Parotid hypersalivation after inferior salivatory nucleus glutamate/NMDA receptor excitation in the rat

Physiol Behav. 2024 Jun 1:280:114564. doi: 10.1016/j.physbeh.2024.114564. Epub 2024 Apr 22.

Abstract

Although salivation is essential during eating behavior, little is known about the brainstem centers that directly control the salivary glands. With regard to the inferior salivatory nucleus (ISN), the site of origin of the parasympathetic preganglionic cell bodies that innervate the parotid glands, previous anatomical studies have located it within the rostrodorsal medullary reticular formation. However, to date there is no functional data that shows the secretory nature of the somas grouped in this region. To activate only the somas and rule out the activation of the efferent fibers from and the afferent fibers to the ISN, in exp. 1, NMDA neurotoxin was administered to the rostrodorsal medullary region and the secretion of saliva was recorded during the following hour. Results showed an increased secretion of parotid saliva but a total absence of submandibular-sublingual secretion. In exp. 2, results showed that the hypersecretion of parotid saliva after NMDA microinjection was completely blocked by the administration of atropine (a cholinergic blocker) but not after administration of dihydroergotamine plus propranolol (α and β-adrenergic blockers, respectively). These findings suggest that the somata of the rostrodorsal medulla are secretory in nature, controlling parotid secretion via a cholinergic pathway. The data thus functionally supports the idea that these cells constitute the ISN.

Keywords: Inferior salivatory nucleus; Parotid; Saliva; Salivary glands; Salivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Atropine / pharmacology
  • Excitatory Amino Acid Agonists / pharmacology
  • Male
  • Medulla Oblongata / drug effects
  • Medulla Oblongata / metabolism
  • Microinjections
  • N-Methylaspartate* / metabolism
  • N-Methylaspartate* / pharmacology
  • Parotid Gland* / drug effects
  • Parotid Gland* / metabolism
  • Propranolol / pharmacology
  • Rats
  • Rats, Wistar
  • Receptors, N-Methyl-D-Aspartate* / metabolism
  • Saliva / metabolism
  • Salivation / drug effects
  • Salivation / physiology
  • Sialorrhea

Substances

  • Receptors, N-Methyl-D-Aspartate
  • N-Methylaspartate
  • Excitatory Amino Acid Agonists
  • Atropine
  • Propranolol
  • Adrenergic beta-Antagonists