The fundamental pattern of chewing induced by the network of neurons called central pattern generator has been reported
to be modified by the information arising from the various oro-facial sensory receptors including muscle spindles of jaw
closing muscles. The cell bodies of primary afferent neurons from these muscle spindles lie in mesencephalic trigeminal
nucleus (MTN) in the brainstem. The aim of the study was to understand whether muscle spindles from jaw-closing
muscles play any role in hard food chewing. Single neuronal discharge of muscle spindle afferents was recorded from the
MTN simultaneous with jaw-movement and electromyograpic (EMG) activities of the left masseter (jaw-closing) muscle
during chewing soft and hard foods (apple and pellet) in awake rabbits. Ten consecutive chewing cycles were taken for
analysis. Discharge of nineteen muscle spindles from seven rabbits was successfully recorded. Muscle-spindle discharge
was significantly higher during the closing phase of jaw-movement for the hard food chewing than for the soft food. The
jaw-closing muscle EMG activity was significantly higher during hard food chewing compared to soft food. The spindle
discharge was higher when the masseter muscle activity was greater for chewing hard food. Significant positive (r=0.822,
p=<0.001) correlation was found between the difference of muscle activity between apple and pellet and the difference
of spindle discharge between apple and pellet. Above findings suggest that the increase of spindle discharge during
hard food chewing may play a role for facilitating jaw-closing muscle activities and thereby provides servo-assistance
to jaw-closing muscles to compensate the hardness of food.
Dental pain is a common health problem that negatively impacts the activities of daily living. Dentine hypersensitivity and pulpitis-associated pain are among the most common types of dental pain. Patients with these conditions feel pain upon exposure of the affected tooth to various external stimuli. However, the molecular mechanisms underlying dental pain, especially the transduction of external stimuli to electrical signals in the nerve, remain unclear. Numerous ion channels and receptors localized in the dental primary afferent neurons (DPAs) and odontoblasts have been implicated in the transduction of dental pain, and functional expression of various polymodal transient receptor potential (TRP) channels has been detected in DPAs and odontoblasts. External stimuli-induced dentinal tubular fluid movement can activate TRP channels on DPAs and odontoblasts. The odontoblasts can in turn activate the DPAs by paracrine signaling through ATP and glutamate release. In pulpitis, inflammatory mediators may sensitize the DPAs. They could also induce post-translational modifications of TRP channels, increase trafficking of these channels to nerve terminals, and increase the sensitivity of these channels to stimuli. Additionally, in caries-induced pulpitis, bacterial products can directly activate TRP channels on DPAs. In this review, we provide an overview of the TRP channels expressed in the various tooth structures, and we discuss their involvement in the development of dental pain.
Nerve conduction study is essential in the diagnosis of focal neuropathies and diffuse polyneuropathies. There are many factors that can affect nerve conduction velocity, and age is one of them. Most of the many studies of this effect, and the values from them, were on Caucasian subjects. Therefore, this study was designed to investigate the effect of age on conduction velocity among healthy Asian Malay subjects by analyzing its influence on the median, ulnar, and sural nerves.