Practice Questions Test 2 (Deck 3) Flashcards
________ accumulations
are a manifestation of derangement in cells
Intracellular accumulations
Accumulations are attributed to what 4 types of abnormalities?
- Abnormal metabolism
- Defect in protein folding or transport
- Lack of an enzyme
- Ingestion of indigestible material
Fatty changes in the liver
and
Resorption Protein Droplets in Renal Tubules
are due to what abnormality?
Abnormal metabolism
Storage diseases like
**GM1 **and GM2 Gangliosidosis
are due to what type of abnormality?
Abnormality in
protein folding or transport
in the storage of lipids
Carbon particles and silica accumulate due to the lack of what?
The lack of an
enzyme
to degrade carbon and silica
Anthracosis is what type of accumulation?
TRICK!
It’s both types of accumulation
Intracellular AND Extracellular
Hepatocytes
Cardiac and Skeletal Muscle
and
Kidneys
are subject to accumulation by what substance?
Lipid accumulation
occurs in
Hepatocytes, Cardiac and Skeletal Muscle, and Kidneys
Glycogen is normally stored in variable amounts in 2 places. What are they?
Glycogen
stored normally in
Hepatocytes and Myocytes
Diabetes mellitus
is an example of a disease that is characterized by
accumulation of what substance?
Diabetes mellitus
Glycogen accumulation
Hyperadrenocorticism (steroid-induced hepatopathy)
is characterized by accumulation of what substance?
Hyperadrenocorticism (steroid-induced hepatopathy)
Glycogen accumulation
Pompe’s Disease
and
EPSSM (Equine Polysaccharide Storage Myopathy)
are examples of
_______ storage diseases
Pompe’s and EPSSM are
Glycogen storage diseases
Pompe’s Disease
is a glycogen storage disease that predisposes
Lapphunds, Shorthorn cattle, and Brahmin cattle
to a defective enzyme called _______.
GAA
is the defective enzyme in
POMPE’S Disease
What glycogen storage disease
affects the cardiomyocytes
and
peripherally displaces contractile elements?
Pompe’s Disease
EPSSM affects
Type ___ muscle fibers
like those in the
- Semitendinosus*
- and*
- Semimembranosus?*
EPSSM
Type 2 muscle fibers
Which glycogen storage disease
causes intracytoplasmic accumulations
of abnormal polsaccharides and subsarcolemmal
glycogen?
EPSSM
Protein accumulations are generally
intra________ accumulations.
Protein accumulations are
intracytoplasmic