Neurology Flashcards

(38 cards)

1
Q

Central Nervous System Intro

A

-Brain and spine
-integrate information from body
-co-ordinate responses
-seat of consciousness

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2
Q

Peripheral nervous system

A

-cranial and spinal nerves
-enervate the body
-autonomic and somatic systems

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3
Q

Blood brain barrier

A

-brain immunologically privileged
-astrocytes wrapped around capillaries
-stops some drugs

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4
Q

Myelin

A

-lipid rich substance coating some neurones
-glial cells produce
(Schwann cells in PNS, oligodendrocytes in CNS)
-saltatory conduction

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5
Q

Role of Neurotransmitters

A

-signal transduction, function of NTs tissue dependant.
-cross synapse and bind complementary receptor, receptor activity is regulated

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6
Q

Ionotropic receptors

A

-ligand gated ion channels
-acts quickly

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7
Q

Metabotropic receptors

A

-GPCR
-slow reaction
-signal cascade (open another ion channel on membrane)

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8
Q

Glutamate Ionotropic Receptor

A

-glutamate major excitatory NT in CNS=75%
-allows excitatory cations through Na+, Ca2+,
-depolarize post-synapse cell action potential propangated
-NMDA, Kainate, AMPA

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9
Q

Excitotoxicity

A

-death and loss of CNS/PNS function
-increased NT levels, glutamate
-excess glutamate Ca2+ influx
-cofactor of endonucleases and proteolytic enzymes

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10
Q

Multiple Sclerosis

A

-Demyelinating disorder of CNS
-chronic inflammatory condition
-0.1% of pop, 2.5 mill worldwide

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11
Q

MS Predisposing Factors

A

-Geography (highest temperature)
-Ethnicity (Caucasians)
-Gender (women x2)
-Genes -HLA-DR15

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12
Q

Vitamin D

A

-deficiency cause MS
-supplements protective
-modulates immune response

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13
Q

Clinical Manifestation of MS

A

-trauma, pregnancy and infection cause symptoms flare (initiate inflammatory response)
-Symptoms depend on which region of CNS effected:
opticospinal MS
Spinal MS
cerebellar MS

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14
Q

Cause of Symptoms of MS

A

-progressive and diffuse disease CNS
-autoreactive immune cells target myelin antigens and destroy them (loss of conductivity)
-neurones apoptose (Ca2+ homeostasis disturbed)

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15
Q

Evaluation and Treatment

A

-McDonald Criteria
-Treatment based on symptoms
modification and
immunosuppressant’s.

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16
Q

Guillain-Barrė Syndrome

A

-Peripheral neuropathy brought about by demyelination
-Infection cause:
 Campylobacter jejuni 30%
 Cytomegalovirus 10%
 Epstein Barr virus.
 Possibly Zika.
-resolves with time 30% ventilator support

17
Q

Cytomegalovirus (CMV)

A

-herpes virus
-60-70% of world
-congenital transmission birth defects
-serious disease in immunocompromised individuals

18
Q

Ion transport in other Neurotransmitters

A

-reuptake of NTs
-Dopamine (DAT) and serotonin (SERT)
-recycles and controls level of NT in synapse
-Reuptake is facilitated via NT sodium symport.
- Sodium and chloride ion
dependant.

19
Q

Parkinson’s Disease Intro

A

-10 millon world wide, 60, 000 annually diagnosed.
-60 years old, usually men
-10% inherited

20
Q

Presentation of Parkinson’s

A
  • complex motor disorder
    -bradykinetic (slowness of voluntary movement)
    -postural abnormalities
    -tremor
    -rigidity
21
Q

Dopamine

A
  • NT important to motor control
    -produced by cells in basal ganglia, substantia nigra
    -Contributes to the action
    selection process.
    -The greater the amount of
    dopamine, the less stimulus is
    required to trigger movement.
22
Q

Substantia nigra in PD

A
  • depleted
    -underactivity of direct motor pathway
    -overactivity of indirect motor pathway
    -loss of dopamine=cognitive symptoms depression 40%
23
Q

Cause of cell death of dopaminergic neurones

A

 Mitochondrial dysfunction.
 Oxidative stress.
 Inflammation

Lewy bodies in SN of PD, protein aggregates

24
Q

L-Dopa

A

-Treatment of PD, also diagnostic
-precursor of dopamine
-dopa decarboxylase converts to dopamine in CNS
-carbidopa adjunct

25
Dopamine Other function s
-Motivation, reward, sexual gratification -mesolimbic pathway reward (addiction -low dopamine=low desire motivation -anticipation increases
26
PD Prognosis
-Progressively reliant and carers -Hoehn and Yarr scale classifies severity (1-5, 5 worst)
27
Future Therapy for PD
Deep brain stimulation? (haemorrhage and infection risk)
28
Serotonin Location
-brain stem and limbic system (raphe nuclei) -platelets (8%) -Gut 90%
29
Serotonin Receptors
-Mainly GPCR (14 receptors 7 classes) -only 5-HT3 not it is a ligand gated ion channel, Na, K and Ca permeable -5-HT1 and 5 inhibitory decrease cAMP - 5-HT2, 3, 4, 6, 7 excitatory, increase cAMP
30
General anxiety disorder (GAD)
-persistent state (>6 months) of anxiety/fear -physical symptoms possible -genetic= HTR2A gene, SLC6A4
31
Selective serotonin reuptake inhibitors (SSRIs)
-8 available in UK -71% of antidepressants are SSRIs -serotonin syndrome possible -citalopram
32
SSRI Other Uses
-modulator of T cell proliferation -Suppresses production of interferon, TNF and Il-6 -impact clotting profiles
33
Protein folding
Folding is reliant on intramolecular interactions: - Ionic bonds - Hydrophobic interactions - Hydrogen bonds - Disulfide bridges Chaperone proteins assist= calreticulin, calnexin, BiP
34
Prions
-infective particles which are comprised of misfolded protein -can spontaneously misfold native protein
35
Prion protein (PrP)
Surface-bound membrane protein which is believed to be involved in cell- cell adhesion and communication. -Cu binding. -Infectious PrP (PrPSc) is able to convert alpha-helices to beta- pleated sheets which causes proteins to aggregate.
36
Prion disease
-neurodegenerative disease [Spongiform encephalopathy] -20 year incubation -fatal  Srapie (sheep)  Mad cow disease (Cattle)  Kuru (human)  vCJD (human)
37
vCJD (Human prion disease)
Genetic responsible to early development. -homozygous methionine at a.a 129 -40% caucasian -Valine longer incubation -life expecatancy 13 months
38