Abstract:Unilateral anterior crossbite (UAC) has been demonstrated to cause masseter hyperactivity via the periodontal trigeminal mesencephalic nucleus (Vme)–trigeminal motor nucleus circuit. Here, we studied activation of motor neurons of the facial nucleus (VII), hypoglossal nucleus (XII), nucleus ambiguus (Amb), and spinal nucleus of the accessory nerve (SNA) in rats with UAC via their similar connections with Vme. An anterograde tracer, biotinylated dextran amine (BDA), was injected into the Vme to identify the cen… Show more
“…As we proposed in our recent publication, UAC elicited hyperactivity of jaw closing muscles, probably through a circuit of periodontal mesencephalic trigeminal afferents (Vme) to trigeminal motor neurons (Vmo; Liu et al, 2017). A similar impact of the Vme on multiple orofacial motor nuclei in the brain stem has also been reported (Liu et al, 2018). Therefore, the UAC model could be used in explorations of Vme-related problems, which are worthy of investigation.…”
Malocclusion is an important risk factor for temporomandibular disorder (TMD), a series of disorders characterized by dysfunction in the orofacial region involving the temporomandibular joint (TMJ) and jaw muscles. We recently showed that experimental unilateral anterior crossbite (UAC) produced masseter hyperactivity through a circuit involving the periodontal proprioception, trigeminal mesencephalic nucleus (Vme), and trigeminal motor nucleus (Vmo). Anxiety is a common complication in patients with TMD. The lateral habenula (LHb) is involved in emotional modulation and has direct projections to the Vme. Therefore, the present research examined whether UAC facilitates excitatory input from the LHb to the Vme and, subsequently, anxiety-like behaviors in rats. The LHb activation was evaluated by the electrophysiological recording, assessment of vesicular glutamate transporter-2 (VGLUT2) mRNA expression, and measurement of anxiety-like behaviors. The effects of LHb activity on Vme were evaluated by electrophysiological recording from Vme neurons and local changes in VGLUT2 protein density. UAC produced anxiety in modeled rats and increased neuronal activity in the LHb. VGLUT2 mRNA expression was also increased in the LHb. Further, VGLUT2-positive boutons were observed in close apposite upon parvalbumin (PV)-labeled Vme neurons. VGLUT2 protein expression was also increased in the Vme. Significantly, injection of VGLUT2-targeted shRNA into the LHb reduced the expression of VGLUT2 protein in the Vme, attenuated UAC-associated anxiety-like behaviors, and attenuated electrophysiological changes in the Vme neurons. In conclusion, we show that UAC activates the LHb neurons as well as the periodontal proprioceptive pathway to provide excitatory input to the Vme and produce anxiety in rats. These findings provide a rationale for suppressing activity of the LHb to attenuate both the physical and psychological effects of TMD.
“…As we proposed in our recent publication, UAC elicited hyperactivity of jaw closing muscles, probably through a circuit of periodontal mesencephalic trigeminal afferents (Vme) to trigeminal motor neurons (Vmo; Liu et al, 2017). A similar impact of the Vme on multiple orofacial motor nuclei in the brain stem has also been reported (Liu et al, 2018). Therefore, the UAC model could be used in explorations of Vme-related problems, which are worthy of investigation.…”
Malocclusion is an important risk factor for temporomandibular disorder (TMD), a series of disorders characterized by dysfunction in the orofacial region involving the temporomandibular joint (TMJ) and jaw muscles. We recently showed that experimental unilateral anterior crossbite (UAC) produced masseter hyperactivity through a circuit involving the periodontal proprioception, trigeminal mesencephalic nucleus (Vme), and trigeminal motor nucleus (Vmo). Anxiety is a common complication in patients with TMD. The lateral habenula (LHb) is involved in emotional modulation and has direct projections to the Vme. Therefore, the present research examined whether UAC facilitates excitatory input from the LHb to the Vme and, subsequently, anxiety-like behaviors in rats. The LHb activation was evaluated by the electrophysiological recording, assessment of vesicular glutamate transporter-2 (VGLUT2) mRNA expression, and measurement of anxiety-like behaviors. The effects of LHb activity on Vme were evaluated by electrophysiological recording from Vme neurons and local changes in VGLUT2 protein density. UAC produced anxiety in modeled rats and increased neuronal activity in the LHb. VGLUT2 mRNA expression was also increased in the LHb. Further, VGLUT2-positive boutons were observed in close apposite upon parvalbumin (PV)-labeled Vme neurons. VGLUT2 protein expression was also increased in the Vme. Significantly, injection of VGLUT2-targeted shRNA into the LHb reduced the expression of VGLUT2 protein in the Vme, attenuated UAC-associated anxiety-like behaviors, and attenuated electrophysiological changes in the Vme neurons. In conclusion, we show that UAC activates the LHb neurons as well as the periodontal proprioceptive pathway to provide excitatory input to the Vme and produce anxiety in rats. These findings provide a rationale for suppressing activity of the LHb to attenuate both the physical and psychological effects of TMD.
“…The dental occlusion contribution to postural control has been proposed to depend on external disturbances [ 39 , 40 ]. Our published data [ 14 , 25 , 35 , 41 ] and the present work bring about supportive evidence. The existence of an ascending pathway mediating proprioception from the periodontal region to the cerebellum provides a possible neuroanatomical basis for the trigeminal mechanism of somatic movement and balance.…”
Section: Discussionsupporting
confidence: 88%
“…This makes it possible for the projections of neurons in the Vme to target many other neurons in the brainstem. The neurons of Vme innervate spindles in the jaw‐closing muscles and periodontal pressoreceptors [ 25 , 35 , 41 , 43 ]. Axons involved in trigeminal proprioception from periodontal mechanoreceptors and spindles in the jaw‐closing muscles directly bypass the trigeminal ganglion and leave their cell bodies in all the rostro‐caudal levels of the entire mesencephalon [ 44 ].…”
Section: Discussionmentioning
confidence: 99%
“…Reports have indicated that there are projections from Vme to the trigeminal motor nucleus, facial nerve nucleus, hypoglossal nerve nucleus, nucleus ambiguous, accessory nerve nucleus, and Vpdm [ 21 , 33 , 34 ]. In UAC treated female rats, the VGLUT1 mRNA expression level of Vme was upregulated [ 25 ] and the VGLUT1 protein expression level of trigeminal motor nucleus, facial nerve nucleus, hypoglossal nerve nucleus, nucleus ambiguous, and accessory nerve nucleus was increased [ 35 ]. It is of dental interest to determine whether the Vpdm‐cerebellum circuit of UAC rats is excited.…”
Occlusion has been proposed to play a role for body posture and balance, both of which are mediated mainly by the cerebellum. The dorsomedial part of the principal sensory trigeminal nucleus (Vpdm) has direct projection to the cerebellum. The experimental unilateral anterior crossbite (UAC) has an impact on the motor nuclei in the brain stem via trigeminal mesencephalic nucleus (Vme). The current aim was to explore whether UAC has an impact on Vpdm‐cerebellum circuit. The inferior alveolar nerve was injected into cholera toxin B subunit (CTb), the cerebellum was injected into fluoro‐gold (FG), and the Vpdm was injected into biotinylated dextran amine (BDA) to identify the activation of Vpdm‐cerebellum circuit by UAC. Data indicated that there were more neuronal nuclei (NeuN)/CTb/FG triple‐labelled neurons and NeuN/CTb/vesicular glutamate transporter 1(VGLUT1) triple‐labelled neurons in the Vpdm, and more NeuN/BDA/ VGLUT1 triple‐labelled neurons in the cerebellum of rats with UAC than in control rats. The VGLUT1 expression in the Vpdm and cerebellum in the UAC group was higher than that in control rats. These findings indicate an excitatory impact of UAC on the Vpdm‐cerebellum pathway and support the role of occlusion for body posture and balance.
“…In the early stage, dentists only focused on the teeth and occlusal relationship, which was generally static and non-functional [4][5][6]. Until the prevalence of functional occlusion in recent years [7,8], the concept of complete dentistry was put forward [9], with the studies on dynamic occlusion and masticatory function valued by interdisciplinary oral researchers [1-3,10-18], especially in the fields of orthodontics [1-3], occlusal reconstruction [10,11], dental implant [12,13], periodontal disease [14,15], dental caries treatment [16], temporomandibular joint disorders (TMD) [17], bruxism [18], etc. Dentists have begun to realize the integrality of the masticatory system (MS) (i.e., the stomatognathic system (SS)), which is generally composed of teeth and occlusion, the temporomandibular joint (TMJ), neuromuscular factors, jaw, periodontal tissue, etc.…”
The physiological homeostasis of the masticatory complex in short-faced patients is too robust to be disintegrated and reconstructed due to the powerful masseter muscle. This study innovatively introduced the botulinum toxin-A (BTX-A) into the field of dental occlusal treatment, providing a novel and minimally invasive therapy perspective for the two major clinical problems in these patients (low treatment efficiency and high rates of complications). In total, 10 adult patients with skeletal low angle seeking occlusal treatment (age: 27.0 ± 6.1 years; 4 males and 6 females) were administered 30–50 U of BTX-A in each masseter muscle and evaluated before and 3 months after injection based on cone-beam computed tomography (CBCT). We found a significant reduction in the thickness of the masseter muscle (MMT) (p < 0.0001). With regards to occlusion, we found a significant increase in the height of the maxillary second molar (U7-PP) (p < 0.05) with significantly flattened occlusal curves (the curve of Spee [COS] (p < 0.01), and the curve of Wilson [COW] (p < 0.05)). Furthermore, the variations in the temporomandibular joint exhibited a significant reduction in the anterior joint space (AJS) (p < 0.05) and superior joint space (SJS) (p < 0.05). In addition, the correlation analysis of the masticatory complex provided the basis for the following multiple regression equation: MMT = 10.08–0.11 COW + 2.73 AJS. The findings from our pilot study indicate that BTX-A, as a new adjuvant treatment attempt of occlusal therapy for short-faced patients, can provide a more favorable muscular environment for subsequent occlusal therapy through the adjustment of the biting force and may contribute to the reconstruction of healthier homeostasis of the masticatory complex. However, further research is required to establish the reliability and validity of these findings.
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