Basal Ganglia Flashcards

1
Q

Basal Ganglia components

A

striatum
globus pallidus
subthalamic nuclei
substantia nigra

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2
Q

Primary function of basal ganglia

A

Planning and programming of movement

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3
Q

Main neurotransmitter

A

GABA

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4
Q

NT b/w striatum and substantia nigra

A

Dopamine

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5
Q

(-) the INHIBITORY INDIRECT pathway

A

D2 receptors

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6
Q

(+) the EXCITATORY DIRECT pathway

A

D1 receptors

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7
Q

Releases GLUTAMATE –> excites globus pallidus, internal segment

A

Subthalamic nucleus

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8
Q

Releases GABA –> (-) thalamus

A

Substantia Nigra Pars Reticulata

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9
Q

Releases Dopamine –> (-) striatum

A

Substantia Nigra Pars Compacta

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10
Q

Releases Ach –> (-) Substantia Nigra Pars Reticulata

A

Striatum

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11
Q

Releases GABA –> (-) subthalamic nucleus

A

Globus Pallidus External Segment

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12
Q

Lesion in the Globus pallidus

A

Inability to maintain posture

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13
Q

Lesion in the Subthalamic Nucleus

A

Wild, flailing movements

hemiballismus

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14
Q

Lesion in the Striatum

A

Quick, continuous, uncontrollable movements (i.e. Huntington disease)

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15
Q

Lesion in the Substantia Nigra

A

Tremors, cogwheel Rigidity, reduced voluntary movements (Akinesia), Postural problems (TRAP) - Parkinson’s Disease

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16
Q

Generates movement plan

A

Pre-Motor Cortex and Supplementary Motor Cortex (BA 6)

17
Q

Executes movement

Epileptic event here causes JACKSONIAN SEIZURES (focal partial seizure)

A

Primary Motor Cortex (BA 4)

18
Q

Caused by functional hemisection of the spinal cord

(+) contralateral loss of pain and temperature sensation beginning 1-2 segments below the lesion

(+) ipsilateral weakness and spasticity in certain muscles groups

A

Brown-Sequard Syndrome

19
Q

(+) degeneration and loss of motor neurons in the motor cortex, spinal cord, brain stem and corticospinal tract

does NOT usually affect sensation

may present with UMN or LMN

A

Amyotrophic Lateral Sclerosis (ALS)

20
Q

Have negative nitrogen balance as they catabolize large amounts of body protein because they are paralyzed below the level of transection

A

Patients w/ Transected Spinal Cords

21
Q

Include Fragile X, Spinocerebellar ataxia type 3, Huntington Disease, Friedreich Ataxia

A

Trinucleotide Repeat Diseases