Early postnatal ozone exposure alters rat nodose and jugular sensory neuron development

• Published in: Toxicological and environmental chemistry Vol. 93; no. 10; pp. 2055 - 2071
• Main Authors: Zellner, Leor C, Brundage, Kathleen M, Hunter, Dawn D, Dey, Richard D
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis Group 01.01.2011; Taylor & Francis Ltd; Taylor & Francis
• Subjects: Age; air; airway neurons; Airways; Animals; Brain; Counting; epithelium; Flow cytometry; Ganglia; inflammation; Neurons; Ozone; pups; rats; Rodents; sensory neurons; substance P
• ISSN: 1029-0486; 0277-2248; 1029-0486
• DOI: 10.1080/02772248.2011.610882

Sensory neurons originating in nodose and jugular ganglia that innervate airway epithelium (airway neurons) play a role in inflammation observed following exposure to inhaled environmental irritants such as ozone (O₃). Airway neurons can mediate airway inflammation through the release of the neuropeptide substance P (SP). While susceptibility to airway irritants is increased in early life, the developmental dynamics of afferent airway neurons are not well characterized. The hypothesis of this study was that airway neuron number might increase with increasing age, and that an acute, early postnatal O₃ exposure might increase both the number of sensory airway neurons as well as the number SP-containing airway neurons. Studies using Fischer 344 rat pups were conducted to determine if age or acute O₃ exposure might alter airway neuron number. Airway neurons in nodose and jugular ganglia were retrogradely labeled, removed, dissociated, and counted by means of a novel technique employing flow cytometry. In Study 1, neuron counts were conducted on postnatal days (PD) 6, 10, 15, 21, and 28. Numbers of total and airway neurons increased significantly between PD6 and PD10, then generally stabilized. In Study 2, animals were exposed to O₃ (2 ppm) or filtered air (FA) on PD5 and neurons were counted on PD10, 15, 21, and 28. O₃-exposed animals displayed significantly less total neurons on PD21 than FA controls. This study shows that age-related changes in neuron number occur, and that an acute, early postnatal O₃ exposure significantly alters sensory neuron development.