- NEURODEGENARATIVE DISEASE
- Lets understand the defination of PD
- PD IS A NEURODEGENENERATIVE DISEASE MARKED BY A PROMINENT HYPOKINETIC MOVEMENT DISORDER THAT IS CAUSED BY LOSS OF DOPAMINERGIC NEURONS FROM THE SUBSTANTIA NIGRA
Revolving aroud the statement and decoding it into simpler terms lets understand it
- WHY NEURODEGENARATIVE?
- HOW IS THE LOSS OF NEURONS CAUSED?
- WHERE IS SUBSTANTIA NIGRA?
To understand the neurodegenarative we have understand the pathogenesis pathway clearly
NOW LETS SEE THE SUBSTANTIA NIGRA
WHAT IT CONTAINS AND WHAT ARE ITS
And now the surrounding structures
THE DISEASE
THIRD WAY IS SUBSTANTIA NIGRA FOLLOWS EXPOSURE TO MPP IS HIGH ,MPP IS FORMED FROM MPTP BY THE ACTION OF (MAO -B) monoamine oxidase B CONVERSION OF THIS MAKES MPP ACCUMUALTES IN THE BASAL GANGLIA AND DESTROYS THEM(NEURONS)
DAMAGE TO THE NIGROSTRIATAL DOPAMINERGIC NEURON SYSTEM
Why it is happening to the neurons we will learn in the pathogenesis!
CAUSE OF THE DISEASE
- IDIOPATHIC(MAIN CAUSE)
- DRUGS (OCCURS SECONDARY TO CHRONIC USE OF MANY DRUGS LIKE PHENOTHIAZINE ,D2 RECEPTOR BLOCKER)
- MPP (METHYL PHENYL PYRIDINIUM)this compond is formed from its precursor which we will discuss later toxic levels of this compond is seen in PD
HYPOKINETIC MOVEMENTS
- AKINESIA (DIFFICULTY IN INTIATING MOVEMENTS)
- BRADYKINESIA(SLOWNESS OF MOVEMENTS)
- DECREASED ASSOCIATED MOVEMENTS(EXPRESSIONLESS FACE OR MASK FACE)
- HYPERKINETIC MOVEMENTS RIGIDITY TREMOR (TREMOR IS OBSERVED ONLY AT REST ONCE MOVEMENTS STARTS TREMOR STOPS RESTING TREMOR) FESTINANT GAIT (TRYING TO CATCH CENTER OF GRAVITY)
- DOPAMINERGIC NEURONS (RED)originating in the substantia nigra normally inhibit the GABAergic output from the straitum
- BOTTOM IMAGE There is selective loss of DOPAMINERGIC NEURONS (dashed RED)
PATHOGENESIS
- PD is associated with protien accumalation and aggregation ,mitochondrial abnormalities,and neuronal loss in the substantia nigra SINCE LETS BECOME FAMILIAR WITH SOME KEY WORDS ,THERE ARE LIST OF GENES WHERE WE HAVE TO BECOME FAMILIAR WITH
- ALPHA SYNUCLEIN
- LRRK2(leucine rich repeat kinase 2)
- parkin gene
- MPTP(1 methyl 4 phenyl 1,2,3,6 tetrahydropyridine)
FIRST PATHOGENESIS
SECOND WAY
TREATMENT
- REPLACEMENT OF DOPAMINE
- ANTICHOLINERGICS
- DEPRENYL
- TRANSPLANTATION OF ADRENAL
- IMPLANTATION OF FETAL BASAL GANGLIA
- TRANSPLANTATION OF GLOMUS CELLS
TREATMENT WILL BE DISCUSSED IN THE NEXT BLOG
LAST THING TO KNOW ABOUT IS LEWY BODIES
These are single or multiple cytoplasmic ,eosinophilic ,round to enlongated inclusions that often have a dense core surrounded by pale halo
DIAGNOSTIC HALLMARK OF DISEASE
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