Sensory Systems: Tactile and Proprioceptive Sensation

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11 Terms

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<p>Modalities and Nerve Endings- Skin sense modalities</p>

Modalities and Nerve Endings- Skin sense modalities

Fine, discriminative touch (2 point discrimination): Require small receptor near surface ( epidermis)

  • Merkel (II), Pinkus (hairy; = Merkel), Meissner (II, hairless skin), Ruffini organs (deeper in dermis)

Vibration sense: Used to appreciate textures, tested with tuning fork

  • Pacinian (“cut onion”, very fast), Meissner (fast)

Pressure: Slower adaptation

  • Pacinian (very fast: good for fast changing but not ideal for slow changing pressure), Merkel (slow)

<p><strong>Fine, discriminative</strong> touch (2 point discrimination): Require small receptor near surface ( epidermis)</p><ul><li><p><strong>Merkel </strong>(II), <strong>Pinkus </strong>(hairy; = Merkel), <strong>Meissner </strong>(II, <strong>hairless </strong>skin), <strong>Ruffini organs </strong>(deeper in dermis)</p></li></ul><p><strong>Vibration </strong>sense: Used to appreciate textures, tested with tuning fork</p><ul><li><p><strong>Pacinian </strong>(“cut onion”, very fast), <strong>Meissner </strong>(fast)</p></li></ul><p>Pressure: Slower adaptation</p><ul><li><p><strong>Pacinian </strong>(very fast: good for fast changing but not ideal for slow changing pressure), <strong>Merkel </strong>(slow)</p></li></ul><p></p>
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Specialized Sensory Endings (all have group II nerve fibers)

Hair shaft receptors

Merkel cell receptors

Meissner's corpuscles

Pacinian corpuscles

Ruffini endings

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Proprioceptors (muscle and joint senses)

Muscle spindles: muscle stretch (length), primary (Ia) and secondary (II) endings

  • primary have larger (faster) axons

Golgi tendon organs: muscle & tendon tension, group Ib

  • almost as fast as primary spindles

Joint receptors: position sense, groups Ib, II

  • several types

<p><strong>Muscle spindles</strong>: muscle <strong>stretch </strong>(length), <strong>primary (Ia</strong>) and <strong>secondary (II</strong>) endings </p><ul><li><p>primary have larger (faster) axons </p></li></ul><p><strong>Golgi tendon organs</strong>: muscle &amp; tendon <strong>tension</strong>, group<strong> Ib</strong></p><ul><li><p>almost as fast as primary spindles </p></li></ul><p><strong>Joint receptors</strong>: <strong>position</strong> sense, groups<strong> Ib, II </strong></p><ul><li><p>several types</p></li></ul><p></p>
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Physiological Properties

Modality-specific - each is tuned to type of mechanical stimulus

Receptive field: defined surface area of skin- can be mapped out on body surface as dermatomes (area of skin where the particular receptor receives stimulus/ differ by receptor and location of skin)

*photoreceptor cells: exact location in visual field

Smaller receptive field = greater sensitivity (fingertips)

Wider receptive field = lower sensitivity (back)

<p><strong>Modality-specific</strong> - each is tuned to type of mechanical stimulus</p><p><strong>Receptive field</strong>: defined surface area of skin- can be mapped out on body surface as <strong>dermatomes </strong>(area of skin where the particular receptor receives stimulus/ differ by receptor and location of skin)</p><p>*photoreceptor cells: exact location in visual field</p><p>Smaller receptive field = greater sensitivity (fingertips)</p><p>Wider receptive field = lower sensitivity (back)</p>
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Spinal Cord Segments

Cervical

Thoracic

Lumbar (anterior)

Sacral (posterior)

<p>Cervical</p><p>Thoracic</p><p>Lumbar (anterior)</p><p>Sacral (posterior)</p>
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Adaptation and Transduction

Adaptation determined by structure and electrical properties of ending

  • changing stimulus- want fast adaptation

  • slow adaptation = “true representation of stimulus”; keeps firing even after stimulation stops

Transduction thought to be by mechanical deformation of ion channel - differs with receptor type

<p><strong>Adaptation </strong>determined by <strong>structure </strong>and <strong>electrical properties of ending</strong></p><ul><li><p>changing stimulus- want fast adaptation</p></li><li><p>slow adaptation = “true representation of stimulus”; <span>keeps firing even after stimulation stops</span></p></li></ul><p><strong>Transduction </strong>thought to be by <strong>mechanical deformation of ion channel</strong> - differs with receptor type</p>
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Central Connections (body) (receptor → medulla)

Name of tracts: “medial lemniscus pathway” (medulla) or “dorsal column pathway” (spinal cord”

1o afferents have cell bodies in DRG

First synapse in spinal cord (posterior horn) for reflexes only (different from pain & temperature)

  • if reflexes not needed, info will continue tract w/o synapses

1o afferents from body ascend in ipsilateral dorsal columns (gracile MEDIAL(receive sensory info from lower body) and cuneate LATERAL (upper body) fasciculus) to medulla (final destination of axon- first synapse if no reflex)

<p>Name of tracts: “medial lemniscus pathway” (medulla) or “dorsal column pathway” (spinal cord”</p><p>1o afferents have <strong>cell bodies in DRG</strong></p><p>First synapse in<strong> spinal cord </strong>(posterior horn)<strong> </strong>for <strong>reflexes only</strong> (different from pain &amp; temperature)</p><ul><li><p>if reflexes not needed, info will continue tract w/o synapses</p></li></ul><p>1o afferents from body <strong>ascend in ipsilateral dorsal columns </strong>(<strong>gracile </strong>MEDIAL(receive sensory info from lower body)<strong> </strong>and<strong> cuneate </strong>LATERAL (upper body)<strong> fasciculus</strong>) to <strong>medulla </strong>(final destination of axon- first synapse if no reflex)</p>
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Central Connections (body) (medulla → VPL)

Synapses in medulla (dorsal column nuclei)

  • nucleus gracilis (lower body) and nucleus cuneatus (upper body) different

2nd order fibers cross midline in medulla (sensory decussation) to form medial lemniscus

  • lower body (gracile) more ventral in tract

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Central Connections (body) (VPL → parietal lobe)

Medial lemniscus ascends to ventral posterior lateral thalamus (VPL)

  • in pons, moves dorsally and laterally; lower body is most lateral (rearrange)

Third order fibers from VPL ascend to postcentral gyrus in somatotopic order

  • same locations as pain & temperature: leg medial; arm dorsal; face ventral (homonculous)

<p>Medial lemniscus<strong> ascends to ventral posterior lateral thalamus (VPL) </strong></p><ul><li><p>in <strong>pons</strong>,<strong> moves dorsally and laterally</strong>; <strong>lower </strong>body is<strong> most lateral</strong> (rearrange)</p></li></ul><p><strong>Third order fibers</strong> from VPL <strong>ascend </strong>to<strong> postcentral gyrus</strong> in somatotopic order </p><ul><li><p>same locations as pain &amp; temperature: <strong>leg medial</strong>; <strong>arm dorsa</strong>l; <strong>face ventral </strong>(homonculous)</p></li></ul><p></p>
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Tactile and Proprioception Pathways for the Face

Primary afferents (CN V) synapse in principal sensory nucleus (of trigeminal) in pons - cell body in trigeminal ganglion

Local reflexes to facial motor nucleus (e.g., blink - V1 afferent)

Second order fibers cross midline (some ipsilateral), join trigeminothalamic tract

  • more dorsal than pain & temperature fibers

Thalamic relay in ventral posterior medial (VPM) nucleus - same as pain & temp

Third order fibers ascend to inferior aspect of postcentral gyrus

Some primary afferents have cell bodies in mesencephalic nucleus (of trigeminal), participate in jaw reflexes

<p>Primary afferents <strong>(CN V)</strong> synapse in <strong>principal sensory nucleus (of trigeminal) in pons</strong> - cell body in trigeminal ganglion</p><p><strong>Local reflexes</strong> to <strong>facial motor nucleus</strong> (e.g., blink - V1 afferent)</p><p><strong>Second order fiber</strong>s cross midline (some ipsilateral), join<strong> trigeminothalamic tract</strong> </p><ul><li><p>more <strong>dorsal </strong>than pain &amp; temperature fibers</p></li></ul><p>Thalamic <strong>relay </strong>in <strong>ventral posterior medial (VPM) nucleus</strong> - same as pain &amp; temp </p><p><strong>Third order fibers ascend </strong>to <strong>inferior</strong> aspect of <strong>postcentral gyrus </strong></p><p>Some primary afferents have cell bodies in <strong>mesencephalic nucleus (of trigeminal)</strong>, participate in <strong>jaw reflexes</strong></p>
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Muscle and Joint Sense Input to Cerebellum

All muscle and joint receptors, some skin receptors (proprioceptors)

  • Primary afferent may travel in dorsal column

First synapses in spinal cord (Clarke's column- lower) or medulla (lateral cuneate nucleus- upper)

  • Clarke’s: relays info from lower body (leg)

  • Lateral cuneate: relays info from upper body (arm)

Destination in ipsilateral cerebellar vermis (most fibers do not cross midline- no decussation)

  • Spinocerebellar tract from lower body (leg)

  • Cuneocerebellar tract from upper body (arm)

Does not participate in perception: info used for muscular coordination

<p>All <strong>muscle and joint receptors</strong>, some <strong>skin receptors</strong> (proprioceptors)</p><ul><li><p>Primary afferent may travel in<strong> dorsal column </strong></p></li></ul><p>First synapses in <strong>spinal cord </strong>(<strong>Clarke's column</strong>- lower) or<strong> medulla</strong> (<strong>lateral cuneate nucleus- </strong>upper)</p><ul><li><p><strong>Clarke’s</strong>: relays info from lower body (<strong>leg</strong>)</p></li><li><p><strong>Lateral cuneate</strong>: relays info from upper body (<strong>arm</strong>)</p></li></ul><p>Destination in <strong>ipsilateral cerebellar vermis </strong>(most fibers do not cross midline- <strong>no decussation</strong>) </p><ul><li><p><strong>Spinocerebellar </strong>tract from lower body (<strong>leg</strong>) </p></li><li><p><strong>Cuneocerebellar </strong>tract from upper body (<strong>arm</strong>) </p></li></ul><p>Does <strong>not participate in perception</strong>: info used for <strong>muscular coordination</strong></p>