Localization of quantitative changes in pulmonary beta-receptors in ovalbumin-sensitized guinea pigs

C. Gatto, T. P. Green, M. G. Johnson, R. P. Marchessault, V. Seybold, D. E. Johnson

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Impaired β-receptor function has been postulated as one factor contributing to airway hyperreactivity in asthmatic patients. Although numerous indirect studies have cast doubt on this theory, none of these previous investigations has been able to directly measure changes in β-receptor number on intrapulmonary structures capable of affecting the physiologic changes seen in this disease state. To help clarify the intrapulmonary location of such changes, a model of allergic bronchoconstriction was prepared by sensitizing guinea pigs to ovalbumin intraperitoneally (ip) 2 wk prior to testing (Group S). A second group of animals was sensitized to ovalbumin, then 2 wk later partially desensitized (Group D) during a 4- to 6-wk period by repeated exposure to increasing doses of nebulized ovalbumin with epinephrine rescue. Control animals received ip administered and nebulized normal saline alone. Pulmonary function assessed by plethysmography revealed an increase in airway resistance to 294 ± 42% (SE) of control in Group S (p < 0.005) and a decrease in dynamic compliance to 76 ± 8% of control in Group D and 39 ± 10% of control in Group S (p < 0.002) after exposure to nebulized ovalbumin. Using L-[3H]dihydroalprenolol ([3H]DHA), β-receptors were autoradiographically localized ad quantitated in lung sections from all 3 groups. Significant decreases (p < 0.02) in 3H-DHA binding were noted in alveolar and conducting airway epithelium, and bronchiolar and vascular smooth muscle in ovalbumin-exposed animals. The structures where decreases in β-receptor density were observed suggest that impaired β-adrenergic function could be partially accountable for the changes in pulmonary function observed in the ovalbumin-exposed guinea pigs, and may indeed be involved in the pathophysiology of certain types of reactive airway disease in humans.

Original languageEnglish (US)
Pages (from-to)150-154
Number of pages5
JournalAmerican Review of Respiratory Disease
Volume136
Issue number1
DOIs
StatePublished - 1987

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

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