Endoplasmic reticulum stress affects mouse salivary protein secretion induced by chronic administration of an α 1 -adrenergic agonist.
Yoko YoshinoTakahiro ImamuraShigeo YamachikaTomoko OhshimaRyoko Ushikoshi-NakayamaHiroko InoueIchiro SaitoYoichi NakagawaPublished in: Histochemistry and cell biology (2022)
Stress stimulates both the sympathetic-adrenomedullary and hypothalamus-pituitary-adrenal axes. Activation of these axes results in the release of catecholamines, which in turn affects salivary secretion. Thus, repetitive stimulation of the α 1 -adrenergic receptor could be useful for studying the effects of chronic stress on the salivary gland. Salivary protein concentration and kallikrein activity were significantly lower in mice following chronic phenylephrine (PHE) administration. Chronic PHE administration led to significantly increased expression of the 78-kDa glucose-regulated protein, activating transcription factor 4, and activating transcription factor 6. Histological analyses revealed a decrease in the size of the serous cell and apical cytoplasm. These results suggest that repetitive pharmacological stimulation of the sympathetic nervous system elicits ER stress and translational suppression. In addition, PHE-treated mice exhibited a decrease in intracellular Ca 2+ influx elicited by carbachol, a muscarine receptor agonist in the submandibular gland. The present findings suggest that chronic psychological, social, and physical stress could adversely affect Ca 2+ regulation.
Keyphrases
- transcription factor
- endoplasmic reticulum stress
- healthcare
- binding protein
- signaling pathway
- single cell
- mental health
- stem cells
- protein protein
- poor prognosis
- drug induced
- high grade
- stress induced
- induced apoptosis
- amino acid
- blood glucose
- heat stress
- metabolic syndrome
- heat shock protein
- insulin resistance
- sensitive detection
- newly diagnosed