Chapter 14 Sensory Processes Flashcards

1
Q

Sensory Receptor Cell Properties

A
  • Sensory receptor cells are specialized cells that transform a stimulus energy into a neural signal
  • Receptors on sensory cells are sensitive to specific modalities
  • Receptors send signals which are amplified in the cell
  • The sensory cell’s output goes to the CNS

3 examples of different sensory modalities:

  • sound (bell ringing)
  • light (light bulb)
  • taste (skunk)
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2
Q

Sensory Receptor Classification

A

Primary function

  1. Exteroreceptors- external environment
  2. Interoreceptors- internal environment (homeostasis)
  3. Proprioceptors- position of the body in space

Receptor type

  1. Mechanoreceptors
  2. Photoreceptors- photons of light
  3. Chemoreceptors- chemical and olfaction
  4. Thermoreceptors- body temperature
  5. Nociceptors- pain
  6. Electroreceptors- electrical field (non humans)
  7. Magnetoreceptors- magnetics fields
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3
Q

Sensory Transduction

A

The process of converting stimulus energy into the energy of a nerve impulse

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4
Q

Intracellular Events in a Receptor Cell

A

Generator potential-when the receptor potential spreads to a spike initiating zone and generates an action potential

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5
Q

Mechanoreception

A
  • Stretch-activated channels
    • Ion channels that can be opened or closed by stretching a cell membrane
  • open by tugging or stretching the cell membrane (cytoskeleton)
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6
Q

Mechanoreception: Crayfish Stretch Receptor

A
  • Tetrodotoxin (TTX) prevents the production of action potentials, but not receptor potentials(blocks voltage gated Na+ channels)
  • The receptor potentials are similar to EPSP’s
  • Dendritic cell membranes are sensitive to stretch and can produce graded receptor potentials
  • These are converted to APs in the spike initiation zone
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7
Q

Insect Mechanoreceptors

A
  • The surface of insect bodies are covered with sensory “bristles” (bristle sensillum)
  • The no mechanoreceptor potential C (NOMPC) receptor is activated as the bristle bends
    • Similar to a v-gated K+ channel, but not v-sensitive
    • ANK repeats are attached to the cytoskeleton
  • Most stretch-activated receptors are nonselective cation channels
    • Usually cause depolarization
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8
Q

Mammalian Mechanoreceptors: Touch

A

All touch receptors are dorsal root ganglion (DRG) cells

Channels responsible for transduction haven’t been identified

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9
Q

Mammalian Mechanoreceptors: Touch

A

DRG neurons have 5 types of endings in the skin

  1. Merkel disk
    • Most important for form & texture
    • 1 neuron goes to several disks
  2. Meissner’s corpuscles
    • 2-6 endings surrounded by myelin & collagen
  3. Paccinian corpuscles
  4. Ruffini endings
  5. Endings around hair follicles
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10
Q

Receptor Adaptation

A

Tonic Receptors

  • Adapt slowly, if ever
  • Muscle stretch & joint proprioceptors
  • ex: mocieptor, proprioceptor
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11
Q

Receptor Adaptation Continued

A

Phasic Receptors

  • Adapt quickly
  • On-off response
  • Tactile stimulus
  • can ignore the stimulus after awhile
  • ex: sense of touch
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12
Q

Crayfish Stretch Receptor Adaptation

A
  • Phasic receptors (above) only produce AP’s during the beginning of a stimulus.
  • Larger depolarizations may cause trains of multiple action potentials.
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13
Q

Mechanisms of Sensory Adaptation

A
  1. Mechanical properties may filter the stimulus. Common in mechanoreceptors
  2. The receptor molecules may “run-down.” Example: bleaching of photopigment
  3. Enzyme cascade may be inhibited by substance accumulation
  4. A change in the electrical properties. Example: increased intracellular Ca2+ levels
  5. The spike initiating zone may become less excitable.
  6. May take place in higher order cells in the nervous system
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14
Q

Vestibular organs & hearing

A
  • Vestibular organs can be used for equilibrium
    • Simplest organ is a statocyst
    • Vertebrates use a type of hair cell
  • Hearing
    • Detection of low frequency vibrations within the air, water, or substrate
    • Tympanal organ – most common insect form
      • Found in many locations
        • Thorax, abdomen, legs, labial palps
    • Vertebrates use hair cells
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15
Q

Organs of Equilibrium: Invertebrates

A

The lobster statocyst contains dense “statoliths” (made of sand or calcified secretions) which rest on hair cells connected directly to axons which go to the brain

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16
Q

Organs of Equilibrium: Invertebrates 2

A

These AP recordings from a single receptor in the statocyst epithelium show how firing rate changes when a specially-trained lobster performs a somersault

17
Q

Organs of Equilibrium: Vertebrates

A

Hair cells

  • Consist of stereocilia (a type of microvillus
    • Some non-mammalian species also have a kinocilium
18
Q

Organs of Equilibrium: Vertebrates 2

A
  • Hair cells
    • Movement may hyperpolarize or depolarize the hair cell
      • Produces a receptor potential
      • Alters neurotransmitter release
      • Regulates sensory neuron response
19
Q

Ear Diagram

A
20
Q

2 endolymph-filled inner ear chambers called the sacculus and the utriculus as well as the semicircular canals are the vertebrate organs of equilibrium

A
21
Q

Static equilibrium (up, down, left, right)

  • Sensed by hair cells within the macula of the sacculus and utriculus
  • Movement of mineralized otoliths bends the stereocilia, giving the animal positional information relative to gravity
  • Otoliths made of calcium carbonate
A
22
Q
  • 3 mutually perpendicular semicircular canals arise from the utriculus.
  • Movement of the head will cause endolymph to distort the hair-cell containing gelatinous cupula lining the inside of the semicircular canals thereby causing a receptor potential.
  • This gives the animal information about dynamic equilibrium.
A
23
Q

Vertebrate Hearing: The Cochlea

A
24
Q

Vertebrate Hearing: The Cochlea Continued

A
  • Cochlear cross-section shows 3 chambers (scala)
  • The hair-cell containing Organ of Corti sits on the basilar membrane of the scala media.
  • Birds: no organ of corti
  • Reptiles: no tectorial membrane
  • Amphibians: no tectorial/basilar membrane
25
Q

Vertebrate Hearing: The Organ of Corti

A
  • Vibration of the ossicles is converted to pressure waves in the perilymph which cause distension of the basilar membrane and deflection of cilia in the overlying hair cells
  • Inner hair cells responsible for audition
  • Outer cells responsible for amplification (electromotility)
26
Q

Vertebrate Hearing: The Organ of Corti Continued

A
  • Stretching the ciliary cell membrane opens ion channels causing receptor potentials.
  • The unusual ionic composition of endolymph means that K+ is a depolarizing ion in this situation.
27
Q

Vertebrate Hearing: Fish and Amphibians

A
  • Weberian apparatus transfers vibrations from the swim bladder to the inner ear
  • APs are generated by hair cells within the inner ear
28
Q

Chemical Senses: Taste and Smell

A
  • Chemoreceptor: the general term for sensory receptors in this family
    • Can be extremely sensitive: the male silkworm moth can detect the pheromone bombykol at concentrations of 1 molecule/ 1017th!
  • Gustatory receptors are taste receptors
    • Taste receptors are divided into 4 categories:
      • (1) sweet (2) sour (3) salt (4) bitter (5) umami
  • Olfactory receptors are smell receptors
    • There are hundreds of different types of olfactory receptors
    • Richard Axel and Linda Buck won the Nobel Prize in Medicine and Physiology for their discovery of olfactory receptors (2004)!
29
Q

The Vertebrate Taste Bud

A
  • The taste bud consists of the receptor cell, basal cells (which generate new receptor cells), and supporting cells
  • Transduction takes place across the apical membrane
  • Receptor cells synapse with afferent neurons which travel to the CNS
30
Q

Taste Bud and Nerve

A
31
Q

Mechanisms of Taste Sensations

A

Signal transduction of a generic gustatory cell

32
Q

Mechanisms of Taste Sensations Salty and Sour

A

Na+ travels through a Na+ channel causing direct depolarization of the apical membrane

H+ travels through cation channels, depolarizing the apical membrane. H+ ions block K+ channels and allow a slow depolarization from Na+ leaking into the cell

33
Q

Mechanisms of Taste Sensations: Sweet

A
  • Alanine (for sweet—like aspartame) works through a G-protein/cAMP-mediated mechanism to close K+ channels allowing for a slow depolarization.
  • Synthetic sweeteners like saccharine activate a receptor which works through phospholipase C to increase DAG and IP3
  • Arginine (for sweet) binds to a ligand-gated nonspecific cation channel.
34
Q

Mechanisms of Taste Sensations Bitter and Umami

A
35
Q

Olfaction

A
  • Olfactory receptors have a variety of locations:
    • Antennae (sensilla)
    • nasal cavities (most vertebrates)
  • Mammals have an olfactory epithelium
  • Some mammals have an additional olfactory area called the vomeronasal organ which is important for communication (territory, reproductive pheromones)
    • vomeronasal receptors are physiologically and molecularly distinct from olfactory receptors in the nasal cavity
36
Q

Olfaction

A

Animals that are particularly dependent upon olfaction have turbinates which are complex nasal cavities

37
Q

Vertebrate and Insect Olfactory Receptors

A
  • Both vertebrate and insect olfactory receptor cells extend cilia into a mucous layer
  • Depolarization is initiated in the cilia that extend from the dendrite
  • Unlike taste buds, olfactory receptor axons directly carry messages to the CNS
38
Q

Olfactory Receptors

A
  • Odorants bind to receptors that act via G-protein mediated 2nd messengers (cAMP) to open ligand-gated cation channels causing membrane depolarization
  • There are about 1000 known olfactory receptor proteins
  • The olfactory cell contains one type of receptor, but it may bind to several odorants
  • The vomeronasal organ uses a different family of receptor proteins
39
Q

Transmission of Olfactory Information

A

Related receptors send their axons to the same part of the olfactory bulb in the brain

Vomeronasal receptor axons go to glomeruli in the accessory olfactory bulb