Monteiro-Riviere N A, Inman A O
Cutaneous Pharmacology and Toxicology Center, North Carolina State University, Raleigh 27606, USA.
Microsc Res Tech. 1997 May 1;37(3):229-41. doi: 10.1002/(SICI)1097-0029(19970501)37:3<229::AID-JEMT8>3.0.CO;2-I.
The isolated perfused porcine skin flap (IPPSF) is a novel alternative, humane in vitro model consisting of a viable epidermis and dermis with a functional microvasculature. For this study, 200 microliters of either 10.0, 5.0, 2.5, 1.25, 0.50, or 0.20 mg/ml of bis (2-chloroethyl) sulfide (HD) in ethanol or ethanol control was topically applied to a 5.0 cm2 dosing area of the IPPSF and perfused for 8 h with recirculating media. HD dermatotoxicity was assessed in the flap by cumulative glucose utilization (CGU), vascular resistance (VR), light microscopy (LM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). HD produced a statistically significant dose relationship for gross blisters and microvesicles. The HD-treated IPPSFs were also characterized by a decrease in CGU and an increase in VR. Light microscopic changes included mild intracellular and slight intracellular epidermal edema, multifocal epidermal-dermal separation, and dark basal cells. Ultrastructural alterations consisted of cytoplasmic vacuoles, pyknotic basal cells, nucleolar segregation, and epidermal-dermal separation occurring between the lamina lucida and lamina densa of the basement membrane. The severity of these changes increased in a dose-dependent manner. Morphologically, the IPPSF appeared similar to human skin exposed to HD with the formation of macroscopic blisters and microscopic vesicles. In conclusion, the IPPSF appears to be an appropriate in vitro model with which to study the pathogenesis of vesicant-induced toxicity.
离体灌注猪皮瓣(IPPSF)是一种新型的、人道的体外模型,由具有功能性微血管系统的活表皮和真皮组成。在本研究中,将200微升浓度为10.0、5.0、2.5、1.25、0.50或0.20毫克/毫升的双(2-氯乙基)硫化物(HD)乙醇溶液或乙醇对照局部涂抹于5.0平方厘米的IPPSF给药区域,并用循环培养基灌注8小时。通过累积葡萄糖利用(CGU)、血管阻力(VR)、光学显微镜(LM)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)评估皮瓣中的HD皮肤毒性。HD对大水泡和微泡产生了具有统计学意义的剂量关系。HD处理的IPPSF还表现为CGU降低和VR增加。光学显微镜下的变化包括轻度细胞内和轻微细胞内表皮水肿、多灶性表皮-真皮分离以及基底细胞变黑。超微结构改变包括细胞质空泡、固缩的基底细胞、核仁分离以及基底膜透明层和致密层之间的表皮-真皮分离。这些变化的严重程度呈剂量依赖性增加。形态学上,IPPSF与暴露于HD的人类皮肤相似,形成了宏观水泡和微观小泡。总之,IPPSF似乎是一种合适的体外模型,可用于研究糜烂剂诱导毒性的发病机制。