Modulation Of Sulfur Mustard-induced Inflammation And Gene Expression By Olvanil In The Hairless Mouse Vesicant Model

References

• Papirmeister B, Feister AJ, Robinson SI, Ford RD. Medical Defense Against Mustard Gas: Toxic Mechanisms and Pharmacological Implications. CRC Press, Boca Raton 1991
   Google Scholar
• Papirmeister B, Gross CL, Petrali JP, Hixson CJ. Pathology produced by sulfur mustard in human skin grafts on athymic nude mice I gross and light microscopic changes. J Toxicol Cutan Ocular Toxicol 1984; 3: 371–408
   Google Scholar
• Mitcheltree LW, Mershon MM, Wall HG, Pulliam JD. Microblister formation in vesicant-exposed pig skin. J Toxicol Cutan Ocular Toxicol 1989; 8: 309–319
   Web of Science ®Google Scholar
• Petrali JP, Oglesby SB, Mills KR. Ultrastructural correlates of sulfur mustard toxicity. J Toxicol Cutan Ocular Toxicol 1990; 9: 193–214
   Web of Science ®Google Scholar
• Smith WJ, Dunn MA. Medical defense against blistering chemical warfare agents. Arch Dermatol 1991; 27: 1207–1213
   Google Scholar
• Smith KJ, Skelton HG, Hobson DW, Reid FM, Blank JA, Hurst CG. Cutaneous histopathologic features in weanling pigs after exposure to three different doses of liquid sulfur mustard. Am J Dermatopathol 1996; 18: 515–520
   PubMed Web of Science ®Google Scholar
• Smith KJ, Smith WJ, Hamilton T, Skelton HG, Graham JS, Okerberg C, Moeller R, Hackley BE, Jr. Histopathologic and immunohistochemical features in human skin after exposure to nitrogen and sulfur mustard. Am J Dermatopathol 1998; 20: 22–28
   PubMed Web of Science ®Google Scholar
• Smith KJ, Casillas R, Graham J, Skelton HG, Stemler F, Hackley BE, Jr. Histopathogic features seen with different animal models following cutaneous sulfur mustard exposure. J Dermatol Sci 1997; 14: 126–135
   PubMed Web of Science ®Google Scholar
• Casillas RP, Mitcheltree LW, Stemler FW. The mouse ear model of cutaneous sulfur mustard injury. Toxicol Methods 1997; 7: 381–397
   Google Scholar
• Babin MC, Ricketts K, Skvorak JP, Gazaway M, Mitcheltree LW, Casillas RP. Systemic administration of candidate antivesicants to protect against topically applied sulfur mustard in the mouse ear vesicant model (MEVM). J Appl Toxicol 2000; 20: S141–S144
   PubMedGoogle Scholar
• Casillas RP, Kiser RC, Truxall JA, Singer AW, Shumaker SM, Niemuth NA, Ricketts KM, Mitcheltree LW, Castrejon LR, Blank JA. Therapeutic approaches to dermatotoxicity by sulfur mustard I. Modulation of sulfur mustard-induced cutaneous injury in the mouse ear vesicant model. J Appl Toxicol 2000; 20: S145–S151
   PubMed Web of Science ®Google Scholar
• Ricketts KM, Santai CT, France JA, Graziosi AM, Doyel TD, Gazaway MY, Casillas RP. Inflammatory cytokine responses in sulfur mustard exposed mouse skin. J Appl Toxicol 2000; 20: S73–S76
   PubMed Web of Science ®Google Scholar
• Sabourin CLK, Petrali JP, Casillas RP. Inflammatory gene expression in sulfur mustard exposed mouse skin. J Biochem Mol Toxicol 2000; 14: 291–302
   PubMed Web of Science ®Google Scholar
• Sabourin CLK, Danne MM, Buxton KL, Casillas RP, Schlager JJ. Cytokine chemokine, and matrix metalloproteinase response after sulfur mustard injury to weanling pig skin. J Biochem Mol Toxicol 2002; 16: 263–272
   PubMed Web of Science ®Google Scholar
• Veronesi B, Sailstad DM, Doerfler DL, Selgrade M. Neuropeptide modulation of chemically induced skin irritation. Toxicol Appl Pharmacol 1995; 135: 258–267
   PubMed Web of Science ®Google Scholar
• Campbell E, Bevan S, Dray A. Clinical applications of capsaicin and its analogues. Capsaicin in the Study of Pain, J Wood. Harcourt Brace & Co, London 1993; 255–269
   Google Scholar
• Kasting GB, Francis WR, Bowman LA, Kinnett GO. Percutaneous absorption of vanilloids: in vivo and in vitro studies. J Pharm Sci 1997; 86: 142–146
   PubMed Web of Science ®Google Scholar
• Zhang Z, Riviere JE, Monteiro-Riviere NA. Topical sulfur mustard induces changes in prostoglandins and interleukin-1a in isolated perfused porcine skin. Vitro Toxicol. 1995; 8: 149–157
   Google Scholar
• Lindsay CD, Rice P. Assessment of the biochemical effects of percutaneous exposure of sulphur mustard in an in vitro human skin system. Hum Exp Toxicol 1996; 15: 237–244
   PubMed Web of Science ®Google Scholar
• Arroyo CM, Schafer RJ, Kurt EM, Broomfield CA, Carmichael AJ. Response of normal human keratinocytes to sulfur mustard: cytokine release. J Appl Toxicol 2000; 20: S63–S72
   PubMed Web of Science ®Google Scholar
• Brain SD. Sensory neuropeptides: their role in inflammation and wound healing. Immunopharmacology 1997; 37: 133–152
   PubMedGoogle Scholar
• Cao T, Pintér E, Al-Rashed S, Gerard N, Hoult JR, Brain SD. Neurokinin-1 receptor agonists are involved in mediating neutrophil accumulation in the inflamed, but not normal, cutaneous microvasculature: an in vivo study using neurokinin-1 receptor knockout mice. J Immunol 2000; 164: 5424–5429
   PubMed Web of Science ®Google Scholar
• Sayers TJ, Wiltrout TA, Bull CA, Denn AC, 3rd, Pilaro AM, Lokesh B. Effect of cytokines on polymorphonuclear neutrophil infiltration in the mouse. prostaglandin-and leukotriene-independent induction of infiltration by IL-1 and tumor necrosis factor. J Immunol 1998; 141: 1670–1677
   Google Scholar
• Zlotnik A, Yoshie O. Chemokines: a new classification system and their role in immunity. Immunity 2000; 12: 121–127
   PubMed Web of Science ®Google Scholar
• Tsuruta J, Sugisaki K, Dannenberg AM, Jr, Yoshimura T, Abe Y, Mounts P. The cytokines NAP-1 (IL-8) MCP-1, IL-1 beta, and GRO in rabbit inflammatory skin lesions produced by the chemical irritant sulfur mustard. Inflammation 1996; 20: 293–318
   PubMed Web of Science ®Google Scholar
• Cowan FM, Broomfield CA, Smith WJ. Suppression of sulfur mustard-increased IL-8 in human keratinocyte cell cultures by serine protease inhibitors: implications for toxicity and medical countermeasures. Cell Biol Toxicol 2002; 18: 175–180
   PubMed Web of Science ®Google Scholar
• McEver RP. Selectins. Curr Opin Immunol 1994; 6: 75–84
   PubMed Web of Science ®Google Scholar
• Rossiter H, Alon R, Kupper TS. Selectins T-cell rolling and inflammation. Mol Med Today 1997; 3: 214–222
   PubMedGoogle Scholar
• Matis WL, Lavker RM, Murphy GF. Substance P induces the expression of an endothelial-leukocyte adhesion molecule by microvascular endothelium. J Investig Dermatol 1990; 94: 492–495
   PubMed Web of Science ®Google Scholar
• Smith CH, Barker JN, Morris RW, MacDonald DM, Lee TH. Neuropeptides induce rapid expression of endothelial cell adhesion molecules and elicit granulocytic infiltration in human skin. J Immunol 1993; 151: 3274–3282
   PubMed Web of Science ®Google Scholar
• Viac J, Guéniche A, Doutremepuich JD, Reichert U, Claudy A, Schmitt D. Substance P and keratinocyte activation markers: an in vitro approach. Arch Dermatol Res 1996; 288: 85–90
   PubMed Web of Science ®Google Scholar
• Quinlan KL, Naik SM, Cannon G, Armstrong CA, Bunnett NA, Ansel JC, Caughman SW. Substance P activates coincident NF-AT- and NF-KB-dependent adhesion molecule gene expression in microvascular endothelial cells through intracellular calcium mobilization. J Immunol 1999; 163: 5656–5665
   PubMed Web of Science ®Google Scholar