| 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 |