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Neurotest 22002 Feedback
Neurotest 22002 Feedback
Neurotest 22002 Feedback
This question is asking how light energy is tranduced (changed) into chemical
energy. Transduction of energy is the function of a receptor, so you would need to
discuss this.
The rods contain a photosensitive compound called rhodposin (visual purple) that
changes its configuration (structure) in response to light energy. Rhodopsin is made
up of an opsin (protein) called scotopsin and 11-cis retinene 1. The action of light is to
convert the 11-cis retinine1 to the all-trans configuration. (A diagram would be useful
here). This results in the separation of the retinene1 and the scotopsin (bleaching).
The shape of the rhodopsin molecule has now changed (Your books go in to more
detail; that is great if you include it, and it certainly does impress me). The change in
the shape of the rhodopsin activates a G-protein called transducin (G t). The
transducin in turn activates the enzyme cGMP phosphodiesterase. This enzyme
normally breaks down cyclic GMP into an inactivation product called 5-GMP. The
function of cyclic GMP is to keep sodium channels open, so that sodium ions can
flow into the cell, causing the inside to be more positive than the outside
(depolarisation). The action of the phosphodiesterase is to lower cGMP, thus
causing a reduction in the number of open sodium ion channels. This causes less
sodium to enter the cell, and result sin hyperpolarisation. Less transmitter substance
is produced which ultimately leads to ganglion cell depolarisation and neural
impulses reaching the brain.
This requires no interpretation to answer. The trick with these questions is to start in
a logical sequence. The best sequence would be receptor – sensory pathways –
cortical areas – interpretation. Smell is different in that the olfactory glomeruli also
play an important role in detection of smell.
The olfactory receptor cells are located in a specialised portion of the nasal mucosa
called the olfactory mucous membrane. This membrane is comprised of 3 cell types,
the supporting cells, the receptor cells, and progenitor cells. The supporting cells
ensure optimal functioning of the receptor cells, and the progenitor cells can develop
into new receptor cells. Each receptor cell has a dendrite that projects into a layer of
mucus that is produced by Bowman’s glands. The receptor cells are neurones that
regenerate in a carefully regulated process. One of the regulatory proteins is bone
morphogenic protein. This protein inhibits this process. The axons of the receptor
cells pierce the cribiform (the spelling of this was varied!) plate of the ethmoid bone
and enter the olfactory bulbs. In the olfactory bulbs, the axons of the receptor cells
synapse with the dendrites of the mitral and tufted cells in complexes called olfactory
glomeruli. The olfactory bulbs also contain periglomerular cells and granule cells.
These cells are important in the process of lateral inhibition. If one olfactory
glomerulus is stimulated, it excites a periglomerular cell which in turn inhibits other
olfactory glomeruli. If a tufted or mitral cell is stimulated, these cells stimulate
granule cells which in turn inhibit lateral branches of the mitral and tufted cells. This
process is called lateral inhibition and serves to sharpen the sensory input to the
olfactory cortex. Axons of mitral and tufted cells pass through the intermediate and
lateral olfactory stria to the olfactory cortex. This is located in the lateral and anterior
orbitofrontal gyri of the frontal lobes. The representation is asymmetrical with greater
representation on the right. There are also fibres that project to the amydala which
deals with the emotional connotations of smell. Fibres also project to the entorhinal
cortex which is concerned with memories associated with smell.
The olfactory receptors can only respond to odours that are dissolved in the mucus
and close enough for detection. There are 10 000 different odours that can be
distinguished by humans, yet there are only 1000 different types of odourant
receptors. There is thus a mechanism in addition to odourant receptors involved in
smell detection. Determination of odour intensity is weak in humans with a 30%
change in concentration of an odour required in order to sense a change in smell
intensity. Smell direction can be localised, due to a time difference in the odour
reaching the nostril. Smell adaptation is well developed, normally specific for a
specific smell. All of the odourant receptors activate a G protein. Some increase
cyclic AMP inside cells, others increase DAG and IP3. The net result is either
opening of sodium or calcium channels that cause depolarisation and initiation of an
action potential. The olfactory glomeruli play an important role in feature detection.
Each OG receives input from only one type of receptor cell, but many odours can
stimulate a certain type of receptor cell and a single odour can be detected by many
different receptor cells. Any one odour can thus activate a different set of OG’s
which ultimately leads to smell detection.
You should also include a word or 2 on sniffing, irritant pain reflexes, and the smell
abnormalities. I also mentioned odourant binding proteins for example. There is
plenty to write an essay on!
Multiple choice answers: Some of the wording may be slightly different to the
final test version, but this does not change the context.
Question : Slowly adapting touch receptors include
Merkel’s disks T
Ruffini endings T
pacinian corpuscles F (rapidly adapting)
Meissner’s corpuscles F (rapidly adapting)
golgi tendon organs F (not touch receptors)
the sense organs for cold are Ruffini endings F (naked nerve
endings)
the sense organs for warmth are Krause’s end-bulbs F(naked nerve
endings)
naked nerve endings are touch receptors T
naked nerve endings are pain receptors T
pressure is sustained touch T
baroreceptors T
pain receptors T
the majority of touch receptors F (most are phasic)
pacinian corpuscles F (phasic)
muscle spindles T
first order neurones mediating cold synapse in lamina I of the dorsal horns T
second order neurones from the nucleus gracilis relay to the thalamus T
second order neurones from the nucleus cuneatus transmit pain sensations F
(fine touch, proprioception etc.)
primary afferent neurones mediating fine touch terminate in the medulla T
secondary afferent neurones mediating warmth sensations cross the mid-line at the
level of the medulla F
(they cross the midline at the level of entry into the spinal cord)
Questions : Sectioning of the right half of the spinal cord at the level of the first
thoracic segment (T1) will result in loss of
SI T
the cingulate gyrus T
the insular cortex T
the reticular system T
the periaqueductal gray T
the cornea is responsible for most of the refractive power of the eye T
a dioptre is a measure of the refractive power of a lens T
accommodation is a process that reduces the curvature of the lens F
(increases curvature)
myopia can be treated using biconvex lenses F
(biconcave)
presbyopia is common in teenagers F
(onset after 40)
the left optic nerve contains fibres that originate in the right nasal hemiretina F
(left optic nerve comes form the left eye only)
the right optic tract contains fibres that originate in the left temporal hemiretina F
(left nasal)
pituitary tumours normally result in homonymous hemianopia F
(heteronymous)
each optic tract subserves half of the field of binocular vision T
heteronymous hemianopia can be caused by destruction of fibres form both nasal
hemiretinas T
afferent neurones that innervate hair cells in the organ of Corti form the auditory
division of CN VIII T
the fibres in the auditory division of CN VIII terminate on the dorsal cochlear nucleus
T
auditory impulses pass via the lateral geniculate body to the auditory cortex F
(medial geniculate – lateral is for vision)
information from both ears converge on each superior olive T
the primary auditory cortex is located in the frontal lobe F
(occipital lobe)