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1.
MJFCT-Mansoura Journal of Forensic Medicine and Clinical Toxicology. 2002; 10 (1): 35-54
in English | IMEMR | ID: emr-60201

ABSTRACT

In the present work, 765 X-ray photographs for males and 450 for females from a sample of clinically healthy Egyptian population in the east of Delta, in the age range of 9-25 years, were examined for epiphyseal union in the regions of the elbow, wrist, hand, knee, ankle, and foot. The epiphysis was considered united if there was complete obliteration of the diaphyseo-epiphyseal space, and non- united if there was no or partial obliteration of diaphyseo- epiphyseal space. The results showed that epiphyseal union occurs over a range of 4-6 years in males and 4-5 years in females, and the union was 1-2 years earlier in females than in males. Comparison of results of the present study with results of other studies performed earlier or in other localities demonstrated the existence of differences in age timing and sequence of union of the studied epiphyses. The differences were more marked on comparing the present study with a study performed on Bengalis than with a study performed on Caucasians. This raises the importance of developing and updating the standards of ages of epiphyseal union for each locality to achieve more accuracy of age estimation by examining bone epiphyses. Examining more than one epiphysis for age estimation is also recommended


Subject(s)
Humans , Male , Female , Epiphyses , Elbow Joint , Knee Joint , Wrist Joint , Ankle Joint
2.
MJFCT-Mansoura Journal of Forensic Medicine and Clinical Toxicology. 2001; 9 (2): 115-128
in English | IMEMR | ID: emr-57785

ABSTRACT

The present work was conducted to study the effect of lead, after in vivo and in vitro exposure, on neutrophil apoptosis in albino rats. For the in vivo study, adult female albino rats, with body weight range of 150-250 g, were randomized into test and control groups, 20 rats/group. Test groups were treated with lead acetate solution in distilled water by intraperitoneal injection at two dose levels [20 mg/kg body weight or 40 mg/kg body weight for either 4 weeks or 12 weeks for each dose level]. Control groups were treated with distilled water by intraperitoneal injection for either 4 weeks or 12 weeks. For the in vitro study, neutrophil cultures were prepared from 20 rats and each test culture was divided into two subdivisions and incubated for 24 hours with lead acetate at 2 concentrations, 20 or 40 mmol/ml cell culture. Control cultures were prepared from other 20 rats. Apoptosis was assessed morphologically by light microscope using Giemsa stain, fluorescence microscope using acridine orange stain and by assessment of DNA fragmentation by agarose gel electrophoresis


Subject(s)
Animals, Laboratory , Female , Apoptosis , DNA Fragmentation , Electrophoresis, Agar Gel , Microscopy, Fluorescence , Rats
3.
MJFCT-Mansoura Journal of Forensic Medicine and Clinical Toxicology. 2001; 9 (2): 141-150
in English | IMEMR | ID: emr-57787

ABSTRACT

The present work was performed to study the effects of subchronic and chronic in vivo exposure to lead on some parameters of T lymphocyte functions; namely, interferon-gamma [IFN-gamma] production and mitogen blastogenesis in albino rats. Adult female albino rats, with body weight range of 150-250 g, were randomized into test and control groups, 20 rats/group. Test groups were treated with lead acetate solution in distilled water by intraperitoneal injection at two dose levels [20 mg/kg body weight or 40 mg/kg body weight for either 4 weeks or 12 weeks for each dose level]. Control groups were treated with distilled water by intraperitoneal injection for either 4 weeks or 12 weeks. The results showed that lead exerted immunomodulatory effects on the studied immune parameters. It decreased gamma-IFN serum levels and enhanced blastogen transformation of lymphocytes in a dose and time-dependent manner. These results showed that lead differently affects T cell subpopulations. Dysregulation of the immune function may be the end result


Subject(s)
Animals, Laboratory , Female , Interferon-gamma , Immune System , Mitogens , T-Lymphocytes , Rats
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