Kumar Aditya, Wiltz Dena C, Grande-Allen K Jane
Department of Bioengineering, MS 142, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Cardiovasc Eng Technol. 2013 Mar 1;4(1):16-25. doi: 10.1007/s13239-012-0114-6.
Gentamicin is a widely employed antibiotic, but may reduce calcium uptake by eukaryotic cells. This study was conducted to determine whether gentamicin reduces calcification by porcine aortic valvular interstitial cells (pAVICs) grown in 2D culture, which is a common model for calcific aortic valve disease (CAVD).
The presence of gentamicin (up to 0.2 mM) in the medium of pAVICs cultured for 8 days significantly lowered calcification and alkaline phosphatase content in a dose-dependent manner compared to pAVICs cultured without gentamicin. Gentamicin also significantly increased cell proliferation and apoptosis at concentrations of 0.1-0.2 mM. Next, gentamicin was applied to previously calcified pAVIC cultures (grown for 8 days) to determine whether it could stop or reverse the calcification process. Daily application of gentamicin for 8 additional days significantly reduced calcification to below the pre-calcification levels.
These results confirm that gentamicin should be used cautiously with studies of calcification, and suggest that gentamicin may have the ability to reverse calcification by pAVICs. Given the nephrotoxicity and ototoxicity of this antibiotic, its clinical potential for the treatment of calcification in heart valves is limited. However, further investigation of the pathways through which gentamicin alters calcium uptake by valvular cells may provide insight into novel therapies for CAVD.
庆大霉素是一种广泛使用的抗生素,但可能会降低真核细胞对钙的摄取。本研究旨在确定庆大霉素是否会减少二维培养的猪主动脉瓣间质细胞(pAVICs)的钙化,二维培养是钙化性主动脉瓣疾病(CAVD)的常见模型。
与未添加庆大霉素培养的pAVICs相比,在培养8天的pAVICs培养基中添加庆大霉素(浓度高达0.2 mM)能以剂量依赖的方式显著降低钙化程度和碱性磷酸酶含量。在0.1 - 0.2 mM浓度下,庆大霉素还能显著增加细胞增殖和凋亡。接下来,将庆大霉素应用于先前已钙化的pAVIC培养物(培养8天),以确定它是否能阻止或逆转钙化过程。连续8天每日应用庆大霉素可使钙化显著降低至钙化前水平以下。
这些结果证实,在钙化研究中应谨慎使用庆大霉素,并表明庆大霉素可能具有逆转pAVICs钙化的能力。鉴于这种抗生素具有肾毒性和耳毒性,其在治疗心脏瓣膜钙化方面的临床潜力有限。然而,进一步研究庆大霉素改变瓣膜细胞钙摄取的途径可能为CAVD的新疗法提供思路。