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Related Concept Videos

Toxicity Testing in Animals01:23

Toxicity Testing in Animals

Toxicity tests in animals are grounded on two main assumptions: first, the effects observed in laboratory animals can be extrapolated to humans, especially when adjusted for body surface area; second, high-dose exposure in animals is essential to identify potential human hazards from lower doses. This is based on the quantal dose-response concept, which faces the challenge of extrapolating results from relatively few test animals to much larger human populations. For example, a 0.01% incidence...
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The hazard rate, also known as the hazard function or failure rate, is a statistical measure used to describe the instantaneous rate at which an event occurs, given that the event has not yet happened. From a probabilistic perspective, it represents the likelihood that a subject will experience the event in a very small time interval, conditional on surviving up to the beginning of that interval. In terms of frequency, the hazard rate can be viewed as the ratio of the number of events to the...
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Studies that assess how a drug is absorbed, distributed, metabolized, and excreted (ADME) at toxic doses are termed toxicokinetics. Understanding toxicokinetics helps predict adverse drug reactions (ADRs) and manage toxicity in humans.Toxicokinetics differs from pharmacokinetics mainly in the dose levels studied, with toxicokinetics focusing on higher toxic doses. The kinetics at these levels can be non-linear due to altered physiological processes. Toxicodynamics examines the relationship...
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Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
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Drug toxicity quantifies the harm a compound causes to an organism, varying by dose and potentially impacting whole systems or specific organs like the liver. Toxic reactions may arise from venomous insect or spider bites, with effects ranging from mild symptoms to severe outcomes such as brain damage or death. Common forms of acute poisoning include ethanol intoxication and overdose of pain or fever medications, with substances like GHB and heroin being particularly lethal at doses close to...
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Related Experiment Video

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In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
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Databases applicable to quantitative hazard/risk assessment--towards a predictive systems toxicology.

Michael Waters1, Marcus Jackson

  • 1ILS, Inc., P.O. Box 13501, Research Triangle Park, NC 27709, USA. mwaters@ils-inc.com

Toxicology and Applied Pharmacology
|August 5, 2008
PubMed
Summary

This study reviews the development and application of several key toxicity databases, including EPA Gene-Tox, GAP, TAP, GAC, and CEBS, for hazard identification and risk assessment. These aggregated datasets enhance toxicological data and inform regulatory decision-making.

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Area of Science:

  • Toxicology
  • Environmental Health
  • Bioinformatics

Background:

  • Quantitative hazard and risk assessment requires robust, distributed databases.
  • Existing databases have evolved to incorporate diverse toxicological data types.

Purpose of the Study:

  • To review the development and application of several federal-supported toxicity databases.
  • To highlight the utility of aggregated datasets for enhancing toxicological information.

Main Methods:

  • Development of the EPA Gene-Tox Database for mutagen detection.
  • Creation of the EPA/IARC Genetic Activity Profile (GAP) Database for carcinogen classification.
  • Construction of the NIEHS Genetic Alterations in Cancer (GAC) and CEBS Knowledgebase.

Main Results:

  • The EPA Gene-Tox Database facilitated collaborative evaluation of short-term tests.
  • The GAP Database has been instrumental in hazard classification of potential human carcinogens.
  • The GAC and CEBS Knowledgebase integrate genomic and dose-response data for comprehensive analysis.

Conclusions:

  • Aggregating data from these diverse databases significantly augments toxicological information.
  • These resources are crucial for advancing hazard identification and risk assessment.
  • The presented databases support regulatory decision-making in environmental health.