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Neuroscience 14a - Introduction to Consciousness Anil Chopra 1. Define consciousness 2. Outline briefly the structure of the reticular formation 3. Explain how the reticular activating system modulates the activity of the cerebral cortex 4. Define the main EEG rhythms and state their functional significance 5. Define the main altered states of consciousness and the 3 observations upon which the Glasgow coma scale is based 6. Give examples of metabolic and non-metabolic causes of coma 7. Distinguish between brain death and persistent vegetative state Consciousness is defined as the level or arousal or state of awareness. There are different level’s of arousal: - Full awakefullness and responsiveness –normal arousal - Obtundation – drowsy and not fully responsive. - Stupor – appears to be asleep, little or no spontaneous activity however rousable when stimulated. - Coma – completely unresponsive and unrousable. Reticular formation This regulates many vital functions including the sleep/awake cycle. It is a polysynaptic network located in the pons, midbrain and upper medulla and is poorly differentiated. It consists of 3 parts: Lateral Reticular Formation Has small neurones Receives information from ascending tracts for touch and pain. Receives vestibular information from median vestibular nerve. Receives auditory information from superior olivary nucleus. Visual information from superior colliculus. Olfactory information via medial forebrain bundle. Paramedian Reticular Formation Has large cells. Receives signals from lateral reticular formation. Projects onto cerebral hemispheres. Nucleus coeruleus contains noradrenergic neurones and projects onto the cerebral cortex. Ventral tegmental nucleus contains dopaminergic neurones that project directly onto the cortex. Cholinergic neurones project onto the thalamus. Raphe nuclei (Median RF) In the midline of the reticular formation Contain serotonergic projections to the brain and spinal cord. Thalamus The thalamus is contained in the mid-part of the diencephalon and is split up into a number of different nuclei which perform 3 main tasks: o Cholinergic projections excite the individual thalamic relay nuclei which lead to activation of the cerebral cortex. o Cholinergic projections to the intralaminar nuclei, which in turn project to all areas of the cortex . o Cholinergic projections to reticular nuclei regulate flow of information through other thalamic nuclei to the cortex. Tuberomammillary nucleus in the hypothalamus projects to the cortex and is involved in maintaining the awake state. This collectively is known as the reticular activating system, which is triggered by sensory input – cholinergic projections to the thalamus which then stimulates the cerebral cortex. Nucleus Group Type Anterior Anterior Dorsal medial (DM) Centromedian (CM) Medial nuclear Diffuse projection Diffuse projection Intralaminar - Other IL nuclei Intralaminar Diffuse projection Ventral anterior (VA) Lateral nuclear Relay Ventral lateral (VL) Lateral nuclear Relay Ventral posterolateral (VPL) Lateral nuclear Relay Ventral posteromedial (VPM) Lateral nuclear Relay Lateral dorsal Lateral (LD) and Lateral nuclear posterior (LP) Input mammillary bodies, hippocampus olfactory cortex, amygdala globus pallidus (inhibitory) pontine and mesencephalic reticular formation Output Function cingulate gyrus memory formation hypothalamus, cingulate and orbitofrontal cortex emotional behavior modulation of basal ganglia diffuse projections to frontal thalamic portion of cortex and other thalamic ascending reticular nuclei activation system Primary, Pre and Basal Ganglia (GPi, motor relay. activation Supplementary motor SNr) facilitates movement cortex (areas 4 & 6) Primary, Pre and Basal Ganglia (GPi, motor relay. activation Supplementary motor SNr) & Cerebellum facilitates movement cortex (areas 4 & 6) cuneate, gracile nuclei, somatosensory relay for somatosensory cortex marginal zone and body, relays info from ALS (areas 1,2,3) substantia gelatinosa and DCML tracts somatosensory relay for spinal and principal somatosensory cortex face, relays sensory info nuclei of V, nucleus (areas 1,2,3), taste cortex (from trigeminothalamic solitarius (area 43) tract) and taste info caudate and putamen Diffuse projection sensory cortex, other thalamic nuclei frontal, parietal and cingulate cortex sensory and emotional info integration visual cortex (area 17), cuneate and lingual gyri via visual relay optic radiations LGN Lateral nuclear Relay retina (60% feedback from cortex) MGN Lateral nuclear Relay inferior colliculus (via auditory cortex (area 41), brachium of the inferior via auditory radiations colliculus) auditory relay Pulvinar Lateral nuclear Diffuse projection reciprocal input from all output areas, superior parietal and temporal colliculus, primary association areas visual cortex integration of sensory information, modulation of spatial attention (?) Diffuse projection thalamic nuclei (excitatory input), collateral projections from cortical feedback to thalamus) Reticular Reticular inhibitory output to thalamic nuclei from which input was received (only thalamic nucleus w/o projection to cortex & w/ inhibitory output) regulate flow of info from thalamus to cortex, part of ascending reticular activating system, modulation of arousal & sleep, generation of oscillations (?) Electroencephalogram – EEG This is a technique used to record the electrical activity of neurones in the brain. Electrodes are placed at a number of points on the heads of patients pick up both action potentials and graded potentials generated in the brain (particularly the superficial cortex). The patterns produced by the EEG consists of waves, each with different patterns that are normally recognisable. - Amplitude: indicates degree of electrical activity. Synchronous firing also results in an increased amplitude. - Frequency: how often they change from maximum to minimum amplitude. Lower frequencies are indicative of less active/responsive states. There are 4 distinctive frequency ranges: Alpha: relaxed awake with eyes open. (8-13Hz) Beta: awake and concentrating on something. (13-30Hz) Theta: early sleep / drowsiness. (4-8Hz) Delta: late stage sleep (0.5-4Hz) Altered States of Consciousness Alertness is measured on the Glasgow Coma Scale. Eyes open none in response to pain in response to speech spontaneous 1 2 3 4 Verbal responses none incomprehensible sounds inappropriate words disoriented speech oriented speech 1 2 3 4 5 Motor responses none extensor response to pain (decerebrate rigidity) flexor response to pain (decorticate rigidity) withdrawal to pain localisation of pain obeys commands 1 2 3 4 5 6 There are different altered states of consciousness: o Concussion or contusion - temporary loss of consciousness lasting for a few minutes. o Confusion – least, sustained disturbance of consciousness – mental processes are slowed. May be inattentive, disoriented, have difficulty carrying out simple commands or speaking. o Stupor – more profound, can only be roused by strong sensory stimuli o Coma – cannot be roused by even strong sensory stimuli. Different from sleep as metabolic activity of brain is depressed & there is total amnesia for period in coma. Causes of Coma - Metabolic alteration: hypoglycaemia, hypoxia, intoxication, overdosing on certain drugs such as sedatives, narcotics. Lesions in Cerebral Hemispheres: only cause coma if they are large and bilateral. Leads to a flat EEG. Lesion in thalamus or brainstem: can be due to a number of reasons e.g. raised intra-cranial pressure. EEG is a slow wave sleep. Persistent Vegetative State Patients who go into an irreversible coma can often enter persistent vegetative stage in which sleep-wake cycles are present even though the patient is unaware of their surroundings. Their brainstem is still able to function so reflexes and postural movements are still present. Individuals in a persistent vegetative state may smile, cry or react to elements of their environment but there is no evidence that they can comprehend their behaviours. Brain Death Brain death is the point at which the entire brain does not function and there is no possibility of it functioning again. The body may be kept alive artificially. This may be caused by disconnection of the cortex from the brainstem or widespread disease in the cerebral hemispheres. The EEG is not normally diagnostic although will be flat. Spinal reflexes may be present.