RESUMEN
The clastogenic effect of the drug cis-diamminedichloroplatinum II (cisplatin, CDDP) was investigated in Wistar rat bone marrow cells. Male rats, 3 per treatment time, aged 4 months and weighing 250-350 g were injected intraperitoneally with 6.0 mg/kg CDDP solution, and the control group received isotonic saline. The animals were sacrificed 6, 12, 18, 24 and 48 h after the injection. The chromosome preparation was obtained from bone marrow cells. Chromatid and chromosome aberrations were investigated in 300 metaphases per animal. A significant increase in number of chromosome aberrations was observed from 6 to 24 h, the majority being of the break and gap type. After 48 h a progressive reduction was observed, without differences from the negative control. These data confirm the mutagenic effect of CDDP in rats demonstrated for mice bone marrow by micronuclei assay, for murine ovary cells and mice spermatocytes.
Asunto(s)
Células de la Médula Ósea , Aberraciones Cromosómicas/genética , Cisplatino/farmacología , Mutágenos/farmacología , Animales , Médula Ósea/efectos de los fármacos , Masculino , Pruebas de Mutagenicidad , Ratas , Ratas WistarRESUMEN
The clastogenic effect of the drug cis-diamminedichloroplatinum II (cisplatin, CDDP) was investigated in Wistar rat bone marrow cells. Male rats, 3 per treatment time, aged months and weighing 250-350 g were injected intraperitoneally with 6.0 mg/Kg CDDP solution, and the control group received isotonic saline. The animals were sacrificed 6, 12, 18, 24 and 48h after the injection. the chromosome preparation was obtained from bone marrow cells. Chromatid and chromosome aberrations were investigated in 300 metaphases per animal. A significant increase in number of chromosome aberration was observed from 6 to 24h, the majority being of the break and gap type. After 48 h a progressive reduction was observed, without differences from the negative control. These date confirm the mutagenic effect of CDDP in rats demonstrated for mice bone marrow by micronuclei assay, for murine ovary cells and mice spermatocytes
Asunto(s)
Animales , Masculino , Ratas , Aberraciones Cromosómicas/genética , Cisplatino/administración & dosificación , Médula Ósea/citología , Cisplatino/farmacología , Médula Ósea , Ratas WistarRESUMEN
The association between anemia during pregnancy and spontaneous preterm birth was studied with a two-stage case-control design in a large, multiethnic cohort. Results of all hematologic measurements were abstracted from the prenatal and delivery records of 1706 of the 26,901 women in the cohort. Among women delivered of infants at term, mean hematocrit value was low during the early phase of the second trimester, stable until near term, then reached a maximum at 40 weeks' gestation. The mean hematocrit value of black women was consistently lower than that of Asian, Mexican, and white women. Anemia (hematocrit value less than the tenth percentile for ethnic group and duration of pregnancy) at any time during the second trimester was positively associated with subsequent spontaneous preterm birth (odds ratio, 1.9; 95% confidence interval, 1.3 to 2.8). Compared with white women, the odds ratios for preterm birth were 2.0 (95% confidence interval, 1.6 to 2.4) for black, 1.2 (95% confidence interval, 0.9 to 1.6) for Asian, and 1.2 (95% confidence interval, 1.0 to 1.5) for Mexican women. Adjustment for second-trimester anemia had minimal influence on the odds ratios. We conclude that anemia during the second trimester was associated with preterm birth. However, it does not account for the large ethnic differences in preterm birth.
Asunto(s)
Anemia , Recien Nacido Prematuro , Complicaciones Hematológicas del Embarazo , Anemia/sangre , Anemia/etnología , Pueblo Asiatico , Población Negra , Estudios de Cohortes , Femenino , Hematócrito , Humanos , Recién Nacido , México/etnología , Embarazo , Segundo Trimestre del Embarazo , Población BlancaRESUMEN
A total of 977 White individuals living in five Brazilian cities, as well as 173 Black individuals from two of these cities have been studied in relation to HLA-A and HLA-B. Allele frequency similarities among these populations are much more impressive than dissimilarities, and the differences, considering putative ancestors, are not remarkable. This limited variability can be only partially explained in terms of racial admixture, estimates of the latter using different alleles in the various populations showing disparate results. Linkage disequilibrium values vary between groups, that for A1-B8 being the most consistent, independent of sample or race. But four other haplotypes observed to be in significant disequilibrium in Portugal showed the same pattern in at least one of the five Brazilian White samples.
Asunto(s)
Antígenos HLA/genética , Polimorfismo Genético , Adulto , Alelos , Brasil , Femenino , Frecuencia de los Genes , Ligamiento Genético , Humanos , MasculinoAsunto(s)
Genética de Población , Matrimonio , Personal Militar , Adolescente , Adulto , Antropometría , Brasil , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
Os autores apresentam sua experiencia com o angiodema hereditario, descrevendo diversos casos no Rio Grande do Sul. As familias acometidas foram investigadas com dosagem de C4, tipagem HLA, grupo sanguineo e Rh. Conclui-se que nao existe relacao entre o surgimento da doenca e antigenos de histocompatibilidade, grupos sanguineos ABO e Rh. A dosagem de C4 e importante na confirmacao do diagnostico clinico
Asunto(s)
Humanos , Masculino , Femenino , Angioedema , Proteínas del Sistema Complemento , Antígenos HLARESUMEN
Ninety-nine Tükuna Indians, inhabitants of the high Amazon, were typed for the HLA antigens. The method used was the microlymphocytotoxicity technique recommended by the NIH. At the same time, cross-matching was performed between the lymphocytes of the 99 Indians and the sera of 240 other multiparous Indians. Later the multiparous sera were cross-matched with a selected panel of Caucasoid individuals. The results showed that the most frequent antigens for th HLA-A locus were A2, Aw24 and Aw31. As for the HLA-B locus, B5, Bw39 and B40 were most frequent. The haplotypes HLA-Aw31-Bw39, and A2-B5 were in linkage disequilibrium. The results of the cross-matching showed 21.3% sera with positive reactions against Indian cells. Ten sera presented antibodies against known HLA antigens; five of them were monospecific, four had two specificities, and one showed three specificities. It was not possible to arrive at any conclusion about the 41 remaining sera. Six sera had positive reactions only with Indians cells.