Lung damage in paraquat poisoning and hyperbaric oxygen exposure: superoxide-mediated inhibition of phospholipase A2.

Paraquat poisoning and hyperbaric oxygen exposure are well established models of oxidative stress in lung. The aim of this study was focused on the contribution of oxygen free radicals and other cytotoxic species, such as lipid hydroperoxides, to the overall toxicity. Adult Wistar rats were injected with paraquat (30 or 60 mg/kg b.w.) or exposed to hyperbaric oxygen (0.2 MPa), and several parameters of lung damage were measured. Both treatments resulted in increased spontaneous lung chemiluminescence, number of lung PMN, malondialdehyde content, lung edema, and pleural liquid. Of note, spontaneous lung chemiluminescence, used to monitor the steady-state concentration of oxygen free radicals in vivo, did not increase significantly after either treatment. The increase in spontaneous lung chemiluminescence started after PMN migration, being both maxima separated by a delay time of 4-6 h. After PMN migrated and became activated in the lung, the survival of the animals started to decline. Thus, PMN can be considered as additional sources of oxygen free radicals supported by the subsequent increase in chemiluminescence. Their role in lung damage was evidenced by the increase in lung edema, augmented pleural liquid, and decreased survival after PMN migration. Lipid hydroperoxide concentration in lung membranes was also increased after either treatment. This increased concentration may be a consequence of an increased rate of lipid peroxidation, initiated by oxidative stress on lipid membranes, or by an inhibition of their catabolism. Ester lipid hydroperoxides normally produced in membranes cannot be catabolized directly by the glutathione peroxidase-reductase system unless phospholipase A2 catalyses the release of free lipid hydroperoxides. In both experimental models, phospholipase A2 activity was decreased to almost negligible values. Betamethasone (1 mg/ml; IV) administered to the rats 3 h before paraquat injection accelerated the decrease in survival and phospholipase A2 inactivation. Inactivation of phospholipase A2, detected in paraquat or oxygen exposed rats, could be attributed to a O2(.-)-driven Fenton reaction. However, phospholipase A2 inactivation by betamethasone pretreatment may be attributed to the presence of lipocortin, a corticosteroid-inducible factor and inhibitor of phospholipase A2. Besides the mechanism underlying the inactivation of phospholipase A2, the increase in lipid hydroperoxides may indicate their role as long-lived cytotoxic species that contribute to the damage already initiated by oxidative stress. Indeed, lipid hydroperoxides are very well known modifiers of membrane physical properties

OPTICAL RANGING IN ENDOSCOPY: TOWARDS QUANTITATIVE IMAGING

Nowadays endoscopic analysis is limited to a direct and qualitative view of internal anatomy. On the other hand, the measurement of the actual size of anatomical objects could be a powerful instrument both in research and in clinical survey. For instance, an important application could be monitoring lesion size, both during diagnosis and in follow-up. The foremost obstacle to quantitative imaging is the incapability of measuring the distance between the endoscopic probe and the anatomical object under examination, since the dimension of the object in the image depends on that distance. This problem has not been solved yet in a satisfactory way. In this Chapter we describe our work to address this problem by means of an optical measurement of the distance between the endoscope distal tip and the anatomical wall. We make use of Fiber Optics Low Coherence Interferometry to realize an absolute distance sensor compatible with endoscope technology. The result is a system integrating a clinical endoscope and an optical distance sensor, equipped with a software that allows an user to acquire an endoscopic image, select a region of interest, and obtain its quantitative measure

Confronto tra metodo manuale e computerizzato nella conta delle particelle intramembrana degli eritrociti dopo Freeze-fracturing nelle distrofie muscolari progressive legate al cromosoma X

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