بسم هللا الرحمن الرحيم ﴿و ما أوتيتم من العلم إال قليال﴾ صدق هللا العظيم االسراء اية 85 BY Dr /Hany M. borg Assistant professor of physiology KFS University Centers Tracts Afferents Receptors Sensation 1) Def., • Sensation is a conscious perception of particular feeling caused by stimulation of certain type of receptor by its adequate stimulus. 2) Classifications: Sensations General Special Organic 1) Special sensations: • Vision, hearing, taste, smell and equilibrium 2) General sensations: • Arise from receptors distributed allover the body • Are classified into; a) Somatic sensations: from somatic structures e.g. skin b) Visceral sensations: from viscera 3) Organic senses: e.g. thirst, hunger and sexual desire Somatic sensations Def, • These sensations arise from somatic structures of all the body i.e. skin and deep tissues e.g. sk ms Types: • They include according to their adequate stimulus: 1. Mechanoceptive sensations: 2 types; – Tactile e.g. touch, pressure, and vibration sensations. – Proprioceptive sensations e.g. sense of position and movement 2. Thermal sensation; cold and warm. 3. Pain sensation Somatic sensations Mechanoreceptive Tactile Touch , pressure &vibration Thermoceptive proprioceptive Position & movement of joints pain According to center of perception 1- Protopathic (crude sensations): • perceived in the thalamus as slow pain, extreme grades of temperature & crude touch. 2- Epicritic (fine sensations): • Perceived in the cortex as fast pain, fine grades of temperature, fine touch & deep sensations BY Dr /Hany M. borg Associate professor of physiology KFS University Def : • Pain is an unpleasant sensory and emotional experience associated with actual or potential tissue damage Significance: 1. Pain is a warning signal for tissue damage. It is the prominent symptom of tissue damage 2. Pain has a protective function. It initiates protective reflexes that; • Get rid of the painful stimulus. • Minimize tissue injury or damage. Painless nature of diabetic foot disease •Pain Rs are morphologically similar but functionally they are specific 1) Morphology: are specific free nerve endings 2) Highly specific i.e. respond to tissue damage only • Classified according to their adequate stimulus into:a) Mechanical Pain Rs: • Respond to strong mechanical trauma e.g. cutting b) Thermosensitive pain Rs: • Respond to excessive changes in temp (above 45°C and below 10°C). c) Chemical Pain Rs: respond to noxious chemical stimuli. d) Polymodal Pain Rs: respond to a combination of mechanical, thermal, and chemical noxious stimuli 3) Distribution: a) Abundant in the skin and some internal tissue such as the periosteum, arterial wall, joint surfaces, and the dura of the tentorium cerebelli. b) Few in deep tissues and all viscera. So, for pain to occur, painful stimulus must by intense and widespread. The deep & visceral pain is poorly localized. c) Brain itself and the parenchymal tissues of the liver, kidneys, and lungs have no pain receptors “pain insensitive structures” 4) Threshold : •It is the lowest intensity of injurious agent needed to stimulate the pain receptors and produced pain sensation •Pain receptors are of high threshold: the pain receptors needs sufficient degree of tissue damage to be stimulated. 5) Adaptation: •Slowly adapting receptors even non adapting receptors •This is very important because it directs the subject to get rid of the injurious agent 6) Mechanism of stimulation: Chemical stimuli Mechanical stimuli Thermal stimuli Strong acids or Alkalies Cutting or pricking temp. > 45 C and < 10 C Tissue damage 1st class K ions, Histamine, Serotonin, and Bradykinin Directly stimulate Pain Receptors Release of Pain Producing Compounds (PPS) 2nd class PGE2, leukotriens and Substance P Sensitize the pain Rs by lowering its threshold to stimuli Tissue Damage Direct stimulators Sensitizers A) According to its mechanism or cause: •Pain is classified into 3 main types; 1. Physiological Pain Also called Nociceptive pain Caused by stimulation of pain receptors by tissues damage e.g. in inflammation 2. Pathological Pain Also called neuropathic pain Caused by damage of nerve pathway 3. Psychogenic Pain In depression and anxiety Difficult to differentiate whether 2ry to or actual cause of pain B) According to its duration: •Both nociceptive and neuropathic pains are classified into 2 types; a) Acute pain: less than 7 weeks b) Chronic pain : more than 7 weeks C) According to the quality or character : •A pain it is classified into 5 types; a) Pricking or Cutting Pain: b) Burning Pain: c) Aching Pain: d) Throbbing Pain: e) Colicky Pain: 1. Pricking pain • Sharp and localized pain. • Of skin origin (mainly) • e.g. in pricking or cutting the skin by sharp object 2. Burning pain • Less well localized, has unpleasant burning nature. • Usually of skin origin • Caused by wide spread irritation of skin 3. Aching pain 4.Throbbing pain 5.Colicky pain • disagreeable pain of dull- aching nature • More diffuse and felt coming from deeper tissues e.g. rheumatic pains • Fluctuation of its intensity with arterial pulsations • localized inflammation in deep tissues e.g. abscess • Comes in cramps, so it has a colicky nature, e.g. intestinal colic and ureteric colic • Spasm of smooth ms in the walls of hollow viscera D) According to site of origin: 3 types; Cutaneous pain • Pain comes from skin and subcutaneous tissues • Usually pricking or burning pain Deep pain • Pain comes from structures deep to the skin e.g. skeletal muscle, joints, and tendons • Usually dull aching or throbbing Visceral pain • Pain comes from internal viscera e.g. stomach • Usually colicky or dull aching Comparisons Between Slow and Fast Pain Acute (Fast) Chronic (Slow) Source Skin only Quality Onset Pricking Within 0.1 sec after stimulation Short (one second) Well –localized Not summated Skin, deep tissues, and viscera Burning One or more seconds after stimulation Long (few minutes) Diffuse Can be summated A-delta Neospinothalamic tract Cerebral cortex Glutamate C Paleospinothalamic tract Thalamus Substance P Duration Localization Summation Afferent Tract Centre Chemical trans. Pathway: Neospinothalamic tract A) 1st order neuron : • A delta afferent fibers • End in lamina I of dorsal horn of spinal cord B) 2nd order neuron : • Axons of neurons lamina I of dorsal horn of spinal cord cross the opposite side in front of central canal and ascend as neospinothalamic in spinal cord and as spinal leminiscus in brain stem • End in posteroventral nucleus of thalamus (PVNT) Pathway: C) 3rd order neuron : • Axons of neurons of PVNT ascend in sensory radiations • End in primary somatic sensory area (area 3,1,2) Note: • The chemical transmitter released at the central end of A delta fibers that carry fast pain is glutamate PVNT Sensory Radiations Spinal Leminiscus Lamina I A delta Receptors Free nerve endings Lateral spinothalamic tract Pathway: Paleospinothalamic tract A) 1st order neuron : • C afferent fibers • End in lamina II and III (called substantia Gelatinosa of Rolandi SGR) of dorsal horn of spinal cord B) 2nd order neuron : • Axons of neurons SGR of dorsal horn of spinal cord cross the opposite side in front of central canal and ascend in spinal cord and as; 1. Spinoreticular tract end in RF of MO and Pons 2. Spinotectal tract end in PAG areas of midbrain 3. Paleospinothalamic tract end in non specific thalamic nuclei (intralaminar and midline) Pathway: C) 3rd order neuron : • Axons of neurons from RF and NSTN of thalamus ascend in sensory radiations • Terminate diffusely in all areas of the cerebral cortex Note: • The chemical transmitter released at the central end of c fibers that carry fast pain is substance P All cortical areas Non-specific nuclei of thalamus Periaqueductal gray area (PAG) in midbrain Reticular formation In MO and Pons SGR Laminae II, III Receptors Free nerve endings Afferent C fibers Paleospinothalamic tracts Significance of Pain Pathways Neospinothalamic Paleospinothalamic a) Rapidly inform the C.N.S about the injurious agent → initiate rapid protective reflexes as flexion withdrawal reflex. a) Continuously inform the C.N.S about the presence of tissue damage → direct the person to remove the injurious agents. b) Determines accurately b) Strong arousal state due the site “locality” of the to potent activation of RAS painful stimuli. c) Initiation of the emotional & autonomic reactions, through RF • N.B. • Damage or removal of the sensory cortex does not lose pain, but the pain become diffuse, ill defined and the nature of the painful stimulus cannot be identified. • So, CC seems to be concerned with the intensity, locality & modality discrimination of the painful stimulus. 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