Pathophysiology, 5th Edition By Lee-Ellen C. Copstead-Test Bank
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Sample
Test
Chapter 3: Cell Structure and Function
Test Bank
MULTIPLE CHOICE
1. Glycolysis
is the metabolic process of breaking down a glucose molecule to form
a. |
CO2 and H2O. |
b. |
2 ATP and 2 pyruvate. |
c. |
30 ATP. |
d. |
oxygen. |
ANS: B
Glycolysis produces a net gain of 2 ATP molecules and breaks
down glucose modules to produce two pyruvate molecules. Oxidative
phosphorylation produces CO2 and H2O.
Oxidative phosphorylation produces 30 ATP molecules. Oxygen is not produced by
glycolysis, but it is necessary for oxidative phosphorylation.
REF: Pg. 34
2. The
benefit of glycolysis is that this phase supplies
a. |
ATP to meet energy needs of
the body. |
b. |
pyruvate to the citric acid
cycle. |
c. |
energy for oxidative
phosphorylation |
d. |
lactate during anaerobic
conditions. |
ANS: B
The benefit of glycolysis is to supply pyruvate to the citric
acid cycle of cellular metabolism, which then produces much ATP. Glycolysis
only produces 2 ATP modules, which is insufficient for energy needs. Glycolysis
does not supply energy for oxidative phosphorylation. Lactate produced during
prolonged anaerobic conditions builds up and can lead to lactic acidosis, which
is an undesirable outcome.
REF: Pg. 34
3. Repolarization
of a neuron after a depolarizing action potential is due to
a. |
activation of the Na+-K+ pump. |
b. |
influx of calcium. |
c. |
efflux of potassium. |
d. |
influx of sodium. |
ANS: C
Repolarization is due to efflux of potassium from the cell. The
Na+-K+ pump maintains cellular volume via osmotic pressure and
helps to maintain resting membrane potential. Calcium influx prolongs the
action potential. Influx of sodium initiates depolarization.
REF: Pg. 45
4. Excitable
cells are able to conduct action potentials because they have
a. |
receptors for
neurotransmitters. |
b. |
tight junctions. |
c. |
ligand-gated channels. |
d. |
voltage-gated channels. |
ANS: D
Voltage-gated channels respond to changes in membrane potential
and are responsible for conducting action potentials. Receptors for
neurotransmitters allow neurotransmitters to bind to the cell membrane but are
not directly responsible for action potentials in excitable cells. Tight
junctions are intercellular connections that help segregate proteins on the
cell membrane and are not involved in conducting action potentials.
Ligand-gated channels respond to binding of a signaling molecule such as a
neurotransmitter, but are not directly responsible for action potentials in excitable
cells.
REF: Pgs. 42-44
5. The
resting membrane potential in nerve and skeletal muscle is determined primarily
by
a. |
extracellular sodium ion
concentration. |
b. |
the ratio of intracellular
to extracellular potassium ions. |
c. |
activation of voltage-gated
sodium channels. |
d. |
activity of
energy-dependent membrane pumps. |
ANS: B
The major determinant of the resting membrane potential is the
difference in potassium ion concentration across the membrane. Extracellular
sodium helps to maintain cell volume and resting membrane potential but it is
not the primary determinant. Activation of voltage-gated sodium channels help
to initiate an action potential. Channels are not linked to an energy source;
ions flow passively across the cell membrane.
REF: Pgs. 42-43
6. An
increase in extracellular potassium ion from 4.0 to 6.0 mEq/L would
a. |
hyperpolarize the resting
membrane potential. |
b. |
make it more difficult to
reach threshold and produce an action potential. |
c. |
hypopolarize the resting
membrane potential. |
d. |
alter the threshold
potential. |
ANS: C
An increase in extracellular potassium hypopolarizes the cell
(makes it less negative) because more K+ ions
stay inside the cell owing to the reduced concentration gradient.
Hyperpolarization of the resting membrane potential (makes it more negative) is
caused by a decrease in extracellular potassium. Hyperpolarization due to a
decrease in extracellular potassium makes it more difficult to reach threshold
and produce an action potential. The threshold for action potential does not
change with a change in extracellular potassium.
REF: Pg. 43
7. GTP-binding
proteins (G proteins) function to
a. |
activate receptors on the
extracellular surface. |
b. |
degrade second-messenger
molecules. |
c. |
activate intracellular
enzyme systems. |
d. |
synthesize ATP. |
ANS: C
G-proteins activate specific target enzymes within the cell and
these enzymes then produce second messenger molecules that trigger specific intracellular
function. Membrane-bound G-protein channels are a component of the cell
membrane; they do not activate other receptors on the extracellular surface.
G-proteins do not degrade second messengers, but instead produce these.
G-proteins do not synthesize ATP.
REF: Pg. 49
8. Phospholipids
spontaneously form lipid bilayers, because they are
a. |
polar. |
b. |
charged. |
c. |
insoluble. |
d. |
amphipathic. |
ANS: D
Phospholipids have a hydrophilic (water-loving) polar end and a
hydrophobic (water-fearing) polar end. This amphipathic nature causes the
lipids to form bilayers. It is the water-loving and water-fearing nature of the
end rather than simply being polar, charged, or insoluble that forms the
bilayers.
REF: Pg. 27
9. Cell-to-cell
communication through secretion of chemical signals into the bloodstream to
target cells throughout the body is called _____ signaling.
a. |
synaptic |
b. |
paracrine |
c. |
endocrine |
d. |
autocrine |
ANS: C
Endocrine signaling is accomplished by specialized endocrine
cells that secrete hormones that travel via the bloodstream to target cells
throughout the body. Synaptic signaling occurs at specialized junctions between
the nerve cell and its target cell; the neuron secretes a chemical neurotransmitter
into a small space between the nerve and target cell. In paracrine signaling
chemicals are secreted into a localized area, and only those cells in the
immediate area are affected. Autocrine signaling occurs when cells respond to
signaling molecules that they secrete and provides feedback to that cell rather
than other cells.
REF: Pg. 47
10. Ribosomes
are very important organelles within the cell that have the function of
a. |
detoxifying substances. |
b. |
synthesizing proteins. |
c. |
converting energy to forms
that can be used. |
d. |
coding for protein
synthesis. |
ANS: B
Ribosomes primary function is the synthesis of proteins.
Lysosomes and peroxisomes detoxify substances. Mitochondria convert energy to
forms that can be used to drive cell reactions. The nucleus contains genomic
DNA that codes for protein synthesis.
REF: Pg. 31
11. The
cardiac drug digitalis enhances myocardial contraction, because it
a. |
increases intracellular
calcium level in cardiac cells. |
b. |
inhibits sodium from entering
cardiac cells. |
c. |
enhances the
sodium-potassium pump. |
d. |
increases the sodium
gradient across the cell membrane. |
ANS: A
Digitalis inhibits the sodium-potassium pump and allows the
accumulation of intracellular sodium, decreasing the sodium gradient across the
cell membrane. This leads to less efficient calcium removal by the
sodium-dependent calcium pump. Increased calcium inside the cardiac cell leads
to more forceful cardiac muscle contraction to treat congestive heart failure
due to cardiac muscle weakness.
REF: Pg. 41
12. The
organelle that contains enzymes necessary for oxidative phosphorylation to
produce ATP is the
a. |
mitochondria. |
b. |
ribosome. |
c. |
lysosome. |
d. |
nucleus. |
ANS: A
The inner membrane of the mitochondria contains many enzymes
that promote oxidative phosphorylation which produces ATP. Ribosomes synthesize
proteins. Lysosomes and peroxisomes detoxify substances. The nucleus contains
genomic DNA that codes for protein synthesis.
REF: Pg. 32
13. Ion
channels open and close in response to all the following except
a. |
mechanical pressure. |
b. |
ligand binding. |
c. |
voltage changes. |
d. |
temperature changes. |
ANS: D
No temperature change channels are present on the cell membrane.
Mechanically gated channels respond to mechanical deformation. Ligand-gated
channels respond to the binding of a signaling molecule (neurotransmitter or
hormone). Voltage-gated channels respond to a change in membrane potential.
REF: Pg. 42
14. Gap junctions
are connecting channels that allow passage of small molecules from one cell to
the next and are especially important for
a. |
distance signaling. |
b. |
tissues requiring
synchronized function. |
c. |
communication within a
cell. |
d. |
passage of large molecules. |
ANS: B
Gap junctions are especially important in tissues in which
synchronized functions are required such as in cardiac muscle contraction. Gap
junctions are channels between adjacent cells, not distant cells. Gap junctions
function to promote communication not within a cell, but between adjacent
cells. Gap junctions allow passage of small molecules, but not large molecules.
REF: Pg. 45
COMPLETION
15. During
conditions of prolonged insufficient oxygen availability (e.g., respiratory or
cardiovascular disease) anaerobic glycolysis accumulated pyruvate can lead to
_____ acidosis.
ANS:
lactic
Pyruvate is converted to lactate and released into the blood
stream, resulting in lactic acidosis.
REF: Pg. 34
16. The
phase of cellular metabolism in which energy is released during breakdown of
nutrient sources is ________.
ANS:
catabolism
Catabolism involves energy release via breakdown of nutrient
sources such as glucose to provide ATP to the cell. In contrast, anabolism
refers to energy-using processes that result in complex molecules such as fats.
REF: Pg. 34
17. Some
individuals inherit a gene that results in dangerously high blood cholesterol
due to impaired ________ of low-density lipoproteins (LDLs).
ANS:
endocytosis
The defective gene inhibits the synthesis of LDL protein
receptors on the cell membrane. This impairs endocytosis of LDL. High levels of
LDL in the blood predispose to atherosclerosis.
REF: Pg. 38
Chapter 4: Cell Injury, Aging, and Death
Test Bank
MULTIPLE CHOICE
1. An
increase in organ size and function due to increased workload is termed
a. |
atrophy. |
b. |
hypertrophy. |
c. |
metaplasia |
d. |
inflammation. |
ANS: B
Increased function of an organ such as the heart or skeletal
muscle results in organ hypertrophy due to cellular enlargement. Atrophy refers
to reduction in size of an organ due to cellular shrinkage. Metaplasia refers
to replacement of one differentiated cell type with another. Inflammation
results from immune response rather than workload.
REF: Pg. 61
2. Apoptosis
is a process that results in cellular
a. |
atrophy. |
b. |
death. |
c. |
proliferation. |
d. |
mutation. |
ANS: B
Apoptosis results in death of a cell when it is no longer
needed. Atrophy refers to reduction in size of an organ due to cellular
shrinkage. Proliferation refers to growth of new cells. Mutation refers to
alteration in the genetic structure of cellular DNA.
REF: Pg. 64
3. All
these cellular responses are potentially reversible except
a. |
necrosis. |
b. |
metaplasia. |
c. |
atrophy. |
d. |
hyperplasia. |
ANS: A
Necrosis refers to death of cells/tissue and is not reversible.
Metaplasia refers to the replacement of one differentiated cell type with
another from persistent injury and is reversible when the injury stops. Atrophy
occurs due to lack of use of an organ and is reversible. Hyperplasia is an
increase in the number of cells from increased physiologic demands or hormonal
stimulation and is reversible.
REF: Pg. 62
4. Necrotic
death of brain tissue usually produces _____ necrosis.
a. |
coagulative |
b. |
caseous |
c. |
liquefactive |
d. |
fat |
ANS: C
Liquefactive necrosis is produced when brain tissue dies, as it
is rich in enzymes and has little connective tissue. Coagulative necrosis
occurs from ischemic injury in any tissue. Caseous necrosis occurs in lung
tissue damaged by tuberculosis. Fat necrosis occurs in adipose (fat) tissue.
REF: Pg. 64
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