Tewari-Singh Neera, Goswami Dinesh G, Kant Rama, Croutch Claire R, Casillas Robert P, Orlicky David J, Agarwal Rajesh
Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Toxicol Appl Pharmacol. 2017 Feb 15;317:25-32. doi: 10.1016/j.taap.2017.01.003. Epub 2017 Jan 11.
Phosgene Oxime (CX), an urticant or nettle agent categorized as a vesicant, is a potential chemical warfare and terrorist weapon. Its exposure can result in widespread and devastating effects including high mortality due to its fast penetration and ability to cause immediate severe cutaneous injury. It is one of the least studied chemical warfare agents with no effective therapy available. Thus, our goal was to examine the acute effects of CX following its cutaneous exposure in SKH-1 hairless mice to help establish a relevant injury model. Results from our study show that topical cutaneous exposure to CX vapor causes blanching of exposed skin with an erythematous ring, necrosis, edema, mild urticaria and erythema within minutes after exposure out to 8h post-exposure. These clinical skin manifestations were accompanied with increases in skin thickness, apoptotic cell death, mast cell degranulation, myeloperoxidase activity indicating neutrophil infiltration, p53 phosphorylation and accumulation, and an increase in COX-2 and TNFα levels. Topical CX-exposure also resulted in the dilatation of the peripheral vessels with a robust increase in RBCs in vessels of the liver, spleen, kidney, lungs and heart tissues. These events could cause a drop in blood pressure leading to shock, hypoxia and death. Together, this is the first report on effects of CX cutaneous exposure, which could help design further comprehensive studies evaluating the acute and chronic skin injuries from CX topical exposure and elucidate the related mechanism of action to aid in the identification of therapeutic targets and mitigation of injury.
二氯苯醚菊酯肟(CX)是一种被归类为糜烂性毒剂的致荨麻剂或荨麻制剂,是一种潜在的化学战和恐怖主义武器。它的暴露会导致广泛而具有破坏性的影响,包括由于其快速渗透和导致立即严重皮肤损伤的能力而导致的高死亡率。它是研究最少的化学战剂之一,目前尚无有效的治疗方法。因此,我们的目标是研究CX经皮肤暴露于SKH-1无毛小鼠后的急性影响,以帮助建立相关的损伤模型。我们的研究结果表明,局部皮肤暴露于CX蒸气会导致暴露皮肤变白,并伴有红斑环、坏死、水肿、轻度荨麻疹和红斑,暴露后数分钟至暴露后8小时内均会出现这些症状。这些临床皮肤表现伴随着皮肤厚度增加、凋亡性细胞死亡、肥大细胞脱颗粒、髓过氧化物酶活性增加(表明中性粒细胞浸润)、p53磷酸化和积累,以及COX-2和TNFα水平升高。局部CX暴露还导致外周血管扩张,肝脏、脾脏、肾脏、肺和心脏组织血管中的红细胞大量增加。这些事件可能导致血压下降,进而导致休克、缺氧和死亡。总之,这是关于CX皮肤暴露影响的第一份报告,有助于设计进一步的综合研究,评估CX局部暴露引起的急性和慢性皮肤损伤,并阐明相关的作用机制,以帮助确定治疗靶点和减轻损伤。