Karna Sandeep
National Institute of Horticultural and Herbal Science, Nongsaengmyeong-ro, Iseo-myeon, Wangju-gun, Jeollabuk-do, Korea.
Pharmacogn Mag. 2017 Jan;13(Suppl 1):S122-S126. doi: 10.4103/0973-1296.203971. Epub 2017 Apr 7.
Prostaglandins (PGs) have short existence because they are rapidly metabolized by NAD-dependent 15-hydroxyprostaglandin dehydrogenase (15-PGDH) to 15-ketoprostaglandins. Inhibition of 15-PGDH causes elevated level of PGE in cellular system. It will be valuable for the therapeutic management of diseases requiring elevated PGE levels, like wound healing.
Ninety-eight plant samples were screened for the discovery of potent 15-PGDH inhibitor. Among them, top five plant extracts as potent 15-PGDH inhibitor were chosen to determine PGE release from HaCaT (Keratinocyte cell line) cell line. Finally, top 15-PGDH inhibitor was selected to evaluate wound healing effect on HaCaT scratch model.
The inhibitory activity for 15-PGDH inhibitors was evaluated using fluorescence spectrophotometer by measuring the formation of NADH at 468 nm following excitation at 340 nm. Cell viability assay and PGE release was evaluated in HaCaT cell line after treatment of 15-PGDH inhibitors. Scratches were made using sterile 200 μL on HaCaT cell and wound-healing effect was evaluated after treatment of 15-PGDH inhibitor.
15-PGDH inhibitors elevated PGE levels in concentration-dependent manner. Ethanol extract of (EEAH), the most potent 15-PGDH inhibitor (IC = 0.62 µg/mL) with least cytotoxicity (IC = 670 µg/ml), elevated both intracellular and extracellular PGE levels. EEAH facilitated wound healing in a HaCaT (Keratinocyte cell line) scratch model.
EEAH might apply to treat dermal wounds by elevating PGE levels via COX-1 induction and 15-PGDH inhibition.
Biological inactivation of 15-PGDH causes elevated level of PGE which will be useful for the management of disease that requires elevated level of PGE. 15-PGDH: 15-hydroxyprostaglandin dehydrogenase, COX: Cyclooxygenase, DTT: Dithiothreitol, DMEM: Dulbecco's modified Eagle's media, EEAH: Ethanol extract of Artocarpus heterophyllus, MRP4: Multidrug resistance 4, PGs: Prostaglandins, PGT: Prostaglandin transporter, SDS: Sodium dodecylsulfate.
前列腺素(PGs)存在时间短暂,因为它们会被NAD依赖性15-羟基前列腺素脱氢酶(15-PGDH)迅速代谢为15-酮基前列腺素。抑制15-PGDH会导致细胞系统中PGE水平升高。这对于治疗需要升高PGE水平的疾病(如伤口愈合)具有重要价值。
筛选98种植物样本以发现强效的15-PGDH抑制剂。其中,选择了五种最强效的15-PGDH抑制剂植物提取物来测定HaCaT(角质形成细胞系)细胞系中PGE的释放。最后,选择最强效的15-PGDH抑制剂来评估其对HaCaT划痕模型的伤口愈合效果。
使用荧光分光光度计通过测量在340nm激发后468nm处NADH的形成来评估15-PGDH抑制剂的抑制活性。在处理15-PGDH抑制剂后,在HaCaT细胞系中评估细胞活力测定和PGE释放。使用无菌200μL在HaCaT细胞上制造划痕,并在处理15-PGDH抑制剂后评估伤口愈合效果。
15-PGDH抑制剂以浓度依赖性方式升高PGE水平。波罗蜜乙醇提取物(EEAH)是最强效的15-PGDH抑制剂(IC = 0.62μg/mL),细胞毒性最小(IC = 670μg/ml),可升高细胞内和细胞外PGE水平。EEAH在HaCaT(角质形成细胞系)划痕模型中促进伤口愈合。
EEAH可能通过诱导COX-1和抑制15-PGDH来升高PGE水平,从而用于治疗皮肤伤口。
15-PGDH的生物失活会导致PGE水平升高,这对于治疗需要升高PGE水平的疾病将是有用的。15-PGDH:15-羟基前列腺素脱氢酶,COX:环氧化酶,DTT:二硫苏糖醇,DMEM:杜氏改良 Eagle培养基,EEAH:波罗蜜乙醇提取物,MRP4:多药耐药蛋白4,PGs:前列腺素,PGT:前列腺素转运体,SDS:十二烷基硫酸钠。