Age-related changes in airway-reactivity-to cholinergic and other agonists are well described in both humans and animals. In animal models these changes are associated with age-related pharmacological and biochemical changes in airway smooth muscle. As the mechanisms responsible for these changes, are not known it is the aim of this proposal to study specific intracellular mechanisms by which these changes occur. Our preliminary data suggests that changes are occurring in receptor coupling to G proteins. The G proteins couple the muscarinic receptor to several intracellular biochemical events. Since the G proteins play such a key regulatory role, it is our hypothesis that alterations occurring in these proteins result in the observed reductions in functional responses to muscarinic stimulation. Experiments are described in which we explore systematically the intracellular events resulting in second messenger generation, which are initiated by muscarinic receptor occupation in tissues from animals of different ages. Initially, we will characterize the muscarinic receptors in guinea pig tracheal tissues to determine which receptor subtypes are present and if the type, density or affinity of these receptors is changed with age. To evaluate the role of the G protein in age-related changes we will first identify which types are present in these tissues, then we will determine if changes are occurring in their structure, quantity or function with age. To test the hypothesis that the primary change is occurring at the level of the G proteins, it we need first to establish which second messenger enzyme systems the G proteins are coupled to. Once the sequence of steps resulting in second messenger generation is defined, we will block specific G proteins and determine second messenger production independently. Comparison of second messenger generation with and without G protein regulation, should provide information as to where in this sequence changes have occurred. These studies will clarify the precise mechanisms by which signal transduction occurs in airway smooth muscle and how these events are related to the changes seen physiologically with age. Many disease states such as chronic obstructive pulmonary disease and asthma, involve abnormalities in airway tone and reactivity. A clear understanding of the mechanism by which airway tone is regulated is a first step towards understanding and treating these diseases.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL043312-03
Application #
3472809
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1989-07-01
Project End
1994-06-30
Budget Start
1991-07-01
Budget End
1992-06-30
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Public Health
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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Deng, M C; Bell, S; Huie, P et al. (1995) Cardiac allograft vascular disease. Relationship to microvascular cell surface markers and inflammatory cell phenotypes on endomyocardial biopsy. Circulation 91:1647-54
Gavett, S H; O'Hearn, D J; Li, X et al. (1995) Interleukin 12 inhibits antigen-induced airway hyperresponsiveness, inflammation, and Th2 cytokine expression in mice. J Exp Med 182:1527-36
Gavett, S H; Chen, X; Finkelman, F et al. (1994) Depletion of murine CD4+ T lymphocytes prevents antigen-induced airway hyperreactivity and pulmonary eosinophilia. Am J Respir Cell Mol Biol 10:587-93
Wills-Karp, M; Uchida, Y; Lee, J Y et al. (1993) Organ culture with proinflammatory cytokines reproduces impairment of the beta-adrenoceptor-mediated relaxation in tracheas of a guinea pig antigen model. Am J Respir Cell Mol Biol 8:153-9
Wills-Karp, M; Gilmour, M I (1993) Increased cholinergic antagonism underlies impaired beta-adrenergic response in ovalbumin-sensitized guinea pigs. J Appl Physiol 74:2729-35
Wills-Karp, M (1993) Age-related changes in pulmonary muscarinic receptor binding properties. Am J Physiol 265:L103-9

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