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Pulpal & Dental Pain

The document discusses the anatomy and physiology of the dental pulp. It describes the components of pulpal tissue including fibers, cells, matrix, nerves and blood vessels. It explains how the pulp functions to maintain dentinal health, provide sensory pathways and initiate repair. It discusses pulp innervation including the types of nerve fibers and neurotransmitters. Pain mechanisms involving the pulp such as neurotrophic substances, nociceptive responses and referred pain are also summarized.

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Ali Al-Qudsi
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100% found this document useful (1 vote)
3K views28 pages

Pulpal & Dental Pain

The document discusses the anatomy and physiology of the dental pulp. It describes the components of pulpal tissue including fibers, cells, matrix, nerves and blood vessels. It explains how the pulp functions to maintain dentinal health, provide sensory pathways and initiate repair. It discusses pulp innervation including the types of nerve fibers and neurotransmitters. Pain mechanisms involving the pulp such as neurotrophic substances, nociceptive responses and referred pain are also summarized.

Uploaded by

Ali Al-Qudsi
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd

PULPAL & DENTAL

PAIN

Oral physiology
Dent 207
Dental pulp
 Specialized connective tissue
 Contained within the tooth
 Enclosed by dentine
 Continuous with the periodontal ligament through:
 Apical foramen
• Narrow – only allows for passage of the neurovascular
bundle
 Small volume
• Total volume in all teeth is 0.40 ml
Pulpodentine complex
 Functions of pulp & dentine are interlinked
 Functions of the pulp
• Maintain dentinal health by supplying nutrients
• Provide a pathway for sensory impulses from
dentine
• Initiate & govern repair of dentine in injury
Odontoblasts
 The layer of specialized cells immediately
adjacent to dentine
 Have processes that penetrate dentine for
varying distances
 Responsible for formation of dentine
 Involved in sensory perception of dentine
Components of pulpal tissue
 Fibers
• Collagen
 Confers rigidity
 Maintains 3D spatial relationship of cells, blood vessels & nerves
• Elastin in blood vessel walls
 Cells
• Odontoblasts
• Fibroblasts
• Undifferentiated mesenchymal cells
• Macrophages, histocytes & lymphocytes
 Amorphous matrix
• Support
 Nerves & blood vessels
Pulp nerves
 Sensory fibers
 Aδ & C fibers
 Types of nerve terminals near blood vessels
• Large fibers
 Contain small vesicles (resemble cholinergic endings)
• Medium fibers
 Numerous small dense-cored vesicles
 Found in pulp horns & pulp chamber
• Small fibers
 Numerous large dense vesicles (purinergic or peptidergic endings)
 Plexus of Raschkow (subodontoblastic plexus)
• Individual axons divide into many branches in the plexus
Pulp nerves during tooth formation
 Fibers near base of dental papilla
 At cap stage
• Fibers form a plexus - to dental follicle – to dental papilla
 At bell stage – unmyelinated
 At eruption - number of fibers & their average size increase -
transition towards myelination
 Continues to increase for a few years after eruption
 Dentine is laid down – pulp reduced in size – nerve plexus
decrease in size
 Ageing pulp
• Decrease in number of axons entering pulp
• Reduction in myelinated fiber size
• Raschkow’s shows little change
Pulp nerves in primary teeth
 Number of axons is less than that in permanent
 Except primary canine
 Number of axons decrease with resorption
until the tooth is shed
Neurotrophic substances
 Nerve growth factors – evidence
• Promote survival of neural crest cells in trigeminal
ganglion
• Produced in the maxillary process to maintain survival of
nerve axons
• No role in directing spread of fibers
• Act on nearby nerves govern late invasion of pulp tissue by
nerve fibers
• Allow permanent teeth to recruit their nerve supply from
branches of axons previously supplying deciduous teeth
• Odontoblastic factors promote extension of new nerve
fibers into the subodontoblastic layer & dentine in
reimplanted teeth
Functions of Aδ fibers
• Myelinated
• Diameter: 1 – 4 µm
• Rapidly conducting (>2 m/s)
• Mediate sharp, piercing pain sensations
• Responsible for dentinal sensitivity
• Respond to any stimuli causing fluid movement in
dentinal tubules
 Drilling, drying & application of osmotic solutions
Functions of C fibers
 Unmyelinated
 Diameter: < 0.5 µm
 Slowly conducting (< 2 m/s)
 Polymodal: activated by
• Thermal
• Mechanical
• Chemical stimuli – histamine & bradykinen
 Mediate dull, longer standing & less well-
localized
Neurotransmitters in dental pulp
 Calcitonin gene-related peptide (CGRP)
 Substance P
 Neurokinin A
Autonomic nerve supply in the pulp
 Sympathetic
 Parasympathetic
Sympathetic
 Majority of autonomic
 Some are cholinergic
• Removal of superior cervical ganglion – some decrease in
cholinesterase staining in the pulp
 In mouse
• ½ in pulp horn
• 1/3 in pulp chamber
• Rest in root canal
 Functions
• Control pulp blood flow
• Regulation of odontogenesis
• Afferent transmission of impulses associated with pain sensation
 Evidences of functions
• Anatomical: near blood vessels & odontoblasts
• Sympathectomy – vasodilatation & changed in dentine apposition
Parasympathetic
 Majority are cholinergic
• Resection of inferior alveolar nerve
 Abolish cholinesterase staining
 Increased rate f tooth eruption (increased intrapulpal
pressure)
Nociceptive response – substance P
 Pulp reacts initially to stimulating dentine
• Electrically
• Mechanically
• Chemically
 C fibers stimulated -
 Retrograde impulse in C branches –
 Release of substance P at terminals –
• Vasodilatation – tissue edema
• Release of histamine – increase capillary permeability &
fluid extravasation
Nociceptive response - bradykinin
 Noxious stimulation of the pulp –
 Bradykinin formation –
• Contribute to vasodilatation
• May stimulate release of encephalins from pulpal
cells
 Encephalins – anti-inflammatory – inhibit
bradykinin release – protective –ve feedback
mechanism
Nociceptive responce – ecosanoid
group
 Are metabolites of arachidonic aid
• Prostaglandins
• Leucotrienes
 PG I2 produced by endothelial cells
• Inhibit platelet aggregation
• Vasodilator
 Thromboxane A2 produced by platelets & fibroblasts
• Stimulate platelet aggregation
 In the pulp
• PG I2, PG F2α , PG E2
• Thromboxane A2
• Leucotrience 12-HETE, LTC4
Nociceptive response – prostaglandins
 Bacterial/mechanical/chemical irritation –
 Increase in prostaglandin F & E (found in high
2α 2

conc. In inflamed pulp)


• Vasodilatation
• Increase pain-producing properties of
 Histamine
 Bradykinin
 Serotonin
Pain relieving drugs
 Aspirin – inhibitor of cyclo-oxygenase –
inhibition of PG synthesis
 Root canal medicaments
• Phenol, p-Chlorophenol, cresol, thymol, guaiacol
• Inhibit synthesis of PG & leucotrienes
• Have antibacterial activity
 Eugenol – more effective than phenols in
inhibition of prostaglandin synthesis
Pulpitis & pulp necrosis
 Injury to dentine (cavity prep.)
• Nerve fibers & odontoblastic processes pulled by
hydrodynamic force –
• Separated from pulpal tissue –
• Damaging nerve fibers & killing of odontoblasts –
• Pain in dentine
Small injury
 In small damaged areas / odontoblastic layer
damage is slight
• Reparative dentine may seal off small damaged
areas
 Blocks re-innervation
 Innervation of adjacent areas is increased
• CGRP from reactive axons promote growth of new
fibers
• When the lesion heals - new fibers disappear
Pulpitis
 Cavity reaches the pulp
• Odontoblastic layer destroyed
• Inflammation occurs locally
• In small lesions, dentine bridge forms – inflammation
resolves & pulp heals (reversible pulpitis)
 Inflammation area demarcated by fibrous tissue
• More severe stimuli / larger lesions – irreversible pulpitis
 Severe inflammation -inflammation area demarcated by fibrous
tissue
 Lack of pain at a later stage of pulpitis
• CGRP-mediated growth of nerve fibers outside
inflammation area
 Hypersensitivity in early pulpitis
 Difficulty in achieving anesthesia a tooth with an inflamed pulp
Pulp necrosis
 More severe pulpal exposure
• Irreversible pulpitis - necrosis occurs
• Necrosis area demarcated by fibrous tissue
• CGRP-mediated growth of nerve fibers outside
necrosis area
 Lesion extends to root apex
• Nerve growth in periapical tissue
• New fibers appear to be involved in pain sensation
Pain of dental origin
 Exposed dentine – sensitivity - pain
• Dental caries or cavity prep.
• Cemental layer wears away
 Any sensation through dentine – pain
 Heat / cold may be perceived as separate sensations?
 Most sensitive areas in dentine as at
• EDJ
• Exposed dentine in cervical root areas
 Nerve fibers to dentine are limited to coronal dentine
 Nerve fibers numerous under cusps
 Nerve fibers extend for a short distance within dentine
 Odontoblastic processes vary in extension through dentine
• Function as receptors
Three theories of dentinal
hypersensitivity
 Odontoblastic processes as receptors
• Odontoblasts are neural crest in origin
 Nerve fibers extend through dentine
• Direct stimulation
• Deformation of odontoblasts by fluid movement promotes
potassium release – action potential in neighboring nerve
fibers
 Hydrodynamic theory
• Movement of fluids through dentinal tubules inward &
outward
• Distortion of nerve endings in Raschkow’s plexus
Referred pain
 Sensation of pain resulting from a deep organ
peripherally in areas derived from the same
somite
• Pain of cardiac origin may be perceived in the arm
 Convergence of somatic & visceral sensory
impulses at one or more of 3 levels
• Prespinal
• Spinal
• Supraspinal
Referred orofacial pain
 In trigeminal, levels are
• Prepontine
• Pontomedullary
• Suprapontine
 No convergence within brain
 Pain within the oral cavity is referred
• Within the distribution of the specific divisions of the trigeminal nerve
• Doesn’t cross midline except in ramifications of nerve terminals
(incisor region)
 Migrainous headache may be due to dental conditions
• Not referred pain
• Because it is vascular in origin

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