Takahashi N, Yuasa S, Hitomi H, Hashimoto M, Kiyomoto H, Uchida K, Shoji T, Hirohata M, Matsuo H
2nd Department of Internal Medicine, Kagawa Medical University.
Nihon Jinzo Gakkai Shi. 1996 Dec;38(12):610-7.
We examined the effects of histamine H2-receptor antagonists on the phosphorus binding ability of phosphate binders. Serum calcium, phosphorus, ALP, PTH and arterial blood pH and bicarbonate were measured during treatment with histamine H2-receptor antagonists accompanied by calcium carbonate in sixteen patients undergoing maintenance hemodialysis. Seven patients receiving histamine H2-receptor antagonists without calcium carbonate were selected as controls. In the sixteen patients receiving calcium carbonate, serum calcium, ALP, PTH and arterial blood pH and bicarbonate were not significantly altered during treatment with histamine H2-receptor antagonists, but serum phosphorus levels increased significantly after four (5.6 +/- 1.1 mg/dl) and eight weeks (5.9 +/- 0.8 mg/dl) of treatment as compared with that before treatment (4.8 +/- 1.2 mg/dl). Furthermore, serum phosphorus levels decreased significantly eight weeks after the discontinuation of treatment with histamine H2-receptor antagonists. In the seven control patients there were no statistical differences in serum calcium and phosphorus levels measured before and after treatment with histamine H2-receptor antagonists. In seven other patients receiving histamine H2-receptor antagonists with calcium carbonate, calcium carbonate was replaced with calcium lactate as the phosphate binder after four weeks of treatment with histamine H2-receptor antagonists. With the 4-week administration of histamine H2-receptor antagonists accompanied by calcium carbonate, the serum phosphorus level increased, similarly to that of the first study (from 6.3 +/- 0.9 to 7.1 +/- 0.5 mg/dl). However, with the substitution of calcium lactate, the serum phosphorus level decreased significantly (6.3 +/- 0.2 and 6.0 +/- 0.9 mg/dl after four and eight weeks, respectively, despite continued administration of histamine H2-receptor antagonists). These results suggest that histamine H2-receptor antagonists significantly affect the phosphorus binding ability of calcium carbonate, but not of calcium lactate. Although the exact mechanism remains obscure, one possible explanation may be related to the rise in pH of the gastric juice. Careful observation of changes in the serum phosphorus level is required in hemodialysis patients receiving calcium carbonate and histamine H2-receptor antagonists. Calcium lactate may be useful as a phosphate binder in such hemodialysis patients.
我们研究了组胺H2受体拮抗剂对磷结合剂磷结合能力的影响。在16例维持性血液透析患者接受组胺H2受体拮抗剂联合碳酸钙治疗期间,测定血清钙、磷、碱性磷酸酶(ALP)、甲状旁腺激素(PTH)以及动脉血pH值和碳酸氢盐水平。选择7例接受组胺H2受体拮抗剂但未联合碳酸钙治疗的患者作为对照。在接受碳酸钙治疗的16例患者中,接受组胺H2受体拮抗剂治疗期间,血清钙、ALP、PTH以及动脉血pH值和碳酸氢盐水平无显著变化,但与治疗前(4.8±1.2mg/dl)相比,治疗4周(5.6±1.1mg/dl)和8周后(5.9±0.8mg/dl)血清磷水平显著升高。此外,停用组胺H2受体拮抗剂8周后,血清磷水平显著下降。在7例对照患者中,组胺H2受体拮抗剂治疗前后测定的血清钙和磷水平无统计学差异。在另外7例接受组胺H2受体拮抗剂联合碳酸钙治疗的患者中,组胺H2受体拮抗剂治疗4周后,将碳酸钙换成乳酸钙作为磷结合剂。在4周给予组胺H2受体拮抗剂联合碳酸钙治疗时,血清磷水平升高,与第一项研究情况类似(从6.3±0.9mg/dl升至7.1±0.5mg/dl)。然而,换成乳酸钙后,血清磷水平显著下降(尽管继续给予组胺H2受体拮抗剂,但4周和8周后分别为6.3±0.2mg/dl和6.0±0.9mg/dl)。这些结果表明,组胺H2受体拮抗剂显著影响碳酸钙的磷结合能力,但不影响乳酸钙的磷结合能力。尽管确切机制尚不清楚,但一种可能的解释可能与胃液pH值升高有关。在接受碳酸钙和组胺H2受体拮抗剂治疗的血液透析患者中,需要仔细观察血清磷水平的变化。乳酸钙可能作为此类血液透析患者的磷结合剂有用。