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E Husztik

Publications and source records attributed to E Husztik.

17 recordsLinked to original sources

The effect of the glucocorticoid Oradexon on endotoxin-induced peritoneal cell response.

Glucocorticoids are important modulators of immune reactions. They are capable of antagonising several effects of the bacterial endotoxin by inhibiting endotoxin-induced leukocyte activation, and the production of cytokines and inflammatory mediators. We earlier demonstrated that the antiglucocorticoid RU 38486 enhances the cytokine production induced by endotoxin and aggravates the course of experimental endotoxic and septic shock. In the present study we investigated the effect of the glucocorticoid Oradexon on the endotoxin-induced peritoneal cell response. For measurement of the peritoneal cell response, male CFLP mice (20-25 g) were injected i.p. with 10 microg/10 g body weight endotoxin (E. coli 026:B6 LPS, Difco Lab, Detroit, lot 110273JB). Dexamethasone (Oradexon, N.V, Organon Oss, The Netherlands) was administered i.p., i.v. or s.c. in a dose of 0.1 mg/10 g body weight, alone or concomitantly with endotoxin. We found that bacterial endotoxin increased the total cell count due to neutrophilia at 24 hours and, due to increases in the number of macrophages and lymphocytes 48 and 72 hours after treatment, respectively. The i.p., i.v., and s.c. injection of Oradexon, increased the total cell count and the macrophage count at 24, 48 and 72 hours. The i.p., s.c. and i.v. injection of Oradexon, concomitantly with endotoxin, reduced the total cell count at 48 and 72 hours, due to decreases in the macrophage count. The i.p., i.v. or s.c. administration of Oradexon concomitantly with LPS decreased the lymphocyte count and the neutrophil count at 24 and 72 hours. These results prove that glucocorticoids are capable of modifying the immune cell reactions induced by endotoxin.

Animals↗

Inhibition of anaphylactic shock by gadolinium chloride-induced Kupffer cell blockade.

Data in the literature concerning the role of macrophages in anaphylaxis are contradictory. In the present study, the effect of macrophage blockade induced by gadolinium chloride (GdCl3) on anaphylactic shock is investigated. Our observations show that GdCl3 prevents lethal anaphylactic shock in mice sensitized to ovalbumin. Gadolinium chloride given i.v. in a dose of 1 mg/100 g body weight 24 or 48 h before the elicitation of anaphylactic shock resulted in 80% survival, compared with the 43% survival in the control group. The same dose of this rare-earth metal salt also greatly reduced the mortality in mice sensitized with ovalbumin containing Bordetella pertussis vaccine, and similarly abrogated the symptoms of anaphylaxis, including the accumulation of serotonin and histamine in the liver. The results suggest that macrophages play an important role in mouse anaphylaxis.

Anaphylaxis↗

Prevention of anaphylactic death by macrophage blockade.

Data in the literature concerning the role of macrophages in anaphylaxis are contradictory. In the present study the effect of macrophage blockade induced by gadolinium chloride (GdCl3) on anaphylactic shock was investigated. Our observations show that GdCl3 prevents the lethal anaphylactic shock of mice sensitized to ovalbumin. GdCl3 given i.v. in a dose of 1 mg/100 g body weight 24 or 48 h before the elicitation of anaphylactic shock resulted in 90% survival, compared to the 43% survival in the control group. The same dose of this rare earth metal salt also greatly reduced the mortality in mice sensitized with ovalbumin containing Bordetella pertussis vaccine, and the symptoms of anaphylaxis including the accumulation of 5-hydroxytryptamine in the liver. Our results suggest that macrophages play an important role in anaphylaxis.

Anaphylaxis↗

Immunologically induced peliosis hepatis in rats.

Peliosis hepatis has been induced immunologically with anti-rat glomerular basal membrane rabbit serum in rats pre-sensitized with a rare earth metal complex, neodymium pyrocatechin disulphonate (NPD). This is the first experimental evidence that peliosis hepatis may develop as a result of an immunological process. It is noteworthy that in this experimental form of peliosis hepatis and in that observed earlier in rats treated with basic polyglutamic acid derivatives, severe defibrination was detected and, as in most human cases, not only the liver but other organs were also involved in the peliotic lesions. Since the rare earth metal compounds, among them the pyrocatechin disulphonate complex of neodymium, depress the reticulo-endothelial activity, a role of the reticulo-endothelial system in the pathogenesis of this experimental form of peliosis hepatis is suggested.

Animals↗

[Cellular mechanism of the blocking of Kupffer cell phagocytosis induced by gadolinium chloride].

Studying the distribution of heterolog erythrocytes labelled by Cr51 in rats, it was established that reticuloendothelial blockade induced by gadolinium chloride first of all can be explained by the decreased phagocytic activity of Kupffer cells. Light-and electronmicroscopic studies have evidenced that gadolinium chloride inhibited phagocytosis of indian ink not only by normal, non activated Kupffer cells but also by those, activated by a reticuloendothelial stimulator, zymosan. These experiments seem to indicate that the blockade of Kupffer cell phagocytosis induced by gadolinium chloride both phases of this process, the surface sticking and engulfing are damaged.

Animals↗

Electron microscopic study of Kupffer-cell phagocytosis blockade induced by gadolinium chloride.

The cellular basis of Kupffer-cell phagocytosis blockade induced by gadolinium chloride was studied in rats. Investigations with heterologous erythrocytes labelled with 51Cr show that the gadolinium chloride-induced reticuloendothelial blockade is due to the depressed phagocytic activity of the Kupffer cells. Our light-microscopic studies indicate that, as a result of the action of gadolinium chloride, the impaired Kupffer-cell phagocytosis is observed not only in normal, non-activated Kupffer cells, but also in those activated with a reticuloendothelial stimulant, Zymosan. Our electron-microscopic investigations suggest that the failure of the Kupffer cells to incorporate carbon during the reticuloendothelial blockage induced by this rare earth metal chloride is due to defects in the surface attachment and in the engulfment phases of phagocytosis.

Animals↗