Institute of Chemistry, University of Campinas-UNICAMP, CP 6154, Campinas, SP 13087-970, Brazil.
J Mater Sci Mater Med. 2013 Sep;24(9):2157-69. doi: 10.1007/s10856-013-4973-7. Epub 2013 Jun 12.
New approaches based on topical treatments are needed for treating pain and impaired dermal blood flow. We used a topical Pluronic F127 hydrogel containing S-nitrosoglutathione (GSNO) as a prodrug to generate free NO, an effector molecule that exerts both dermal vasodilation and antinociceptive effects. GSNO-containing hydrogels underwent gelation above 12 °C and released free NO at rates that were directly dependent on the GSNO concentration in the range of 50-150 mM. The topical application of this material led to dose-response dermal vasodilation in healthy volunteers and to a reduction of up to 50 % of the hypernociception intensity in Wistar rats that were subjected to inflammatory pain. Mechanistic investigations indicated that the antinociceptive effect of the topical F127/GSNO hydrogels is produced by the local activation of the cGMP/PKG/KATP channel-signaling pathway, which was stimulated by the free NO that diffused through the skin. These results expand the scope of the biomedical applications of this material and may represent a new approach for the topical treatment of inflammatory pain.
需要新的局部治疗方法来治疗疼痛和受损的皮肤血流。我们使用含有 S-亚硝基谷胱甘肽(GSNO)的局部普朗尼克 F127 水凝胶作为前药来产生游离的 NO,这是一种效应分子,具有皮肤血管扩张和抗伤害感受作用。含有 GSNO 的水凝胶在 12°C 以上凝胶化,并以直接依赖于 GSNO 浓度的速率释放游离的 NO,范围在 50-150 mM 之间。该材料的局部应用导致健康志愿者的皮肤血管舒张呈剂量反应,并且使接受炎症性疼痛的 Wistar 大鼠的超敏反应强度降低高达 50%。机制研究表明,局部 F127/GSNO 水凝胶的抗伤害感受作用是通过皮肤扩散的游离 NO 局部激活 cGMP/PKG/KATP 通道信号通路产生的。这些结果扩展了这种材料的生物医学应用范围,并可能代表治疗炎症性疼痛的新的局部治疗方法。