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  • Brain.  (1)
  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Brain. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (216 pages)
    Edition: 1st ed.
    ISBN: 9781483287768
    Series Statement: Pergamon Studies in Neuroscience Series
    Language: English
    Note: Front Cover -- Interleukin-1 in the Brain -- Copyright Page -- Table of Contents -- Foreword -- Chapter 1. Location of interleukin-1 in the nervous system -- 1.1. IL-1 in the peripheral nervous system -- 1.2. IL-1 and the hypothalamo-pituitary-adrenocortical axis -- 1.3. IL-1 in the central nervous system -- 1.4. Summary -- Acknowledgements -- References -- Chapter 2. Brain interleukin-1 receptors: mapping, characterization and modulation -- 2.1. Anatomical mapping of IL-1α receptors -- 2.2. Cellular localization of IL-1 receptors -- 2.3. Characterization of IL-1 receptors in the brain -- 2.4. Effect of LPS injection in mice genetically responsive and unresponsive to LPS -- 2.5. Conclusion -- Acknowledgements -- References -- Chapter 3. lnterleukin-1β activation of the central nervous system -- Introduction -- 3.1. Bidirectional network between the nervous and immune systems -- 3.2. Importance of cytokine-induced glucocorticoid secretion -- 3.3. IL-1 activation of the hypothalamic-pituitary-adrenal (HPA) axis -- 3.4. CNS mechanism for IL-1 activation of the HPA axis -- 3.5. Other CNS effects of IL-1 -- 3.6. Future directions -- 3.7. Summary -- Acknowledgements -- References -- Chapter 4. Electrophysiological studies of the effects of interleukin-1 and α-interferon on the EEG and pituitary-adrenocortical activity -- 4.1. Introductory statement -- 4.2. Interleukin-1 -- 4.3. α-Interferon -- 4.4. Concluding Comments -- Acknowledgements -- References -- Chapter 5. The immune-hypothalamo-pituitary adrenal axis: Its role in immunoregulation and tolerance to self-antigens -- 5.1. Introduction -- 5.2. Plasma adrenocorticotropin and corticosterone responses to NDV and bacterial endotoxin -- 5.3. Origin or ACTH after NDV or LPS administration -- 5.4. Involvement of macrophages in LPS-induced ACTH and CORT responses -- 5.5. Involvement of cytokines?. , 5.6. Site of action -- 5.7. Mechanism of action -- 5.8. Functional significance -- 5.9. Self-tolerance to auto-antigens -- 5.10. Conclusions -- Acknowledgements -- References -- Chapter 6. The pyrogenic action of cytokines -- 6.1. Introduction -- 6.2. Fever -- 6.3. The neuromodulation of fever -- 6.4. Putative mediators of fever -- 6.5. Cytokine signal transduction from blood to brain -- 6.6. Conclusions -- 6.7. Summary -- Acknowledgments -- References -- Chapter 7. Metabolic responses to interleukin-1 -- 7.1. Introduction -- 7.2. Central control of thermogenesis -- 7.3. Afferent signals mediating thermogenesis -- 7.4. Evidence for central action of cytokines in thermogenesis -- 7.5. Mechanisms of action of IL-1 -- 7.6. Endogenous inhibitors of IL-1 action -- 7.7. Impaired responses to IL-1 -- 7.8. Summary and implications -- Acknowledgements -- References -- Chapter 8. Behavioural effects of cytokines -- 8.1. Cytokines induce sickness behaviour -- 8.2. Acute versus chronic effects of cytokines -- 8.3. Role of prostaglandins and CRF in behavioural effects of cytokines -- 8.4. Central versus peripheral targets in behavioural effects of cytokines -- 8.5. Processes opposing behavioural effects of cytokines -- 8.6. Conclusions -- Acknowledgements -- References -- Chapter 9. lnterleukin-1 involvement in the regulation of sleep -- 9.1. Introduction -- 9.2. Sleep -- 9.3. IL-1 and sleep -- 9.4. Inhibition of IL-1 effects by a specific IL-1β receptor antagonist -- 9.5. IL-1 fragments and biological activity -- 9.6. Additional evidence implicating IL-1 in sleep regulation -- 9.7. Perturbations to homeostasis: sleep deprivation and IL-1 -- 9.8. Interactions of sleep with regulatory mechanisms for IL-1 -- 9.9. Role of CRF in IL-1-induced responses and in sleep-wake regulation -- 9.10. Interactions of IL-1 and αMSH in sleep-wake regulation -- 9.11. Conclusions. , References -- Chapter 10. Regulation of the synthesis of nerve growth factor (NGF) by interleukin-1 (IL-1): facts and questions -- 10.1. Introduction to the physiology and pathophysiology of NGF and related neurotrophic molecules -- 10.2. Macrophage-derived IL-1 upregulates NGF mRNA after lesion of a peripheral nerve -- 10.3. Possible role of IL-1 for the physiological regulation of NGF mRNA levels in the central nervous system -- 10.4. A second endogenous source of IL-1 might play a role during the first phase of NGF mRNA induction after peripheral nerve lesion -- 10.5. Conclusions -- Acknowledgements -- References -- Chapter 11. Cytokines and neuronal degeneration -- 11.1. Introduction -- 11.2. Neurodegenerative disorders and cytokine abnormalities within the nervous system -- 11.3. Neurodegenerative disorders and cytokine abnormalities in the peripheral immune system: the model of cerebellar mutant mice -- References -- INDEX.
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  • 2
    ISSN: 1432-2013
    Keywords: Rats ; Diet ; Thermogenesis ; Noradrenaline ; Blood flow ; Brown adipose tissue
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 1. The influence of noradrenaline on regional blood flow was determined using radioactive microspheres in rats maintained on either stock diet or a palatable cafeteria diet. 2. Cardiac output and blood flow to brain, lungs, liver and skeletal muscle were similar for rats on the two diets. 3. Blood flow to total dissectable brown adipose tissue in control and cafeteria rats represented 1 and 2% of cardiac output respectively but these values rose to 7 and 15.5% during infusion of noradrenaline. 4. Arterial oxygen content was similar for all groups but the oxygen content of venous blood draining the interscapular brown adipose tissue fell to 6 ml O2/100 ml blood in control rats and 1 ml/100 ml in cafeteria rats after noradrenaline. 5. The total oxygen consumption of brown adipose tissue was calculated and found to account for 42% of the response to noradrenaline in control rats and 74% in cafeteria animals. The increments in the oxygen consumption of other tissues were almost identical in both groups and so all the diet-induced changes in thermogenic capacity can be attributed to increases in brown adipose tissue metabolism. 6. These findings demonstrate the quantitative importance of brown adipose tissue in diet-induced thermogenesis and confirm the similarities between diet and non-shivering thermogenesis.
    Type of Medium: Electronic Resource
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