Insight · Reading the evidence

Kyung-A OhSoma Books

How small a force can a tooth feel?

The sense behind holding half a peanut with less than 1 N

Teeth feel forces far smaller than 1 N (about the weight of a tangerine) through mechanoreceptors in the periodontal ligament (PDL) around their roots1,2.

For most of these receptors, the range of greatest sensitivity is 1 N or less at the front teeth and 4 N or less at the back teeth, so it is smaller toward the front3.

The force needed for a person to notice a tooth being pressed is far smaller still: a periodontology textbook gives 1–2 g (about 0.01–0.02 N)1, and one study found a mean of about 0.11 N2.

The force the front teeth use to hold half a peanut (under 1 N) also falls within the receptors’ most sensitive range4,5, and the researchers concluded that this sense is used mainly when food is held and handled lightly5.

The idea that this sense extends as far as memory or cognition, however, is still a hypothesis.

Contents of this article
  1. Tracing tooth sensation with half a peanut
    1. How much force do the front teeth use to hold a peanut?
    2. Where does a tooth feel such a small force?
    3. How does tooth sensation become jaw-muscle force?
    4. What changes when the periodontal tissues are anesthetized?
  2. Evidence
  3. Frequently asked questions
  4. References
  5. Cite this page
  6. Related reading

Tracing tooth sensation with half a peanut

How much force do the front teeth use to hold a peanut?

The front teeth hold half a peanut with a force of less than 1 N4,5. When a Swedish research group asked people to hold half a peanut between their central incisors and then split it, splitting took 16–19 N, more than twenty times the holding force4. One newton (1 N) is roughly the weight of a tangerine resting in your palm. Teeth feel more than pain. When we bite, they also feel how much force is on them, and that sense reaches down to very small forces. The jaw muscles produce the force, but sensation at the tooth root also helps to gauge forces this small5,6.

Table 1 Forces when holding and splitting with the incisors. The newton (N) is the unit of force; 1 N is about the weight of a 100 g object (site calculation). A tangerine weighs 76–120 g (USDA FoodData Central, tangerine FDC 169105).

PhaseForceAlso observed
Holding4Under 1 N; 0.36–0.76 N across participants (biscuit and peanut alike)Steady during each hold and similar from one attempt to the next
Splitting4Peanut: 16.0–19.0 N across participantsMore than twenty times the holding force (site calculation)

Where does a tooth feel such a small force?

A tooth feels such small forces mainly through sensory receptors in the periodontal ligament (PDL) that surrounds its root1,6. A tooth is not attached directly to the bone. Between the root and the bone lies a gap a few hairs wide (0.15–0.38 mm)7,8. In each tooth, the PDL that fills this gap holds several hundred mechanoreceptors, which turn force into nerve signals6.

Even a single incisor has several hundred of these sensory endings6, and most of them respond most keenly to changes in force below 1 N, less than the weight of a tangerine3. That is precisely the level of force the incisors used to hold the peanut.

A gap a few hairs wide holds this much sensation. That is why I see the inside of the mouth not as a small space, but as one as vast and intricate as the universe. That space is built a little differently at each tooth: toward the molars, the force used to hold a peanut and the range in which most receptors are sensitive grow larger together3,9.

The force at which a person first notices a tooth being pressed is far smaller still: the periodontology textbook gives 1–2 g1. The value varies from study to study and from person to person2, but on average it stays far below the force used to hold a peanut.

Holding force by tooth, the range where most receptors are most sensitive, and the force first felt on a natural tooth Horizontal chart for four teeth (central incisor, canine, second premolar, first molar): an orange dot marks the force used to hold half a peanut and a band marks the range where most periodontal mechanoreceptors are most sensitive. Holding forces are 0.60, 0.77, 1.15 and 1.74 N; the sensitive range is 1 N or less for the front teeth (central incisor, canine) and 4 N or less for the back teeth (premolar, molar). The left end of each band fades out because a logarithmic axis cannot show 0 N. A separate row shows the force at which a natural tooth is first felt (tooth type not specified): the textbook value of 1–2 g (about 0.01–0.02 N) as a hollow bar and one study's mean of about 0.11 N (22 people) as a hollow dot (in that study, values ranged from 1.2 to 26.2 g across participants, so most of the textbook range falls within them). The sensitive range comes from nerve recordings and the first-felt force from people's responses, so they are different measurements. Placing the results side by side is the site's choice. Central incisorHolding force 0.60 N Front teeth: 1 N or less CanineHolding force 0.77 N Front teeth: 1 N or less Second premolarHolding force 1.15 N Back teeth: 4 N or less First molarHolding force 1.74 N Back teeth: 4 N or less Natural teeth: force first felt (tooth type not specified) Textbook: 1–2 g (≈0.01–0.02 N) One study (n = 22): mean ≈0.11 N 1 N 4 N Force (N), log scale Range where most PDL receptors are most sensitive Force used to hold half a peanut (20 people) Force first felt (textbook, passive detection) Force first felt, mean (one study) Data: Johnsen et al. 2007 · Trulsson 2006 · Hämmerle et al. 1995 · Jacobs 2015 (Lindhe, 6th ed.); redrawn by the site from reported values. Sensitive range: nerve recordings. Force first felt: people's responses (varies by study and person). Putting the results together is the site's choice.
Graph 1 Force used to hold half a peanut with each tooth (20 people), the range in which most periodontal mechanoreceptors are most sensitive, and the force at which a pressed natural tooth is first felt. The researchers explained the differences in holding force between teeth in terms of the different sensitive ranges of periodontal sensation in the front and back teeth9. The sensitive range comes from nerve recordings and the force first felt from people’s responses, so they are different measurements; the force first felt varies by study and by person: 1–2 g in the textbook, and a mean of 11.5 g (range 1.2–26.2 g across participants) in one study, and most of the textbook range (1.2–2 g) falls within that study’s range. The three kinds of values come from different publications1,2,3,9; combining them in one graph is the site’s choice. The horizontal axis is logarithmic.
Read the graph as text
ToothFront or backForce used to hold half a peanut (20 people)Range where most receptors are most sensitive
Central incisorFront teeth0.60 N1 N or less
CanineFront teeth0.77 N1 N or less
Second premolarBack teeth1.15 N4 N or less
First molarBack teeth1.74 N4 N or less
Natural teeth (tooth type not specified)Not specifiedForce first felt: 1–2 g in the textbook (about 0.01–0.02 N, passive force detection); mean about 0.11 N in one study (22 people; range 1.2–26.2 g across participants)Not applicable

The canine is grouped with the front teeth; its sensitive range was not measured separately. The sensitive range starts at 0 N: for the front teeth the text of the review (Trulsson 2006) gives 0–1 N, and for the back teeth the review gives only an upper limit of 4 N. The sensitive range comes from nerve recordings and the force first felt from people's responses, so they are different measurements. The force first felt varies by study and by person; most of the textbook range (1.2–2 g of its 1–2 g) lies within one study's range across participants (1.2–26.2 g). Holding force, sensitive range and force first felt come from different publications; putting them together is the site's choice.

How does tooth sensation become jaw-muscle force?

Sensory signals from the teeth travel along the trigeminal nerve to the brainstem10 and are used to regulate the force of the jaw muscles5. An occlusion textbook explains that the brainstem’s chewing rhythm generator (a central pattern generator) uses this information to choose the most suitable chewing movement10. According to the pathway mapped in animal studies, the signal then passes to the motor neurons of the jaw-closing muscles11. When the muscles change their force, that change reaches the PDL again, so in effect the signal travels a full loop. This loop is the site’s summary, weaving together textbook explanations and a number of experiments.

A touch of less than 1 N at the tip of an incisor travels along the trigeminal nerve to the brainstem and comes back as force in the jaw-closing muscles. This loop is the site’s summary, and the details of the last stretch, from the brainstem to the motor neurons, rest on animal studies.

The teeth seem to be one thing and the jaw muscles another. Yet even while holding just half a peanut, the two do not move separately. I read this loop as one of the smallest scenes showing that the body is connected.

The whole loop. Pick a step to light up only that part.

Half apeanut PDLreceptors position marker(not thickness) PDL anesthesia:reduced signal Inferior alveolar nerve(branch of V3) Trigeminal ganglion Brainstem Trigeminal nuclei ·chewing rhythmgenerator Nucleus positions:schematicMotor-side detail:animal data Jaw-closing muscle(masseter etc.) Muscle spindles Jaw-closing force reaches the incisor;force change sensed again Link to wider brain functions(memory, cognition):still a hypothesis Seen from the patient's left; face on the left Lower jaw (public CBCT data, one person) andskull with upper jaw (anatomical atlas model):from two different people, aligned as stated in the creditsPeanut-hold pose: computed sensory signal motor signal Force on the incisor (same scale) Hold under 1 N Split 16–19 N After anesthesia: holdingforce up; unsteady in someexperiments · splittingforce: same size
Peanut PDL position marker PDL anesthesia:reduced signal Inferioralveolar nerve (branch of V3) Trigeminal nerve Brainstem Motor side: animal data Jaw muscles Muscle spindles Link to memory and cognition:still a hypothesis Patient's left side,face on the left Force on the incisor (same scale) Hold under 1 N Split 16–19 N After anesthesia: holding force up;unsteady in some experiments ·splitting force: same size Lower jaw (public CBCT data, one person) andskull with upper jaw (anatomical atlas model):from two different people, aligned as stated in the creditsPeanut-hold pose: computed
  • Textbook anatomy and human experiments (some details from animal data)
  • Experiments that reduced periodontal sensation
  • Still a hypothesis
  • Gray: other sensory input (muscle spindles)
Figure 1Concept visualization · The loop in which sensation at the tooth root travels through the trigeminal nerve and brainstem and comes back as force in the jaw muscles. This loop is the site's summary, weaving together textbook explanations and a number of experiments. Press the step buttons above the figure to light up one step at a time. Solid lines show textbook and human-experiment findings (the details from the brainstem to the motor neurons come from animal data), blue lines show experiments that reduced periodontal sensation, and the dotted line shows what is still a hypothesis. The gray line shows other sensory input, such as from muscle spindles.

Anatomy: lower jaw, teeth and inferior alveolar canal from ToothFairy2 CBCT (Bolelli et al.) — the upper ramus (condyle, coronoid process) completed from Z-Anatomy · skull (including the facial bones and upper jaw), upper teeth, brainstem, nerves and masseter from Z-Anatomy (Gauthier Kervyn, Marcin Zielinski; based on BodyParts3D) · root entry position from 7T MRI (Edlow et al., CC0) · root direction from HCP1065 (Yeh 2022, Human Connectome Project data). Lower jaw (public CBCT data, one person) and skull with upper jaw (anatomical atlas model) are from two different people, aligned as stated under “Modifications” in the credits. The peanut-holding pose is computed. The positions of the trigeminal ganglion, nerve roots and trigeminal nuclei are schematic, as are the short connections from the ganglion to each opening. Adapted from the original data. This figure is licensed under CC BY-SA 4.0.

Full credits
  • ToothFairy2 dataset (University of Modena and Reggio Emilia · Radboud University), CC BY-SA 4.0. Case ToothFairy2P_091, labels 1 (mandible), 3 (left inferior alveolar canal) and 31–38 (left lower teeth) only. Bolelli F et al., Med Image Anal 2026;104095, https://doi.org/10.1016/j.media.2026.104095 · Bolelli F et al., CVPR 2025, https://doi.org/10.1109/CVPR52734.2025.00494 · Lumetti L et al., IEEE Access 2024, https://doi.org/10.1109/ACCESS.2024.3408629
  • Z-Anatomy (Gauthier Kervyn, Marcin Zielinski), CC BY-SA 4.0: skull (skull base, frontal, parietal, nasal, lacrimal, ethmoid, maxilla, palatine, vomer, inferior nasal conchae, zygomatic), upper teeth (11–17, 21–27), brainstem, nerve curves, masseter, completion of the upper ramus. Many shapes are based on BodyParts3D, © The Database Center for Life Science, CC BY 4.0.
  • Edlow BL, Mareyam A, Horn A, et al. 7 Tesla MRI of the ex vivo human brain at 100 micron resolution. OpenNeuro ds002179, https://doi.org/10.18112/openneuro.ds002179.v1.1.0, CC0.
  • Tractography: HCP1065 atlas, Yeh FC (2022), CC BY-SA 4.0, https://doi.org/10.1038/s41467-022-32595-4. Data were provided in part by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University. · WU-Minn HCP Consortium Open Access Data Use Terms
  • Modifications: rendered with a new camera, translucency and outlines, the top of the skull faded; the lower jaw rotated and shifted to sit closed against the skull (the mismatch between the two datasets was shared among connected structures, such as the condyle's position in the jaw joint and the relation of the upper and lower teeth, according to how much each can move or adapt; this is a fitted relation, not one person's anatomy); as part of that fit, the upper jaw with its teeth moved back by 3.9 mm and the upper incisors and canines tilted by 4° (the maxilla's shift tapers to zero below the orbit and also moves the distal part of the maxillary nerve that runs through the upper jaw); the peanut-holding pose is computed (the lower jaw protruded, with the condyle about 8 mm forward, and opened by about 5°, computed for this model's bone shape); the right half of the lower jaw, teeth 41–48 and the right temporal bone are not drawn (hidden in the side view); the insertion of the (atlas) masseter moved to that jaw position and vertices inside the bone pushed out by up to 3.4 mm; arrows, text and the peanut added.
  • License: CC BY-SA 4.0, https://creativecommons.org/licenses/by-sa/4.0/
Read the figure as text
  1. ① Contact and sensing When the peanut touches the incisors, the mechanoreceptors in the PDL respond. At the incisors, most of them are most sensitive to force changes of 1 N or less.
  2. ② From brainstem to jaw muscle The signal travels along the trigeminal nerve to the brainstem and feeds into the activity of the jaw-closing muscles. Other sensory input, such as from muscle spindles, comes in as well. The detailed wiring from the brainstem to the motor neurons rests on animal data.
  3. ③ From holding to splitting First the peanut is held with under 1 N, then split with 16–19 N. While it is held, the PDL senses the force changes again.
  4. ④ With PDL sensation reduced When the periodontal tissues were anesthetized, the holding force grew larger and, in some experiments, unsteady. The size of the splitting force stayed the same, but one study found that the time taken to split the peanut and the rate at which force rose both changed.

Links in the figure

  • Peanut contact → PDL
  • PDL → Trigeminal nerve (signal)
  • Trigeminal nerve → Brainstem
  • Brainstem → Jaw-closing muscle (regulates activity)
  • Jaw-closing muscle → Hold
  • Hold → Split
  • Hold → PDL (force change sensed again)
  • Muscle spindles etc. → Trigeminal nerve
  • PDL anesthesia → Trigeminal nerve (reduced signal, blue line)
  • PDL anesthesia → After anesthesia (blue line)
  • PDL → Wider brain functions (still a hypothesis, dotted line)

What changes when the periodontal tissues are anesthetized?

When the periodontal tissues are anesthetized, the force used to hold a peanut grows larger, and the morsel often slips from the incisor tips4,5. Some experiments found that the force also became unsteady, but in the largest one (45 people) it did not become more unsteady4,5,9,12. Anyone who has tried to pick up a small bead while wearing thick gloves will recognize the picture. The size of the splitting force stayed the same4,5,9, but in one study (15 people) splitting the peanut took longer and the force rose more slowly13.

When the sensation was briefly reduced, holding became clumsy, but the large splitting force stayed the same. The researchers concluded that this sense is used mainly when food is held and handled lightly, rather than when it is bitten hard5.

Holding and splitting force, and with periodontal sensation reduced Force chart on a logarithmic axis. Top row (normal sensation): a short bar for the holding force, 0.36–0.76 N across participants, far from a bar for the splitting force, 16.0–19.0 N across participants, with the note 'More than 20× apart'. Bottom row (periodontal sensation reduced, in blue): a dotted outline bar at the usual holding position with a short arrow to the right, labeled 'larger (no value in the abstract)', and a small wave mark labeled 'unsteady'. The arrow shows direction only: the abstract gives no value, and the same group's review shows the values only in a figure. The splitting force is drawn as an outline bar at the same position, labeled 'no effect'. Normal sensation HoldSplit 0.36–0.76 N16.0–19.0 N More than 20× apart PDL sensation reduced (local anesthesia) HoldSplit Larger (no value in the abstract) Unsteady No effect 1 N 10 N Force (N), log scale Dashed bar: where the usual holding force sits; arrow and wave: direction only (no value in the abstract). Bars and numbers: reported values. Data: Trulsson & Johansson 1996b, redrawn by the site; "20×" is the site's calculation.
Graph 2 Forces used by the incisors to hold and split half a peanut, normally and with periodontal sensation reduced by local anesthesia4. Each range shows the spread across participants, and the horizontal axis is logarithmic. The arrow for the holding force after anesthesia shows direction only: the abstract gives no value, and the same group’s review shows the values only in a figure5.
Read the graph as text
ConditionHolding forceSplitting force (peanut)
Normal sensationUnder 1 N; 0.36–0.76 N across participants16.0–19.0 N across participants (more than twenty times the holding force; site calculation)
Periodontal sensation reduced (local anesthesia)Larger and unsteady (no value in the abstract)No effect

Data: Trulsson & Johansson 1996b. The arrow and the wave mark for the holding force after anesthesia show direction only: the abstract gives no value, and the same group's review (Trulsson & Johansson 1996a) shows the values only in a figure.

Table 2 What changed when periodontal sensation was reduced (local anesthesia)

Experiment (participants)What changed
Holding and splitting a morsel with the incisors4,5Holding force larger and unsteady. The morsel often slipped from the incisor tips. No effect on the splitting phase
Half a peanut, incisors to molars (4 people)9Holding force larger and more unsteady at every tooth. No clear change in the splitting phase
Biscuit and peanut (15 people)13Before anesthesia biscuits split at about 9 N and peanuts at about 18 N on average; after anesthesia, splitting a peanut took longer and the force rose more slowly, so the force profiles for the two foods could no longer be told apart
Show the other experiments
Experiment (participants)What changed
Chewing (14 people; infiltration and PDL injections on the chewing side)14Number of chewing strokes unchanged; timing of masseter (a chewing muscle) activity changed. The researchers estimate that periodontal sensation contributes about 20% of the muscle activity in the jaw-closing phase
45 people in three anesthesia groups (reference group: 20 people from an earlier study with the same task)12Holding force higher in the incisor and nerve-block groups. Holding and splitting forces did not become more unsteady, and splitting force did not differ between groups. With repetition, force tended to recalibrate
Another research group, holding a light sensor between the incisors (20 people)15When seated, the minimum force needed to keep the sensor from dropping rose from a mean of 0.63 N to 1.87 N
Another research group, periodontal tissues and mucosa anesthetized on the chewing side (11 people)16Reduced ability to break up and mix peanuts

To return to the half peanut we began with: that light force of less than 1 N fell within the range in which most of the sensory receptors at the tooth root are most sensitive, and when that sensation was reduced, the change centered on that same light hold. In the next article, I plan to read the evidence on how this loop changes with implants, which have no PDL.

The mouth is not the only window into the body. Still, I think it is one of the high-resolution ones: a window that can feel even forces far smaller than 1 N.

This note covers the PDL, the second station on the Somatic Dentistry evidence map. Definition: Somatic Dentistry is a perspective within dentistry that reads how sensation and movement in the teeth and mouth connect with the rest of the body, distinguishing connections established by anatomy, those observed in human studies and those that are still hypotheses. What is Somatic Dentistry? · Evidence map: PDL (coming soon)

Evidence

  • What this article can say. When people hold food with their incisors, they tend to use the small range of forces to which periodontal mechanoreceptors are most sensitive, and reducing periodontal sensation makes the holding force larger.
  • What this article cannot say. It does not show that the PDL alone sets the force, that the anesthesia results reflect the effect of the PDL alone, or that training this sense improves health or brain function.

The table below collects, for each of the four questions in the text, the supporting evidence alongside contrary results and limitations; evidence beyond those questions (the FAQ and the analogies) is in the last row. Each cell starts with the broadest sources: textbooks, then reviews and systematic reviews, human studies, animal studies and hypotheses. Textbooks are ordered by how directly they state the row’s claim rather than by citation count; other sources in the same tier are ordered by citation count (OpenAlex, retrieved October 11, 2026). In the supporting-evidence column, each cell shows representative sources, and the rest can be expanded. In the contrary-results column, textbooks come first, and the rest can be expanded. “Same research line” marks publications with Trulsson as an author. There are five grades: established (textbook), human studies, animal data, hypothesis and editorial interpretation.

Table 3 The four questions in the text and further evidence

Question in the textSupporting evidenceContrary results and limitationsGrade
How much force do the front teeth use to hold a peanut?
Under 1 N; splitting takes more than twenty times that
  • Textbook Klineberg & Eckert, ch. 10 (same research line: written by Svensson and Trulsson, who ran the experiments): the holding force with the incisors is below 1 N. For molars it gives about 2–3 N, which differs from the 1.74 N for the first molar in Johnsen et al. 20076
  • Review Trulsson & Johansson 1996a (same research line): when holding food between the incisors, people spontaneously use low forces matched to the sensitive range of periodontal sensation (the abstract gives no number for this force)5
  • Human study Trulsson & Johansson 1996b (same research line): the force for holding half a peanut or a biscuit is under 1 N (0.36–0.76 N across participants); the force for splitting a peanut is 16.0–19.0 N across participants4
3 more (3 human studies)
  • Human study Johnsen et al. 2007 (same research line): the force for holding half a peanut is 0.60 N at the central incisor and 1.74 N at the first molar (20 people)9
  • Human study Svensson & Trulsson 2009 (same research line): peanuts split at about 18 N and biscuits at about 9 N (15 people)13
  • Human study Oguz et al. 2026 (another research group, another method): the minimum force needed to hold a light sensor between the incisors averages 0.63 N when seated (20 people)15
  • Textbook Okeson (ch. 2, pp. 23–35): treats force mainly as maximum bite force and does not address the small forces of this row10
  • Experimental conditions These were laboratory tasks with few participants, and the instructions are reported differently in different sources. The 1996b abstract says no instruction was given about force4, the textbook chapter co-written by Trulsson says participants were asked to use as little force as possible while holding6, and the incisor-to-molar study told participants not to use more force than necessary9
2 more contrary results and limitations
  • Same task, other questions The same hold-and-split task has been used in studies without Trulsson as an author to look at jaw-muscle pain17, development in children18, teeth after root-end surgery19 and implants20
  • Same research line The textbook chapter and the hold-and-split human studies in this row all have Trulsson as an author; the only value from another research group is Oguz et al. 2026, with a different method
Human studies
Where does a tooth feel such a small force?
Mainly by the PDL mechanoreceptors around the root. The receptors’ most sensitive range (nerve recordings) and the force a person first feels (people’s responses) are different measurements
  • Textbook Lindhe (chapter by Jacobs): the tactile function of teeth is mainly determined by PDL receptors, and the force at which a pressed tooth is first felt (passive force detection) is 1–2 g (about 0.01–0.02 N)1
  • Textbook Klineberg & Eckert, ch. 10 (same research line): each tooth’s PDL holds several hundred highly sensitive touch receptors, which let us perceive forces on the teeth as touch6
  • Review Trulsson 2006 (same research line): recordings from single nerve fibers show that most receptors are most sensitive to force changes of 1 N or less at the front teeth and 4 N or less at the back teeth3
  • Human study Hämmerle et al. 1995: when a natural tooth is pressed with steadily increasing force, the force at which this is first felt averages 11.5 g (about 0.11 N), ranging from 1.2 to 26.2 g across participants; implants need on average 8.75 times that (22 people)2
4 more (2 textbooks, 1 review, 1 human study)
  • Textbook Ten Cate: the PDL is soft connective tissue between the cementum covering the root and the alveolar bone of the socket wall, 0.15–0.38 mm wide7
  • Textbook Newman & Carranza: periodontal mechanoreceptors finely discriminate differences in pressure21
  • Review Trulsson & Johansson 1996a (same research line): human periodontal signals were recorded from the inferior alveolar nerve, which supplies the lower teeth, and most (15 of 19) of the receptors analyzed in the front teeth were most sensitive to force changes below 1 N5
  • Human study Johnsen et al. 2007 (same research line): the holding force rises from 0.60 N at the central incisor to 1.74 N at the first molar, which the researchers explain by the different sensitivity of front and back periodontal sensation (20 people)9
  • Textbook Newman & Carranza: there is little evidence of proprioceptive sense organs within the PDL21
  • Systematic review Song et al. 2022: concludes that implants, which have no PDL, also give a sense of touch (osseoperception), though thresholds are higher than for natural teeth22
  • Human study Enkling et al. 2007: with a single implant opposed by a natural tooth, detecting a thin foil was about as good as between natural teeth (62 people)23
  • Varies by study and person The force first felt is 1–2 g in the textbook (passive force detection on a pressed tooth) and a mean of 11.5 g, 1.2–26.2 g across participants, in one study, so most of the textbook range (1.2–2 g) lies within that study’s range across participants (the two sources above)
1 more limitation
  • Site composition Graph 1 places results of different kinds of measurement side by side (holding force, sensitive range, force first felt)
Established, human studies
How does tooth sensation become jaw-muscle force?
It travels along the trigeminal nerve to the brainstem and regulates jaw-muscle force. The whole loop (Figure 1) is the site’s summary
  • Textbook Okeson: sensory signals from the face and mouth enter the brainstem through the trigeminal nerve, and receptors in the mouth, including those in the PDL, continually feed back information that guides muscle activity. The brainstem’s chewing rhythm generator uses this information to choose the most suitable chewing movement10
  • Textbook Lindhe (chapter by Jacobs): this path through the trigeminal nerve to the brainstem is a sensory feedback pathway that refines jaw movements, and periodontal touch information serves mainly to fine-tune biting and chewing forces rather than to provide protection1
  • Review Lund & Kolta 2006: the basic chewing rhythm is generated by a central pattern generator in the brainstem (pons and medulla), and sensory feedback modifies its output; oral touch receptors, muscle spindles of the jaw-closing muscles and PDL mechanoreceptors have especially strong effects24
8 more (3 reviews or systematic reviews, 2 human studies, 2 animal studies, 1 hypothesis)
  • Review Trulsson 2006 (same research line): periodontal signals are used in the fine motor control of the jaw3
  • Review Trulsson & Johansson 1996a (same research line): people rely on these signals to regulate the jaw muscles mainly when they first contact, handle and hold food5
  • Systematic review Piancino et al. 2017: reviewing 51 human and animal studies, concludes that periodontal mechanoreceptors are deeply involved in activating and coordinating the chewing muscles25
  • Human study Grigoriadis et al. 2019 (same research line): the researchers estimate that periodontal sensation contributes about 20% of muscle activity in the jaw-closing phase (14 people)14
  • Human study Naser-ud-Din et al. 2010 (another research group): tapping the incisors evoked a periodontal mechanoreceptor reflex in the masseter (28 people)26
  • Animal study Morimoto et al. 1989 (rabbits): a thin strip between the molars increased jaw-closing muscle activity, and this facilitation comes mainly from periodontal receptors and muscle spindles together27
  • Review of animal data Yoshida et al. 2017 (mostly cat data): the mesencephalic trigeminal nucleus in the brainstem receives input from the PDL and muscle spindles and relays it mainly to the jaw-closing motor neurons11
  • Hypothesis Oh 2026 (the editor’s hypothesis paper): the dotted line in Figure 1. The idea that tooth sensation is linked to memory or cognition was proposed in this paper and is not a conclusion established in people28
  • Textbook Ten Cate: whether the jaw-opening reflex is needed for chewing or serves only a protective role is not known7
  • Human study Naser-ud-Din et al. 2010: a muscle-spindle reflex appeared as well, and both reflexes weakened during simulated chewing (28 people)26
  • Animal study Hidaka et al. 1997: in anesthetized rabbits making cortically induced chewing movements, cutting the dental nerves slowed the rapid rise in force, but force was still adjusted to the hardness of the object being chewed29
1 more limitation
  • Site summary The whole loop from the PDL to the jaw muscles (Figure 1) weaves together textbook explanations and experiments, and the details of the last stretch from the brainstem to the motor neurons rely on animal data
Established, human studies, animal data (brainstem details), hypothesis (dotted line in Figure 1)
What changes when the periodontal tissues are anesthetized?
The holding force rises. Some experiments found it became unsteady and the largest (45 people) did not; the splitting force kept its size, though one study found splitting took longer
  • Textbook Klineberg & Eckert, ch. 10 (same research line): without periodontal information (local anesthesia, complete dentures, implant-supported prostheses) holding forces are not only higher but also more variable6
  • Textbook Lindhe (chapter by Jacobs): anesthesia raises the threshold at which a tooth senses touch (perception, not force control)1
  • Review Trulsson & Johansson 1996a (same research line): without periodontal information the control of holding force is severely impaired, and few nerve fibers signal the fast, strong force used to bite through food5
9 more (1 textbook, 1 review, 7 human studies)
  • Textbook Newman & Carranza: losing PDL mechanoreceptors can impair the control of muscle activity (receptor loss, not anesthesia)21
  • Review Trulsson 2006 (same research line): when these receptors are lost, as in people with implants, important sensory and motor functions are lost or impaired (receptor loss, not anesthesia)3
  • Human study Trulsson & Johansson 1996b (same research line): with anesthesia the holding force is larger and unsteady and the morsel often slips from the incisor tips, while the splitting phase is unaffected4,5
  • Human study Johnsen et al. 2007 (same research line): at every tooth from incisor to molar the size and unsteadiness of the holding force increased, with no clear change in the splitting phase (4 people)9
  • Human study Svensson & Trulsson 2009 (same research line; splitting time and rate): after anesthesia splitting a peanut took longer and the force rose more slowly (15 people)13
  • Human study Kumar et al. 2017 (same research line): holding force rose in the incisor and nerve-block groups (45 people; the reference group was 20 people from an earlier study)12
  • Human study Grigoriadis et al. 2019 (same research line): the number of chewing strokes stayed the same, but the timing of masseter activity changed (14 people; infiltration and PDL injections)14
  • Human study Yoshida et al. 2015 (another research group, another task): anesthetizing the periodontal tissues and mucosa on the chewing side reduced the ability to break up and mix peanuts (11 people)16
  • Human study Oguz et al. 2026 (another research group, another method): the minimum force needed to keep a sensor from dropping rose from a mean of 0.63 N to 1.87 N when seated (20 people; splitting not measured)15
  • Review Türker 2002: in human chewing experiments any stimulus engages several sensory systems together, so stimulating one system alone is not yet possible30
  • Human study Hellsing 1980: anesthetizing the jaw joint and the periodontal receptors in 8 people with natural teeth and 5 with complete dentures did not noticeably change their ability to produce maximum bite force or a requested incisor bite force. The author suggests that well-learned, preprogrammed movements can run without peripheral feedback31
  • Human study Kumar et al. 2017 (45 people): the unsteadiness of holding and splitting forces did not increase, splitting force did not differ between groups, and force tended to recalibrate with repetition12
  • Human study Higaki et al. 2016: in a task of holding about 27.5 N with the first molar for 30 seconds, performance was similar after anesthesia (5 people; not a small-force task, and force was matched to visual and auditory cues)32
2 more contrary results and limitations
  • Site interpretation Because of the limit noted by Türker 2002, the anesthesia results cannot be attributed to the PDL alone. The area actually anesthetized also differed: infiltration and PDL injections in Grigoriadis et al. 2019, periodontal tissues and mucosa in Yoshida et al. 2015
  • Replication The four hold-and-split human studies cited here (1996, 2007, 2009, 2017) and one chewing study from the same line (2019) all have Trulsson as a co-author, and the PubMed search for this article found no record of another group repeating a study that combined periodontal anesthesia with the hold-and-split task. Two experiments by other groups (Yoshida et al. 201516, Oguz et al. 202615) used different tasks or methods but point the same way
Established, human studies
Further evidence (FAQ, analogies, conversions)
Implant sensation, brain function, and analogies that give a sense of scale
  • Textbook Klineberg & Eckert, ch. 10: an implant is attached directly to bone and has no PDL, so there are no such mechanoreceptors close to it6
  • Textbook Lindhe (chapter by Jacobs): after implants are placed, the force first felt rises to 50–100 g1
  • Systematic review Song et al. 2022: concludes that implants also give a sense of touch (osseoperception)22
5 more (3 human studies, 1 hypothesis, 1 analogy)
  • Human study Hämmerle et al. 1995: pressure on an implant is first felt only at, on average, 8.75 times the force needed for a natural tooth (22 people)2
  • Human study Enkling et al. 2007: with a single implant opposed by a natural tooth, thin-foil detection was about as good as between natural teeth (62 people)23
  • Human study Higaki et al. 2016: anesthetizing the periodontal tissues while holding force with a molar reduced prefrontal blood flow (5 people)32
  • Hypothesis Oh 2026: the link between tooth sensation and brain function was proposed in the editor’s hypothesis paper28
  • Analogies and conversions 1 N is about the weight of a 100 g object and one tangerine weighs 76–120 g (USDA FoodData Central; site calculation). One hair is about 80 µm thick8, so the PDL is 2–5 hairs wide (site calculation). The thick-gloves analogy comes from everyday experience
  • Human study Higaki et al. 2016 did not measure memory or cognition
  • Analogy Analogies and conversions are not evidence; they are the site’s way of giving a sense of scale
Established, human studies, hypothesis, editorial interpretation
Show the evidence for every statement

Table 4 Claims table: the evidence grade and sources of the 32 main factual statements in the text (numbers refer to the reference list)

ClaimEvidence gradeSource no. · DOI
Periodontal touch information is used mainly for the fine control of biting and chewing forces, not for protectionEstablished1 ISBN 978-0-470-67248-8
Teeth feel the forces placed on them as touch (periodontal receptors provide the conscious perception of force)Established1 ISBN 978-0-470-67248-8; 2 doi:10.1034/j.1600-0501.1995.060203.x; 6 doi:10.1016/b978-0-7234-3809-0.00010-3
The force at which a pressed tooth is first felt is 1–2 g (about 0.01–0.02 N) in the textbook, and 50–100 g for implantsEstablished1 ISBN 978-0-470-67248-8
A loop from tooth sensation through the trigeminal nerve, brainstem and jaw muscles back to the teeth (Figure 1; the site's summary of textbooks and studies)Editorial interpretation1 ISBN 978-0-470-67248-8; 4 doi:10.1007/BF00230428; 5 doi:10.1016/s0301-0082(96)00016-0; 10 ISBN 978-0-323-58210-0; 11 doi:10.2334/josnusd.16-0845; 26 doi:10.1177/0022034509352842; 27 doi:10.1007/BF00247900
Toward the molars the holding force and the receptors' sensitive range grow together (two results placed side by side)Editorial interpretation1 ISBN 978-0-470-67248-8; 2 doi:10.1034/j.1600-0501.1995.060203.x; 3 doi:10.1111/j.1365-2842.2006.01629.x; 9 doi:10.1007/s00221-006-0719-9
The receptors' most sensitive range (nerve recordings) and the force a person first feels (people's responses) are different measurements, and the force first felt varies by study and personEditorial interpretation1 ISBN 978-0-470-67248-8; 2 doi:10.1034/j.1600-0501.1995.060203.x; 3 doi:10.1111/j.1365-2842.2006.01629.x; 4 doi:10.1007/BF00230428
When a natural tooth was pressed with steadily increasing force, the force at which this was first felt averaged 11.5 g (about 0.11 N); implants needed 8.75 times that (22 people)Human studies2 doi:10.1034/j.1600-0501.1995.060203.x
Most periodontal mechanoreceptors are most sensitive to force changes of 1 N or less at the front teeth and 4 N or less at the back teethHuman studies3 doi:10.1111/j.1365-2842.2006.01629.x
The force for holding half a peanut or a piece of biscuit with the central incisors is under 1 N (0.36–0.76 N across participants) and steadyHuman studies4 doi:10.1007/BF00230428
The force for splitting half a peanut is 16.0–19.0 N across participantsHuman studies4 doi:10.1007/BF00230428
With the periodontal tissues anesthetized, the holding force is larger and unsteady and the morsel slips out, while the splitting phase is unaffectedHuman studies4 doi:10.1007/BF00230428; 5 doi:10.1016/s0301-0082(96)00016-0
1 N is about the weight of a 100 g object, and the splitting force is more than twenty times the holding force (site calculation)Editorial interpretation4 doi:10.1007/BF00230428
1 N is about the weight of a tangerine resting in the palm (one tangerine 76–120 g; analogy)Editorial interpretation4 doi:10.1007/BF00230428; fdc.nal.usda.gov
The anesthesia result is compared with picking up a small bead in thick gloves (analogy)Editorial interpretation4 doi:10.1007/BF00230428; 5 doi:10.1016/s0301-0082(96)00016-0; 9 doi:10.1007/s00221-006-0719-9
Human periodontal signals were recorded from the inferior alveolar nerve, which supplies the lower teeth. The researchers concluded that this sense is used mainly when food is first contacted, handled and heldHuman studies5 doi:10.1016/s0301-0082(96)00016-0
Each tooth's PDL holds several hundred highly sensitive touch receptors; none lie close to an implantEstablished6 doi:10.1016/b978-0-7234-3809-0.00010-3
Whether the jaw-opening reflex is needed for chewing or serves only a protective role is not knownEstablished7 ISBN 978-0-323-48524-1
The PDL is soft connective tissue between root and bone, 0.15–0.38 mm wideEstablished7 ISBN 978-0-323-48524-1
The PDL is as wide as a few hairs side by side (one hair about 80 µm; analogy)Editorial interpretation7 ISBN 978-0-323-48524-1; 8 doi:10.1155/2020/2476890
The force for holding half a peanut rises from 0.60 N at the central incisor to 1.74 N at the first molar; with anesthesia it rises and becomes unsteady at every toothHuman studies9 doi:10.1007/s00221-006-0719-9
The brainstem's chewing rhythm generator chooses the chewing movement from the information the teeth and PDL feed backEstablished10 ISBN 978-0-323-58210-0
Sensory signals from the teeth and mouth enter the brainstem (pons) along the trigeminal nerveEstablished10 ISBN 978-0-323-58210-0
The mesencephalic trigeminal nucleus in the brainstem receives input from the PDL and muscle spindles and relays it mainly to the jaw-closing motor neuronsAnimal data11 doi:10.2334/josnusd.16-0845
With anesthesia, splitting a peanut takes longer and the force rises more slowly (before anesthesia, biscuits split at about 9 N and peanuts at about 18 N)Human studies13 doi:10.1111/j.1600-0722.2009.00691.x
Implants also give a sense of touch, known as osseoperception (systematic review of human and animal studies)Human studies22 doi:10.1111/joor.13296
With a single implant opposed by a natural tooth, detecting a thin foil was about as good as between natural teeth (62 people)Human studies23 doi:10.1111/j.1600-0501.2006.01321.x
In mammals, a pattern generator in the brainstem (pons and medulla) generates the chewing rhythm, and feedback from oral touch receptors, muscle spindles and PDL mechanoreceptors modifies it especially strongly (review)Animal data24 doi:10.1007/s00455-006-9027-6
Periodontal mechanoreceptors are deeply involved in activating and coordinating the chewing muscles (systematic review of 51 human and animal studies)Animal data25 doi:10.1016/j.archoralbio.2017.02.010
In rabbits, the facilitation of jaw-closing muscle activity comes mainly from periodontal receptors and muscle spindles togetherAnimal data27 doi:10.1007/BF00247900
The idea that tooth sensation is linked to memory or cognition (the editor's hypothesis paper)Hypothesis28 doi:10.1016/j.nbas.2026.100169; 32 doi:10.1038/srep36893
With the periodontal tissues anesthetized, prefrontal blood flow fell, but memory and cognition were not measured (5 people)Human studies32 doi:10.1038/srep36893
Somatic Dentistry is a perspective within dentistry that reads how sensation and movement in the teeth and mouth connect with the rest of the body, distinguishing connections established by anatomy, those observed in human studies and those that are still hypotheses.Editorial interpretationSite definition C (editor's decision, October 11, 2026; definition page)

Frequently asked questions

What is the periodontal ligament? It is the soft connective tissue that fills the space between the tooth root and the bony wall of its socket in the jaw. It is 0.15–0.38 mm wide7, and in each tooth it holds several hundred sensitive mechanoreceptors that turn forces on the tooth into nerve signals6.

Do implants have this sense too? An implant is attached directly to the bone and has no PDL, so there are no such mechanoreceptors close to it6. The periodontology textbook states that a press of 1–2 g is noticed on a natural tooth, whereas an implant needs 50–100 g1. In a study of 22 people, pressure on a natural tooth was noticed at about 11.5 g (about 0.11 N) on average, while an implant needed 8.75 times as much on average2. On the other hand, one study (62 people) found that with a single implant opposed by a natural tooth, detecting a thin foil was about as good as between natural teeth23, and a systematic review concluded, on the basis of brain adaptation and nerve fibers around implants, that implants also give a sense of touch (osseoperception)22.

Is chewing hard food good for the brain? The studies in this article do not show that. What they measured was force control in the jaw, and the human study (5 people) in which prefrontal blood flow fell when the periodontal tissues were anesthetized while a force was held with a molar did not measure memory or cognition32. The link between tooth sensation and brain function is an idea I proposed in a hypothesis paper, not a conclusion established in people28.

References

1. Jacobs R. From Periodontal Tactile Function to Peri-implant Osseoperception. In: Lang NP, Lindhe J, editors. Clinical Periodontology and Implant Dentistry. 6th ed. Wiley Blackwell; 2015. Ch. 6, pp. 112–121. ISBN 978-0-470-67248-8. https://books.google.com/books?vid=ISBN9780470672488
2. Hämmerle CH, Wagner D, Brägger U, Lussi A, Karayiannis A, Joss A, et al. Threshold of Tactile Sensitivity Perceived with Dental Endosseous Implants and Natural Teeth. Clinical Oral Implants Research. 1995;6(2):83–90. https://doi.org/10.1034/j.1600-0501.1995.060203.x
3. Trulsson M. Sensory‐motor Function of Human Periodontal Mechanoreceptors. Journal of Oral Rehabilitation. 2006;33(4):262–273. https://doi.org/10.1111/j.1365-2842.2006.01629.x
4. Trulsson M, Johansson RS. Forces Applied by the Incisors and Roles of Periodontal Afferents during Food-Holding and -Biting Tasks. Experimental Brain Research. 1996b;107(3):486–496. https://doi.org/10.1007/BF00230428
5. Trulsson M, Johansson RS. Encoding of Tooth Loads by Human Periodontal Afferents and Their Role in Jaw Motor Control. Progress in Neurobiology. 1996a;49(3):267–284. https://doi.org/10.1016/s0301-0082(96)00016-0
6. Svensson KG, Trulsson M. Physiological Considerations of Oral Implant Function. In: Klineberg I, Eckert SE, editors. Functional Occlusion in Restorative Dentistry and Prosthodontics. Elsevier; 2016. Ch. 10, pp. 131–141. ISBN 978-0-7234-3809-0. https://doi.org/10.1016/b978-0-7234-3809-0.00010-3
7. Nanci A. Ten Cate’s Oral Histology: Development, Structure, and Function. 9th ed. Elsevier; 2018. Ch. 9, pp. 475–476, 492–498. ISBN 978-0-323-48524-1. https://shop.elsevier.com/books/ten-cates-oral-histology/nanci/978-0-323-48524-1
8. Leerunyakul K, Suchonwanit P. Evaluation of Hair Density and Hair Diameter in the Adult Thai Population Using Quantitative Trichoscopic Analysis. BioMed Research International. 2020;2020:2476890. https://doi.org/10.1155/2020/2476890
9. Johnsen SE, Svensson KG, Trulsson M. Forces Applied by Anterior and Posterior Teeth and Roles of Periodontal Afferents during Hold-and-Split Tasks in Human Subjects. Experimental Brain Research. 2007;178(1):126–134. https://doi.org/10.1007/s00221-006-0719-9
10. Okeson JP. Management of Temporomandibular Disorders and Occlusion. 8th ed. Elsevier; 2020. Ch. 2, pp. 23, 26–35. ISBN 978-0-323-58210-0. https://shop.elsevier.com/books/management-of-temporomandibular-disorders-and-occlusion/okeson/978-0-323-58210-0
11. Yoshida A, Moritani M, Nagase Y, Bae YC. Projection and Synaptic Connectivity of Trigeminal Mesencephalic Nucleus Neurons Controlling Jaw Reflexes. Journal of Oral Science. 2017;59(2):177–182. https://doi.org/10.2334/josnusd.16-0845
12. Kumar A, Castrillon E, Trulsson M, Svensson KG, Svensson P. Fine Motor Control of the Jaw Following Alteration of Orofacial Afferent Inputs. Clinical Oral Investigations. 2017;21(2):613–626. https://doi.org/10.1007/s00784-016-1939-4
13. Svensson KG, Trulsson M. Regulation of Bite Force Increase during Splitting of Food. European Journal of Oral Sciences. 2009;117(6):704–710. https://doi.org/10.1111/j.1600-0722.2009.00691.x
14. Grigoriadis A, Kumar A, Åberg MK, Trulsson M. Effect of Sudden Deprivation of Sensory Inputs From Periodontium on Mastication. Frontiers in Neuroscience. 2019;13:1316. https://doi.org/10.3389/fnins.2019.01316
15. Oguz EE, Ucan GO, Akcan SK, Mihmanli A, Cetinkaya NB, Weisskircher H-W, et al. Periodontal Mechanoreceptor Contribution to Minimal Holding Force Between Incisor Teeth. Journal of Oral Rehabilitation. 2026. https://doi.org/10.1111/joor.70300
16. Yoshida E, Fueki K, Wakabayashi N. Influence of Intra-Oral Sensory Impairment by Anaesthesia on Food Comminution and Mixing in Dentate Subjects. Journal of Oral Rehabilitation. 2015;42(6):401–406. https://doi.org/10.1111/joor.12276
17. Al Sayegh S, Borgwardt A, Svensson KG, Kumar A, Grigoriadis A, Christidis N. Effects of Chronic and Experimental Acute Masseter Pain on Precision Biting Behavior in Humans. Frontiers in Physiology. 2019;10:1369. https://doi.org/10.3389/fphys.2019.01369
18. Almotairy N, Kumar A, Noirrit-Esclassan E, Grigoriadis A. Developmental and Age-Related Changes in Sensorimotor Regulation of Biting Maneuvers in Humans. Physiology & Behavior. 2020;219:112845. https://doi.org/10.1016/j.physbeh.2020.112845
19. Al-Manei K, Almotairy N, Al-Manei KK, Kumar A, Grigoriadis A. Oral Fine Motor Control of Teeth Treated with Endodontic Microsurgery: A Single-Blinded Case-Control Study. Journal of Endodontics. 2021;47(2):226–233. https://doi.org/10.1016/j.joen.2020.10.022
20. Winitsky N, Naimi-Akbar A, Smedberg J-I, Grigoriadis A. Oral Fine Motor Control in Patients With Anterior Maxillary Single Implants, Freestanding Teeth and Teeth Connected in 3-Unit Bridges: An Experimental In Vivo Study. Clinical Oral Implants Research. 2026;37(8):922–930. https://doi.org/10.1111/clr.70136
21. Newman MG, Takei HH, Klokkevold PR, Carranza FA, editors. Newman and Carranza’s Clinical Periodontology. 13th ed. Elsevier; 2019. Ch. 26, p. 337.e1. ISBN 978-0-323-52300-4. https://shop.elsevier.com/books/newman-and-carranzas-clinical-periodontology/newman/978-0-323-52300-4
22. Song D, Shujaat S, Politis C, Orhan K, Jacobs R. Osseoperception Following Dental Implant Treatment: A Systematic Review. Journal of Oral Rehabilitation. 2022;49(5):573–585. https://doi.org/10.1111/joor.13296
23. Enkling N, Nicolay C, Utz K-H, Jöhren P, Wahl G, Mericske-Stern R. Tactile Sensibility of Single-Tooth Implants and Natural Teeth. Clinical Oral Implants Research. 2007;18(2):231–236. https://doi.org/10.1111/j.1600-0501.2006.01321.x
24. Lund JP, Kolta A. Generation of the Central Masticatory Pattern and Its Modification by Sensory Feedback. Dysphagia. 2006;21(3):167–174. https://doi.org/10.1007/s00455-006-9027-6
25. Piancino MG, Isola G, Cannavale R, Cutroneo G, Vermiglio G, Bracco P, et al. From Periodontal Mechanoreceptors to Chewing Motor Control: A Systematic Review. Archives of Oral Biology. 2017;78:109–121. https://doi.org/10.1016/j.archoralbio.2017.02.010
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27. Morimoto T, Inoue T, Masuda Y, Nagashima T. Sensory Components Facilitating Jaw-Closing Muscle Activities in the Rabbit. Experimental Brain Research. 1989;76(2):424–440. https://doi.org/10.1007/BF00247900
28. Oh K-A. The DentoNeural Axis: A Piezo Channel-Mediated Mechanosensory Pathway Linking Tooth Loss to Cognitive Decline. Aging Brain. 2026;10:100169. https://doi.org/10.1016/j.nbas.2026.100169
29. Hidaka O, Morimoto T, Masuda Y, Kato T, Matsuo R, Inoue T, et al. Regulation of Masticatory Force during Cortically Induced Rhythmic Jaw Movements in the Anesthetized Rabbit. Journal of Neurophysiology. 1997;77(6):3168–3179. https://doi.org/10.1152/jn.1997.77.6.3168
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31. Hellsing G. On the Regulation of Interincisor Bite Force in Man. Journal of Oral Rehabilitation. 1980;7(5):403–411. https://doi.org/10.1111/j.1365-2842.1980.tb00459.x
32. Higaki N, Goto T, Ichikawa T. Periodontal Tactile Input Activates the Prefrontal Cortex. Scientific Reports. 2016;6:36893. https://doi.org/10.1038/srep36893

This article explains research. It is not a diagnosis or treatment advice for any individual.

Cite this page

Reviewed by the editor October 11, 2026 · not yet published. Citation details will be finalized on publication.

APA

Oh, K.-A. (2026, October 11). How small a force can a tooth feel? Somatic Dentistry. https://somaticdentistry.org/en/insights/peanut-hold/

BibTeX
@online{oh2026peanutholden,
  author       = {Oh, Kyung-A},
  title        = {How small a force can a tooth feel?},
  date         = {2026-10-11},
  organization = {Soma Books},
  url          = {https://somaticdentistry.org/en/insights/peanut-hold/},
  langid       = {english},
  note         = {Reviewed by the editor October 11, 2026 · not yet published}
}