[en] Continuing studies of the sublethal effects of tritium on freshwater species emphasize the potential for genetic transmission of suppressed immune competence in offspring of parental rainbow trout (Salmo gairdneri) exposed to tritium (0, 0.04, 0.4, 40.0 rads) during embryogenesis. We plan to determine the relative biological effectiveness of tritium beta irradiation when compared to ⁶⁰Co gamma irradiation using the relatively radiosensitive immune process of rainbow trout. During FY 1979, we concluded genetic effects studies and prepared a manuscript for open literature publication summarizing FY 1977 and FY 1978 studies on the permanence of suppression of the primary immune response in rainbow trout sublethally irradiated during embryogenesis. We are also studying the potential effects of beryllium and lithium on aquatic systems. Because of mining and refining subsequent to the use of these metals in the construction of fusion reactors, increased levels of each are likely to be encountered in surface waters. Studies included an evaluation of potential toxicity of lithium on embryological life stages of rainbow trout and an assessment of fate and effects in artificial stream habitats. Levels of lithium necessary to cause an observed effect would have to be at least three orders of magnitude above observed background. Studies initiated in FY 1978 include evaluation of effects of low-level magnetic fields on embryologic development of rainbow trout. The objective of these studies to provide data useful in assessing potentially harmful effects of low-level magnetic fields encountered by attendant personnel working in the transport and hot cell areas of fusion reactors. This approach is less costly than using mammalian systems, provides large numbers of experimental organisms for meaningful statistical analysis and permits examination of potential latent effects in a representative vertebrate

[en] Background: Lead remains a considerable occupational and public health problem, which is known to cause a number of adverse effects in both men and women. Conflicting reports have appeared on lead induced nephrotoxicity in experimental studies in the past. There is hardly any work on its teratogenic effects on kidney. Present study was therefore designed to investigate the effects of lead acetate on developing kidney. Methods: Twelve mice were used as experimental model and were divided into two groups of six animals each; group A served as control group and B was used as an experimental group. Lead acetate (10 mg/kg) dissolved in 0.02 ml of distilled water was administered as a single daily dose orally to group B whereas weight related amount of distilled water was given to group A for the entire period of experiment. On 18 day of gestation foetuses were dissected free of uterine wall under the dissecting microscope and were sacrificed; kidneys were removed and fixed in 10% formalin, dehydrated in ascending grades of alcohol, cleared in xylene and infiltrated with filtered paraffin. The paraffin blocks were made and five micron thin sections were obtained using a rotary microtome. The sections were stained with Hematoxylin and eosin and, PAS; these were examined under light microscope. Results: Significant decrease in cortical thickness was observed which varied from 578.6 +- 1.4 mu m in group A to 515.6 +- 5 mu m in group B (p<0.001). Diameter of renal corpuscles varied from 57.7 +- 0.07 mu m in group A to 50.5 +- 0.07 mu m in group B (p<0.001). Moderate cortical tubular atrophy showing thickening of endothelial basement membrane in glomeruli, desquamated epithelium with degenerated nuclei in proximal and distal tubules were observed in group B in contrast to group A. Conclusion: The results of the investigation indicated that lead acetate administration to the dams produced deleterious effects on the developing kidney in mice. (author)

[en] The CT and MR findings are reported for a patient diagnosed as having teratoma of the posterior fossa with onset in the form of intracranial hypertension. The objective of this article is to report the detection of the lesion, as well as its origin in the closure defect of the cranial cavity with the formation of a cutaneous fistula, and review the recent literature

[en] The long-term risks induced by radiation are of much concern to patients and clinicians alike. As an example, perceived radiation risks are frequently cited in a woman's decision to choose a radical mastectomy over lumpectomy + radiation. In consequence, the actual radiation risks are often considerably overstated, or unreasonably downplayed. In this lecture we will discuss just what is known about the long term risks following radiotherapy, both from the human experience and from the laboratory. We will discuss risks both to the patient and to radiotherapy personnel. A good deal is known about the carcinogenic effects of high and low doses of radiation, in large part thanks to the careful study of the survivors of the atomic bombing in Japan, as well as studies of individuals exposed to medical x rays. It is possible to make an estimate, which is probably good to within a factor of, perhaps, three to five, of the cancer risks faced by a patient of a particular age and sex who is going to undergo a particular radiotherapeutic regimen. It is also possible to make an estimate of the risks faced by radiotherapy and nursing staff exposed to low doses. Brachytherapy related risk estimates are likely to be somewhat more uncertain, due to the poorly known sparing effects of the low dose rates used; for the radiotherapy personnel in brachytherapy, because of the doses which can be received, the risks can be quite significant. A recent complication in external-beam radiotherapy is the advent of high-energy linacs, which can produce a significant fast neutron dose which, dose for dose, may be ten to fifty times more carcinogenic than gamma rays. Data relating to the risks of hereditary effects of radiation come almost entirely from laboratory experiments in animals. Studies involving several million mice form the basis of most of our current understanding of hereditary effects. The results of these studies indicate that radiation is a relatively inefficient mutagen. The first generation of offspring of survivors of Hiroshima and Nagasaki show no statistically significant increase in hereditary effects, but the numbers are small, and not inconsistent with risk estimates based on animal data. These data will be discussed, and we will try to conclude just what can currently be reasonably said about hereditary risks to a young patient facing the radiotherapy decision. Finally, risks from prenatal radiation exposure are now of little relevance to radiotherapy patients, but are certainly of considerable relevance to radiotherapy personnel, particularly those involved in brachytherapy. The developing embryo and fetus are extremely radiosensitive and, at certain stages of gestation, risk estimates far exceed those for carcinogenic or hereditary effects

[en] Objective: To observe the effect of ethanol vapours on chick embryos regarding developmental defects and hatch ability characteristics. Methods: An experimental study was performed in the Department of Anatomy at the Regional Center of College of Physicians and Surgeons, Islamabad, from February, 2006 to February, 2007. Chicken eggs after having been exposed to ethanol vapours produced in a specially designed glass chamber, were dissected on day 7, day 10 and day 22 or on hatching and compared with age-matched controls. A breathalyser was used for monitoring level of ethanol vapours inside the incubator. Results: The results show that experimental group had comparatively more cases of delayed and assisted hatchings as well as growth retardation resulting into failure of retraction of yolk sac, as compared to the controls. Conclusion: Ethanol vapour exposure increases the risks of developmental defects with increasing embryonic age. Increased duration of exposure, causes delayed hatching and more assisted hatchings. Newly hatched alcohol exposed chicks showed diminished locomotor activity and poor balance. (author)

No abstract available

[en] Purpose: To evaluate the effectiveness and safety of covered stents for the management of iatrogenic arterial injury. Materials and Methods: Between 03/1998 and 12/2009, 31 patients underwent selective covered stent implantation after iatrogenic arterial injury. 12/31 of these patients (38.7 %) were hemodynamically unstable. Six different endovascular covered stent types were utilized. The primary endpoints of this study were technical and clinical success and rates of minor and major complications. Results: Initial angiograms demonstrated active extravasation in 19 (61.3 %) patients and pseudoaneurysms in 12 (38.7 %) patients. The following sites of bleeding origin were detected: axillary artery, subclavian artery, common iliac artery, external iliac artery, internal iliac artery, common femoral artery, superficial femoral artery, popliteal and fibular artery, femoro-popliteal and popliteo-crural bypasses, common hepatic artery, aberrant hepatic artery, cystic and gastroduodenal artery. In all patients bleeding was effectively controlled by covered stent implantation resulting in an immediate technical success of 100 %. Clinical success attributed to covered stent implantation was documented in 30 of the 31 patients (96.8 %). Major complications included death in four patients (11.1 %), acute thrombosis with arm ischemia in one patient (2.8 %) and stent fracture with associated pseudoaneurysm in another patient (2.8 %). In 2/31 patients (6.5 %) covered stent failure was detected and successfully treated by implantation of a second covered stent. Conclusion: Emergency and elective implantation of covered stents may be used for minimally invasive and effective management of iatrogenic arterial injury. (orig.)

[en] Present article is devoted to embryotoxicity and teratogenicity of 2-bromo-7-methyl-5-oxo-5 h-1,3,4-thiadiazole [3,2-a] pyrimidine. It has been shown that 2-bromo-7-methyl-5-oxo-5 H-1,3,4-thiadiazole [3,2-a] pyrimidine has no embryotoxic and teratogenic effects in experiments on rats. (author)

No abstract available

[en] Although fetal development is known to be sensitive to environmental agents, relatively little epidemiologic research has addressed this concern. Effects on pregnancy outcome of self-reported parental exposure to pesticides and to radiation were examined using data from the National Natality and Fetal Mortality Surveys, large national probability samples of live births and stillbirths occurring in 1980. In case-control analyses, maternal exposure to pesticides at home or work was associated with increased risk of stillbirth (odds ratios (ORs) = 1.5-1.6). Paternal pesticide exposure was associated with stillbirth (ORs = 1.2-1.4) and delivery of small-for-gestational-age infants (ORs = 1.4-2.0). A small increased risk of stillbirth (OR = 1.3) was found in relation to either parent's reported exposure to radiation. In spite of limitations in the quality of exposure data and the possibility of biased recall related to pregnancy outcome, associations of reported pesticide exposure to either parent with risk of stillbirth and small-for-gestational-age infants warrant further evaluation