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1. |
PERSPECTIVES ON CANADIAN FIELD STUDIES EXAMINING THE POTENTIAL OF PULP AND PAPER MILL EFFLUENT TO AFFECT FISH REPRODUCTION |
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Journal of Toxicology and Environmental Health,
Volume 51,
Issue 4,
1997,
Page 305-352
T. G. Kovacs,
R. H. Voss,
S. R. Megraw,
P. H. Martel,
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摘要:
The results and interpretations of published Canadian field studies on the reproductive status of fish in waters receiving pulp and paper mill effluent discharges were reviewed. Most of the information was obtained from indicator measurements such as gonad size, fecundity, and serum steroid levels in wild fish sampled at reference and effluent-exposed sites. Difficulties in selecting appropriate sampling sites, natural variability, and the ecological relevance of the indicator measurements were identified as major complicating factors for the interpretation of the field data. Consequently, it was not possible to conclude to what extent, if any, widespread effects on fish reproduction are being caused by pulp and paper mill effluents or that specific manufacturing processes are causing such effects. Further research on the normal variability and predictive capability of reproductive indicators, for example, using an integrated approach (i.e., laboratory testing, mesocosm studies, and field work), is recommended.
ISSN:0098-4108
DOI:10.1080/00984109708984029
出版商:Taylor & Francis Group
年代:1997
数据来源: Taylor
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2. |
OZONE-INDUCED DNA STRAND BREAKS IN GUINEA PIG TRACHEOBRONCHIAL EPITHELIAL CELLS |
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Journal of Toxicology and Environmental Health,
Volume 51,
Issue 4,
1997,
Page 353-367
Shiaw-Fen Ferng,
C. Elizabeth Castro,
AbdelmonemA. Afifi,
Eliezer Bermudez,
MohammadG. Mustafa,
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摘要:
Ozone (O3), the major oxidant of photochemical smog, is thought to be genotoxic and a potential respiratory carcinogen or promoter of carcinogenic processes. Because of oxidative reactions with the mucus in the upper airway, O3reaction products are able to penetrate into the tracheobronchial epithelial (TE) cells. The carcinogenic effects of O3on the TE cells are especially of interest since most previous studies have focused on the morphology or permeability changes of tracheas only. Therefore, the objective of this study was to examine the potential O3genotoxicity in TE cells after an in vivo exposure, using DNA strand breaks as an index. Two-month-old male Dunkin-Hartley guinea pigs, specific pathogen free, 4 in each group, were exposed to 1.0 ppm 03 for 0, 12, 24, 48, 72, or 96 h. Animals exposed to filtered air without 03 exposure were used as controls. After O3exposure, the trachea with two main bronchi was removed from each animal, and TE cells were isolated and employed for determination of DNA strand breaks by fluorometric analysis of DNA unwinding (FADU). The statistical significance level was set at a=.05. Compared with controls, ozone exposure did not alter the TE cell yield or viability, but caused an increase in protein content in tracheal lavage and an increase in DNA strand breaks. The amount of DNA left in the alkali lysate of TE cells found at 72 h exposure was significantly decreased from controls for 3 different alkali incubation times. An increase of the double-stranded DNA left in the alkali lysate of TE cells was observed at 96 h of exposure and approached the value of 24 h of exposure. The same pattern was seen with all 3 different alkali incubation times at 15°C. One Qd unit was estimated to correspond to 100 strand breaks per cell. The Qd was also used as an indicator for 03 damage. Compared to controls, the Qd increases significantly after 1 ppm 03 exposure for 72 h, regardless of the alkali incubation time at 15°C.
ISSN:0098-4108
DOI:10.1080/00984109708984030
出版商:Taylor & Francis Group
年代:1997
数据来源: Taylor
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3. |
GROWTH-RELATED SIGNALING IN VASCULAR SMOOTH MUSCLE CELLS OS DEREGULATED BY TCDD DURING THE G0/G1, TRANSITION |
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Journal of Toxicology and Environmental Health,
Volume 51,
Issue 4,
1997,
Page 369-386
ThomasJ. Weber,
Yang-Yi Fan,
RobertS. Chapkin,
KennethS. Ramos,
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摘要:
Experiments have been conducted to examine the impact of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on growth-related signaling in vascular smooth muscle cells (SMCs). A 40% reduction of peak DNA synthesis was observed in SMCs only when TCDD was added during the G0/G1, transition of the cell cycle. Enhanced phosphorylation of several endogenous proteins during this period was coincident with increased tyrosine kinase activity as early as 15 min following TCDD challenge. No changes in protein phosphorylation status occurred in cells treated with TCDD during the C,/S transition or during 5 phase. Cotreatment of quiescent SMCs with 10 nM TCDD and serum for 3 h reduced serum-inducible binding activity to a 12-O-tetradecanoyl phorbol 13-acetate responsive element (TRE) by approximately 40%. No alterations of constitutive TRE binding were observed in quiescent SMCs treated with TCDD for up to 5 h. These data show that mitogen-related signaling in vascular SMCs is modulated by TCDD selectively during the G0/G1transition, and these effects influence the growth behavior of these cells.
ISSN:0098-4108
DOI:10.1080/00984109708984031
出版商:Taylor & Francis Group
年代:1997
数据来源: Taylor
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4. |
SYSTEMIC TOXICITY OF DERMALLY APPLIED CRUDE OILS IN RATS |
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Journal of Toxicology and Environmental Health,
Volume 51,
Issue 4,
1997,
Page 387-399
MaureenH. Feuston,
CarlR. Mackerer,
C. A. Schreiner,
CarrieE. Hamilton,
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摘要:
Two crude oils, differing in viscosity (V) and nitrogen (N) and sulfur (S) content, were evaluated for systemic toxicity. In the Crude I (low V, low N, low S) study, the material was applied to the clipped backs of rats at dose levels of 0, 30, 125, and 500 mg/kg. In the Crude II (high V, high N, moderate S) study, the oil was applied similarly at the same dose levels. The crude oils were applied for 13 wk, 5 d/wk. Exposure sites were not occluded. Mean body weight gain (wk 1-14) was significantly reduced in male rats exposed to Crude II; body weight gain of all other animals was not adversely affected by treatment. An increase in absolute (A) and relative (R) liver weights and a decrease in A and R thymus weights were observed in male and female rats exposed to Crude II at 500 mg/kg; only liver weights (A and R) were adversely affected in male and female rats exposed to Crude I. In general, there was no consistent pattern of toxicity for serum chemistry endpoints; however, more parameters were adversely affected in Crude II-exposed female rats than in the other exposed groups. A consistent pattern of toxicity for hematology endpoints was observed among male rats exposed to Crude I and male and female rats exposed to Crude II. Parameters affected included: Crudes I and II, red blood cell count, hemoglobin, and hematocrit; Crude II, platelet count. Microscopic evaluation of tissues revealed the following treatment-related findings: Crude I, treated skin, thymus, and thyroid; Crude II, bone marrow, treated skin, thymus, and thyroid. The LOEL (lowest observable effect level) for skin irritation and systemic toxicity (based on marginal effects on the thyroid) for both crude oils was 30 mg/kg; effects were more numerous and more pronounced in animals exposed to Crude II. Systemic effects are probably related to concentrations of polycyclic aromatic compounds (PAC) found in crude oil.
ISSN:0098-4108
DOI:10.1080/00984109708984032
出版商:Taylor & Francis Group
年代:1997
数据来源: Taylor
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5. |
BILIARY ELIMINATION OF ORAL 2,4-DBCHLQROPHEN-OXYACETBC ACID AND ITS METABOLITES ON MALE AND FEMALE SPRACUE-DAWLEY RATS, B6C3F1 MICE, AND SYRIAN HAMSTERS |
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Journal of Toxicology and Environmental Health,
Volume 51,
Issue 4,
1997,
Page 401-413
RobertJ. Griffin,
Jean Salemme,
James Clark,
Page Myers,
LeoT. Burka,
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摘要:
The role of biliary elimination in the metabolic disposition of 2,4-D was evaluated in male and female Sprague-Dawley rats, B6C3F1 mice, and Syrian hamsters. Following cannulation of the bile duct, an intragastric (ig) dose of 2,4-D (200 mg/kg) was administered and bile was collected at 30- or 60-min intervals for up to 6 h. Bile flow rates were constant in rats, increased in mice, and decreased in hamsters throughout the collection periods. Total recovery of radioactivity was greatest in male mice (about 7% of administered dose over 4 h). Female mice and rats of both sexes excreted about 3% over the same interval and male and female hamsters about 1%. About 71–88% of the activity in bile was parent compound. The glycine conjugate of 2,4-D was found in bile from mice, rats, and hamsters and the taurine conjugate in bile from mice. The only sex-dependent difference in the metabolite profile was in mice. Male mice excreted twice as much glycine conjugate as female mice. An additional minor metabolite (4–7%) was present in rat and mouse bile. This was tentatively identified as 2,4-D-glucuronide based on its hydrolysis by β-glucuronidase. One more very minor metabolite (3%) was detected in rat bile but was not characterized due to its lability. The results of this study indicate that there are species-dependent differences in the biliary elimination of 2,4-D but not sex-dependent differences.
ISSN:0098-4108
DOI:10.1080/00984109708984033
出版商:Taylor & Francis Group
年代:1997
数据来源: Taylor
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