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The DIAGNOdent, a device used in caries detection, uses a laser to excite fluorescence from pigments in carious tooth structure. In clinical use assessing occlusal surfaces, distance and tooth structure may separate the instrument's tip from the fluorescent source.The aim of this in vitro study was to examine the effect of distance and tooth structure on laser fluorescence (LF) readings.In one set of experiments, a porphyrin pigmentin oil suspension was used as a LF signal source. Thin slices of enamel and dentin were obtained from extracted molars. Pigment-induced LF readings were obtained when these slices were placed between the porphyrin pigment and the LF instrument's tip. The effect of either demineralized or intact tooth tissue on pigment-induced LF readings was assessed.In other experiments on extracted molars with small occlusal caries, LF readings were taken from pit/fissure sites before and after removal of the occlusal surface.LF readings are proportional to pigment con-centration and inversely proportional to the distance between the suspension and the instrument's tip. Enamel, demineralized enamel,dentin, and demineralized dentin all caused significant reductions in LF signal, all readings being taken with the same tip-pigment distance. Demineralized enamel (white with intact surface) caused the most reduction.After sectioning of carious teeth, there was a significant increase in LF readings.The results of this study indicate that distance and the presence of tooth structure between the carious lesion and the instrument's tip reduce LF readings. These results indicate that anatomic factors interfere with the LF device's ability to assess occlusal caries. DIAGNOdent readings should not be relied on when making diagnostic decisions.

All biological tissues are three dimensional and contain structures that span a range of length scales from nanometres through to hundreds of millimetres. These are not ideally suited to current three-dimensional characterization techniques such as X-ray or transmission electron tomography. Such detailed morphological analysis is critical to understanding the structural features relevant to tissue function and designing therapeutic strategies intended to address structural deficiencies encountered in pathological states. We show that use of focused ion beam milling combined with scanning electron microscopy can provide three-dimensional information at nanometre resolution from biologically relevant volumes of material, in this case dentine., (© 2010 The Authors Journal compilation © 2010 The Royal Microscopical Society.)

Objective: The aim of this study is to examine the influence of electrostatics in determining the ability of charged material to adhere to dentin surfaces., Design: Deep dentin slices were obtained from third molars. In one set of experiments the effect of a cationic polymer (polyquaternium-6) application on dentin staining with the cationic dye (toluidine blue) was assessed using a colour analyser and photography. In other experiments the effect of cationic polymer treatment on adhesion of cationic and acidic anionic 0.5 microm latex beads was assessed using scanning electron microscopy and quantification of dentin surface bead attachment. In both experiments dentin discs were split in half and the effect of cationic polymer was compared to water treatment., Results: Water-treated dentin was stained an intense blue after application of toluidine blue. Cationic polymer pretreatment significantly reduced the intensity of dye staining. SEM examination of dentin treated with cationic beads showed a dense coverage of beads. In contrast, dentin that was pretreated with cationic polymer was virtually free of cationic beads. Acidic anionic bead treatment left a coating of beads on the dentin surface. Pretreatment with the cationic polymer prior to anionic bead application caused a significant reduction in bead coverage., Conclusions: Dentin treatment with a cationic polymer inhibits the staining of dentin by cationic dye and adherence of cationic beads. Acid functional anionic beads adhere to the dentin surface but the pattern of adherence is altered by cationic polymer application. Electrostatic forces may influence the attachment of therapeutic materials to dentin surfaces., (Copyright 2009 Elsevier Ltd. All rights reserved.)

Dentinal sensitivity is a common complaint of patients. Removal of cementum or enamel leaves the dentin exposed allowing various stimuli to produce fluid movement through the dentinal tubules. These fluid movements are believed to activate pulpal sensory nerves leading to pain. Various therapeutic approaches have been investigated to treat this problem. Resins, fluoride compounds and oxalate solutions have been used to block the dentinal tubules. KNO3 and SrCl2 are active ingredients in desensitizing tooth pastes but neither compound reduces the permeability of dentine. The ability of various solutions to decrease hypertonic (3M NaCl) evoked nerve activity was tested in the canine teeth of anesthetized cats. Excitatory and desensitizing solutions were placed into a deep dentinal cavity prepared over the incisal pulp horn. An electrode used to record nerve activity was also placed into this deep cavity. KNO3 and other K+ ion containing solutions elicit a biphasic effect on nerve activity. Immediately following application of these solutions into the deep dentinal cavity there is a brief burst of high frequency spike activity. Following this brief period of excitation, the intradental nerves are silent and respond weakly to hypertonic NaCl. CaCl2 and other divalent cation solutions also inhibit hypertonic NaCl induced nerve activity, but have a weaker effect than that exerted by K+. These observations can be explained based on the effects of various ions on nerve excitability. Increasing the K+ ion concentration in the vicinity of the dentinal nerve terminal depolarize and activates the nerve fibers. Following a prolonged period of depolarization the action potential mechanism is inactivated. Divalent cation solutions stabilize the nerve membrane without changing the membrane potential. Desensitizing solutions do not decrease nerve activity by an effect on pulpal blood flow. This experimental model does not entirely explain the clinical action of these desensitizing agents. The role of inflammation in hypersensitivity and dental pain is currently being investigated.

Nerve activity was recorded from deep dentinal cavities in the canine teeth to assess the possible influence of potassium and divalent cations in decreasing this activity in hypersensitive teeth. The decreased activity after the topical application of 0.756 mol/l KCl to the cavity was primarily due to the cation. KCl elicited a biphasic response from intradental nerves, an initial transient excitatory response followed by a prolonged inhibitory period. During the inhibitory period 3 mol/l NaCl, an effective excitatory stimulus, failed to evoke intradental nerve activity. However, with time the response to 3 mol/l NaCl eventually recovered to its previous control level. Close, intra-arterial injection of KCl showed the same biphasic response and time-course of intradental nerve activity as with topical application. Therefore, whether KCl was applied topically or injected its effectiveness in altering the nerve activity was similar. Pretreatment of the dentinal cavity with CaCl2, MgCl2 or SrCl2 greatly reduced the response of intradental nerves to KCl. Therefore these divalent cations seem to have a depressant action on pulpal nerve fibres. The mechanism of action of KCl seems to be an alteration of K+ concentration immediately surrounding the intradental nerves which presumably depolarizes the nerve fibre membrane and elicits an initial firing of action potentials. Because of the persisting high levels of extracellular potassium a sustained depolarized state occurs that results in an inactivation of the action potential. Divalent cations appear to depress the excitability of the nerve cell membrane without altering membrane potential. Such ionic agents could be used in conjunction with KCl as a possible treatment for hypersensitive teeth.

Intradental nerve activity (INA) was recorded from cat canine teeth to determine whether solutions altering intradental nerve sensitivity were strongly correlated to the osmotic concentration of the solution or via a more direct action on intradental nerve excitability. The effects of various ionic and non-ionic solutions were tested in both deep and shallow dentinal cavities. With saline in the deep dentinal cavity a very low firing rate or resting nerve spike (action potentials) activity was recorded. When 3 M NaCl was placed in the same or similar cavity a high discharge rate of nerve spike activity was obtained. This 3 M NaCl elicited activity was utilized to determine the inhibitory or excitatory effects of various test agents on the intradental nerves. The following agents: MgCl2, MgSO4, and CaCl2 were inhibitory to the INA response elicited by 3 M NaCl. Non-ionic solutions of urea or sucrose failed to evoke INA and they were also minimally effective in altering 3 M NaCl elicited activity. Shallow cavities were utilized to maintain the tubular structure of dentin relatively intact. In the shallow cavity preparations hypertonic sucrose or urea failed to evoke INA, even when dentin was etched with 50% citric acid for 2 min. The results suggest that the osmolarity of these solutions is a poor indicator of the INA.

Tooth sensitivity is a common dental pain condition where sufferers experience brief episodes of sharp well-localized pain when their teeth are subjected innocuous stimuli such as cold, air-currents and probing with a metallic instrument. In this review, we will make no attempt to describe all the treatments that have been developed to treat tooth sensitivity. We will review the basic anatomic and physiological mechanisms responsible for sensitivity. The insights into the dental lesions responsible for tooth sensitivity, as well as the physiological processes linking stimuli and pain generation have suggested several treatments and preventive strategies. Unfortunately, many tooth sensitivity treatments fail to perform better than placebos in clinical trials that seek to assess the effect of agents on pain symptoms. In the case of the most commonly used self-applied desensitizing agent, potassium salts, the mechanism of action established by laboratory and animal models may not apply to clinical use. Thus results obtained with laboratory and animal models must be applied with care to clinical use. Clinical literature suggests that tooth sensitivity is the symptomatic manifestation of significant dental problems, such as wear and other forms of non-carious tooth structure loss. These conditions are increasing in frequency as people age, retaining their natural teeth longer. They are frequently the consequences of aggressive oral hygiene practices and diets rich in acids. Treatments directed at the underlying causes rather than the symptoms of tooth sensitivity would hinder the development of these lesions and provide researchers with objective targets for assessing therapeutic efficacy. [ABSTRACT FROM AUTHOR]

A personal narrative is presented which explores the authors' experience with tooth sensitivity and their research on this topic.