Bradykinin stimulates tumor necrosis factor and interleukin-1 release from macrophages

Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many inflammatory diseases. The potential ability of bradykinin to stimulate release of tumor necrosis factor and interleukin-1 from macrophages was e...

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Published in:FEBS letters Vol. 247; no. 2; pp. 189 - 192
Main Authors: Tiffany, Carol W., Burch, Ronald M.
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 24-04-1989
Elsevier
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Abstract Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many inflammatory diseases. The potential ability of bradykinin to stimulate release of tumor necrosis factor and interleukin-1 from macrophages was examined. Bradykinin stimulated release of both cytokines from P388-D1 and RAW264.7 murine macrophages. Studies with selective agonists and antagonists suggest that cytokine release is mediated by a B 1 kinin receptor.
AbstractList Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many inflammatory diseases. The potential ability of bradykinin to stimulate release of tumor necrosis factor and interleukin‐1 from macrophages was examined. Bradykinin stimulated release of both cytokines from P388‐D1 and RAW264.7 murine macrophages. Studies with selective agonists and antagonists suggest that cytokine release is mediated by a B1 kinin receptor.
Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many inflammatory diseases. The potential ability of bradykinin to stimulate release of tumor necrosis factor and interleukin-1 from macrophages was examined. Bradykinin stimulated release of both cytokines from P388-D1 and RAW264.7 murine macrophages. Studies with selective agonists and antagonists suggest that cytokine release is mediated by a B 1 kinin receptor.
Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many inflammatory diseases. The potential ability of bradykinin to stimulate release of tumor necrosis factor and interleukin‐1 from macrophages was examined. Bradykinin stimulated release of both cytokines from P388‐D1 and RAW264.7 murine macrophages. Studies with selective agonists and antagonists suggest that cytokine release is mediated by a B 1 kinin receptor.
Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many inflammatory diseases. The potential ability of bradykinin to stimulate release of tumor necrosis factor and interleukin-1 from macrophages was examined.
Author Tiffany, Carol W.
Burch, Ronald M.
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  fullname: Burch, Ronald M.
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Issue 2
Keywords Interleukin-1
Bradykinin antagonist
Tumor necrosis factor
Bradykinin
Cytokine
Macrophage
Cell culture
Radiolabelling
Interleukin
Peptide hormone
Stimulation
Language English
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Elsevier
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Snippet Bradykinin and related kinins have been implicated in the initiation and maintenance of inflammation. Cytokines appear to be the primary mediators of many...
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SubjectTerms Analytical, structural and metabolic biochemistry
Animals
Biological and medical sciences
Bradykinin
Bradykinin - analogs & derivatives
Bradykinin - pharmacology
Bradykinin antagonist
Cell Line
Cytokine
Fundamental and applied biological sciences. Psychology
Interleukin-1
Interleukin-1 - metabolism
Lipoprotein Lipase - antagonists & inhibitors
Macrophage
Macrophages - metabolism
Mice
Prostaglandins E - biosynthesis
Protein hormones. Growth factors. Cytokines
Proteins
Receptors, Bradykinin
Receptors, Neurotransmitter - physiology
Tumor necrosis factor
Tumor Necrosis Factor-alpha - metabolism
Title Bradykinin stimulates tumor necrosis factor and interleukin-1 release from macrophages
URI https://dx.doi.org/10.1016/0014-5793(89)81331-6
https://onlinelibrary.wiley.com/doi/abs/10.1016%2F0014-5793%2889%2981331-6
https://www.ncbi.nlm.nih.gov/pubmed/2541011
https://search.proquest.com/docview/15263476
https://search.proquest.com/docview/78936261
Volume 247
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