Toxicology of the human environment : the critical role of free radicals /

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Bibliographic Details
Imprint:London ; New York : Taylor & Francis Limited, 2000.
Description:xvi, 494 p. : ill. ; 24 cm.
Language:English
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/4486610
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Other authors / contributors:Rhodes, Christopher J.
ISBN:0748409165 (alk. paper)
Notes:Includes bibliographical references and index.
Table of Contents:
  • List of contributors
  • List of abbreviations
  • 1. Introduction
  • Part I. Spin-trapping
  • 2. Chemistry of spin-trapping
  • 2.1. Introduction
  • 2.2. Types of spin-trap
  • 2.3. Selection criteria
  • 2.4. Structural assignment considerations
  • 2.5. Conclusions
  • 3. Spin-trapping: problems and artefacts
  • 3.1. Introduction
  • 3.2. The redox reactivity of spin-traps and reagents involved in the radical cation mechanism; inverted spin-trapping
  • 3.3. The Forrester--Hepburn mechanism; nucleophilic addition--oxidation
  • 3.4. Detection of spin adducts in biochemical/biological systems
  • 3.5. Cycloaddition as a possible cause of artefacts
  • 4. In vivo spin-trapping--from chemistry to toxicology
  • 5. Ex vivo detection of free radicals
  • 5.1. Background
  • 5.2. Ex vivo spin-trapping of short-lived free radicals
  • 5.3. Nitrogen monoxide (nitric oxide, NO[superscript .], NO)
  • 5.4. Conclusion
  • Part II. Nitroxides
  • 6. The metabolism of nitroxides in cells and tissues
  • 6.1. Introduction and overview
  • 6.2. Reduction of nitroxides in mammalian cells
  • 6.3. Cellular oxidation of hydroxylamines
  • 6.4. The toxicity of nitroxides
  • 6.5. Applications of the metabolism of nitroxides
  • 7. Clinical uses of nitroxides as superoxide-dismutase mimics
  • 7.1. Introduction
  • 7.2. Structural features and chemical properties of nitroxides
  • 7.3. In vitro and in vivo toxicity
  • 7.4. In vitro radioprotection by nitroxides
  • 7.5. In vivo radioprotection by nitroxides
  • 7.6. Protection against redox-cycling chemotherapy drugs
  • 7.7. Nitroxides as functional imaging probes
  • 7.8. Summary
  • 8. Nitroxide skin toxicity
  • Abstract
  • 8.1. Introduction
  • 8.2. Materials and methods
  • 8.3. Results
  • 8.4. Discussion
  • 8.5. Conclusion
  • Part III. Toxic role of specific agents
  • 9. Biological oxidations catalyzed by iron released from ferritin
  • 9.1. Introduction
  • 9.2. Iron-catalyzed oxidations
  • 9.3. Biological sources of catalytic iron
  • 9.4. Antioxidant defences for iron-mediated toxicity
  • 9.5. Conclusions
  • 10. The toxicology of iron
  • 10.1. Introduction
  • 10.2. Human conditions and diseases involving iron toxicity
  • 10.3. From oxygen via iron to the hydroxyl radical
  • 11. The role of free radicals in the toxicology of airborne particulate pollutants
  • 11.1. Introduction
  • 11.2. Silica toxicity
  • 11.3. Coal
  • 11.4. Asbestos
  • 11.5. Man-made mineral fibres
  • 11.6. Zeolites
  • 11.7. Smoke
  • 11.8. Traffic air pollution
  • 11.9. Nutritional and physiological antioxidants
  • 11.10. Pharmacological antioxidants
  • 11.11. Conclusion
  • 12. Free radical mechanisms of ethanol toxicity
  • 12.1. Introduction
  • 12.2. Mechanisms involved in causing oxidative damage by alcohol
  • 12.3. Free radical-mediated processes in organ damage by alcohol
  • 12.4. Role of free radical-mediated mechanisms in alcohol toxicity
  • 12.5. Conclusions
  • 13. The role of cytokines in the inflammatory response
  • 13.1. Introduction
  • 13.2. Activation of TNF-[alpha] by THP-1 exposed to H-MG
  • 13.3. Nitrosyl chloride in keratinocytes exposed to HD
  • 14. Duplicity of thiols and thiyl radicals: protector and foe
  • Abstract
  • 14.1. Introduction
  • 14.2. Background to the muon spectroscopy technique
  • 14.3. Experimental section
  • 14.4. Structural studies of thiyl radicals
  • 14.5. Reactivity of thiyl radicals
  • 14.6. Evidence for actual biological significance of thiyl radicals
  • 14.7. Conclusions
  • 15. Synergistic effect of carbon tetrachloride and 1,2-dibromoethane
  • 15.1. Introduction
  • 15.2. Carbon tetrachloride and 1,2-dibromoethane interactions
  • 15.3. Conclusions
  • 16. Reactive oxygen species in physiology and toxicology
  • Abstract
  • 16.1. Production of free radicals
  • 16.2. Biological sources of free radicals
  • 16.3. Toxicity of reactive oxygen species
  • 16.4. Oxidant stress and signaling
  • 16.5. Oxidative stress and inflammation
  • 16.6. Oxidative stress in apoptosis, necrosis and cell growth
  • 16.7. Oxidative stress and carcinogenesis
  • Part IV. Free radicals in specific disease states
  • 17. The role of free radicals in chemical carcinogenesis
  • Abstract
  • 17.1. Introduction
  • 17.2. Stimulation of the arachidonic acid cascade, oxygen radical generation, and chemical carcinogenesis
  • 17.3. Metabolism of polycyclic aromatic hydrocarbons, free radicals, and chemical carcinogenesis
  • 17.4. Metal-induced free radical generation and metal salt carcinogenesis
  • 17.5. Endogenous oxygen radical generation and carcinogenesis
  • 17.6. Conclusions
  • 18. Free radical involvement in cardiovascular and respiratory diseases
  • Abstract
  • 18.1. Heart disease
  • 18.2. Lung diseases
  • Part V. Free radicals in the diet
  • 19. NMR evaluation of thermally-induced peroxidation in culinary oils
  • 19.1. Introduction
  • 19.2. Materials and methods
  • 19.3. Results
  • 19.4. Discussion
  • Part VI. Chemical models
  • 20. The structure and electronic properties of oxy intermediates in the enzymatic cycle of cytochrome P450s
  • 20.1. Introduction
  • 20.2. Theoretical and technical aspects
  • 20.3. Results and discussion
  • 20.4. Conclusions
  • 21. Spin-trapping--applications to photochemical and photobiological problems
  • 21.1. Introduction
  • 21.2. Photochemistry of photosensitizers
  • 21.3. Free radical and EPR
  • 21.4. Spin-trapping in photochemical systems
  • 21.5. Spin-trapping of oxygen-centered radicals
  • 21.6. Spin-trapping of radicals from photosensitizing chemicals
  • 22. Thermodynamic considerations of free radical reactions
  • 22.1. Introduction
  • 22.2. Reduction
  • 22.3. Oxidation
  • 22.4. pH dependence of reduction potentials
  • 22.5. Measurement of reduction potentials
  • 22.6. Redox enzymes
  • 22.7. Drugs, oxygen and metals
  • 23. The use of QSAR for the prediction of free radical toxicity
  • 23.1. Introduction
  • 23.2. Identification of compounds likely to form free radicals
  • 23.3. Acute toxicity
  • 23.4. Skin sensitisation
  • 23.5. Teratogenicity
  • 23.6. Mutagenicity
  • 23.7. Conclusions
  • Index