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69 Cards in this Set

  • Front
  • Back

Concentration of ions (K/Na/Ca/Cl)

Out:In


K/ 1:20


Na/ 10:1


Ca/ 10000:1


Cl/ 12:1

Pacinian Corpuscle

Sense vibration

Ruffini Endings

Responds to skin stretch

Free nerve endings

Pain and temperature

Meissner's Corpuscle

Flutter and stroking movements

Merkel Receptors

Sense steady pressure and texture

Mechanoreceptors


Adaptation & Receptive field

Diameter of 4 axons thickness

group 1: Aalpha:


13-20 micrometers/ 80-120 m/s


used for proprrioception



group 2: Abeta:


6-12 micrometers/ 35-75 m/s


used for mechanoreceptors



group 3: Adelta:


1-5 micrometers/ 5-30 m/s


used for pain/temperature



group 4: C:


0.2-1.5 micrometers/ 0.5-2 m/s


used in temperature, pain, itch

Dorsal Column-Medial Lemniscal Pathway?

This is the major route for touch and proprioceptive sensations ascend to the cortex

Lemniscus?

Means a band of white nerve fibers in the brain

Damage to posterior parietal cortex

(association area essential for perception of spatial perception of sensation)


leads to Tactile Agnosia: can't recognized objects by feeling them

Retinal cells

Retinal Layers

Cellular pigmented epithelium

Phototransduction in Rods

Depolarization in the dark: dark current (cGMP-gated Na+ channel)


Hyperpolarization in the light


Rhodopsin: Opsin + Retinal


Opsins are receptors that activate by light causing a conformational change on Retinal (11-cis to all-trans)

3 Opsins in Cones

Red, green and blue

What NT is secreted in the dark

Glutamate as a result of depolarization of cells in the dark


go on to depolarize IPL of bipolar cell, then OPL of them onto ganglion cells which generate an AP

2 kinds of Bipolar cells

ON: respond to Glutamate by hyperpolarizing (light ON at the center)


,so depolarized when light is on


OFF: respond to Glutamate by hyperpolarizing (light OFF from the center)


,so depolarized when light is off

Example of direct and indirect pathways

Retinal Processing picture

"PhBAG"


Photoreceptors -> (Horizontal) -> Bipolar -> Amacrine -> Ganglion

Purpose of on/off ganglion cells

Detect differences in illumination in a receptive field

Best stimuli for an on/off ganglion cell

light/dark center pattern


(They are sensitive and responsive to contrast!)

integration of presynaptic inhibition

3 major types of great ape ganglion cells

P (Parvo) - Type: 90%


M (Magno) - Type: 5%


nonM-nonP (K-type): 5%



some P and K type cells are color-sensitive ganglion cells


(color-opponent center-surround receptive field)

Mechanoreceptors

M-type cells

-Lack of color opponency


-do not send color info to brain


-large receptive field


-respond and adapt fast


*motion detection, but low-resolution image

P-type cells

-color-opponency


-sends color info to brain


-response has no adaptation


-conduction speed is slower than M-type


*Object shape and color detection, with detailed images

K-type cells

-color-opponency


-sends color info to brain


-contributes to color vision


*physiological properties not yet clear

Parallel Processing

Simultaneous input from 2 eyes


for depth and distance


info about light and dark (On/Off ggl. cells)


different receptive fields and properties of retinal ggl cells (M/P/K type)

Nonthalamic Targets of the optic tract (3)

Hypothalamus: biological rhythms like sleep and wakefulness



Midbrain's pretectum: size of the pupil



Midbrain's Sup. Colliculus: visual reflexes, tracking, or reading left to right for example

Superior colliculus

receives 10% of optic fibers, and is involved in Saccadic eye movements and attention

2 visual systems

Primitive


(eye and head movements, reaching hands and other simple behaviors)



Mammalian


(Speech and thinking in words: consciousness, and other complex behaviors)

damage to each visual system

to primitive: person is not aware of vision


to mammalian: abolishes perception

Segregation of eye input by ganglion cell types in LGN

Receptive fields of LGN

Retinotopy

Map of the visual field onto a target structure:


Retina -> LGN -> striate cortex



perception here is related to the brains interpretation of distributions of neural activity, not a snapshot of reality

Gen features of cerebral cortex

Anatomy of striate cortex

Simple Cells

analyze shape, are orientation-selective, but not very sensitive to color

Complex cells

detect movement and not color regardless of position in the receptive field

Hypercomplex cells

Has stopping properties in larger receptive fields

Dorsal stream

Part of interconnected systems in the visual cortex involved in perception of spatial locations, visual disparity (depth) and movement

Ventral stream

anatomical pathway for perception of form and color

Damage in the MST


(of dorsal stream)

leads to "snapshot vision" of motion perception

Magnocellular LGN neurons project to

layer IVC-alpha

Parvocellular LGN neurons project to

layer IVC-beta

Koniocellular LGN axons bypass

layer IV to make synapses in layers II and III

basis of stereopsis

-binocular disparities for depth perception


-layer IVC innervates binocular neurons in superficial layers

What are receptive fields of the striate cortex

-input of K cells to II, III


(Koniocellular in LGN)


-input of M cells to IVC-alpha


(Magnocellular in LGN)


-input of P cells to IVC-beta


(Parvocellular in LGN)

Cortical receptive fields physiology

Layer IVCalpha: insensitive to the wavelength


Layer IVCbeta: center-surround color opponency


Outside IVC: not center-surround



(found upon Hubel and Wiesel's work in the 60's that won them a nobel prize in 1981)

Orientation selectivity

orientation-selective neurons where layers II to VI have the same orientation selectivity for vertical outlines

What is the great impact of Hubel and Wiesel to neurobiology?

1) ocular dominance columns


2) describing how visual signals are processed by the brain to generate edge detectors, motion detectors, stereoscopic depth detectors and color detectors: building blocks of the visual scene



(Detection of lines or bars of the simple cell)

Direction selectivity

some neurons fire AP's more strongly to a bar moving to one specific direction

Simple cell picture

Hypercomplex cells

exhibit end stopping properties:


when a cells response increases as a stimulus expands to fill the receptive field, and then responds less when the stimulus exceeds the size of the receptive field

3 classes of cells in V1

building blocks of the visual scene:



simple cells (line/bar/edge detectors)


complex cells (orientation detectors)


hypercomplex cells (patterns/length/corners/angle detectors)

Color blobs of the striate cortex

are cytochrome oxidase mitochondrial enzyme in cell metabolism, which receive input from K-cells of the LGN for color as well as some P and M LGN neurons

Blob cells

-are color detectors (light wavelength-sensitive)


-monocular, no orientation, no direction selectivity

***3 parallel pathways to visual cortex

A cortical module

2 by 2 block in V1 of striate cortex containing ocular dominance columns, orientation columns, and color blobs to fully analyze a portion of the visual field

Steps of hearing

Dorsal Stream

A system of interconnected regions of visual cortex involved in the perception of spatial locations, visual disparity (depth) and movement, beginning with the striate cortex (primary) and ending with the posterior parietal cortex by way of extrastriate cortex.


Receiving projections mostly from M-cell pathway

Ventral Stream

A system of interconnected regions of the visual cortex involved in the perception of form (3D object) amd color, beginning with the striate cortex and ending with the inferior temporal cortex by way of the extrastriate cortex.


Receiving projections mostly from P cell and blob pathways

receiving projections of dorsal stream

Mostly from M cell pathwaya

receiving projections of ventral stream

mostly from P cell and blob pathways

Achromatopsia

caused by damage to area V4 (part of Ventral stream)


leading to partial or complete loss of color vision as well as shapes of objects (color cone receptors in the retina are normal)

Area IT

is the major output of V4 and responds to a wide variety of colors and abstract shapes, like faces and hands

damage to ventral stream

leads to inability to recognize objects. faces, textures or colors.


although they can still perceive movement


so can see form from motion, so patients with this visual agnosia can recognize their friends by the way they walk

"Where" and "What" streams

Where: dorsal stream (M-ovement)


What: ventral stream (P-erception)