瑞舒伐他汀
二甲双胍
奥美拉唑
医学
药理学
美托洛尔
西酞普兰
他汀类
氨氯地平
内科学
内分泌学
糖尿病
血清素
血压
受体
作者
Moshe Salai,Dalia Sömjen,Roy Gigi,O. Yakobson,Sara Katzburg,Oleg Dolkart
出处
期刊:The bone & joint journal
[British Editorial Society of Bone and Joint Surgery]
日期:2013-11-01
卷期号:95-B (11): 1575-1580
被引量:27
标识
DOI:10.1302/0301-620x.95b11.31158
摘要
We analysed the effects of commonly used medications on human osteoblastic cell activity in vitro, specifically proliferation and tissue mineralisation. A list of medications was retrieved from the records of patients aged > 65 years filed in the database of the largest health maintenance organisation in our country (> two million members). Proliferation and mineralisation assays were performed on the following drugs: rosuvastatin (statin), metformin (antidiabetic), metoprolol (β-blocker), citalopram (selective serotonin reuptake inhibitor [SSRI]), and omeprazole (proton pump inhibitor (PPI)). All tested drugs significantly stimulated DNA synthesis to varying degrees, with rosuvastatin 5 µg/ml being the most effective among them (mean 225% (SD 20)), compared with metformin 10 µg/ml (185% (SD 10)), metoprolol 0.25 µg/ml (190% (SD 20)), citalopram 0.05 µg/ml (150% (sd 10)) and omeprazole 0.001 µg/ml (145% (SD 5)). Metformin and metoprolol (to a small extent) and rosuvastatin (to a much higher extent) inhibited cell mineralisation (85% (SD 5)). Our results indicate the need to evaluate the medications prescribed to patients in terms of their potential action on osteoblasts. Appropriate evaluation and prophylactic treatment (when necessary) might lower the incidence and costs associated with potential medication-induced osteoporosis.
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