Literature DB >> 19543559

Lansoprazole is an uncompetitive inhibitor of tissue-nonspecific alkaline phosphatase.

Mélanie Delomenède1, René Buchet, Saïda Mebarek.   

Abstract

Lansoprazole, a known H(+)/K(+)-ATPase inhibitor, is currently used as a therapeutical option for the initial treatment of gastroesophageal reflux disease. Recently, lansoprazole has been found to be an inhibitor of cytosolic PHOSPHO1 (a phosphatase which hydrolyses phosphocholine and phosphoethanolamine), providing a possible therapeutical target to cure pathological mineralization. Since PHOSPHO1 is present inside matrix vesicles, we tested the effect of lansoprazole on matrix vesicles containing several key enzymes for the mineralization process including tissue-nonspecific alkaline phosphatase. We found that lansoprazole can inhibit in an uncompetitive manner tissue-nonspecific alkaline phosphatase. A K(i) value of 1.74 +/- 0.12 mM has been determined for the inhibition of tissue-nonspecific alkaline phosphatase by lansoprazole. Lansoprazole, currently used for treating gastroesophageal disease, by inhibiting PHOSPHO1 and tissue-nonspecific alkaline phosphatase could prevent hydroxyapatite-deposition disease and could serve as an adjunct treatment for osteoarthritis.

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Year:  2009        PMID: 19543559

Source DB:  PubMed          Journal:  Acta Biochim Pol        ISSN: 0001-527X            Impact factor:   2.149


  5 in total

1.  NT5E mutations and arterial calcifications.

Authors:  Cynthia St Hilaire; Shira G Ziegler; Thomas C Markello; Alfredo Brusco; Catherine Groden; Fred Gill; Hannah Carlson-Donohoe; Robert J Lederman; Marcus Y Chen; Dan Yang; Michael P Siegenthaler; Carlo Arduino; Cecilia Mancini; Bernard Freudenthal; Horia C Stanescu; Anselm A Zdebik; R Krishna Chaganti; Robert L Nussbaum; Robert Kleta; William A Gahl; Manfred Boehm
Journal:  N Engl J Med       Date:  2011-02-03       Impact factor: 91.245

Review 2.  Inorganic Pyrophosphate Deficiency Syndromes and Potential Treatments for Pathologic Tissue Calcification.

Authors:  Douglas Ralph; Koen van de Wetering; Jouni Uitto; Qiaoli Li
Journal:  Am J Pathol       Date:  2022-02-16       Impact factor: 5.770

3.  Oral proton pump inhibitors disrupt horizontal cell-cone feedback and enhance visual hallucinations in macular degeneration patients.

Authors:  Anne M Hanneken; Norbert Babai; Wallace B Thoreson
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-02-27       Impact factor: 4.799

4.  Pharmacological inhibition of PHOSPHO1 suppresses vascular smooth muscle cell calcification.

Authors:  Tina Kiffer-Moreira; Manisha C Yadav; Dongxing Zhu; Sonoko Narisawa; Campbell Sheen; Boguslaw Stec; Nicholas D Cosford; Russell Dahl; Colin Farquharson; Marc F Hoylaerts; Vicky E Macrae; José Luis Millán
Journal:  J Bone Miner Res       Date:  2013-01       Impact factor: 6.741

5.  Proton Pump Inhibitors Inhibit PHOSPHO1 Activity and Matrix Mineralisation In Vitro.

Authors:  Katherine A Staines; Katherine Myers; Kirsty Little; Stuart H Ralston; Colin Farquharson
Journal:  Calcif Tissue Int       Date:  2021-07-02       Impact factor: 4.333

  5 in total

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