Lack of a role for creatine phosphate kinase in sulphur mustard-induced cytotoxicity

• Published in: Human & experimental toxicology 2007-11, Vol.26 (11), p.891-897
• Main Authors: Nelson, P., Burczyk, A., Sawyer, T.W.
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Biological & chemical weapons; Biological and medical sciences; Cell culture; Cells, Cultured; Chemical and industrial products toxicology. Toxic occupational diseases; Chemical Warfare Agents - toxicity; Chemoprevention; Chick Embryo; Creatine - pharmacology; Creatine Kinase - metabolism; Dose-Response Relationship, Drug; Gas, fumes; Keratinocytes - drug effects; Keratinocytes - enzymology; Kinases; Medical sciences; Mustard Gas - toxicity; Neurons; Neurons - drug effects; Neurons - enzymology; Neuroprotective Agents - pharmacology; Phosphocreatine - pharmacology; Skin; Toxicity; Toxicology
• ISSN: 0960-3271; 1477-0903
• DOI: 10.1177/0960327107084043

Several compounds involved in the creatine phosphate kinase (CPK) pathway were evaluated for their protective effects against the chemical warfare (CW) agent sulphur mustard (HD), in primary chick embryo neuron and first passage human skin keratinocyte cultures. High concentrations of both creatine and creatine phosphate were found to be protective under all culture conditions and increased the LC50 of HD in both culture systems up to ~250%. Little difference was observed in the protective activity of these compounds in undifferentiated versus differentiated neuronal culture, or in proliferating versus differentiating cultures of keratinocytes. The protective effect of these compounds was found to be strictly prophylactic in nature. Although a modest decline in HD half-life was measured in buffer containing creatine phosphate, this did not account for the protective effects of this compound. In contrast to historical literature reporting 90—100% HD-induced CPK inhibition of purified enzyme, less than 30% of CPK activity was found to be inhibited by HD in both human keratinocytes and in swine blood plasma. Incubation of keratinocyte cultures with creatine or creatine phosphate prior to HD exposure did not alter CPK activity, compared with HD-only treated cultures. Although high mM concentrations of both creatine and creatine phosphate exert significant protective effects against HD, these results do not support a role for CPK in its toxicity or in the development of medical countermeasures against this CW agent. Human & Experimental Toxicology (2007) 26, 891—897.