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VetBooks.ir  Chapter 8





             Toxicokinetics in Veterinary Toxicology



             Deon van der Merwe, Ronette Gehring and Jennifer L. Buur







             INTRODUCTION                                       human food chain. Kinetic parameters, such as duration
                                                                of internal exposure and tissue concentrations, are
             The epithelial barriers that form the body’s interface with
                                                                therefore  useful  metrics  for  assessing  risk.
             the environment, and the cellular barriers that separate
                                                                Mathematical models are used to characterize these para-
             internal organs and tissues, have to be permeable to a
                                                                meters by describing changes in toxicant concentrations
             wide variety of chemicals to allow nutrient absorption
                                                                over time. Models are most often used as predictive tools
             and waste product elimination. The permeability of these
                                                                following exposure to toxicants, but they can also be used
             physiological barriers, however, also allows toxicants to  as an aid to understanding the underlying physiological
             penetrate. Exposure to toxicants through ingestion, inhala-
                                                                mechanisms of chemical absorption, transport and elimina-
             tion, and dermal contact may therefore result in harmful
                                                                tion. Various types of toxicokinetic models have been
             absorption. The degree of adverse effects following expo-
                                                                developed and the appropriateness of a specific model type
             sure to a toxicant is dependent on the rate and extent of
                                                                depends on the available data and the model’s purpose
             absorption into the body, distribution to susceptible
                                                                (Riviere, 2011). One of the key challenges to the successful
             organs and tissues, and specific interactions with biologi-
                                                                use of models is identifying the appropriate conditions for
             cal targets. Living organisms are adapted to toxicant
                                                                its application. Two fundamentally different types of toxico-
             exposure through the development of transport and elimi-
                                                                kinetic models are recognized: traditional (also called “clas-
             nation mechanisms that prevent the build-up of harmful
                                                                sic”) toxicokinetic models, and physiologically based
             chemical concentrations in organs and tissues.
                                                                toxicokinetic (PBTK) models. Traditional toxicokinetic
                Toxicokinetics refers to the movement and fate, also
                                                                models are mathematical descriptions of concentration/time
             referred to as the disposition, of toxicants. The term is
                                                                profiles that are constructed without assuming that the com-
             most commonly used when describing the time course of
                                                                partments and functions used in the models are directly rep-
             absorption, distribution, and elimination (including bio-
                                                                resentative of physical structures or physiological processes.
             transformation and excretion) of toxicants in an organism.
                                                                The selection of compartments and functions are therefore
             Toxicokinetics is closely related to pharmacokinetics, and
                                                                solely dependent on their ability to describe experimentally
             may even be viewed as the same discipline, with the only
                                                                observed concentration/time profiles. PBTK models, on the
             difference being the class of compound (toxicant or
                                                                other hand, are mathematical simulations of kinetic pro-
             pharmaceutical) that is involved. Compared to typical
                                                                cesses in organs and tissues. The mathematical constructs
             pharmaceutical exposure, exposure to toxicants is often
                                                                therefore represent actual organs, tissues, and physiological
             uncontrolled and variable, and very large doses may be
                                                                processes.
             involved. Toxicants are also more likely to cause lesions
             and abnormal physiological function that may alter the
             toxicant disposition, compared to exposures to pharma-  UNDERLYING PHYSIOLOGY
             ceutical drugs below toxic levels. When very large doses
                                                                Absorption
             are involved, kinetic processes that can become saturated
             are more likely to reach their maximum rates, resulting in  Most hazardous substances must gain access to the systemic
             altered disposition.                               circulation to exert their toxic effects through interaction
                Predicting tissue concentrations over time is essen-  with one or more internal organs. Notable exceptions are
             tial for the prediction of adverse effects (Andersen  those compounds that cause a local reaction at the site
             et al., 2006). It is also needed to prevent unwanted  of exposure. Absorption is the process whereby toxic sub-
             xenobiotic residues in animal tissues from entering the  stances gain entrance to the body from the external
             Veterinary Toxicology. DOI: http://dx.doi.org/10.1016/B978-0-12-811410-0.00008-8
             Copyright © 2018 Elsevier Inc. All rights reserved.                                            133
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