1/75
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
medial longitudinal fissure
separates the right and left cerebral hemispheres
transverse fissure
separates the cerebellum and the cerebrum
cruciate/ansate sulcus
separates the frontal and parietal lobes in sheep brain
central sulcus
separates the frontal and parietal lobes in the human brain
lateral sulcus
separates the temporal lobe from the other cerebral lobes
frontal lobe
motor function, language production, personality, working memory, higher-order thinking
parietal lobe
somatosensation
occipital lobe
primary visual perception
temporal lobe
primary auditory sensation, language comprehension
insula lobe
taste, pain, interoception
limbic lobe
emotion, memory, olfaction
midbrain
stimulus orientation and auditory perception
pons
acts as a bridge between the cerebellum and the brain stem
medulla
responsible for life functions such as breathing, HR, BP, reflexes and sleep
cerebellum
motor memory and coordination, posture, balance
spinal cord
neuron axons that carry sensory and motor information
cerebral peduncles
communication pathways between the brain stem and the cerebrum
infundibulum
facilitates communication between the hypothalamus and the pituitary gland
pituitary gland
endocrine gland that contributes to the maintenance of homeostasis by influencing growth, metabolism, and reproductive processes
trapezoid body
helps determine the spatial direction of sound
pyramidal tracts
contain motor fibers that carry information for muscle movement
optic chiasm
crosses visual field information to corresponding hemisphere so that it is processed into a single image
optic tracts
carry contralateral visual field information to the lateral geniculate nucleus
mammillary bodies
emotion and memory
rhinencephalon
olfactory processing center
pyriform area/lobe
smell perception
olfactory tract
connects the olfactory bulbs to the cortex for processing smells
rhinal fissure
separates the pyriform area of the rhinencephalon from the rest of the cerebrum
dura mater
physically protects the brain
arachnoid mater
contains CSF and filters it back into the blood
pia mater
maintains the blood-brain barrier
cingulate gyrus
involved in emotion, learning, and memory
hippocampus
learning, memory, spatial orientation/navigation
fornix (and fimbria)
transmits information from the hippocampus to the mammillary bodies
hypothalamus
maintains homeostasis by regulating hormones, body temperature, and appetite/thirst; involved in emotion and memory
thalamus
relays sensory and motor information to the cerebrum
lateral ventricles
produce, circulate, and store CSF
3rd ventricle
produce, circulate, and store CSF
cerebral aqueduct
produce, circulate, and store CSF
4th ventricle
produce, circulate and store CSF
corpus callosum
connects the left and right cerebral hemispheres
pineal body
secretes melatonin that plays a role in the sleep-wake cycle
superior colliculus
responsible for visual orientation to stimuli
inferior colliculus
responsible for auditory perception
internal capsule
relays information between the putamen and the caudate nuclei of the basal ganglia
corona radiata
carry sensory and motor information between the cerebrum and the brain stem
caudate nucleus
part of the dorsal striatum of the basal ganglia which is involved in initiating movement, suppressing unwanted movement, reward, and motivation
putamen
part of the dorsal striatum of the basal ganglia which is involved in initiating movement, suppressing unwanted movement, reward, and motivation
sheep vs. human CNS
smaller cerebral cortex in sheep
sheep spinal cord extends posteriorly (quadrupedal), human spinal cord extends inferior (bipedal)
nervous system adapted to these forms of movement over evolutionary time
larger olfactory bulb to cerebrum size ratio in sheep
processing smells in environment more important for sheep than humans
less prominent temporal and occipital lobes in sheep
humans have better vision, and language and emotion processing than sheep
both have sulci and gyri
larger surface area of neural tissue in both animal cortexes
cerebrospinal tract (CST) pathway
primary motor cortex (located in pre-central gyrus) → cerebral peduncles in the midbrain → pyramids in the medulla → spinal cord → upper motor neurons → lower motor neurons → skeletal muscle fibers → voluntary movement
cerebrospinal fluid (CSF) flow
choroid plexus in lateral ventricles produces CSF → 3rd ventricle where more CSF is produced → cerebral aqueduct → 4th ventricle where even more CSF is produced → some through central canal of spinal cord, most into subarachnoid space → arachnoid granulations → dural sinuses → blood
mouse spinal cord sections
ventral horns have large motor neuron cell bodies in them
ventral horns look larger in the lumbar sections because more motor neurons are needed to innervate the lower limbs since they contain lots of musculature
less white matter in sacrum and coccyx sections because most axons exit the spinal cord in prior sections
white matter (outside) = oligodendrocytes that produce myelin for axons in CNS, grey matter (inside) = cell bodies
PowerLab
an analog-to-digital converter, meaning that it takes a continuous and smooth analog signal input and converts it into a discrete digital signal output that is easier to interpret in the Lt software
PowerLab input
input sensors- responsible for collecting physiological data and transferring it to the PowerLab hardware in the form of an electrical, analog signal
pulse transducer- detects changes in pressure from the pulse of the finger and converts that information into an electrical analog signal that serves as input for the PowerLab hardware to convert into a digital signal that is ultimately used by the Lt software to calculate heart rate
bioamplifier- measures and magnifies the amplitude of small physiological voltages
Bio Amp cable- brings afferent information to the Powerlab
Powerlab output
stimulating bar electrode- used to deliver a stimulus to a nerve or muscle
sampling rate
how many times per second an analog signal is sampled to create a digital signal
ECGs are typically 1000 samples per second while slowly changing signals like breathing are typically 200 samples per second
motor unit
a group of muscle fibers that is innervated by a single LMN
large muscles have multiple motor units and thus multiple LMNs innervating them
neuromuscular junction (NMJ)
facilitates neurotransmitter release and binding that leads to muscle contraction
AP reaches the synapse → calcium ions enter pre-synaptic neuron terminal and bind with synaptic vesicles → ACh is released into the synaptic cleft and diffuses across it → ACh binds with nAChRs → nAChRs open → sodium ions enter and depolarize the postsynaptic muscle cell → calcium ions are released into the muscle cell cytoplasm from the SR → muscle contraction → acetylcholinesterase breaks down ACh remaining in cleft
disorders affecting muscle contraction
amyotrophic lateral sclerosis (ALS), myasthenia gravis, botulism, and muscular dystrophy
amyotrophic lateral sclerosis (ALS)
progressive degeneration of motor neurons
DNA-binding protein dysfunction that results in its mislocalization and aggregation that leads to degeneration
can affect both the CNS (UMNs) and the PNS (LMNs)
myasthenia gravis
an autoimmune disorder in which antibodies attack nAChRs on muscle cells making it difficult for muscle contraction to occur
causes facial drooping, muscle weakness, fatigue
botulism
involves the neurotoxin botulinum A that causes muscle paralysis by entering the presynaptic neuron terminal of NMJs and preventing the formation of synaptic fusion complexes so that ACh is not released into the synaptic cleft and muscle contraction does not occur
muscular dystrophy
genetic condition caused by a gene mutation that makes muscle fibers leaky to calcium ions resulting in excess intracellular calcium ion concentration that damages the mitochondria of muscle cells which leads to muscle cell death and muscular atrophy
surface EMG measure and analysis
use electrodes placed on the skin over the muscle of interest to detect the electrical activity produced when the muscle is activated → Bio Amp carries electrical analog signal from electrodes to PowerLab hardware → bioamplifier amplifies the analog signal → PowerLab converts analog signal into digital signal that is displayed in the Lt software as a waveform
an EMG can be analyzed based on the timing of contractions versus relaxation, the pattern of motor unit recruitment, and the amplitude of its resulting waveforms which reflects the strength of contractions
increase in amplitude when force of contraction increases because more motor units are recruited to increase contraction → more motor neurons firing → more electrical activity detected
electromyography (EMG)
EMG is a technique that measures the electrical activity of skeletal muscles
EMGs are recorded either using surface electrodes placed on the skin or needle electrodes inserted into the muscle through the skin
EMGs represent the overall electrical activity of the different motor units within the muscle
stronger EMG signal = more motor units firing
root mean square (RMS)
square each voltage value so they are all positive → average together the squared values → take the square root of that average
quantifies the overall magnitude of the EMG signal which provides an estimate of muscle activation → higher RMS = larger EMG signal = greater muscle activation and vice versa
muscle coactivation
contraction of an agonist (primary muscle) results in minor activity in the antagonist (opposing muscle)
thought to help stabilize joints
biceps contraction has a large amplitude EMG signal paired with a small amplitude EMG signal from the triceps
surface vs. intramuscular EMG
surface EMG
records the overall electrical activity of the muscle
limited application in clinical settings but can be used for performance analysis and monitoring of muscle activation
less accurate, more general information
can be affected by presence of adipose tissue
non-invasive but restricted to superficial muscles
intracellular EMG
records the individual electrical activity of a motor unit within a muscle
produces consistent and accurate information useful for clinical diagnosis
invasive
biopotentials
voltages produced by physiological processes that involve excitable cells (i.e. muscle contraction or nerve stimulation)
compound action potential (CAP)
the sum of the action potentials recorded from a whole nerve that contains numerous nerve fibers
represents the overall electrical activity of an entire nerve
compared to an individual action potential from one nerve fiber
shape does not correspond to the form of a single intracellular AP recording (monophasic)
artifact a result of current that spreads passively through water contained in tissues
recorded by using two external electrodes (1 reference, 1 recording) that measure the changes in polarity between them as the signal passes beneath them (+ then 0 then - → biphasic)
low signal strength (2-4 mV CAP vs. 80-100 mV AP)
evoked EMG
an evoked EMG because stimulated nerve to cause it to fire CAPs and then also recorded EMG
different from previous lab because recording electrical activity of an intentionally stimulated nerve over milliseconds versus recording electrical activity of a voluntarily activated muscle over seconds
as nerve stimulation increased, the evoked EMG amplitude increased until reaching a maximum response where it stopped increasing
amplitude determined by the number and frequency of nerve fibers firing
maximum response reached when all nerve fibers are firing at their highest possible frequency
at lower levels of stimulation myelinated fibers that are larger in diameter and have a higher NCV are stimulated first
greater diameter = lower internal resistance = current spreads more easily and more quickly through axon = lower stimulation threshold so recruited first
myelination = higher membrane resistance = less current leakage = current spreads farther
nerve conduction velocity
the rate at which an AP travels along a nerve
impacted by axon diameter (determines internal resistance, lower = higher NCV) and myelination (determines membrane resistance, higher = higher NCV)
calculated by comparing distance traveled to time it took to travel that distance
stimulation spot at elbow distance from stimulation spot at wrist / latency of elbow - latency of wrist
earthworm median and lateral fibers
earthworms have a ventral nerve cord that contains a median giant nerve fiber and two lateral giant nerve fibers that lie on either side of the medial giant nerve fiber as well as segmental sensory and motor fibers that do not run along the complete length of the animal
“giant” because they achieve speed via their large diameter rather than via myelination
each giant fiber is made up of individual cells (1 per segment) that are electrically coupled through gap junctions → rapid conduction of APs from cell-to-cell behavior of a single continuous fiber
lateral fibers are extensively linked to one another via cross-connections so behave like a single fiber
allow the earthworm to respond rapidly to threatening situations with a variety of escape behaviors
earthworm APs recording
same extracellular recording set-up as PNS function lab except this specific set-up is measuring the evoked EMG of a single nerve fiber versus a whole nerve, so APs are all-or-nothing and not graded CAPs
recording set-up
reference (-) electrode followed by recording (+) electrode
differential amplifier used to amplify the small changes in voltages between the two electrodes
depolarization under reference electrode = positive inflection, depolarization under recording electrode = negative deflection, no difference between membrane potential under electrodes = zero deflection → biphasic
extracellular recording so cannot determine exact membrane potential of nerve fibers only if they fired an AP or not
electrodes placed closer to the nerve likely to have a higher amplitude, reversing electrodes (recording then reference) would flip polarity of biphasic signal (- then +), and increasing distance between stimulating and recording electrodes increases latency
ground electrode helps to reduce electrical interference called “noise” from the recording equipment and from the environment
stimulating set-up
red cable (+ anion) anterior to black cable (- anion)
ground cable connecting to mat worm is on
determining earthworm measurments
threshold is determined by gradually increasing strength of stimulus until an AP occurs
affected by myelination, nerve diameter, membrane properties (differences in membrane potential, ion channel distribution)
different from worm to worm due to fiber distance to electrode and tissue condition
latency determined by measuring time it takes AP to occur after stimulation has occurred
affected by NCV (higher HCV = lower latency) and distance between stimulator and recording electrodes
different from worm to worm due to NCV differences
nerve conduction velocity is determined by comparing distance traveled by signal to electrode with latency
affected by axon diameter, myelination, temperature, tissue condition, membrane properties
different from worm to worm due to nerve fiber diameter, temperature, tissue condition, and accuracy of electrode placement and distance measurements
refractory period is determined by decreasing time in between two stimuli until only one action potential occurs instead of two → absolute refractory period when impossible for another AP to occur
bidirectionality and orthodromic direction
bidirectionality shown in lab by eliciting an AP from the medial giant fiber in both the orthodromic and antidromic directions
orthodromic direction is determined by the anatomical connections of neurons and their normal function (i.e. the medial giant fiber in earthworms controls reflex response of head so propagates anterior to posterior)