PMID- 24820768 OWN - NLM STAT- MEDLINE DCOM- 20150219 LR - 20220331 IS - 1432-1041 (Electronic) IS - 0031-6970 (Linking) VI - 70 IP - 8 DP - 2014 Aug TI - Interaction of magnesium oxide with gastric acid secretion inhibitors in clinical pharmacotherapy. PG - 921-4 LID - 10.1007/s00228-014-1694-x [doi] AB - PURPOSE: Magnesium oxide (MgO), a short-term osmotic laxative, is converted into MgCl2 under acidic condition in the stomach and then Mg(HCO3)2 in the intestinal tract, where Mg(HCO3)2 induces the water exudation into the intestine. This indicates that the laxative effect of MgO could be attenuated under the suppressed gastric acid secretion. In this study, the possible interaction of MgO with gastric acid secretion inhibitors was evaluated by using electronic patient records of MgO dosage levels. METHODS: Defecation was controlled with MgO alone in some patients after colon surgery (n = 67) and after total gastric resection (n = 4). Some other patients were treated with a combination use of MgO and H2 receptor antagonist (H2RA) (n = 14) or proton pump inhibitor (PPI) (n = 27). The possible drug interaction of MgO with H2RA or PPI was evaluated by comparing dosage levels of MgO used in controlling defecation. RESULTS: In controlling defecation, the daily dosage levels of MgO in patients taking H2RA or PPI and patients with total gastric resection were significantly higher than those patients taking MgO alone after colon surgery. The ratios of good constipation control (controlled well at the dosing level of 1,000 mg MgO) in patients taking H2RA or PPI were significantly lower than that in patients treated with MgO alone. In an in vitro study, the solubility of MgO at pH 4.5 was quite low, as compared with that at pH 1.2. CONCLUSIONS: When patients received H2RA or PPI, the laxative effect of MgO is decreased possibly due to the low solubility of MgO at the higher gastric pH and less generation of MgCl2 and Mg(HCO3)2. Higher dosing level of MgO or another laxative should be used in patients taking H2RA or PPI, as well as the case of patients with total gastric resection. FAU - Yamasaki, Miho AU - Yamasaki M AD - Department of Pharmacy, Chugoku Rosai Hospital, 1-5-1 Hiro-Tagaya, Kure, Hiroshima, 737-0193, Japan, yakuzai@chugokuh.rofuku.go.jp. FAU - Funakoshi, Sachiyo AU - Funakoshi S FAU - Matsuda, Shohei AU - Matsuda S FAU - Imazu, Tomoko AU - Imazu T FAU - Takeda, Yoshiaki AU - Takeda Y FAU - Murakami, Teruo AU - Murakami T FAU - Maeda, Yorinobu AU - Maeda Y LA - eng PT - Controlled Clinical Trial PT - Journal Article DEP - 20140513 PL - Germany TA - Eur J Clin Pharmacol JT - European journal of clinical pharmacology JID - 1256165 RN - 0 (Histamine H2 Antagonists) RN - 0 (Laxatives) RN - 0 (Proton Pump Inhibitors) RN - 3A3U0GI71G (Magnesium Oxide) SB - IM MH - Aged MH - Aged, 80 and over MH - Drug Interactions MH - Drug Therapy, Combination MH - Female MH - Gastric Acid/*metabolism MH - Histamine H2 Antagonists/*administration & dosage MH - Humans MH - Hydrogen-Ion Concentration MH - Laxatives/*administration & dosage MH - Magnesium Oxide/*administration & dosage MH - Male MH - Middle Aged MH - Proton Pump Inhibitors/*administration & dosage EDAT- 2014/05/14 06:00 MHDA- 2015/02/20 06:00 CRDT- 2014/05/14 06:00 PHST- 2014/02/25 00:00 [received] PHST- 2014/05/01 00:00 [accepted] PHST- 2014/05/14 06:00 [entrez] PHST- 2014/05/14 06:00 [pubmed] PHST- 2015/02/20 06:00 [medline] AID - 10.1007/s00228-014-1694-x [doi] PST - ppublish SO - Eur J Clin Pharmacol. 2014 Aug;70(8):921-4. doi: 10.1007/s00228-014-1694-x. Epub 2014 May 13.