Spry Malinda L, Vanover Jillian C, Scott Timothy, Abona-Ama Osama, Wakamatsu Kazumasa, Ito Shosuke, D'Orazio John A
Markey Cancer Center, Lexington, KY, USA.
Pigment Cell Melanoma Res. 2009 Apr;22(2):219-29. doi: 10.1111/j.1755-148X.2008.00536.x. Epub 2008 Dec 12.
We previously reported that topical application of forskolin to the skin of fair-skinned MC1R-defective mice with epidermal melanocytes resulted in accumulation of eumelanin in the epidermis and was highly protective against UV-mediated cutaneous injury. In this report, we describe the long-term effects of chronic topical forskolin treatment in this animal model. Forskolin-induced eumelanin production persisted through 3 months of daily applications, and forskolin-induced eumelanin remained protective against UV damage as assessed by minimal erythematous dose (MED). No obvious toxic changes were noted in the skin or overall health of animals exposed to prolonged forskolin therapy. Body weights were maintained throughout the course of topical forskolin application. Topical application of forskolin was associated with an increase in the number of melanocytes in the epidermis and thickening of the epidermis due, at least in part, to an accumulation of nucleated keratinocytes. Together, these data suggest in this animal model, short-term topical regular application of forskolin promotes eumelanin induction and that over time, topical forskolin treatment is associated with persistent melanization, epidermal cell accumulation, and skin thickening.
我们之前报道过,将福斯高林局部应用于具有表皮黑素细胞的白皮肤MC1R缺陷小鼠的皮肤上,会导致真黑素在表皮中积累,并对紫外线介导的皮肤损伤具有高度保护作用。在本报告中,我们描述了在该动物模型中慢性局部应用福斯高林的长期影响。通过每日应用,福斯高林诱导的真黑素生成持续了3个月,并且通过最小红斑剂量(MED)评估,福斯高林诱导的真黑素对紫外线损伤仍具有保护作用。在接受长期福斯高林治疗的动物的皮肤或整体健康状况中未观察到明显的毒性变化。在局部应用福斯高林的整个过程中,动物体重保持稳定。局部应用福斯高林与表皮中黑素细胞数量的增加以及表皮增厚有关,这至少部分是由于有核角质形成细胞的积累所致。总之,这些数据表明,在该动物模型中,短期局部定期应用福斯高林可促进真黑素的诱导,并且随着时间的推移,局部应用福斯高林治疗与持续的黑素化、表皮细胞积累和皮肤增厚有关。