Free radicals, such as hydrogen and hydroxyl radicals, are produced in aqueous solution after X-irradiation. 1) They react with body tissues and generate lipid peroxidation, DNA lesions and enzyme inactivation, all of which are mediators of radiation damage. [2][3][4][5] Nitric oxide is another free radical induced by irradiation.6,7) Nitric oxide induces vasorelaxation and inhibition of platelet aggregation and thus, can improve hypertension or prevent thrombosis. In contrast, nitric oxide can also have cytotoxic effects. Administration of Nomeganitroarginine methyl ester (L-NAME), which is the nitric oxide synthase (NOS) inhibitor, can prevent enteritis after irradiation. 8) This suggests that nitric oxide may be related to irradiation-induced injury. However, early endothelial injury following radiation exposure causes kidney damage with hypertension, capillary thrombosis and death from renal failure. Hypertension and thrombosis could be caused by a deficit of NOS and indeed, the administration of a nitric oxide emission reagent increases survival time after irradiation. 9) Therefore, it is unclear whether nitric oxide affects protection or injury after irradiation, and its relationship to radiation damage has not been examined.Our continuing research of the radioprotective action of sulfur compounds has been reported over a number of years. [10][11][12][13][14][15] Of the sulfur compounds we have studied, S-2-aminoethylisothiourea 2HBr (AET) 12) is a representative drug in the research of experimental radiation damage protectors. Although AET has an effect on the NOS inhibitor, [16][17][18][19] the relationship between radiation damage protection and inhibition of NOS has not been clarified. This study investigated the role of nitric acid in relation to radiation damage, by examining changes in mouse serum nitrate concentrations after irradiation. The mechanisms of radiation damage protection mediated by AET were also clarified. MATERIALS AND METHODS Laboratory AnimalsFive-week-old male ICR strain mice (Charles River Japan, Inc., Yokohama, Japan) were given nutritional chow (MF; Oriental Yeast Co., Ltd., Tokyo, Japan) and water ad libitum. Mice weighing 32Ϯ3 g (about six-week-old) were used throughout the studies.Irradiation Method Irradiation experiments were carried out by a soft X-ray irradiator (Softex M-100WE; Softex Co., Ltd., Tokyo, Japan). Mice were placed in a circular polystyrene cage (diameter: 150 mm, depth: 23 mm) and covered with a net (mesh: 10 mm), then put on a revolving stage at a distance 400 mm below the source. The animals were wholebody irradiated from the dorsum, using various doses (19.6-31.5 Gy) at 70 kVp, 10 mA, a 10 mm acrylic filter and 0.8 Gy/min. Dose rate of the experiments was determined by a Victoreen model 500 dosimeter, using a model 500-6 A type probe.The irradiation groups were irradiated at doses described in the Results. The non-irradiation group served as a control.Methods for Coordination and Injection of the Drug Lipopolysaccharide E. coli (LPS; Difco Laboratories, D...

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We report the anomalous solubility of the pharmaceutical salt irsogladine maleate, which is associated with phase dissociation. The anomalous solubility was demonstrated by the similarity of solubility and miscibility between the salt and its base in ethanol solvent. The phase dissociation was revealed and confirmed by distinguishing irsogladine maleate and its free base using single-crystal X-ray analysis. Herein, the crystal structures of irsogladine maleate and its base were reported for the first time, and the plausible mechanism for phase dissociation was established based on the structural correlations between those phases.