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1.
J Appl Toxicol ; 28(6): 765-72, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18300328

ABSTRACT

Deoxynivalenol (DON) is a mycotoxin food contaminant found in several cereal grains. The literature on the liver toxicity of DON in vivo is conflicting and does not clearly characterize its hepatotoxic effects. Cultured rat liver clone-9 cells were used as a model to assess the hepatotoxic potential of DON. The cell cultures, seeded onto 96-well plates, were treated at confluence with varying concentrations of DON (0-100 microg ml(-1)) for 48 h at 37 degrees C in 5% CO2. After the treatment period, the cells were assayed for a number of hepatotoxic endpoints that included cytotoxicity, double-stranded DNA (ds-DNA) content, oxidative stress and mitochondrial function. The concentration-dependent toxicity of DON, as measured by cytotoxicity and ds-DNA content, was observed over the entire concentration range studied beginning at 0.5 microg ml(-1). DON also induced a significant concentration-dependent increase in oxidative stress at DON concentrations starting at 10 microg ml(-1). The mitochondrial function of the treated cells decreased with the increasing concentration of DON exposure, but it was not statistically different from that of the control value. Liver histopathology observed at 3, 24 and 72 h following a single intraperitoneal administration dose of DON (10 mg kg(-1) BW) to adult male rats is consistent with early mild hepatotoxicity. The overall results of this study suggest that acute DON exposure has early mild cytotoxic effects on hepatocytes in vivo that are expressed as severe effects in rat liver clone-9 cells in vitro.


Subject(s)
Chemical and Drug Induced Liver Injury/pathology , Food Contamination , Hepatocytes/drug effects , Trichothecenes/toxicity , Animals , Cell Line , Cell Survival/drug effects , Cells, Cultured , Clone Cells , DNA/biosynthesis , DNA/genetics , Male , Mitochondria, Liver/drug effects , Oxidative Stress/drug effects , Rats , Rats, Sprague-Dawley
2.
Neurotoxicol Teratol ; 30(4): 349-81, 2008.
Article in English | MEDLINE | ID: mdl-17826946

ABSTRACT

The reliable detection, measurement, and interpretation of treatment-related developmental neurotoxicity (DNT) effects depend on appropriate study design and execution, using scientifically established methodologies, with appropriate controls to minimize confounding factors. Appropriate statistical approaches should be optimized for the specific endpoints in advance, analyzing effects across time and functional domains as far as possible. If available, biomarkers of exposure are useful to assess the bioavailability of toxicants to the dam and offspring in utero and after birth. Finally, "weight of evidence" principles are used to aid assessment of the biological significance of differences from concurrent controls. These effects should be interpreted in light of available information from historical controls, positive controls, maternal and offspring systemic toxicity, and other relevant toxicological data. This review provides a framework for the integration of all these types of information in the interpretation of DNT studies.


Subject(s)
Biomedical Research/methods , Biomedical Research/standards , Data Interpretation, Statistical , Neurotoxicity Syndromes , Animals , Disease Models, Animal , Female , Humans , Male , Neurotoxicity Syndromes/etiology , Pregnancy , Prenatal Exposure Delayed Effects , Risk Assessment
3.
J Appl Toxicol ; 27(5): 421-33, 2007.
Article in English | MEDLINE | ID: mdl-17345587

ABSTRACT

The oral toxicity of a single administration by gavage (10, 20 or 30 mg kg(-1) body weight) of colchicine (COL) was determined in young, mature male and female Sprague-Dawley rats. The effect of COL was evaluated in the presence or absence of additional treatment variables that included vehicle and lipopolysaccharide (LPS) pre-exposure. The vehicle for COL was either Half and Half cream (H & H) or saline, and each group included pretreatment with either saline or a low, minimally toxic dose (83 microg kg(-1) body weight) of LPS. Colchicine toxicity in both male and female age-matched rats was characterized by progressively more severe dose-related clinical signs of toxicity. These included mortality, decreased body weight and feed intake during the first several days after dosing, with recovery thereafter in surviving animals. There were differences in the severity of the toxic response to COL between male and female rats. The most notable sex-related difference was in COL lethality. Female rats were two times more susceptible to the lethal effects of COL than male rats. Saline or H & H delivery vehicles did not result in any apparent qualitative or quantitative differences in COL toxicity. LPS pretreatment significantly potentiated COL lethality in both males and females, although the potentiation in males was greater than in females. LPS pretreatment modestly increased the COL induced anorexic effect in surviving males, but not in surviving female animals. LPS did not appear to modulate either the body weights or clinical signs of COL induced toxicity in surviving males or females.


Subject(s)
Colchicine/toxicity , Lipopolysaccharides/toxicity , Administration, Oral , Animals , Body Weight/drug effects , Colchicine/administration & dosage , Female , Lethal Dose 50 , Male , Pharmaceutical Vehicles , Rats , Rats, Sprague-Dawley , Sex Factors
4.
Neurotoxicol Teratol ; 27(3): 417-27, 2005.
Article in English | MEDLINE | ID: mdl-15939202

ABSTRACT

A one and a half day workshop on behavioral testing was conducted in order to discuss experimental procedures and practices that may help enhance the utility of behavioral data as a reliable index of neurotoxicity and in the safety evaluation of chemical substances. The workshop was open to participation by all sectors of the neuroscience community including academia, government, testing laboratories, and industry. The level of confidence with which changes in behavior can reliably signal adverse effects on the nervous system depends, in part, on the scientific quality of the data generated. With an emphasis on education and problem solving, the workshop focused on the practical aspects and scientific rationale underlying valid and high quality testing. In behavioral testing, there are numerous experimental factors that may impact on the quality of data. These include such elements as experimental design, selection of test methods, the care and precision in the conduct of behavioral testing, procedures to minimize bias and potential confounds, appropriateness of statistical analyses, and data interpretation. In plenary session investigators experienced in behavioral testing discussed the significance of these various experimental factors to data quality, outlined problematic issues, and presented a synopsis of approaches for addressing each of the factors as outlined in a draft of a primer developed by the Interagency Committee on Neurotoxicology (ICON). During the remainder of the workshop, open discussions in small breakout groups were used to address the problematic issues identified by the plenary speakers and explore alternative approaches for dealing with them. Finally, all workshop participants were reconvened in plenary session for summation of breakout group discussions and final recommendations. Information from the workshop was used to form the basis of this manuscript and will be used to help finalize a behavioral test methods primer being drafted by the ICON. The overall conclusions from the workshop were that consensus can be reached on the fundamentals of behavioral assessment, and that aspects of behavioral assessment including experimental design, test method selection, training, validation, control of confounds, data variability, data analysis, and data interpretation need to be carefully considered in the planning and conduct of behavioral safety assessments.


Subject(s)
Behavior, Animal/drug effects , Behavior/drug effects , Neurotoxicity Syndromes/psychology , Animals , Data Interpretation, Statistical , Dose-Response Relationship, Drug , Humans , Neurotoxicity Syndromes/epidemiology , Research Design , Risk Assessment , Toxicology , Workforce
5.
Lab Anim (NY) ; 32(7): 34-40, 2003.
Article in English | MEDLINE | ID: mdl-19760848

ABSTRACT

The noise level in an animal facility is an important environmental variable that can adversely affect animal welfare, as well as experimental data. The authors describe the strategy they used to record, evaluate, and control excess noise and vibration during a period of renovation, while maintaining the operation of a research facility.


Subject(s)
Animal Welfare , Animals, Laboratory , Housing, Animal/standards , Noise/prevention & control , Vibration , Animals
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