Laboratory of Stress Medicine, Department of Nautical Medicine, Second Military Medical University, Shanghai, People's Republic of China.
Cell Mol Life Sci. 2011 Apr;68(8):1405-14. doi: 10.1007/s00018-010-0526-0. Epub 2010 Sep 19.
Glucocorticoids (GCs) are routinely believed to take effect through genomic mechanisms, which are also largely responsible for GCs' side effects. Beneficial non-genomic effects of GCs have been reported as being independent of the genomic pathway. Here, we synthesized a new type of GCs, which took effect mainly via non-genomic mechanisms. Hydrocortisone was conjugated with glycine, lysine and phenylalanine to get a bigger molecular structure, which could hardly go through the cell membrane. Evaluation of the anti-inflammatory efficacy showed that hydrocortisone-conjugated glycine (HG) and lysine could inhibit neutrophil degranulation within 15 min. HG could inhibit IgE-mediated histamine release from mast cells via a non-genomic pathway, and rapidly alleviate allergic reaction. Luciferase reporter assay showed that HG would not activate the glucocorticoid response element within 30 min, which verified the rapid effects independent of the genomic pathway. The work proposes a novel insight into the development of novel GCs, and provides new tools for experimental study on non-genomic mechanisms.
糖皮质激素(GCs)通常被认为通过基因组机制发挥作用,而这些机制在很大程度上也是 GCs 产生副作用的原因。已有报道称,GC 的有益的非基因组效应不依赖于基因组途径。在这里,我们合成了一种新型 GCs,它主要通过非基因组机制发挥作用。将氢化可的松与甘氨酸、赖氨酸和苯丙氨酸结合,得到一个更大的分子结构,使其很难穿过细胞膜。抗炎疗效评估表明,氢化可的松-甘氨酸(HG)和赖氨酸在 15 分钟内即可抑制中性粒细胞脱颗粒。HG 可以通过非基因组途径抑制 IgE 介导的肥大细胞释放组胺,从而迅速缓解过敏反应。荧光素酶报告基因检测表明,HG 在 30 分钟内不会激活糖皮质激素反应元件,这验证了非基因组途径的快速作用不依赖于基因组途径。这项工作为新型 GCs 的开发提供了新的思路,并为非基因组机制的实验研究提供了新的工具。