House-dust mite allergen and ozone exposure decreases histamine H3 receptors in the brainstem respiratory nuclei

Toxicol Appl Pharmacol. 2010 Sep 15;247(3):204-10. doi: 10.1016/j.taap.2010.06.014. Epub 2010 Jun 30.

Abstract

Allergic airway diseases in children are a common and a growing health problem. Changes in the central nervous system (CNS) have been implicated in contributing to some of the symptoms. We hypothesized that airway allergic diseases are associated with altered histamine H3 receptor expression in the nucleus tractus solitarius (NTS) and caudal spinal trigeminal nucleus, where lung/airway and nasal sensory afferents terminate, respectively. Immunohistochemistry for histamine H3 receptors was performed on brainstem sections containing the NTS and the caudal spinal trigeminal nucleus from 6- and 12-month-old rhesus monkeys who had been exposed for 5 months to house dust mite allergen (HDMA)+O3 or to filtered air (FA). While histamine H3 receptors were found exclusively in astrocytes in the caudal spinal trigeminal nucleus, they were localized to both neuronal terminals and processes in the NTS. HDMA+O3 exposure significantly decreased histamine H3 receptor immunoreactivity in the NTS at 6 months and in the caudal spinal trigeminal nucleus at 12 months of age. In conclusion, exposing young primates to HDMA+O3 changed histamine H3 receptor expression in CNS pathways involving lung and nasal afferent nerves in an age-related manner. Histamine H3 receptors may be a therapeutic target for allergic asthma and rhinitis in children.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aging / immunology
  • Aging / metabolism
  • Animals
  • Disease Models, Animal
  • Inhalation Exposure / adverse effects*
  • Macaca mulatta
  • Ozone / toxicity*
  • Pyroglyphidae / immunology*
  • Receptors, Histamine H3 / analysis
  • Receptors, Histamine H3 / biosynthesis*
  • Respiratory Hypersensitivity / immunology*
  • Respiratory Hypersensitivity / metabolism
  • Solitary Nucleus / drug effects*
  • Solitary Nucleus / growth & development
  • Solitary Nucleus / immunology
  • Solitary Nucleus / metabolism
  • Trigeminal Nucleus, Spinal / drug effects
  • Trigeminal Nucleus, Spinal / growth & development
  • Trigeminal Nucleus, Spinal / immunology
  • Trigeminal Nucleus, Spinal / metabolism

Substances

  • Receptors, Histamine H3
  • Ozone