Tissue Distribution
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Distribution or translocation of the toxicant follows via the bloodstream to reactive sites, including storage depots.
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The selective deposition of foreign chemicals in various tissues depends on receptor sites.
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The ease of chemical distribution depends largely on its water solubility.
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Polar- or aqueous-soluble agents tend to be excreted by kidneys; lipid-soluble chemicals are more likely to be excreted via bile and get accumulated in fat depots.
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Knowledge of the translocation characteristics of poisons is necessary for proper selection of organs for analysis.
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Highest concentration of a poison is not necessarily found in the organ in which it exerts its greatest effect.
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Substances absorbed from the gut may be transported either in association with plasma proteins or circulatory erythrocytes.
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Following their absorption, toxic substances will first reach the liver via hepatic portal system.
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Hence, hepatic damage is frequently observed. However, substances that are entering after pulmonary and subcutaneous exposure may also cause hepatic damage.
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Some toxic agents are selectively deposited in certain tissues and organs like
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iodine in thyroid
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lead, fluorine and strontium in skeletal tissue
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arsenic in hair and nails
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halogenated hydrocarbons in adipose tissue
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primaquine in liver
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mercurials, aminoglycosides, certain antifungal drugs in kidneys
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paraquat in lungs
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This affinity for the toxic agent does not necessarily result in the development of pathological lesions in these tissues.
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However, they are of importance while conducting toxicological analysis.
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The concentration of a xenobiotic in the tissues/organs is directly proportional to the free xenobiotic concentration in plasma, which further depends on its binding to plasma proteins.
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Protein bound xenobiotic will serve as a depot since bound toxicant cannot cross the capillary wall. This also serves to lower the intensity of toxic effects.
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Last modified: Tuesday, 27 December 2011, 12:58 AM