3. Smallest in size while largest part of the
hindbrain.
Its control is IPSILATERAL.
Homotypical
Important functions are to maintaining
tone, posture and equilibrium of the body
It is the in adults the weight ratio of
cerebellum to cerebrum is approximately
1 : 10 and in infants 1 : 20.
CEREBELLUM: latin SMALL BRAIN
4. Weight is approx 150 gm in an adult.
ie. About 10% of the weight of the cereberal
hemisphere
cerebellar cortex has about 50% of surface area
of the cerebral cortex
The cerebellum lies dorsal to the pons and medulla,
from which it is separated by the fourth ventricle.
It is seperated from the cerebrum by TENTORIUM
CEREBELLI.
17. ANTERIOR AND
POSTERIOR LOBE IS
MAINLY DEVIDED INTO 3
PARTS THESE ARE;
(a)LATERAL ZONE
(b)INTERMEDIATE ZONE
(c)VERMIS ZONE
Functional regions of cerebellum
20. The white matter consists of:
(a) Afferent fibres entering the cerebellum from
outside.
(b) Projection fibres from the cerebellar cortex
to the cerebellar nuclei.
(c) Association fibres interconnecting different
parts of the cerebellar cortex.
(d) Commissural fibres connecting the two
cerebellar hemispheres.
(e) Fibres from the cerebellar nuclei (and some
from the cerebellar cortex) to centres outside
the cerebellum.
22. 2. Basket Cells –(inhibitory, GABA)
contact Purkinje soma (“basket” around it)
Each basket cell may synapse with 70 purkinje
fibres.
inhibitory to purkinje cells.
location: inner molecular layer
23. 3.Purkinje (inhibitory – GABA)
characteristic cell of cerebellum
Flasked shaped cell bodies
Dendrites arise from neck
of the flask.
Axon moves downward
Through the granular layer
To enter the white matter.
Their end synapse with
Neurons in cerebellar nuclei.
INHIBITYORY in nature.
24. 4. Granule cell
Very small , numerous,
spherical neurons
Occupy the greater part of
granular layer.
Having 3-5 dendrites
Claw like endigs,
contacted by mossy fibres.
the only excitatory neuron.
The spaces not occupied
by these cells in the
granular layer are called
cerebellar islands
25. 5. Golgi Cells –(inhibitory, GABA).
contacts granule cell within “glomeruli”
(inhibitory) –
glial capsule and specificity of connections.
location: granule cell layer
26. Complex synapsis
structure
About 10 um in
diameter
Surrounded by
neuroglial cell
STRUCTURE OF GLOMERULI
These synapse are
axodendritic and
excitatory
27. Core is formed by expandaded
terminartion of mossy fibre
Termination is also called ROSETTE
Also receive synapse with granule and
golgi cell
28. Neurons in the Cerebellar Cortex Are
Organized into Three Layers
29.
30.
31. Histologically afferents fibres are of two
distinct types.
(a) Mossy fibres:
Excitatory fibre
These fibres terminate in the granular
layer of the cortex, within glomeruli.
They branch profusely within the granular
layer, each branch ending in an expanded
terminal called a rosette
All fibres entering the cerebellum,
afferent inputs; mossy fibres pass
through granule cells to reach Purkinje cells.
32. (b) Climbing fibres:
Excitatory fibre
olivo-cerebellar fibres end predominantly as
climbing fibres
terminations of axons reaching the cerebellum
from the inferior olivary complex
They pass through the granular layer, and the
Purkinje cell layer, to reach the
molecular layer.
climbing fibres as they appear to climb up
along the Purkinje cell dendrites
33. CONNECTIONS OF CEREBELLUM
Inferior cerebellar
peduncle-
also called the restiform body
connect posterolateral part of
the medulla with spinal cord,
contain both afferent and
efferent fibers,,
Peduncles: Three peduncles
34. Middle cerebellar peduncle -
connect with pons,
contain afferent fibers
Its fibres, which arise in pontine nuclei, cross to
the opposite side
Superior cerebellar peduncle -
•connect with midbrain,
•contain mostly efferent fibers
consists mainly of fibres arising in cerebellar nuclei
(mainly the dentate nucleus)
•The right and left peduncles are connected by a
thin lamina of white matter, the superior (or
anterior) medullary velum
40. The cerebellum receives direct afferents from the
spinal cord and from various centres in the
brainstem. The main afferents are
(1) Spinocerebellar. These terminate
predominantly in the paleocerebellum.
(2) Pontocerebellar. These are part of the cortico-
ponto-cerebellar pathway. They end
predominantly in the neocerebellum.
(3) Olivocerebellar. These end mainly in the
neocerebellum and partly in the paleocerebellum.
.
41. (5) Reticulocerebellar fibres from the reticular
formation of the pons and of the medulla.
The cerebellum also receives fibres from the
tectum, the arcuate nuclei, the accessory cuneate
nucleus, and from the sensory nuclei of the
trigeminal nerve.
(4) Vestibulocerebellar, from the vestibular nuclei,
and also direct fibres of the vestibular nerve
43. The main efferents of the cerebellum are :
(1) Cerebellorubral, to the red nucleus of the
opposite side.
(2) Cerebellothalamic, to the thalamus of the
opposite side.
(3) Cerebellovestibular, to the
vestibular nuclei.
(4) Cerebelloreticular, to the reticular
formation.
Some fibres from the cerebellum also
reach the inferior olivary nucleus, the
nucleus of the oculomotor nerve, and the
tectum.
45. Connections between Cerebellum
and Spinal Cord
Spinocerebellar pathways convey to the
cerebellum proprioceptive information necessary
for controlling muscle tone and for maintaining
body posture. These pathways also carry
exteroceptive impulses.
(a) Direct pathways from spinal cord to
cerebellum
ventral spinocerebellar tract, and the dorsal
spinocerebellar.
Rostral spinocerebellar tract and the
cuneocerebellar tract .
46. (b) Indirect pathways from spinal cord to
cerebellum
• Spino-olivo-cerebellar;
• Spino-reticulo-cerebellar;
• Spino-vestibulo-cerebellar; and
• Spino-tecto-cerebellar pathways.
(c) Cerebello-spinal pathways
The cerebellum can influence the spinal cord
through the following pathways:
• Cerebello-rubro-spinal;
• Cerebello-vestibulo-spinal;
• Cerebello-reticulo-spinal;
• Cerebello-tecto-spinal; and
• Cerebello-thalamo-cortico-spinal.
47. Connections between Cerebellum and
Cerebral Cortex
(b) Cortico-olivo-cerebellar;
(c) Cortico-reticulo-cerebellar;
(d) Cortico-rubro-cerebellar;
(e) Cortico-tecto-cerebellar; and
(f) Cortico-spino-cerebellar.
(a)cortico-ponto-cerebellar
48. ARTERIAL SUPPLY OF CEREBELLUM
SUPERIOR CEREBELLAR ARTERY –
Branch of BASILAR ARTERY
Supply the superior surface of the cerebellum.
ANTERIOR INFERIOR CEREBELLAR ARTERY
Branch of BASILAR ARTERY
Supply the anterior part of inferior surface of
the cerebellum.
POSTERIOR INFERIOR CEREBELLAR ARTERY
Branch of VERTEBRAL ARTERY
Supply the posterior part of inferior surface of
the cerebellum.
59. Ataxia
• May affect limbs,
trunk, gait
(depends on part
of cerebellum
involved)
• Gait ataxia cause
due to lesion in
anterior lobe.
• Defective timing of
sequential
contraction of
agonist /antagonist
muscles
60. Ataxia
• Results in a
disturbance in
smooth
performance of
voluntary acts
• Without cerebellar
modulation, skilled
movements originating
in cerebral cortex are
inaccurate, poorly
controlled
63. • Asynergia=
lack of synergy
of various
muscles while
performing
complex
movements (
movements
are broken up
into isolated,
successive
parts--
decomposition
of movement)
65. Cerebellar Dysarthria
• Hemisphere lesions are associated with speech
disorders more often than vermal lesions
• Abnormalities in articulation and prosody (together
or independent)
• “scanning”, “slurring”, “staccato”, “explosive”,
“hesitant”, “garbled”
• Scanning speech is jerky and explosive.
71. Features of Cerebellar Dysfunction
• Hypotonia
• Ataxia
• Dysarthria
• Tremor
• Ocular Motor Dysfunction
• Adiadochokinesia
• Scanning and jerky speech
72. • postural instability
• delayed initiation and termination of motor
actions
• inability to perform continuous, repetitive
movements
• errors in smoothness and direction of a
movement
• lack of coordingation or synergy of movement,
especially complex movements
• lack of motor plasticity or learning
73. Tremors
• rhythmic, alternating, or oscillatory movements
• can be a normal exaggeration of movement, a primary
disorder, or a symptom of a cerebellar disorder or
Parkinson's disease
• Diagnosis is usually clinical
• Treatment varies by etiology
74. General features
• Resting tremor : maximal at rest, decreases with
activity; usually a symptom of Parkinson's disease
• Postural tremor : maximal with limb in a fixed position
against gravity; gradual onset suggests physiologic or
essential tremor; acute onset suggests toxic /
metabolic disorder
• Intention tremor : maximal during movement toward a
target (finger-to-nose testing) ; suggests a cerebellar
disorder but may result from other diseases (MS,
Wilsons)
75. • Physiologic tremor: present normally -- usually so
slight that it is noticeable only under certain
conditions ; predominantly postural, fine and rapid
movements.
• most visible when hands are outstretched
• Amplitude may be increased (enhanced) by
• Anxiety
• Stress
• Fatigue
• Metabolic disorders (eg, hyperadrenergic states
such as alcohol or drug withdrawal or
thyrotoxicosis)
76. Certain drugs (eg, caffeine, other
phosphodiesterase inhibitors, β-adrenergic
agonists, corticosteroids)
Alcohol and other sedatives usually
suppress it.
77. Oculomotor dysfunction
•Nystagmus frequently seen in cerebellar
disorders
• To and fro oscillatory movements of eye ball,
• Gaze-evoked nystagmus, upbeat nystagmus,
rebound nystagmus, opticokinetic nystagmus may
all be seen in midline cerebellar lesions
78. •Cerebellar CONGENITAL affective disorder
• Impaired executive function,
• personality, emotional and behavioral changes
• Grammatical errors inspeech
• Patchy memory loss
• Show inattention
• Ataxic or unsteady gait
80. Used to detect Infraction,Tumours,Calcification,
and Haemorrhage.
In this procedure, X-RAY beam traces an arc at
Multiple angle around a section of the head.
Resulting transverse section reproducedby the
computer on its mnitor screen.
Generates 3D view,
Hypodense(dark) and hyperdense(bright) appears
CT SCAN:
X-RAY COMPUTEDTOMOGRAPHY
82. •Provide superior imaging than CT-SCAN
•Used to confirm diagnosis of Neoplasm,
Vascular disease, posterior cranial fossa lession,
Cervicomedullary lesion or intracranial pressure
Disorder.
•Body is exposed to high magnetic field which permis
Protons in the tissue to arrange themselves in the
Related field
• then a pulse of radiowaves `reads` these ion pattern
And a coloured image is form on the monitor
• no risk of ionizing radition
MRI:
MAGNETIC RESONANCE IMAGING