Berman Marvin D, Carey Martin C
Department of Medicine, Harvard Medical School, Boston, Massachusetts; Division of Gastroenterology, Brigham and Women's Hospital, Boston, Massachusetts; Harvard Digestive Diseases Center, Boston, Massachusetts.
Department of Medicine, Harvard Medical School, Boston, Massachusetts; Division of Gastroenterology, Brigham and Women's Hospital, Boston, Massachusetts; Harvard Digestive Diseases Center, Boston, Massachusetts
Am J Physiol Gastrointest Liver Physiol. 2015 Jan 1;308(1):G42-55. doi: 10.1152/ajpgi.00277.2014. Epub 2014 Oct 30.
Metastable and equilibrium phase diagrams for unconjugated bilirubin IXα (UCB) in bile are yet to be determined for understanding the physical chemistry of pigment gallstone formation. Also, UCB is a molecule of considerable biomedical importance because it is a potent antioxidant and an inhibitor of atherogenesis. We employed principally a titrimetric approach to obtain metastable and equilibrium UCB solubilities in model bile systems composed of taurine-conjugated bile salts, egg yolk lecithin (mixed long-chain phosphatidylcholines), and cholesterol as functions of total lipid concentration, biliary pH values, and CaCl2 plus NaCl concentrations. Metastable and equilibrium precipitation pH values were obtained, and average pKa values of the two carboxyl groups of UCB were calculated. Added lecithin and increased temperature decreased UCB solubility markedly, whereas increases in bile salt concentrations and molar levels of urea augmented solubility. A wide range of NaCl and cholesterol concentrations resulted in no specific effects, whereas added CaCl2 produced large decreases in UCB solubilities at alkaline pH values only. UV-visible absorption spectra were consistent with both hydrophobic and hydrophilic interactions between UCB and bile salts that were strongly influenced by pH. Reliable literature values for UCB compositions of native gallbladder biles revealed that biles from hemolytic mice and humans with black pigment gallstones are markedly supersaturated with UCB and exhibit more acidic pH values, whereas biles from nonstone control animals and patients with cholesterol gallstone are unsaturated with UCB.
为了理解色素胆结石形成的物理化学过程,尚未确定胆汁中未结合胆红素IXα(UCB)的亚稳相图和平衡相图。此外,UCB是一种具有重要生物医学意义的分子,因为它是一种有效的抗氧化剂和动脉粥样硬化的抑制剂。我们主要采用滴定法来获得UCB在由牛磺酸结合胆汁盐、蛋黄卵磷脂(混合长链磷脂酰胆碱)和胆固醇组成的模型胆汁系统中的亚稳溶解度和平衡溶解度,这些溶解度是总脂质浓度、胆汁pH值以及CaCl2和NaCl浓度的函数。获得了亚稳沉淀pH值和平衡沉淀pH值,并计算了UCB两个羧基的平均pKa值。添加卵磷脂和升高温度会显著降低UCB的溶解度,而胆汁盐浓度和尿素摩尔水平的增加则会提高溶解度。NaCl和胆固醇浓度的广泛变化没有产生特定影响,而仅在碱性pH值下添加CaCl2会使UCB的溶解度大幅降低。紫外可见吸收光谱与UCB和胆汁盐之间的疏水和亲水相互作用一致,这些相互作用受pH值的强烈影响。天然胆囊胆汁中UCB成分的可靠文献值表明,来自溶血小鼠和患有黑色色素胆结石的人类的胆汁中UCB明显过饱和,且pH值更酸性,而来自无结石对照动物和胆固醇胆结石患者的胆汁中UCB不饱和。