Sensory Physiology Chapter 10.

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Presentation transcript:

Sensory Physiology Chapter 10

Sensory Organs (Receptors) Monitor the internal and external environment Transmit peripheral signals to CNS for processing Critical for homeostasis

Types of Sensors Structural Design Primary Sensors Dendritic endings of sensory neurons Stimulation directly evokes APs in neuron Secondary Sensors Specialized sensory cell Stimulation of sensor induces release of neurotransmitter to sensory neuron. Figs 10.4, 10.7

Types of Sensory Receptors Functional Types Chemoreceptors respond to changes in chemical concentration Mechanoreceptors Respond to mechanical energy (touch, pressure vibration) Photoreceptors Respond to light Thermoreceptors respond to temperature changes Nociceptors respond to tissue damage (pain)

Sensory Adaptation Fig 10.1 Response of sensors to constant stimulation Phasic receptors exhibit sensory adaptation firing rate of receptor (# AP’s) decreases with constant stimulus Tonic receptors exhibit little adaptation maintain constant firing rate as long as stimulus is applied Fig 10.1

Four Steps to Sensation Stimulation application of stimulus Must be strong enough to induce AP in sensory neuron Sensors most sensitive to one particular stimulus modality (adequate stimulus) Transduction induction of an action potential Stimulation of sensor induces graded potentials in sensors generator potentials, or receptor potentials If strong enough depolarization, AP results ↑ stimulus strength above threshold  ↑ AP firing rate Figs 10.2, 10.3

Four Steps to Sensation Conduction relay of information through a sensory pathway to specific region of CNS Usually three neurons in sensory pathway 1st order neuron from stimulation point to CNS 2nd order neuron e.g., from entry into CNS to thalamus 3rd order neuron e.g., from thalamus to perception site Perception Detection of environmental change by CNS Evaluation of nature of change and magnitude Fig 8.20

Acuity Acuity = ability to discriminate size, shape of an object in the environment Determined by size of receptive field area of the body that, if stimulated, will cause a response from a sensory neuron  receptor density,  receptive field size, acuity easier to define borders of an object Fig 10.5

Classification of Sensory Input Somatesthetic senses sensors located over wide areas of the body Information usually conducted to the spinal cord first (then possibly the brain) Special Senses Changes detected only by specialized sense organs in the head Information conducted directly to the brain

Somatesthetic Senses Touch and Pressure Heat and Cold Limb movements Pain

Somatesthetic Senses: Sensor Structure Free nerve endings heat, cold, pain Expanded dendritic endings Ruffini endings and Merkel's disks (touch) Encapsulated endings Meissner's corpuscles, Krause's corpuscles, Pacinian corpusles (touch and pressure) Bundled receptors Spindle fibers, Golgi tendon organs Figs 10.4, 12.26

Somatosensory Information Conduction Two possible destinations for sensory information upon entering the spinal cord: Part of spinal reflex arc Relayed up ascending to somatosensory cortex Fig 12.26

Special Senses Taste Smell Hearing Equilibrium Vision

Taste (Gustation) Detection of chemical concentrations in the oral cavity Taste buds - chemoreceptors contain microvilli that project to the external surface When chemicals come into contact with these hairs, buds release NT to sensory neurons  APs Travel to the parietal lobe (inferior postcentral gyrus) Fig 10.7

Taste (Gustation) Different tastes derived from activation of different signaling pathways within the cells Salty (high [Na+]) Sour (high [H+]) Sweet (organic molecules) Bitter (toxins) Umami (glutamate) Fig10.8

Smell (Olfaction) Fig10.9 Detection of chemicals in air Modified bipolar neurons (chemoreceptors) Ciliated receptors located in nasal epithelium respond to chemicals in air APs travel to olfactory bulb Synapse with mitral cells (2nd order) in glomeruli Each glomerulus receives signals from one type of receptor Info Relayed to olfactory cortex (temporal lobe) and medial limbic system Fig10.9

Smell (Olfaction) Defines much of food flavor ~1000 different genes for olfactor receptor proteins Humans can distinguish among a great variety of odors (10,000) Combinatory effect of odorants binding to different receptors

Hearing Fig 10.13 Neural perception of vibrations in the air Hair cells - mechanoreceptors vibrations bend stereocilia Opens/closes physically gated ion channels alters release of NT to sensory neurons Fig 10.13

Anatomy of the Ear Fig 10.17 Outer Ear - air-filled Middle Ear - air-filled Inner Ear - fluid-filled

Outer (External) Ear Fig 10.17 Pinna (Auricle) collects and channels sound waves External Auditory Meatus entrance into the skull Tympanic Membrane vibrates when struck by sound waves Fig 10.17

Middle Ear Figs 10.17, 10.18 Air-filled chamber Eustachian tube connects middle ear to pharyx Auditory ossicles act as sound amplifiers malleus - against tympanic membrane incus stapes - linked to oval window Figs 10.17, 10.18

Inner Ear Figs 10.17, 10.19 Fluid-Filled Two regions: Vestibular apparatus equilibrium Cochlea hearing Figs 10.17, 10.19

Cochlea Three snail-shaped tubes filled with fluid Outer canals (continuous) scala vestibuli – superior Links to oval window scala tympani – inferior Links to round window inner canal = Cochlear Duct floor - organ of Corti Figs 10.19, 10.20, 10.22

Organ of Corti Fig 10.22 Hair cells Basilar membrane embedded in supporting cells Basilar membrane Flexible, vibratory Tectorial membrane covers hair cells stereocilia imbedded in membrane Fig 10.22

Conduction of Sound Figs 10.22, 10.23 Fluid pressure waves cause basilar membrane to vibrate Hair cells move against tectorial membrane Stimulates neurotransmitter release to sensory neurons Auditory nerve Signals conducted to auditory cortex (temporal lobe) Figs 10.22, 10.23

Equilibrium Fig 10.13 Changes in position and motion of the head balance and coordination of body movement Hair cells - mechanoreceptors Fig 10.13

Vestibular Apparatus Fig 10.12 Fluid-filled compartments in the inner ear Semi-circular canals Rotation of the head Otolith organs linear movement of head and orientation relative to gravity Sensory information relayed via the vestibular nerve to the cerebellum and medulla Fig 10.12

Semicircular Canals Figs 10.12, 10.15 Fluid-filled circular tubes oriented in three planes Bell-shaped ampulla at one end of each canal contains hair cells covered with gel-like cupula Rotation of head in one direction generates inertial pressure in fluid bends cupula stimulates hair cells stimulates vestibular neurons Figs 10.12, 10.15

Otolith Organs Two fluid-filled chambers (utricle and saccule) Macula – mound of hair cells covered with otolithic membrane jelly like membrane otoliths (CaCO3 crystals) linear movement or tilting of head causes otolithic membrane to sag bends hair cells stimulates vestibular neurons Figs 10.12, 10.14

Vision Fig 10.25 Perception of electromagnetic radiation narrow portion of the EM spectrum Photoreceptors stimulated by photons of light contain photopigments undergo chemical changes in response to light induces metabolic changes in photoreceptors leading to receptor potentials Fig 10.25

Anatomy of the Eye Fig 10.26 Three distinctive layers of tissue Sclera - outer layer Choroid - middle layer Retina - inner layer

Sclera Fig 10.26 “White” of the eye Tough connective tissue Protects inner structures Maintains eye shape Cornea (anterior portion) transparent: lets light pass into the eye fixed lens (bends light) covers the anterior cavity filled with aqueous humor Fig 10.26

Choroid Fig 10.26 Contains blood vessels for the eye Specialized structures anteriorly: Iris Ciliary Muscle Lens Fig 10.26

Iris Fig 10.26, 10.27 Thin ring of pigmented muscle in front of lens pupil - opening in muscle Muscles alter pupil size, thus amount of light passing Radial muscles - open pupil in dim light (sympathetic) Circular muscles - close pupil in bright light (parasympathetic) Fig 10.26, 10.27

Ciliary Muscles and Lens solid but pliable transparent body used to focus light on the retina Ciliary Muscle ring-shaped smooth muscle linked to lens by suspensory ligaments adjusts shape of lens to focus light Fig 10.32

Accommodation Changing lens shape to focus light from objects at different distances on the retina Far objects light from narrow range of angles ciliary muscles relax, lens stretched less convex, less bending of light Near objects light from wide range of angles ciliary muscles contract, lens recoils more convex, more bending of light Fig 10.33

Refraction of Light Fig 10.30 Light bends when passing between mediums with different densities Four different refractive mediums in the eye cornea aqueous humor lens vitreous humor (btw lens and retina) bending of light leads to projection on the retina lens is responsible for focusing the image Fig 10.30

Retina Figs 10.29, 10.30 Inner layer of the eye Contains photoreceptors rods and cones Fovea centralis point where light is focused high density of cones Optic disk where optic nerve joins the eye no photoreceptors - “blind spot” Figs 10.29, 10.30

Retina Cells Fig 10.35 Photoreceptors Bipolar cells Ganglion cells deepest layer rods and cones Bipolar cells modified neurons receive signals from cells transfer signals to ganglion cells Ganglion cells sensory neurons conduct signals to CNS via the optic nerve Fig 10.35

Photoreceptors Fig 10.36 rods - light intensity cones - color more numerous than cones highly sensitive to light low light levels detected low visual acuity cones - color less sensitive to light need high light levels to respond high visual acuity Fig 10.36

Photoreceptors Each photoreceptor has two segments Inner segment metabolic machinery synaptic endings Outer segment contains layers of internal membranes containing photopigments rhodopsin - rod cells photopsins - cone cells Figs 10.36, 10.37, 10.40

Phototransduction Fig 10.39 photoreceptors synapse with bipolar cells bipolar cells synapse with ganglion cells in absence of light, photoreceptors release inhibitory NT hyperpolarize bipolar cells inhibit bipolar cells from releasing excitatory NT to ganglion cells Fig 10.39

Phototransduction Fig 10.39 when stimulated with light, photoreceptors STOP releasing inhibitory NT bipolar cells depolarize release excitatory NT to ganglion cells ganglion cells undergo APs Fig 10.39

Conduction of Light Fig 10.30 Cornea and aqueous body Pupil - adjust light level Lens - focus light Vitreous body Retina (fovea centralis) Fig 10.30

Transduction of Light Figs 10.35. 10.43 Rods and Cones cease release of inhibitory NT bipolar cells depolarize release excitatory NT Ganglion cells depolarize AP in optic nerve Signal conducted to visual cortex in occipital lobe Figs 10.35. 10.43