S1: topography of the nervous system Flashcards

1
Q

Describe grey matter

A

Composed of cell bodies and dendrites
Highly vascular
Contains axons (far less prevalent than white matter) allowing it to communicate with white matter
PNS equivalent of grey matter = ganglion

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2
Q

Describe white matter

A

Composed of axons with their supporting cells
White due to presence of myelin
PNS equivalent of white matter = peripheral nerve

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3
Q

Define nucleus (grey matter)

A

Collection of functionally related cell bodies

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4
Q

Define cortex (grey matter)

A

Folded sheet of cell bodies found on the surface of a brain structure

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5
Q

Define fibre (white matter)

A

An axon in association with its supporting cells

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6
Q

Define the three types of fibres

A

Association fibres = connect cortical regions within the same hemisphere
Commissural fibres = connect left and right hemispheres
Projection fibres = connect the cerebral hemispheres with the cord/brainstem and vice versa

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7
Q

Describe the segments of the spinal cord

A

31 segments, each supplying a given dermatome and myotome on each side
Cord has a central core of grey matter and outer shell of white matter
Segment connects with spinal nerve through dorsal and ventral roots

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8
Q

Define funiculus

A

A segment of white matter containing multiple distinct tracts
Impulses travel in multiple directions

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9
Q

Define tract

A

Anatomically and functionally defined white matter pathway connecting two distinct regions of grey matter
Impulses travel in one direction

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10
Q

Define fasciculus

A

Subdivision of a tract supplying a distinct region of the body

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11
Q

Outline the 3 main parts of the brainstem

A

Midbrain (mesencephalon): eye movements and reflex responses to sound and vision
Pons: feeding and sleep
Medulla: cardiovascular and respiratory centres, contains a major motor pathway (medullary pyramids)

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12
Q

List the important gyri and sulci

A

Central sulcus: separates frontal and parietal lobes
Precentral gyrus: contains primary motor cortex
Postcentral gyrus: contains primary sensory cortex
Lateral/sylvian fissure: separates temporal from frontal/parietal lobes
Parieto-occipital sulcus: separates parietal from occipital lobe
Calcarine sulcus: primary visual cortex surrounds this

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13
Q

Outline key features on the inferior aspect of the brain

A

Optic chiasm: a site where fibres in the visual system cross over
Uncus: medial part of temporal lobe that can herniate, compressing the midbrain
Medullary pyramids: location of descending motor fibres
Parahippocampal gyrus: key cortical region for memory encoding

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14
Q

Outline key features of the brain in the midline

A

Corpus callosum: fibres connecting the two cerebral hemispheres
Thalamus: sensory relay station projecting to sensory cortex
Cingulate gyrus: cortical area important for emotion and memory
Hypothalamus: essential centre for homeostasis
Fornix: major output pathway from the hippocampus
Tectum: dorsal part of the midbrain involved in involuntary responses to auditory and visual stimuli
Cerebellar tonsil: part of the cerebellum that can herniate and compress the medulla

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15
Q

Describe the function of the ventricles

A

Cavities filled with CSF
Each contain the choroid plexus, which is highly vascular and makes a total of 600-700ml of CSF per day (most made in the lateral ventricles)

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16
Q

Describe the function of the CSF

A

Both metabolic and mechanical functions

  • contains glucose (& maybe hormones)
  • shock absorbs the brain and renders it effectively weightless
17
Q

Describe the flow of CSF through the brain ventricles

A

From the lateral ventricles, the CSF circulates through the interventricular foramen into the third ventricle
CSF drains from the third ventricle to the fourth ventricle via the cerebral aqueduct
In the fourth ventricle, the CSF can drain through the lateral and median apertures (direct holes of the brain, which permits the CSF to drain into the subarachnoid space; negligible drainage via the spinal cord central canal)
CSF is reabsorbed at the arachnoid granulations

18
Q

What happens if there is blockage of the ventricular system?

A

Leads to upstream dilatation and potential damage to structures surrounding the dilated ventricles
Cerebral aqueduct is a common place for such occlusions
-would cause dilatation of the lateral and third ventricles but with a normal fourth ventricle (downstream)

19
Q

Describe the process of neurulation

A

Process of formation of the neural tube, induced by the notochord
Elevation of the neural folds
Fusion of the folds in the midline
When the folds fuse, the neural crest cells detach and migrate to their ultimate destinations
Neural tube zips up rostrally and caudally
-process fails in the rostral direction: anencephaly
-process fails in the caudal direction: spina bifida

20
Q

Outline the three major swellings on the rostral neural tube

A

Prosencephalon – becomes the forebrain
Mesencephalon – becomes the midbrain
Rhombencephalon – becomes the hindbrain

21
Q

What are the divisions of the prosencephalon?

A

Telencephalon – becomes most of the cerebral hemisphere

Diencephalon – becomes thalamus, hypothalamus and optic nerve/retina

22
Q

What are the divisions of the rhombencephalon?

A

Metencephalon – forms the pons and cerebellum

Myelencephalon – forms the medulla

23
Q

Describe the fundamental relationship between the sensory and motor systems

A

Motor structures tend to sit anteriorly, and sensory structures tend to sit posteriorly
This pattern exists due to the development of the basal and alar plates in the neural tube
1) Notochord induces the ventral (anterior) portion of the neural tube to become the basal plate – gives rise to motor neurones
2) Alar plate forms in the absence of influences – gives rise to inter- and sensory neurones

24
Q

Describe the development of the cauda equina

A

The spine grows faster than the spinal cord, particularly at the lumbar levels
Lower portions of the cord are stretched, drawing out the cauda equina

25
Q

Outline how neural tube defects can predispose to hydrocephalus

A

Tethering of the cord at the site of the defect
As the spine grows, the cord cannot move within the vertebral canal, resulting in the brainstem being pulled down through the foramen magnum and becoming occluded

26
Q

Describe the developmental basis of neural tube defects

A

Failure of the neural tube to ‘zip up’ in the cranial or caudal directions
Failure of closure in the cranial direction involves the brain eg. anencephaly
Failure of closure in the caudal direction involves the spine/spinal cord eg. classic spina bifida
All of these disorders have failure of development of the posterior vertebral arches at one or more levels (neural tube is partly responsible for inducing the migration of the sclerotome from somites to form the posterior bony arch)

27
Q

Describe craniorachischisis

A

Entire neural tube remains open
Failure of both brain and spinal cord to form
Incompatible with life

28
Q

Describe anencephaly

A

Cranial neural tube fails to close
Failure of brain to form
Children may be born alive but do not live for long

29
Q

Describe myelocoele

A

Spinal cord fails to develop
Usually associated with a CSF filled cyst
Children frequently have neurological deficits and are susceptible to meningitis due to presence of exposed neural tissue

30
Q

Describe myelomeningocoele

A

CSF-filled cysts containing the spinal cord
Transilluminates relatively poorly (due to prescence of solid tissue in the cyst)
Children may have neurological deficits & repair is necessary

31
Q

Describe meningocoele

A

Presence of CSF filled cyst
Cord is sited within the vertebral canal
Transilluminates brilliantly & children tend to have a good neurological prognosis
Cyst will need repair as it predisposes to infection

32
Q

Describe spina bifida occulta

A

Only anomaly is the lack of the posterior vertebral arch
May manifest as a tuft of hair or skin marking over the defect
Not associated with significant neurological problems
Occurs in about 10% of the population

33
Q

What should be taken to prevent neural tube defects?

A

Folic acid
400mg daily to be taken from around 3 months before conception until week 12 of pregnancy
Mechanism of action of folate in preventing neural tube defects is unknown

34
Q

What is the neural crest?

A

A highly specialised population of cells derived from the point at which the neural folds fuse when the surface ectoderm is reconstituted
Become detached from the ectoderm and then migrate to their distant targets

35
Q

Outline cells derived from the neural crest

A
Primary sensory neurones 
Autonomic postganglionic neurones 
Enteric neurones 
Schwann cells 
Cells of the adrenal medulla 
Melanocytes 
Leptomeninges 
Head mesenchyme
36
Q

Outline tissues receiving a significant contribution from the neural crest

A

Thymus
Thyroid
Parts of the heart (eg. spiral septum)
Parts of the teeth

37
Q

Describe Di George syndrome

A
Neural crest cell disorder 
Immunodeficiency (due to involvement of the thymus)
Facial anomalies 
Heart anomalies 
Hypocalcaemia
38
Q

Describe Hirschprung’s disease

A

Lack of enteric neurones in sections of the large intestine

This leads to hypomotility and constipation