Involvement of histaminergic inputs in the jaw-closing reflex arc

Abstract

Histamine receptors are densely expressed in the mesencephalic trigeminal nucleus (MesV) and trigeminal motor nucleus. However, little is known about the functional roles of neuronal histamine in controlling oral-motor activity. Thus, using the whole-cell recording technique in brainstem slice preparations from Wistar rats aged between postnatal days 7 and 13, we investigated the effects of histamine on the MesV neurons innervating the masseter muscle spindles and masseter motoneurons (MMNs) that form a reflex arc for the jaw-closing reflex. Bath application of histamine (100 μM) induced membrane depolarization in both MesV neurons and MMNs in the presence of tetrodotoxin, whereas histamine decreased and increased the input resistance in MesV neurons and MMNs, respectively. The effects of histamine on MesV neurons and MMNs were mimicked by an H1 receptor agonist, 2-pyridylethylamine (100 μM). The effects of an H2 receptor agonist, dimaprit (100 μM), on MesV neurons were inconsistent, whereas MMNs were depolarized without changes in the input resistance. An H3 receptor agonist, immethridine (100 μM), also depolarized both MesV neurons and MMNs without changing the input resistance. Histamine reduced the peak amplitude of postsynaptic currents (PSCs) in MMNs evoked by stimulation of the trigeminal motor nerve (5N), which was mimicked by 2-pyridylethylamine but not by dimaprit or immethridine. Moreover, 2-pyridylethylamine increased the failure rate of PSCs evoked by minimal stimulation and the paired-pulse ratio. These results suggest that histaminergic inputs to MesV neurons through H1 receptors are involved in the suppression of the jaw-closing reflex although histamine depolarizes MesV neurons and/or MMNs.

Histamine 1 receptor-Gβγ-cAMP/PKA-CFTR pathway mediates the histamine-induced resetting of the suprachiasmatic circadian clock

“…Drugs and chemicals utilized in the present study were from Sigma-Aldrich (St. Louis, MO) or Tocris Bioscience (Bristol, UK). The solutions of histamine (100 μM; [ 26 – 28 ]), 2-pyridylethylamine (100 μM; [ 29 – 33 ]) and amthamine (20 μM; [ 34 – 36 ]) were prepared in ACSF or HEPES-buffered saline. The solutions of bumetanide (10 μM; [ 16 , 37 , 38 ]), CFTR inh -172 (50 μM; [ 39 – 41 ]), gallein (100 μM; [ 42 – 44 ]), H89 (10 μM; [ 45 – 47 ]), KT5720 (1 μM; [ 48 – 50 ]), bicuculline (30 μM; [ 51 – 53 ]) and strychnine (1 μM; [ 54 – 56 ]) were prepared by diluting the stock solutions with ACSF or HEPES-buffered saline; the solvent of stock solutions was dimethyl sulphoxide and its final concentration was 0.01–0.003 %.…”