|
a. 6 |
||
|
b. 7 |
||
|
c. 8 |
||
|
d. 9 |
|
a. Afferent; efferent |
||
|
b. Entry; exit |
||
|
c. Sensory; response |
||
|
d. Peripheral; central |
|
a. Peripheral nerves and central nerves |
||
|
b. Sensory nerves and response nerves |
||
|
c. The brain and the spinal cord |
||
|
d. White matter and grey matter |
|
a. 3 |
||
|
b. 4 |
||
|
c. 5 |
||
|
d. 6 |
|
a. Eye movement |
||
|
b. Facial sensation |
||
|
c. Hearing |
||
|
d. All of the above |
|
a. The front |
||
|
b. The back |
||
|
c. The sides |
||
|
d. The bottom |
|
a. -2 |
||
|
b. +2 |
||
|
c. -4 |
||
|
d. +4 |
|
a. Nucleus |
||
|
b. Golgi complex |
||
|
c. Endoplasmic reticulum |
||
|
d. All of the above |
|
a. Myelin sheath |
||
|
b. Cell body |
||
|
c. Cell wall |
||
|
d. Dendrites |
|
a. Covalet |
||
|
b. Ionic |
||
|
c. Van der Waals |
||
|
d. All of the above |
|
a. A single action potential of large magnitude |
||
|
b. A large number of action potentials |
||
|
c. No change in magnitude of action potential compared to a weak stimulus |
||
|
d. No change in number of action potentials compared to a weak stimulus |
|
a. positive inside and negative outside; negative inside and positive outside |
||
|
b. negative inside and positive outside; positive inside and negative outside |
||
|
c. negative inside and negative outside; positive inside and positive outside |
||
|
d. positive inside and positive outside negative inside and negative outside |
|
a. 1; 2 |
||
|
b. 2; 1 |
||
|
c. 2; 3 |
||
|
d. 3; 2 |
|
a. At the myelin sheath |
||
|
b. At the cell body |
||
|
c. At the dendrites |
||
|
d. At the node of Ranvier |
|
a. 1 |
||
|
b. 2 |
||
|
c. 3 |
||
|
d. 4 |
|
a. That the potassium concentration inside the nerve must reach a certain threshold level |
||
|
b. That the action potential is strongest at the beginning of the axon and weakest at the end of the axon |
||
|
c. That the strength of the stimulus must reach a certain threshold level |
||
|
d. That action potential from several axons can merge to reach a threshold level for propagation |
|
a. Cerebral synapses |
||
|
b. Electrical synapses |
||
|
c. Neuromuscular junctions |
||
|
d. Excitatory ion synapses |
|
a. Bioelectricity is not found in muscle cells. |
||
|
b. At rest, most cells have a potential between -40 to -80mV. |
||
|
c. Cell membranes can separate charged ions. |
||
|
d. Cell membranes are electrical insulators. |
|
a. The myelin sheath around the nerve fibers are damaged. |
||
|
b. The dendrites of the nerve cells are damaged. |
||
|
c. Plaque forms around the synapses of the nerve cells. |
||
|
d. The ion channels in the nerve cell membrane have stopped working. |
|
a. From dendrites to cell body to axon |
||
|
b. From cell body to dendrites to axon |
||
|
c. From axon to dendrites to cell body |
||
|
d. From dendrites to axon to cell body |
|
a. Adenosine triphosphate (ATP) |
||
|
b. Inositol trisphosphate (IP₃) |
||
|
c. Cyclic adenosine monophosphate (cAMP) |
||
|
d. Ca²⁺ |
|
a. 2-hydroxy-5-methyllaurophenoxime (HMLO) |
||
|
b. Cocaine |
||
|
c. Tetrahydrocannabinol (THC) |
||
|
d. None of the above |
|
a. Nitric oxide |
||
|
b. Ca2+ |
||
|
c. Na2+ |
||
|
d. Both A and B |
|
a. To trigger neurotransmitter release when the concentration of Ca2+ inside the presynaptic neuron increases |
||
|
b. To trigger neurotransmitter release when the concentration of Ca2+ inside the presynaptic neuron decreases |
||
|
c. To trigger neurotransmitter release when the concentration of Ca2+ outside the presynaptic neuron increases |
||
|
d. To trigger neurotransmitter release when the concentration of Ca2+ outside the presynaptic neuron decreases |
|
a. A neurotransmitter that is released into the synaptic gap |
||
|
b. Neurotransmitter receptors on the membrane of the postsynaptic neuron |
||
|
c. Gap junction connections between the presynaptic and postsynaptic membrane |
||
|
d. Synaptic vesicles in the presynaptic neuron |
|
a. Electrical synapses conduct nerve impulses faster. |
||
|
b. The signal in the presynaptic neuron remains unchanged after it has passed to the postsynaptic neuron. |
||
|
c. Signals can move in either direction in an electrical synapse. |
||
|
d. All of the above |
|
a. It results in ion channels of the postsynaptic membrane to open or close. |
||
|
b. It directly transfers the nerve impulses from the presynaptic membrane to the postsynaptic membrane. |
||
|
c. It deforms the postsynaptic membrane, which results in the formation of a nerve impulse. |
||
|
d. None of the above |
|
a. Both are located on post-synaptic membranes. |
||
|
b. G-proteins bind to both. |
||
|
c. Both are activated by the attachment of a neurotransmitter. |
||
|
d. Both have ion channels. |
|
a. They are always diphenyl trichloroethane (DTT). |
||
|
b. They are always 2,4-dichlorophenoxyacetic acid (2,4-D). |
||
|
c. They are always acetylcholine. |
||
|
d. None of the above |
|
a. The gap ensures that the nerve impulse flows only in one direction. |
||
|
b. There cannot be direct contact between two nerves. |
||
|
c. The gap allows for spatial or temporal summation. |
||
|
d. The gap allows the nerves to filter out unimportant background stimuli. |
|
a. Levels of extracellular excitatory amino acids decrease. |
||
|
b. Intracellular calcium increase. |
||
|
c. Intracellular caspases increase. |
||
|
d. Neurons become more susceptible to free radical damage. |
|
a. Anterograde degeneration |
||
|
b. Retrograde degeneration |
||
|
c. Degeneration of presynaptic terminals |
||
|
d. All of the above |
|
a. Cerebrum |
||
|
b. Hippocampus |
||
|
c. Hypothalamus |
||
|
d. Pons |
|
a. The action potential charge becomes too high and kills the neuron. |
||
|
b. The neuronal membrane becomes damaged from the nerve impulses. |
||
|
c. Too much glutamate causes neurons to take in too much calcium and causes intracellular enzymes to release damaging free radicals. |
||
|
d. All of the above |
|
a. Initiation of the gene expression that causes axon elongation |
||
|
b. Macrophages to remove fragments of degenerating axon and myelin |
||
|
c. Nogo to aid the newly formed axons |
||
|
d. Both A and B |
|
a. Glia growth factor (GGF) |
||
|
b. Nerve growth factor (NGF) |
||
|
c. Dendrite growth factor (DGF) |
||
|
d. Synaptic growth factor (SGF) |
|
a. Fetal stem cells |
||
|
b. Adult brain stem cells |
||
|
c. Both A and B |
||
|
d. None of the above |
|
a. During the early embryonic stage |
||
|
b. During the early fetal stage |
||
|
c. During the late fetal stage |
||
|
d. During the early postnatal period |
|
a. Only stem cells can undergo cell division. |
||
|
b. Only neuroblasts can undergo cell division. |
||
|
c. Both A and B |
||
|
d. None of the above |
|
a. 5 |
||
|
b. 6 |
||
|
c. 7 |
||
|
d. 8 |
|
a. Netrins; semaphorin |
||
|
b. Slit; robo |
||
|
c. Attractin; repellin |
||
|
d. Robo; repellin |
|
a. Fatty acids |
||
|
b. Enzymes |
||
|
c. Ribosomal RNA |
||
|
d. Transcription factors |
|
a. 2 |
||
|
b. 3 |
||
|
c. 4 |
||
|
d. 5 |
|
a. Sonic Hedgehog (Shh) |
||
|
b. Homeobox (Hox) |
||
|
c. Devo |
||
|
d. Both A and B |
|
a. 2 |
||
|
b. 3 |
||
|
c. 4 |
||
|
d. 5 |
|
a. Primitive streak elongates to form the primitive pit, which elongates to become the notochord. |
||
|
b. Primitive pit elongates to form the primitive streak, which elongates to become the notochord. |
||
|
c. Primitive pit elongates to form the notochord, which elongates to become the primitive streak. |
||
|
d. Notochord elongates to form the primitive pit, which elongates to become the primitive streak. |
|
a. It affects intellectual ability. |
||
|
b. It causes impairment of social responsiveness. |
||
|
c. It is caused by a genetic defect only. |
||
|
d. There is no cure. |
|
a. There is no cure. |
||
|
b. It affects males only. |
||
|
c. It is caused by a mutation in the X chromosomes only. |
||
|
d. It affects intellectual ability. |
|
a. Preganglionic neurons located in particular spinal cord segments preferentially connect with ganglion cells projecting from certain targets, like the eyes. |
||
|
b. Selective synapse formation is based on differential affinities of the pre- and postsynaptic elements. |
||
|
c. Selective synapse formation ensures that neurons do not innervate nearby glial or connective tissue cells. |
||
|
d. All of the above |
|
a. Periderm |
||
|
b. Endoderm |
||
|
c. Ectoderm |
||
|
d. Mesoderm |
|
a. Caudate nucleus |
||
|
b. Putamen |
||
|
c. Globus pallidus |
||
|
d. All of the above |
|
a. Third and fourth ventricle |
||
|
b. Lateral and fourth ventricle |
||
|
c. Third and interventricular foramen |
||
|
d. Lateral ventricle and interventricular foramen |
|
a. 10 |
||
|
b. 17 |
||
|
c. 24 |
||
|
d. 31 |
|
a. To carry information from the optic nerve to the brain |
||
|
b. To process sound |
||
|
c. To carry information between the two hemispheres of the brain |
||
|
d. To carry information from the cerebral cortex to the cerebellum |
|
a. It carries the input and output of the cerebral cortex. |
||
|
b. It consists of 3 fiber bundles. |
||
|
c. Outputs are conducted via the superior cerebellar peduncles. |
||
|
d. Inputs are conducted via the inferior and middle cerebellar peduncles. |
|
a. An average healthy adult has 140ml of CSF. |
||
|
b. CSF is produced from lymphatic fluid. |
||
|
c. The circulation of CSF is aided by the pulsations of the choroid plexus and by the motion of the cilia of ependymal cells. |
||
|
d. CSF acts as a cushion that protects the brain from shocks and supports the venous sinus. |
|
a. The ventral root consists of axon from the motor and visceral efferent fibers. |
||
|
b. The dorsal root receives information from the skin, skeletal muscles, and joints. |
||
|
c. Both the dorsal and ventral root eventually come together to form the spinal nerve. |
||
|
d. All of the above |
|
a. It is not connected to the spinal cord. |
||
|
b. It contains the inferior olive. |
||
|
c. It regulates respiration. |
||
|
d. None of the above |
|
a. After exiting the retina, it bundles together to form the optic nerve. |
||
|
b. This is the region where the blind spot of the retina is located. |
||
|
c. It is identified by its appearance as a black disk on the retina. |
||
|
d. None of the above |
|
a. The cerebellum |
||
|
b. The occipital lobe |
||
|
c. The cerebral cortex |
||
|
d. The parietal lobe |
|
a. Information about pain only |
||
|
b. Information about temperature only |
||
|
c. Information about both pain and temperature |
||
|
d. Information about crude touch, pain, and temperature |
|
a. Information about pain only |
||
|
b. Information about temperature only |
||
|
c. Information about both pain and temperature |
||
|
d. Information about crude touch, pain, and temperature |
|
a. Conveys information from the skin to the central nervous system |
||
|
b. Conveys information from the visceral organs to the central nervous system |
||
|
c. Conveys information from the face to the central nervous system |
||
|
d. Conveys information from the limbs to the central nervous system |
|
a. 11 |
||
|
b. 21 |
||
|
c. 31 |
||
|
d. 41 |
|
a. The associated pain occurring in the visceral organs when pain is perceived in the cutaneous layer |
||
|
b. Pain in the visceral organs that is perceived as cutaneous pain |
||
|
c. Pain created by injury to certain parts of the brain that is perceived as cutaneous pain |
||
|
d. Pain created by injury to certain parts of the spinal cord that is perceived as cutaneous pain |
|
a. Connective tissue |
||
|
b. Capsule |
||
|
c. Ligaments |
||
|
d. All of the above |
|
a. The somatic sensory cortex is located in the parietal lobe. |
||
|
b. The somatic sensory cortex consists of 3 regions. |
||
|
c. The somatic sensory cortex responds to stimuli from the eyes. |
||
|
d. The somatic sensory cortex is not found in primates. |
|
a. Sensitization is also called hyperalgesia. |
||
|
b. Sensitization occurs when people become hypersensitive to allergens. |
||
|
c. Sensitization is caused by a genetic mutation. |
||
|
d. Sensitization can occur after brain damage. |
|
a. Cheek |
||
|
b. Fingertip |
||
|
c. Belly |
||
|
d. Toe |
|
a. The Ruffini corpuscle |
||
|
b. The Merkel complex |
||
|
c. Golgi tendon organs |
||
|
d. The Meissner corpuscle |
|
a. Optic nerve head |
||
|
b. Retina |
||
|
c. Optic chiasm |
||
|
d. Optic disc |
|
a. 5Hz – 5kHz |
||
|
b. 10Hz – 10kHz |
||
|
c. 15Hz – 15kHz |
||
|
d. 20Hz – 20kHz |
|
a. 2 |
||
|
b. 4 |
||
|
c. 6 |
||
|
d. 8 |
|
a. All over |
||
|
b. Posterolateral edges |
||
|
c. Mediolateral edges |
||
|
d. Tip |
|
a. To interpret sound |
||
|
b. To interpret head position |
||
|
c. To coordinate head eye movements |
||
|
d. To integrate sound information received from the two ears |
|
a. The otolith organs |
||
|
b. The cochlear |
||
|
c. The malleus |
||
|
d. The spiral organ |
|
a. Round window; tympanic membrane; concha |
||
|
b. Tympanic membrane; concha; round window |
||
|
c. Concha; tympanic membrane; round window |
||
|
d. Tympanic membrane; round window; concha |
|
a. Basilar membrane > scala tympani > round window |
||
|
b. Basilar membrane > round window > scala tympani |
||
|
c. Tympanic membrane > 3 bones of middle ear > oval window |
||
|
d. Tympanic membrane > oval window > 3 bones of middle ear |
|
a. The label line hypothesis |
||
|
b. The interactive hypothesis |
||
|
c. The ensemble hypothesis |
||
|
d. The across-neuron hypothesis |
|
a. The lens |
||
|
b. The vitreous humor |
||
|
c. The cornea |
||
|
d. The rods and cones |
|
a. Attention deficit hyperactivity disorder (ADHT) |
||
|
b. Tourette's syndrome |
||
|
c. Autism |
||
|
d. Parkinson’s disease |
||
|
e. Schizophrenia |
|
a. 1 |
||
|
b. 2 |
||
|
c. 3 |
||
|
d. unlimited |
|
a. The cerebral cortex |
||
|
b. The cerebellum |
||
|
c. The basal ganglia |
||
|
d. The brain stem |
|
a. The premotor cortex |
||
|
b. The supplementary motor area |
||
|
c. The primary motor cortex |
||
|
d. All of the above |
|
a. Preganglionic neurons |
||
|
b. Parasympathetic division |
||
|
c. Sympathetic division |
||
|
d. Both A and B |
|
a. Muscle atrophy |
||
|
b. Fibrillation |
||
|
c. Hyporeflexia |
||
|
d. All of the above |
|
a. Red nucleus |
||
|
b. Rubrospinal tract |
||
|
c. Tectospinal tract |
||
|
d. Both A and B |
|
a. Pulling your elbow away when you bang it against the table |
||
|
b. Lifting your arms when given an unexpectedly heavy book |
||
|
c. A knee jerk when the doctor taps just beneath your knee cap |
||
|
d. All of the above |
|
a. Premotor cortex |
||
|
b. Primary mortor cortex |
||
|
c. Frontal lobe |
||
|
d. Both A and B |
|
a. A chemical synapse |
||
|
b. An electrical synapse |
||
|
c. Both A and B |
||
|
d. None of the above |
|
a. Hippocampus |
||
|
b. Temporal lobes |
||
|
c. Thalamus |
||
|
d. All of the above |
|
a. 3 |
||
|
b. 4 |
||
|
c. 5 |
||
|
d. 6 |
|
a. Sympathetic |
||
|
b. Parasympathetic |
||
|
c. Enteric |
||
|
d. All of the above |
|
a. Amygdala |
||
|
b. Formix |
||
|
c. Cingulate gyrus |
||
|
d. Parahippocampal gyrus |
|
a. 2 |
||
|
b. 3 |
||
|
c. 4 |
||
|
d. 5 |
|
a. Aphasia is the inability to move the muscles of the mouth, tongue, larynx, and pharynx for speech. |
||
|
b. Aphasia is the inability to comprehend or produce language. |
||
|
c. Aphasia is the inability to recognize different textures. |
||
|
d. Aphasia is the inability to recognize different tastes. |
|
a. Facts |
||
|
b. Events |
||
|
c. Skills and habits |
||
|
d. Both A and B |
|
a. Stimuli perceived on the right side is interpreted by the left hemisphere and vice versa. |
||
|
b. Both hemispheres are needed for a stimuli presented on the right to be described in vocal words. |
||
|
c. Both A and B |
||
|
d. None of the above |
|
a. Cognition is a function of association cortices. |
||
|
b. Association cortices receive and integrate information from a variety of sources. |
||
|
c. Two functions of association cortices are stimuli identification and the planning of appropriate behavioral responses to those stimuli. |
||
|
d. All of the above |
|
a. Cerebral cortex |
||
|
b. Insula |
||
|
c. Central sulcus |
||
|
d. None of the above |