pathophysiology of the cerebellum

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PATHOPHYSIOLOGY OF THE CEREBELLUM. Department of Pathophysiology Faculty of Medicine in Pilsen Charles University. STRUCTURE OF THE CEREBELLUM. B. Cortex - stratum moleculare (A) - stratum gangliosum (B) - stratum granulosum (C) White matter Cerebellar nuclei - nc. dentatus - PowerPoint PPT Presentation

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PATHOPHYSIOLOGY OF THE CEREBELLUM

PATHOPHYSIOLOGY OF THE CEREBELLUM

Department of PathophysiologyFaculty of Medicine in Pilsen

Charles University

Department of PathophysiologyFaculty of Medicine in Pilsen

Charles University

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STRUCTURE OF STRUCTURE OF THE THE CEREBELLUMCEREBELLUM

• Cortex - stratum moleculare (A)- stratum gangliosum (B)- stratum granulosum (C)

• White matter

• Cerebellar nuclei - nc. dentatus- nc. emboliformis- nc. globosus- nc. fastigii

AA

BB

CC

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excitatory synapse inhibitory synapse

climbing fibre

mossy fibre

stratum moleculare

stratum gangliosum

stratum granulosum

cerebellarnuclei

white matter

stellatecell

basketcell

Purkinjecell

granulecells

efferent cerebellarpathways

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FUNCTION OF THE CEREBELLUMFUNCTION OF THE CEREBELLUM

1. Archicerebelum (vestibulocerebellum): - equilibrium maintenance, head and eye movement coordination

2. Paleocerebelum (spinocerebellum):- muscle tone regulation

3. Neocerebelum (corticocerebellum):- movement coordination

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CAUSATIONS OF CEREBELLAR CAUSATIONS OF CEREBELLAR DISORDERSDISORDERS

• inborn developmental defects – often accompanied with affections of the brain-stem

• trauma• intoxications - acute or chronic ethanol intoxication• vascular causations – ischemia, hemorrhagia• cerebellar tumours• sclerosis multiplex• inflammations – cerebelitis• hereditary spinocerebelar degenerations

A) autosomal recessive: - Friedreich‘s ataxia- ataxia treleangiectatica- abetalopoproteinemia- ataxia with isolated vitamin-E deficiency

B) autosomal dominant: - spinocerebelar ataxia SCA1 – SCA 7- episodic ataxia type 1 and 2 (EA-1, EA-

2)

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MANIFESTATIONS OF CEREBELLAR MANIFESTATIONS OF CEREBELLAR DISORDERSDISORDERS

– EXTINCTION SYNDROME– EXTINCTION SYNDROMECerebellar ataxia:Cerebellar ataxia:

• posture disorders – titubations, falls (especially rearwards – posture disorders – titubations, falls (especially rearwards – independent on head position), posture with wide basisindependent on head position), posture with wide basis

• ambulation disorders – wobble, retropulsions and propulsionsambulation disorders – wobble, retropulsions and propulsions

• hypermetriahypermetria

• movement coordination disordersmovement coordination disorders

• adiadochokinesisadiadochokinesis

• speaking disorders – because of adiadochokinesis of orofacial speaking disorders – because of adiadochokinesis of orofacial musclesmuscles

Tremor Tremor –– intention (during goal-directed movement intention (during goal-directed movementss))

Disorders of muscular toneDisorders of muscular tone – – hypertonia of trunk extensors and hypertonia of trunk extensors and hypotonia of limb muscleshypotonia of limb muscles

Defects of cognitive functionsDefects of cognitive functions

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MANIFESTATIONS OF CEREBELLAR MANIFESTATIONS OF CEREBELLAR DISORDERSDISORDERS

– IRRITATION SYNDROME– IRRITATION SYNDROME

Opposite to the extinction syndrome, similar to Opposite to the extinction syndrome, similar to parkinsonismparkinsonism

• increased plastic tone of flexorsincreased plastic tone of flexors

• flexion holding of the trunk and limbsflexion holding of the trunk and limbs

• static tremorstatic tremor

• hypokinesis or akinesishypokinesis or akinesis

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Animal model of cerebellar Animal model of cerebellar disorder: Lurcher mutant micedisorder: Lurcher mutant mice

Animal model of cerebellar Animal model of cerebellar disorder: Lurcher mutant micedisorder: Lurcher mutant mice

Heterozygots (+/Lc) – Lurcher mutants:

• complete loss of cerebellar Purkinje cells within 3 months of postnatal life - excitotoxic apoptosis

• secondary decrease of number of cerebellar granule cells and inferior olivary neurons

• cerebellar ataxia, deterioration of cognitive functions, higher CNS excitability, higher sensitivity to neurotoxic agents

Unaffected homozygos (+/+) - wild type: completely healthy

Affected homozygots (Lc/Lc): not viable

- a natural model of olivocerebellar degeneration, a mutation of the 2-glutamate receptor gene- used for investigation of consequences of the neurodegeneration and of therapeutic methods

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Cerebellum of Lurcher mutant miceCerebellum of Lurcher mutant mice

Nissl staining +/+Nissl staining +/+ Nissl staining +/LcNissl staining +/Lc

anticalbindin +/+ (P21)anticalbindin +/+ (P21) anticalbindin +/Lc (P21)anticalbindin +/Lc (P21)

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Apoptosis of Purkinje cells in Lurcher mutant miceApoptosis of Purkinje cells in Lurcher mutant mice

Fluorescent doublestaining: Lucifer Yellow, DiD oil (Kröger a Wagner, 1998)

1 3

2 4

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excitatory synapse inhibitory synapse

climbing fibre

mossy fibre

stratum moleculare

stratum gangliosum

stratum granulosum

cerebellarnuclei

white matter

stellatecell

basketcell

Purkinjecell

granulecells

efferent cerebellarpathways

12

excitatory synapse inhibitory synapse

climbing fibre

mossy fibre

stratum moleculare

stratum gangliosum

stratum granulosum

cerebellarnuclei

white matter

stellatecell

basketcell

Purkinjecell

granulecells

efferent cerebellarpathways

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MOTOR COORDINATION TESTSMOTOR COORDINATION TESTS

Fall – ability to land on all four limbs

Horizontal bar – ability to hold on a horizontal wire

Ladder – ability to hold on a slanting ladder

Bridge – ability to hold on a narrow horizontal bridge

Rotarod – ability to hold on a rotating cylinder

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Mouse model of cerebellar ataxiaMouse model of cerebellar ataxia

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• The mouse is hang with its frontal limbs on a horizontal wire.

• Criterion of the success trial: to stay on the bar for 60 s, or to leave the apparatus actively

HORIZONTAL BARHORIZONTAL BAR

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HORIZONTAL BARHORIZONTAL BAR

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LADDERLADDER

• The mouse is placed into the middle of a slanting ladder (head up position).

• Criterion of the success trial: to stay on the ladder for 60 s, or to leave the apparatus actively

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LADDERLADDER

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BRIDGEBRIDGE

• The mouse is placed transversally into the middle of a narrow horizontal bridge.

• Criterion of the success trial: to stay on the bar for 120 s, or to leave the apparatus actively

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BRIDGEBRIDGE

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• The mouse is placed on a rotating cylinder (head in the direction of rotation).

• Criterion of the success trial: to stay on the bar for 60 s, or to leave the apparatus actively

ROTARODROTAROD

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ROTARODROTAROD

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EVALUATION OF MOTOR EVALUATION OF MOTOR COORDINATION TESTSCOORDINATION TESTS

0

10

20

30

40

50

60

70

80

90

100

hrazda žebřík rotarod

% WT Lc

Mean success rate in motor coordination tests in wild type (WT) and Lurcher mutant mice (Lc) - in % of trials

bar ladder rotarod

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THE ENDTHE END

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