Abstract
Leukocytes contain both nicotinic and muscarinic receptors, and while activation of nicotinic receptors suppresses immune/inflammatory responses, the role of muscarinic receptors in immunity is unclear. We examined the effects of a muscarinic receptor antagonist (atropine) and agonist (oxotremorine), administered chronically through miniosmotic pumps, on immune/inflammatory responses in the rat. Results show that while oxotremorine stimulated, atropine inhibited the antibody and T-cell proliferative responses. Moreover, atropine also suppressed the turpentine-induced leukocytic infiltration and tissue injury, and inhibited chemotaxis of leukocytes toward neutrophil and monocyte/lymphocyte chemoattractants. Thus, activation of nicotinic and muscarinic receptors has opposite effects on the immune/inflammatory responses.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Abscess / chemically induced
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Abscess / immunology
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Animals
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Antibody Formation / drug effects
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Antibody Formation / physiology*
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Atropine / pharmacology*
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Cells, Cultured / drug effects
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Chemokine CCL2 / pharmacology
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Chemotaxis, Leukocyte / drug effects
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Inflammation / physiopathology*
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Lymphocyte Activation / drug effects
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Lymphocyte Activation / physiology*
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Male
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Muscarinic Agonists / pharmacology*
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Muscarinic Antagonists / pharmacology*
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Oxotremorine / pharmacology*
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Rats
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Rats, Inbred Lew
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Receptors, Muscarinic / drug effects
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Receptors, Muscarinic / physiology*
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Receptors, Nicotinic / physiology
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Specific Pathogen-Free Organisms
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T-Lymphocytes / drug effects
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T-Lymphocytes / immunology*
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Turpentine / toxicity
Substances
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Ccl2 protein, rat
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Chemokine CCL2
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Muscarinic Agonists
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Muscarinic Antagonists
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Receptors, Muscarinic
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Receptors, Nicotinic
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Oxotremorine
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Atropine
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Turpentine