Book contents
- Frontmatter
- Contents
- List of contributors
- Preface
- Part I Physiology and pathophysiology of nerve fibres
- Part II Pain
- Part III Control of central nervous system output
- 18 Synaptic transduction in neocortical neurones
- 19 Cortical circuits, synchronization and seizures
- 20 Physiologically induced changes of brain temperature and their effect on extracellular field potentials
- 21 Fusimotor control of the respiratory muscles
- 22 Cerebral accompaniments and functional significance of the long-latency stretch reflexes in human forearm muscles
- 23 The cerebellum and proprioceptive control of movement
- 24 Roles of the lateral nodulus and uvula of the cerebellum in cardiovascular control
- 25 Central actions of curare and gallamine: implications for reticular reflex myoclonus?
- 26 Pathophysiology of upper motoneurone disorders
- 27 Modulation of hypoglossal motoneurones by thyrotropin-releasing hormone and serotonin
- 28 Serotonin and central respiratory disorders in the newborn
- 29 Are medullary respiratory neurones multipurpose neurones?
- 30 Reflex control of expiratory motor output in dogs
- 31 Abnormal thoraco-abdominal movements in patients with chronic lung disease
- 32 Respiratory rhythms and apnoeas in the newborn
- 33 Cardiorespiratory interactions during apnoea
- 34 Impairment of respiratory control in neurological disease
- 35 The respiratory muscles in neurological disease
- Part IV Development, survival, regeneration and death
- Index
20 - Physiologically induced changes of brain temperature and their effect on extracellular field potentials
from Part III - Control of central nervous system output
Published online by Cambridge University Press: 04 August 2010
- Frontmatter
- Contents
- List of contributors
- Preface
- Part I Physiology and pathophysiology of nerve fibres
- Part II Pain
- Part III Control of central nervous system output
- 18 Synaptic transduction in neocortical neurones
- 19 Cortical circuits, synchronization and seizures
- 20 Physiologically induced changes of brain temperature and their effect on extracellular field potentials
- 21 Fusimotor control of the respiratory muscles
- 22 Cerebral accompaniments and functional significance of the long-latency stretch reflexes in human forearm muscles
- 23 The cerebellum and proprioceptive control of movement
- 24 Roles of the lateral nodulus and uvula of the cerebellum in cardiovascular control
- 25 Central actions of curare and gallamine: implications for reticular reflex myoclonus?
- 26 Pathophysiology of upper motoneurone disorders
- 27 Modulation of hypoglossal motoneurones by thyrotropin-releasing hormone and serotonin
- 28 Serotonin and central respiratory disorders in the newborn
- 29 Are medullary respiratory neurones multipurpose neurones?
- 30 Reflex control of expiratory motor output in dogs
- 31 Abnormal thoraco-abdominal movements in patients with chronic lung disease
- 32 Respiratory rhythms and apnoeas in the newborn
- 33 Cardiorespiratory interactions during apnoea
- 34 Impairment of respiratory control in neurological disease
- 35 The respiratory muscles in neurological disease
- Part IV Development, survival, regeneration and death
- Index
Summary
Temperature is an important factor for nervous activity. In physiological conditions we expect the temperature-regulating mechanisms of the homeothermic animal to prevent large temperature changes. However, in addition to the well-documented changes in brain temperature during feeding and sleeping (Abrams & Hammel, 1964), we have recently observed other, surprisingly large variations of brain temperature in behaving rats (Moser, Mathiesen & Andersen, 1993). There are also indications that brain temperature may change appreciably in man, both during exercise and after cooling of the facial skin (Nielsen, 1988). Furthermore, drugs and anaesthesia may cause the temperature of the brain to drop appreciably.
In the present short survey, we review the temperature changes that can be recorded from the brain of freely moving rats and the consequences such changes have on field and unitary potentials.
Field potentials and brain temperature in freely moving rats
In rats swimming in a Morris water maze (Morris, 1984) at 18°C (Moser et al., 1993), we noticed quite large and fast changes of simultaneously recorded hippocampal field potentials (Fig. 20.1 A, B). There was an increased latency of both the field excitatory postsynaptic potential (f-EPSP) and the population spike. Surprisingly, the latter increased greatly in amplitude. The slope of the f-EPSP, measured at its maximum, was reduced. All field potential changes depended on the temperature of the water, but were still quite large at the usually employed temperature of 25°C.
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- The Neurobiology of DiseaseContributions from Neuroscience to Clinical Neurology, pp. 221 - 230Publisher: Cambridge University PressPrint publication year: 1996