SAAD Centre for Pharmacy and Diabetes, School of Pharmacy and Pharmaceutical Science, Ulster University, Coleraine, County Londonderry, Northern Ireland, BT52 1SA, UK.
School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, India.
Inflammation. 2019 Dec;42(6):2032-2036. doi: 10.1007/s10753-019-01065-3.
Hypoxia inducible factor (HIF)-prolyl hydroxylase (PHD) inhibitors are shown to be protective in several models of inflammatory bowel disease (IBD). However, these non-selective inhibitors are known to inhibit all the three isoforms of PHD, i.e. PHD-1, PHD-2 and PHD-3. In the present report, we investigated the associated changes in levels of PHDs during the development and recovery of chemically induced colitis in mice. The results indicated that in the experimental model of murine colitis, levels of both, PHD-1 and PHD-2 were found to be increased with the progression of the disease; however, the level of PHD-3 remained the same in group of healthy controls and mice with colitis. Thus, the findings advocated that inhibitors, which inhibited all three isoforms of PHD could not be ideal therapeutics for IBD since PHD-3 is required for normal gut function. Hence, this necessitates the development of new compounds capable of selectively inhibiting PHD-1 and PHD-2 for effective treatment of IBD.
缺氧诱导因子(HIF)脯氨酰羟化酶(PHD)抑制剂在几种炎症性肠病(IBD)模型中显示出保护作用。然而,这些非选择性抑制剂已知会抑制所有三种同工型的 PHD,即 PHD-1、PHD-2 和 PHD-3。在本报告中,我们研究了在化学诱导的结肠炎小鼠发展和恢复过程中 PHD 水平的相关变化。结果表明,在实验性小鼠结肠炎模型中,随着疾病的进展,发现 PHD-1 和 PHD-2 的水平均升高;然而,健康对照组和结肠炎小鼠的 PHD-3 水平保持不变。因此,研究结果表明,抑制所有三种同工型的 PHD 的抑制剂不可能是 IBD 的理想治疗方法,因为 PHD-3 是肠道正常功能所必需的。因此,这需要开发能够选择性抑制 PHD-1 和 PHD-2 的新型化合物,以有效治疗 IBD。