Phillips R H, Whitehead M W, Lacey S, Champion M, Thompson R P, Powell J J
Gastrointestinal Laboratory, The Rayne Institute, St. Thomas' Hospital, London, UK.
Helicobacter. 2000 Sep;5(3):176-82. doi: 10.1046/j.1523-5378.2000.00028.x.
The aim of this study was to compare the dissolution, bioavailability, and anti-Helicobacter pylori activity of bismuth subnitrate and colloidal bismuth subcitrate. This could, first, provide insights into the mechanism of action of bismuth and, second, help to develop optimal therapeutic strategies.
Solubility and aquated size of bismuth species were determined in human gastric juice, while absorption into blood and urinary excretion of bismuth was determined in volunteers. Activity against H. pylori was determined in vitro in the presence and absence of antibiotics, while H. pylori eradication was compared in vivo.
Bismuth from colloidal bismuth subcitrate was at least 10% soluble and ultrafilterable and was absorbed in volunteers (>0.5%), whereas that from bismuth subnitrate was insoluble and not absorbed (<0.01%). Colloidal bismuth subcitrate was active against H. pylori (mean inhibitory concentration, </=12.5 microg/ml), while bismuth subnitrate was inactive (>400 microg/ml); neither was synergistic with antibiotics. With in vivo triple therapy, bismuth subnitrate was as effective as colloidal bismuth subcitrate in eradicating H. pylori (74% and 70% eradicated, respectively).
Colloidal bismuth subcitrate, unlike bismuth subnitrate, is partially soluble, absorbed in humans, and directly toxic to H. pylori in vitro. Surprisingly, however, these preparations had similar efficacy in vivo against H. pylori within triple therapy, suggesting that bismuth compounds may also exhibit indirect antimicrobial effects. We propose that this is an effect on the gastric mucus layer. Nonabsorbable bismuth compounds should be preferentially considered in bismuth-based therapies against H. pylori, as they would minimize toxicity while maintaining efficacy.
本研究旨在比较次硝酸铋和枸橼酸铋钾的溶出度、生物利用度及抗幽门螺杆菌活性。这首先有助于深入了解铋的作用机制,其次有助于制定最佳治疗策略。
测定铋化合物在人胃液中的溶解度和水化粒径,同时在志愿者中测定铋的血药吸收和尿排泄情况。在有或无抗生素存在的情况下,体外测定对幽门螺杆菌的活性,并在体内比较幽门螺杆菌的根除情况。
枸橼酸铋钾中的铋至少10%可溶且可超滤,并在志愿者体内被吸收(>0.5%),而次硝酸铋中的铋不溶且未被吸收(<0.01%)。枸橼酸铋钾对幽门螺杆菌有活性(平均抑制浓度,≤12.5μg/ml),而次硝酸铋无活性(>400μg/ml);两者均不与抗生素协同。在体内三联疗法中,次硝酸铋和枸橼酸铋钾根除幽门螺杆菌的效果相当(分别为74%和70%)。
与次硝酸铋不同,枸橼酸铋钾部分可溶,可被人体吸收,且在体外对幽门螺杆菌有直接毒性。然而,令人惊讶的是,在三联疗法中,这些制剂在体内对幽门螺杆菌的疗效相似,这表明铋化合物可能也具有间接抗菌作用。我们认为这是对胃黏液层的作用。在基于铋的抗幽门螺杆菌治疗中,应优先考虑不吸收的铋化合物,因为它们在保持疗效的同时可将毒性降至最低。