Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons

The effects of acidic pH on several voltage-dependent ion channels, such as voltage-dependent K⁺ and Ca²⁺ channels, and hyperpolarization-gated and cyclic nucleotide-activated cation (HCN) channels, were examined using a whole-cell patch clamp technique on mechanically isolated rat mesencephalic trigeminal nucleus neurons. The application of a pH 6.5 solution had no effect on the peak amplitude of voltage-dependent K⁺ currents. A pH 6.0 solution slightly, but significantly inhibited the peak amplitude of voltage-dependent K⁺ currents. The pH 6.0 also shifted both the current-voltage and conductance-voltage relationships to the depolarization range. The application of a pH 6.5 solution scarcely affected the peak amplitude of membrane currents mediated by HCN channels, which were profoundly inhibited by the general HCN channel blocker Cs⁺ (1 mM). However, the pH 6.0 solution slightly, but significantly inhibited the peak amplitude of HCN-mediated currents. Although the pH 6.0 solution showed complex modulation of the current-voltage and conductance-voltage relationships, the midpoint voltages for the activation of HCN channels were not changed by acidic pH. On the other hand, voltage-dependent Ca²⁺ channels were significantly inhibited by an acidic pH. The application of an acidic pH solution significantly shifted the current-voltage and conductance-voltage relationships to the depolarization range. The modulation of several voltage-dependent ion channels by an acidic pH might affect the excitability of mesencephalic trigeminal nucleus neurons, and thus physiological functions mediated by the mesencephalic trigeminal nucleus could be affected in acidic pH conditions.

EFFECTS OF NERVE INJURY ON THE EXPRESSION OF Trk RECEPTOR PROTEINS LOCALIZED ON THE TRIGEMINAL MESENCEPHALIC NEURONS / 神经解剖学杂志

Immunofluorescence histochemistry combined with retrograde tracing technique was employed to observe the effects of masseteric nerve transection on the expression of Trk ( tropomyosin-related kinase) receptor proteins, namely TrkA, TrkB and TrkC in the trigeminal mesencephalic nucleus ( Me5 ) of the rat. At 7 and 14 days following transection of masseteric nerve through which Fluorogold (FG) was applied to identify the Me5 neurons innervating masseter, brain sections were immunohistochemically processed to detect the three Trk isoforms in FG-labeled Me5 neurons. With the percentage of double-labeled neurons to the total number of FG-labeled neurons as the index,we demonstrated ( 1 ) a significant increase in the percentage of TrkA-immunoreactive (IR) Me5 neurons at both 7 and 14 days after nerve transection, (2) no significant, but gradual, increase in the percentage of TrkB-IR Me5 neruons with longer survival time post transection and ( 3 ) little change of TrkC expression. The current findings indicate that axotomy differently affected the expression of the individual Trk receptors and these expression patterns may reflect an adaptation of the Me5 neurons to the peripheral nerve injury.

Synaptic connection and GABA-immunoreactivity of periodontal afferent terminals and their presynaptic endings in the trigeminal motor nucleus of the rat / 대한해부학회지

Periodontal-masseteric reflex is implicated in the control of jaw movement and masticatory force during chewing foods. This study is aimed to investigate the synaptic arrangement of mesencephalic periodontal afferents in the trigeminal motor nucleus and to identify the neurotransmitter involved in the presynaptic control of them through the intra-axonal staining of horseradish peroxidase combined with postembedding immunogold methods. Most of the labeled terminals showed synaptic contacts with the small sized dendritic shafts or distal dendrites, while synaptic contacts with the somata or proximal dendrites were not observed. More than one third of the analyzed labeled boutons received presynaptic input from pleomorphic vesicles containing ending (p-ending). About 11% of labeled boutons showed synaptic triads. All the analyzed boutons made synaptic contacts with one to four neuronal profiles and those showing synaptic contact with five or more were not observed. Labeled terminals were larger than presynaptic p-endings. A large number of the analyzed p-endings showed GABA like immunoreactivity. These observations provide evidence that periodontal afferent terminals show very simple and characteristic synaptic arrangements in the trigeminal motor nucleus and that p-endings presynaptic to them may use GABA as a neurotransmitter for presynaptic inhibition.