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NATS 1860 2nd Semester Midterm Exam.docx

8 Pages

Natural Science
Course Code
NATS 1860
Keith Schneider

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NATS 1860 2 nd Semester Midterm Exam Information Brain Framework: - We have sensory inputs (vision, hearing, and touch) that feed the inputs into higher brain areas that make decisions, store them into memory and have them function for other uses. - In the case of light, light enters our eye, that then follows to the visual cortex, that then goes into the planning and decisions and is interchangeable to the working memory that can then be used for long term memory and emotions or motor control o The same process occurs with Ears in terms of the auditory cortex and skin in terms of the somato cortex. Sensory and Motor Maps: - These are two-dimensional surfaces that are developed through electric brain stimulation in order to figure out which locations do which actions - These maps are all distorted in the sense that they represent how much neural activity is coming or going from rather than the physical area of the body - Neurons are one nerve cell whereas some nerves typically have millions of connections to other nerve cells o Axons are the main part of the nerve cell that come out of the nerve cell and connect at synapses with other cells.  Axons originate at axon hillocks which are small protrusions of the soma o Soma is the body of the nerve cell where axons come from and dendrites enter (or leave)  In order to measure cell activity, you insert an electrode into the soma o Dendrites and axons have different functions from the nerve cells o The Dendrites and Axons are how the nerve cell dispatches and receives its information. - Neuron membranes are made from two layers of lipid molecules o One layer seeks water, and the other layer avoids water.  Large protein molecules form channels through the membrane.  Channels open and close to let particular ions through. Spikes and Action Potential - This occurs when there are the proper conditions for cells to release and break through their chemical from outside of the cell to the inside of the cell - This is done through an aspect of ionic charge and forces o The diffusion force occurs when there is a higher to lower concentration o Once there is an equilibrium of negative and positive charges, the cell returns to norms - The two ions used for spikes are Na+ and K+ (Sodium and Potassium) o Na+ is outside of the cell o K+ is inside of the cell - Depolarization occurs when there is a higher amount of positive charge within the cell than there is negative o This occurs when the ionic channels of the cell open and allow the outside Na+ to flow into the cell, causing a diffusion of cells and sending out a spike (Action Potential)  The action potential occurs because of a created threshold.  A cell can fire a maximum of 300 spikes per second. o When the cell reaches threshold, the Sodium channels open, allowing sodium to enter the cell and depolarize it.  Afterwards, the channels for sodium close and the channels that allow potassium to leave open. The reduction of potassium allows the cell to balance out  Finally, the cell is ready to be fired again. - Hyperpolarization occurs when the cell flows K+ out, however is not replenished with enough Na+. When this occurs, there is no reaction in the cell. - Spikes are the same size, and the only thing that differs is how often the spikes are fired, which depends on the amount of stimulation on that specific cell. o The spikes travel down from the axon to the synapses.  It starts from the bottom, travels through the axon, and goes up. o Each spike lasts about 1ms and cannot be fired for another 2ms o Humans require myelin for proper function of spikes in the sense that myelin helps spikes jump from one gap to another. - Once the action potential goes through, it latches onto the dendrites or somas of other bodies. o Synapses contain neurotransmitters that signal our brain when the action potential comes into contact.  GLU (Glutamate) is an important neurotransmitter that opens sodium ion channels in order to open sodium ion channels  This causes EPSP (Excitatory Post-Synaptic Potential) in which the spikes are generated at the cell body and transferred up the axons.  EPSP adds electrodes  GABA (Gamma acid) is the important neurotransmitter that opens potassium channels in the post-synaptic neuron  This allows to hyperpolarize the cell and causes IPSP (Inhibitory Post-Synaptic Potential)  IPSPs subtract from ESPS  If EPSP subtracted by IPSP still results in the depolarization to threshold (more positive than negative in the cell) a spike will be fired o Spikes cause calcium to flow out of the synapses and send signals to the brain - Excitation and Inhibition is present everywhere in the brain where one cell re-excites another cell and this relies on constant cooperation within the brain Photoreceptors and the Retina - The blind spot is where the nerve exits – the retina is at the back of the eye and is organized backwards. - Neurons get stimulated by light: o Photoreceptors are specialized neurons that have proteins in their membranes (photopigments) that evolved to capture photons of light in such wavelength that we can see - We have Rods and Cones: o Rods are specialized for night vision in the sense that they’re sensitive to light, but do not code for colour o Cones are used for seeing daytime vision in term of brighter intense sensitivity to light.  50% of cones are red  45% of cones are green  5% of cones are blue o Colour blindness occurs when there is a certain amount of cones defective or missing  Largely females are responsible for transferring colour blindness and males more commonly have colour blindness (since CB is a hereditary disorder with the X)  People with colour blindness aren’t blind to colour, they simply cannot discriminate against them. - M and P Ganglion Cells o These cells deliver all of their information through a chiasmic method – right side of the primary visual cortex from the left side of the receptive field, and vice cersa o These are the photoreceptors that connect to other cells. They send their axons out of the retina and into the brain. o M cells are for motion, they have a larger receptive field, have bigger cells, and respond to a larger area on the retina  They respond to the intensity of light, but do not carry colour information. They’re active on both rods and cones and can carry information both during the day and night  M cells have low resolution, but have a higher response rate.  This is because we need faster response to motion than to details to avoid predators o P cells (Pattern) have very small receptive fields, are usually smaller than M cells, but have very high detail in imprinting pagers.  They carry colour information, and because of this are good for high spatial resolution. However, because of that information it usually takes longer for that information to reach the brain. - Receptive fields are the area (both inhibitory and excitatory) of a retina that determines how much action potential the ganglion cells send out from the retina to the brain o Receptive fields are marked blue for inhibitory and red for excitatory. o M cells have a larger receptive field than P cells. o Therefore, when there is light hitting only the red zone, there will be more action potential than if light hits both excitatory and inhibitory.  This is due to the competition of depolarization and hyperpolarization between the two areas. o Cone adaptation is a result of viewing one colour for a long period of time, resulting in inversion (our retinas making up for the loss of light)  This is a result of cells fatiguing due to an ionic imbalance, and thus ceasing to fire as strongly - The Retina delivers its information through the ganglion cells from the visual point to the cortex at the back of the brain. o The information goes to the V1 (first visual area of the cortex) Visual Cortex and Orientation - Cells respond to specific orientations based on where the excitatory zones line up and have the light shined on them. o Therefore, a specific orientation will result in the greatest amount of action potential.  In vertical aligned retinal cells the best excitation will occur from a rectangular light, for vertical – vertical, etc. - Orientation cells sense bars, lines, and edges. - There are 12 different orientations represented in V1 that detect specific lines in order to transfer them to further areas of the visual field that eventually builds an image in the brain o Our brain reorganizes information based on vertical and horizontal lines. - Motion Selective V1 Neurons come in the form of MT cells that gather their information from M cells o They respond to a particular direction of the object-motion-path  Each of these cells have a preferred direction  If the motion direc
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