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Bone Abstracts (2014) 3 OC3.6 | DOI: 10.1530/boneabs.3.OC3.6

Osteoclasts, gastric hormones and HIF

Skeletal effects of the gastrin receptor antagonist netazepide in H+/K+ATPase beta-subunit deficient mice

Kristin Matre Aasarød1, Masoud Ramezanzadeh Koldeh2, Mats Peder Mosti1, Astrid Kamilla Stunes1, Bjørn Ivar Viggaklev1, Janne Elin Reseland3, Vidar Beisvåg1, Arne Kristian Sandvik1,5, Bjørn Helge Skallerud2, Unni Syversen1,4 & Reidar Fossmark1,5


1Department of Cancer Research and Molecular Medicine, NTNU, Trondheim, Norway; 2Department of Structural Engeneering, NTNU, Trondheim, Norway; 3Department of Biomeaterials, Institute for Clinical Dentistry, UiO, Oslo, Norway; 4Department of Endocrinology, St. Olav’s Hospital, Trondheim, Norway; 5Department of Gastroenterology and Hepatology, St Olav’s Hospital, Trondheim, Norway.

Epidemiological studies suggest that patients using proton pump inhibitors (PPIs) have increased fracture risk. We have previously shown that H+/K+ATPase beta-subunit knockout (KO) mice have reduced BMD, BMC and mechanical bone strength compared to WT. Like users of PPIs, these mice have elevated serum gastrin levels due to high gastric pH. We wanted to study whether elevated gastrin influences bone quality in these mice.

Female KO and WT mice aged 6 weeks were randomly assigned to subcutaneous injection of either a gastrin receptor antagonist (netazepide 40 mg/kg per 2 weeks) or vehicle (polyethylene glycol) for 1 year. Whole body BMD and BMC were measured by DXA at initiation and before termination. Blood drawn at termination was analyzed for gastrin, RANKL, OPG, osteocalcin, leptin and sclerostin. Right femurs were examined with μCT and 3-point bending tests. The study was approved by the local Animal Welfare Committee.

KO mice had significantly (P<0.5) lower BMD (0.080 vs 0.070 g/cm2) and BMC (0.82 vs 0.61 g) at termination, while no significant differences between KO mice receiving netazepide and vehicle were observed. Cortical thickness, cortical area fraction, trabecular thickness and trabecular BMD were significantly higher in WT compared to KO mice, and significantly higher in KO mice receiving netazepide than in the vehicle group. Stiffness was significantly higher in WT compared to KO, and tended to be higher in the KO group receiving netazepide (P=0.06). Breaking force tended to be higher in WT than KO mice (P=0.08), but no differences were seen between the netazepide and vehicle groups. Serological bone markers did not differ significantly between any of the groups.

The gastrin receptor antagonist netazeptide partly prevents bone loss and deterioration of bone quality in H+/K+ATPase KO mice. Hypergastrinemia therefore, could play a part in the osteoporotic process in mice lacking the gastric proton pump.

Volume 3

European Calcified Tissue Society Congress 2014

Prague, Czech Republic
17 May 2014 - 20 May 2014

European Calcified Tissue Society 

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