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1.
Reprod Toxicol ; 15(5): 487-94, 2001.
Article in English | MEDLINE | ID: mdl-11780956

ABSTRACT

To evaluate the potential of unleaded gasoline vapor for developmental toxicity, a sample was prepared by slowly heating API 94-02 (1990 industry average gasoline) and condensing the vapor. The composition of this vapor condensate, which comprises 10.4% by volume of the starting gasoline, is representative of real-world exposure to gasoline vapor encountered at service stations and other occupational settings and consists primarily of volatile short chain (C4-C6) aliphatic hydrocarbons (i.e. paraffins) with small amounts of cycloparaffins and aromatic hydrocarbons. A preliminary study in rats and mice resulted in no developmental toxicity in either species. However, a slight reduction in maternal body weight gain in rats led to the selection of rats for this guideline study. Groups of pregnant rats (n = 24/group) were exposed to unleaded gasoline vapor at concentrations of 0, 1000, 3000, or 9000 (75% lower explosive limit) ppm equivalent to 0, 2653, 7960, or 23,900 mg/m3, for 6 h/day on gestation days 6-19. All rats were sacrificed on gestation day 20. No maternal toxicity was observed. Developmentally, there were no differences between treated and control groups in malformations, total variations, resorptions, fetal body weight, or viability. The maternal and developmental NOAEL is 9000 ppm. Under conditions of this study, unleaded gasoline vapors did not produce evidence of developmental toxicity.


Subject(s)
Air Pollutants/toxicity , Embryonic and Fetal Development/drug effects , Gasoline/toxicity , Administration, Inhalation , Air Pollutants/analysis , Animals , Atmosphere Exposure Chambers , Dose-Response Relationship, Drug , Female , Gasoline/analysis , Inhalation Exposure , No-Observed-Adverse-Effect Level , Pregnancy , Random Allocation , Rats , Rats, Sprague-Dawley , Volatilization , Weight Gain/drug effects
2.
J Cell Sci ; 113 Pt 23: 4221-30, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11069767

ABSTRACT

p125 focal adhesion kinase (p125FAK) is a cytoplasmic tyrosine kinase that is activated upon engagement of integrin cell adhesion receptors, and initiates several signaling events that modulate cell function in vitro. To determine the biologic role of p125FAK in malignant astrocytic tumor cells, U-251MG human malignant astrocytoma cells were stably transfected with p125FAK cDNA using the TET-ON system, and stable clones isolated that exhibited an estimated 5- or 20-fold increase in p125FAK expression on administration of 0.1 or 2.0 microg/ml doxycycline, respectively. In vitro studies demonstrated that induction of p125FAK resulted in a 2- to 3-fold increase in cell migration, increased p130CAS phosphorylation, localization of exogenous p125FAK to focal adhesions, and a 2-fold increase in soft agar growth. To determine the role of p125FAK in vivo, clones were injected stereotactically into the brains of scid mice. A 4.5-fold estimated increase in p125FAK expression was induced by administration of doxycycline in the drinking water. Analysis of xenograft brains demonstrated that, upon induction of p125FAK, there was a 1.6- to 2.8-fold increase in tumor cell number, and an increase in mAb PCNA-labeling of tumor cells in the absence of a change in the apoptotic index. Compared to normal brain, the expression of p125FAK was elevated in malignant astrocytic tumor biopsies from patient samples. These data demonstrate for the first time that p125FAK promotes tumor cell proliferation in vivo, and that the underlying mechanism is not associated with a reduction in apoptosis.


Subject(s)
Astrocytoma/pathology , Brain Neoplasms/pathology , Focal Adhesions/enzymology , Protein-Tyrosine Kinases/metabolism , Proteins , Agar , Animals , Anti-Bacterial Agents/pharmacology , Astrocytoma/enzymology , Biopsy , Brain Neoplasms/enzymology , Cell Division/physiology , Cell Movement/physiology , Crk-Associated Substrate Protein , Doxycycline/pharmacology , Enzyme Activation/drug effects , Enzyme Activation/physiology , Focal Adhesion Kinase 1 , Focal Adhesion Protein-Tyrosine Kinases , Gene Expression Regulation, Neoplastic , Humans , Mice , Mice, SCID , Neoplasm Transplantation , Phenotype , Phosphoproteins/metabolism , Phosphorylation , Protein-Tyrosine Kinases/analysis , Protein-Tyrosine Kinases/genetics , Retinoblastoma-Like Protein p130 , Transplantation, Heterologous , Tumor Cells, Cultured/cytology , Tumor Cells, Cultured/enzymology , Tumor Cells, Cultured/transplantation , Vitronectin/metabolism
3.
Toxicol Sci ; 48(1): 21-9, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10330680

ABSTRACT

The carcinogenic and chronic toxicity potential of commercial hexane solvent was evaluated in F-344 rats and B6C3F1 mice (50/sex/concentration/species) exposed by inhalation for 6 h/day, 5 days/week for 2 years. Target hexane vapor concentrations were 0, 900, 3000, and 9000 ppm. There were no significant differences in survivorship between control and hexane-exposed groups, and clinical observations were generally unremarkable. Small, but statistically significant decreases in body weight gain were seen in rats of both sexes in the mid- and high-exposure groups and in high-expsoure female mice. The only noteworthy histopathological finding in rats was epithelial cell hyperplasia in the nasoturbinates and larynx of exposed groups. This response was judged to be indicative of upper respiratory tract tissue irritation. No significant differences in tumor incidence between control and hexane-exposed rats were found. In mice, uterine tissue from the high-exposure females exhibited a significant decrease in the severity of cystic endometrial hyperplasia compared to controls. An increase in the combined incidence of hepatocellular adenomas and carcinomas was observed in high-exposure female mice. The incidence of liver tumors was not increased in the mid- or low-exposure female mice or in male mice exposed to hexane. An increased incidence of pituitary adenomas was observed in female, but not male mice. This finding was not believed to have been treatment-related because the incidence in the control group was unusually low, and the incidence in exposed groups was not dose-related and was within the historical control range. No other neoplastic changes judged to be treatment-related were observed in tissues from male or female mice. In conclusion, chronic exposure to commercial hexane solvent at concentrations up to 9000 ppm was not carcinogenic to F-344 rats or to male B6C3F1 mice, but did result in an increased incidence of liver tumors in female mice.


Subject(s)
Hexanes/toxicity , Solvents/toxicity , Adenoma, Liver Cell/chemically induced , Adenoma, Liver Cell/pathology , Administration, Inhalation , Animals , Body Weight/drug effects , Carcinogenicity Tests , Carcinoma, Hepatocellular/chemically induced , Carcinoma, Hepatocellular/pathology , Endometrium/drug effects , Endometrium/pathology , Epithelial Cells/drug effects , Epithelial Cells/pathology , Female , Hematologic Tests , Hexanes/administration & dosage , Hyperplasia/chemically induced , Hyperplasia/pathology , Liver Neoplasms/chemically induced , Liver Neoplasms/pathology , Male , Mice , Rats , Rats, Inbred F344 , Sex Distribution , Solvents/administration & dosage , Survival Rate , Turbinates/drug effects , Turbinates/pathology
5.
Int J Rehabil Res ; 3(3): 321-6, 1980.
Article in English | MEDLINE | ID: mdl-6450185

ABSTRACT

Television programming covering disability over a ten year span, 1967-68 and 1977-78, was studied to determine similarities and differences. Variables identified for comparisons included network, program type, disability, time slot, and length of programming. The largest frequency of programs occurred on NBC in 1968. However, in 1978 the largest frequency occurred on the Public Broadcasting System. This can be partially explained by the increased numbers of programs on PBS overall and their traditional concern with public interest and service programming. The commercial networks historically have been in the business of entertaining and portray disability more so in that fashion. Movies head the list in 1968. However, in 1978, dramatic series and children's programming head the list followed by news documentaries and telethon. Paraplegia was the most frequent disability portrayed in 1968 followed by mental illness, drug addiction and emotional disability. In 1978 mental illness headed the list followed by alcoholism, emotional disability and physically handicapped. Paraplegia in 1968 can be accounted for by the program "Ironside" that featured a paraplegic detective. Mental illness and emotional disturbance seem to be consistent targets over the decade for popular programming in prime time.


Subject(s)
Disabled Persons , Television , Humans , Time Factors , United States
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