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1.
Toxicol Sci ; 45(2): 137-45, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9848120

ABSTRACT

Topical application of certain petroleum middle distillates (PMD) to mice produces skin tumors after long latency, and initiation/promotion protocols indicate that this effect is associated with their tumor promoting activity. Since induction of sustained, potentiated epidermal hyperplasia is predictive of promoting activity, five compositionally distinct PMD [hydrodesulfurized kerosene (API 81-07); hydrodesulfurized PMD (API 81-10); odorless light petroleum hydrocarbons; severely hydrotreated light vacuum distillate (LVD); and lightly refined paraffinic oil (LRPO)] were assessed for their effects on epidermal hyperplasia. PMD were administered (2 x/week for 2 weeks) to skin of CD-1 mice. Four quantitative biomarkers of epidermal hyperplasia were evaluated: epidermal thickness, number of nucleated epidermal cells per unit length of basement membrane, labeling (BrdUrd) index of epidermal cells, and induction of epidermal ornithine decarboxylase (ODC) activity. As positive controls, 12-O-tetradecanoylphorbol-13-acetate (TPA) and n-dodecane were utilized. PMD-induced skin irritation was evaluated visually and/or histopathologically. All five PMD produced dose-dependent, skin irritation and epidermal hyperplasia. On a weight basis the magnitude of the maximal PMD-induced effects was similar to that produced by n-dodecane, but > 1000-fold less than that produced by TPA. Epidermal hyperplasia and subacute skin irritancy produced by the five PMD were similar. Of the four short-term markers of tumor promotion assessed, labeling index and epidermal ODC activity were predictive of the relative promoting activities of those PMD for which tumorigenicity bioassay data are available, i.e., API 81-07 > API 81-10 > LRPO. An apparent discrepancy to the predictability of epidermal ODC activity occurred with LRPO:toluene [1:1 (v/v)]. This mixture is nontumorigenic, yet significantly induced epidermal ODC activity. This mixture, however, produced severe epidermal toxicity that precluded any meaningful analysis of short-term biomarkers in relationship to biological activity.


Subject(s)
Carcinogens/toxicity , Dermatitis, Irritant/etiology , Petroleum/toxicity , Skin/drug effects , Administration, Topical , Animals , Biomarkers , Cell Division/drug effects , Dermatitis, Irritant/pathology , Enzyme Induction , Female , Hyperplasia/chemically induced , Mice , Mutagenicity Tests , Ornithine Decarboxylase/biosynthesis , Salmonella typhimurium/drug effects , Salmonella typhimurium/genetics , Skin/enzymology , Skin/pathology
3.
Environ Health Perspect ; 102(1): 82-7, 1994 Jan.
Article in English | MEDLINE | ID: mdl-9719673

ABSTRACT

Nine refinery streams were tested in both chronic and initiation/promotion (I/P) skin bioassays. In the chronic bioassay, groups of 50 C3H/HeJ mice received twice weekly applications of 50 microl of test article for at least 2 years. In the initiation phase of the I/P bioassay, groups of CD-1 mice received an initiating dose of 50 microl of test article for 5 consecutive days, followed by promotion with 50 microl of phorbol-12-myristate-13-acetate (0.01% w/v in acetone) for 25 weeks. In the promotion phase of the I/P bioassay, CD-1 mice were initiated with 50 microl of 7,12-dimethylbenzanthracene (0.1% w/v in acetone) or acetone, followed by promotion with 50 microl of test article twice weekly for 25 weeks. The most volatile of the streams, sweetened naphtha, and the least volatile, vacuum residuum, were noncarcinogenic in both assays. Middle distillates, with a boiling range of 150 degrees-370 degrees C, demonstrated carcinogenic activity in the chronic bioassay and acted as promoters but not initiators in the I/P bioassay. Untreated mineral oil streams displayed initiating activity and were carcinogenic in the chronic bioassay, presumably due to the presence of polycyclic aromatic hydrocarbons of requisite size and structure. A highly solvent-refined mineral oil stream lacked initiating activity. These results indicate that the I/P bioassay, which takes 6 months to complete, may be a good qualitative predictor of the results of a chronic bioassay, at least for petroleum streams. Furthermore, the I/P bioassay can provide insight into possible mechanisms of tumor development.


Subject(s)
Carcinogens/toxicity , Petroleum/toxicity , Skin Neoplasms/chemically induced , Alkanes/toxicity , Animals , Biological Assay , Carcinogenicity Tests , Extraction and Processing Industry , Male , Mice , Mice, Inbred C3H , Mineral Oil/toxicity , Random Allocation , Skin Tests , Tetradecanoylphorbol Acetate/toxicity , Time Factors
4.
Am Ind Hyg Assoc J ; 44(12): 948-50, 1983 Dec.
Article in English | MEDLINE | ID: mdl-6660195

ABSTRACT

This study examined formaldehyde vapor exposures that occurred in the gross anatomy laboratories of a major medical school during a 12-week study period. Formaldehyde samples were collected using personal sampling pumps to draw air through midget impingers containing a 0.1% solution of sodium bisulfite dissolved in deionized water as the absorbing medium. Breathing zone and ambient air samples were collected and analyzed from 8 laboratories on a rotating basis. Analysis was via the chromotropic acid method recommended by the National Institute for Occupational Safety and Health. It was found that 44% of all breathing zone samples were greater than the 1.0 ppm ceiling value for occupational exposure recently recommended by the American Conference of Governmental Industrial Hygienists. Only 11% of ambient air samples were in excess of 1.0 ppm.


Subject(s)
Air Pollutants/analysis , Anatomy/education , Formaldehyde/analysis , Laboratories , Volatilization
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