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 ![]() |