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Biomedical subjects

J Vilas

Publications and source records attributed to J Vilas.

7 recordsLinked to original sources

Immune and biochemical responses of the polychaete Eurythoe complanata exposed to sublethal concentration of copper.

A series of immunoassays, enzyme activity tests and growth rate analyses were conducted on the free living polychaete Eurythoe complanata after 21 day exposure to 0.2 mg.L-1 sublethal nominal concentration of Cu2+ (CuSO45H2O). The immunological assessment was further made immediately after 15 and 30 day post-exposure. Immune cytological parameters, coelomocyte viability and differential coelomocyte counts showed significant differences between exposed an non-exposed worms. Coelomocyte responses to antigenic mouse red blood cells (MRBC), such as formation of secretory (SR) and erythrocyte rosettes (ER), and phagocytosis evidenced significant impairments in the immunological defenses related to copper contamination, related to a two fold increase in Cu-carcass tissue concentration (13.70 +/- 1.50 micrograms.g-1 dry wt, n = 6). The normal immune functions were reestablished upon depuration as tissue Cu content approached basal levels (7.40 +/- 1.70 micrograms.g-1 dry wt, n = 6). Neither enzyme activity of coelomic transaminases as indicators of tissue damage, nor growth rate indexes (carcass tissue RNA/DNA and protein/DNA ratios) were affected by copper exposure. In conclusion, the immunoassays yielded highly sensitive results compared to biochemical markers, suggesting the potential usefulness of immune parameters as environmental stress indicators for sediment/aquatic bioassays with the polychaete Eurythoe complanata.

Animals↗

[Arginase deficiency, congenital hypothyroidism and hepatic fibrosis].

A new case of arginase deficiency in a newborn is reported. In contrast with previous cases, this infant showed severe protein intolerance of early onset. Diagnosis was based on the assay of urea cycle enzymes in a postmortem liver sample and on arginase activity in erythrocytes of parents and sister of the patient. "Pedigree" shows that arginase deficiency in this family presents a dramatic course. Congenital hypothyroidism with athyreosis, moderate hepatic fibrosis and megamitochondria are present in the same subject. Possible significance of these findings is briefly discussed.

Congenital Hypothyroidism↗

A new case of arginase deficiency in a Spanish male.

A new case of arginase deficiency is reported in a male newborn from Spain. In contrast with the majority of the earlier cases, this infant showed severe protein intolerance of early onset. The diagnosis was based on the assay of the urea cycle enzymes in a postmortem liver sample. Levels of erythrocyte arginase were also determined in the parents and in a sister of the patient, and were consistent with heterozygosity. From a study of the pedigree it appears that arginase deficiency in this family presents a dramatic course.

Amino Acid Metabolism, Inborn Errors↗