Neurophysiology
Outline
Basal Ganglia:
I. terms: (Kingsley p. 286-287)

 1. Corpus Striatum: putamen, globus pallidus, & caudate nuclei

 2. basil ganglia: this term has been used to describe this area of the brain.
  A.  components:
    a. caudate nucleus
    b. putamen
    c. globus pallidus (paleostriatum or pallidum)
    d. nucleus accumbens (frequently considered part of the limbic system)
    e. substantia nigra (frequently not included as basal ganglia)
    f. subthalamic nuclei: (frequently not included as basal ganglia)
    g. claustrum (usually included but not by Kingsley)
    h. some put the amygdala in this group

 3. lentiform nucleus: putamen & globus pallidus
  A. grouping these structures is probably not appropriate.  P 249 Kiernan

 4. external capsule: white matter lateral to the lentiform nucleus

 5. claustrum: gray matter immediately lateral to the putamen

 6. extreme capsule: white matter that separates the claustrum from the insula

 7. internal capsule: runs between the caudate nucleus & putamen
 

II. neostriatum (striatum): includes the caudate, putamen, and nucleus
     accumbens (NA)

 1. this is the newest part of the basal ganglia (from telencephalon)

 2. Caudate nucleus: p. 249-250
   A. parts include the head & tail (tale terminates at the amygdala)

 3.  the most ventral striatum is called the nucleus accumbens (NA)

 4. afferents to the striatum
  A. cerebral cortex (corticostriate fibers)
  B. thalamus: (thalamostriate) fibers originate in intralaminar nuclei
  C. substantia nigra (nigrostriate) from the pars compacta (midbrain)
  D. amygdala: fiber from here synapse in the NA & caudate (via stria
       terminalis)

 5. efferents from the striatum (cells release GABA primarily)
  A. globus pallidus (striopallidal fibers)
  B. substantia nigra (strionigral fibers) axons end in both parts of the
       substantia Nigra (pars compacta & pars reticulata)
 

III. pallidum (paleostriatum): is the globus pallidus

 1. situated between the putamen & the internal capsule

 2. it can be divided into 2 divisions
   A. lateral (GPl)
   B. medial (GPm)
     a. functionally identical to substantia nigra pars reticulata

 3. afferents to the globus pallidus
  A. striatum
  B. substantia nigra
  C. subthalamic nucleus

 4. efferents from the globus pallidus (cells release GABA primarily)
  A. thalamus
  B. habenular nuclei: part of the diencephalon (posterior thalamus)
  C. pallidofugal fibers also project to the superior colliculus (midbrain)
  D. brainstem reticular formation (p. 183 lower)
  E. subthalamic nucleus
 

IV. substantia nigra (SN): just dorsal to BP

1. two parts are described in our text
  A. pars compacta:
    a. neurons here produce lots of dopamine
    b. efferent axons travel to the
      ?striatum (forebrain) via the nigrostriatal pathway
      ?amygala
      ?prefrontal cortex

  B. pars reticulata: this is probably a detached segment of the globus
       pallidus
    a. neurons probably make & release GABA
    b. efferent axons project to the
      ?thalamus
      ?S. colliculus
 

V. Pyramdal & extrapyramidal systems
  1. Pyramidal system: an old fashioned term referring to the corticospinal &
      corticobulbar tracts

  2. extrapyramidal system: movement areas outside the pyramidal system
    A. including the reticulospinal, vestibulospinal, & basal ganglia
 
 

Dyskinesia & Disease of the Basal Ganglia:

I. Dyskinesia involves a loss of voluntary control of movements with no
    paralysis, paresis, or apraxia.

II. there are two categories of dyskinesia
 1. hyperkinesia: unplanned spontaneous movements
   A. choreiform movements: brisk jerky movements involving several muscle
         groups.

   B. athetosis: slow writhing movements usually of the hands, face, or tongue
      a. side effect of antipsychotic medications (extrapyramidal side effects)
      b. seen in tardive dyskinesia

   C. dystonic movements: prolonged contractions of the neck, trunk, or limbs
        that lead to abnormal postures & twisting
      a. idiopathic torsion dystonia:
      b. spasmodic torticollis:

   D. myoclonus: sudden spasms of the muscle usually lifting & flailing the
        arms
      a. seen in degenerating brain diseases e.g., spongiform encephalopathies
      b. nocturnal myoclonus:
      c. ballism: irregular flinging movements of the limbs

   E. tics: stereotyped (repetitive) involuntary movements (often are twitches)
      a. seen in Gilles de al Tourette syndrome

   F. tremor: rhythmical alternating movements that can effect any part of the
         body

   G. akathisia: restless agitation (can’t sit still)

 
 2. hypokinetic dyskinesia:
  A. bradykinesia: a poverty or slowness of movements
 
 

III. diseases effecting the basal ganglia:

 1.  Parkinson's disease due primarily to degeneration of dopamine neurons
     in the substantia nigra pars compacta
  A. a loss of pigmented cells in other brain areas may occur (e.g. locus
       Ceruleus & dorsal motor nucleus of the vagus)

  B. This disease results in
    a. bradykinesia:

  C. This cause of abnormal dopamine cell loss in the substantia nigra is still a
       mystery
    a. toxins, faulty metabolism, or infections have been implicated
     ->encephalitis lethargica:

  D. treatment usually involves some sort of DA agonist
    a. L-dopa is used to treat Parkinson's
    b. deprenyl (MAO inhibitor) looks promising.

  E. surgical procedure are also used for treatment
    a. brain lesions: destroying part of the globus pallidus
 

 2. Huntington’s disease
  A. a genetic disorder with symptoms appearing in mid life

  B. it alters the brain in the following ways
    a. degeneration of the caudate N and putamen mostly
    b. some cells in the cortex also die

  C. This produces uncontrollable movements (choreiform)
     a. early in the disease process they may seem restless or fidgety
     b. eventually patients are in constant motion & finally athetosis or dystonia

  D. progressive mental deterioration also occurs

  E. changes in personality often occur
 

3. cerebral palsy: effects this area of the brain
  A. movement disorder due to brain injury occurring near or during birth
 
4. Wilson’s disease:
  A. caused by a genetic error in copper metabolism
  B. symptoms occur between ages 10 & 25 & include the following

5. tardive dyskinesia: permanent brain damage due to antipsychotic meds.

6. abulia: a loss of will power & initiative
  A. seen in people with caudate nucleus lesions

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