Alzheimer's disease Flashcards
what is the main risk factor for Alzheimer’s?
age
is there a genetic link to Alzheimer’s?
- genes include: APEN, APP –> genetic link to getting early onset Alzheimer’s (8%)
- ApoE –> genetic link to late onset Alzheimer’s (most common)
what are the symptoms of Alzheimer’s?
- memory loss (short term)
- disorientation/confusion
- language problems
- personality changes
- poor judgement
in the amyloid hypothesis, what is the normal physiology?
- Amyloid precursor protein (APP) cleaved by alpha-secretase
- sAPP alpha released and C83 fragment remains
- C83 then digested by gamma-secretase
- products then removed
in the amyloid hypothesis, what is the pathophysiology?
- APP cleaved by beta-secretase
- sAPP beta released, leaving C99 fragment
- C99 is digested by gamma-secretase releasing beta-amyloid protein
- beta-amyloid protein forms toxic aggregates
- toxic aggregated cause neurodegeneration
what are tau proteins? what are they important for physiologically?
- tau protein is a soluble protein present in axons
- important for assembly and stability of microtubules
what happens in pathophysiology?
- tau gets hyperphosphorylated
- hyperphosphorylated tau is insoluble –> self aggregates
- self aggregates from neurofibrillary tangles = neurotoxic
- tangles result ultimately in microtubule instability and neurotoxic damage to neurones
what are microglia cells used for?
- specialised CNS immune cells
- like macrophages
what is the pathophysiology in inflammation hypothesis?
- inc release of inflammatory mediators and cytotoxic proteins
- inc. phagocytosis
- dec. levels of neuroproteins
what are the main treatment drugs for AD?
4 drugs
- 3 acetylcholinesterases (Donepezil, Rivastigmine, Galantamine)
- NMDA (glutamate) receptor blocker (Memantine)
what is important to remember with these drugs?
none of these drugs affect disease progession, just symptoms
describe donepezil
- reversible cholinesterase inhibitor
- long plasma half life
- inc. levels of Ach
- effective in treating symptoms
- effects only last for around a year
describe rivastigmine
- inhibits both isoforms
- pseudo-reversible AChE and BChE inhibitor
- 8hr half life
- transdermal patch
describe galantamine
- reversible cholinesterase inhibitor
- half life = 7/8 hours
- can also activate neuronal nicotininc AChR (agonist effects)
= alpha 7 nAChR agonist
what is memantine?
- non competitive NMDA receptor blockade
- NMDA-R activated by glutamine
- only for late stage