polar than DC. Sulfation reduced the ability of DC to destroy large unilamellar liposomes by a factor of 10. Thus, sulfation abolishes the effects of DC on the intestine by enhancing the polarity of this molecule. The enhancement of intestinal solute and water absorption by SDC requires further study.
为了确定硫酸化如何改变二羟基胆汁酸的生物学特性,我们比较了3-硫酸脱氧胆酸盐(SDC)和脱氧胆酸盐(DC)对大鼠和兔肠道的影响。5 mM DC可诱导大鼠水和电解质分泌并抑制葡萄糖吸收,而SDC可增强空肠和回肠的水和溶质吸收。SDC对兔回肠无影响。在大鼠空肠中,DC导致黏膜损伤并增强黏膜通透性,而SDC无此作用。在兔回肠的体外实验中,10 mM SDC增强净钠通量并降低净残留通量,而0.5 mM DC降低净钠通量并诱导氯离子分泌。两种胆汁酸均增加短路电流和电位差并降低组织电导。在反相高效液相色谱中,SDC比DC极性更强。硫酸化使DC破坏大单层脂质体的能力降低了10倍。因此,硫酸化通过增强该分子的极性消除了DC对肠道的影响。SDC对肠道溶质和水吸收的增强作用需要进一步研究。