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Kinetics of peptide‐induced release of inflammatory mediators by the urinary bladder
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Objective
To investigate the release of inflammatory mediators by the urinary bladder in response to exposure to pro‐inflammatory peptides.
Materials and methods
Isolated guinea pig urinary bladder was incubated with 10 &mgr;mol/L each of substance P (SP), neurokinin A (NKA), calcitonin gene‐related peptide (CGRP), vasoactive intestinal peptide (VIP), octreotide acetate (a long‐acting analogue of somatostatin, SOM), or bradykinin (BK), and the release of histamine, prostaglandin (PG) E
2
, PGF
2
&agr;
and leukotriene B
4
(LTB
4
) was determined during 0–5, 5–30 and 30–120 min after addition.
Results
Substance P, NKA, VIP and BK stimulated the release of histamine, while CGRP and SOM suppressed the release to below the spontaneous rates. All peptides, except CGRP and SOM, stimulated the release of PGE
2
between 0 and 30 min, and only VIP failed to stimulate the release of PGF
2
&agr;
within 5 min of exposure. Substance P, NKA, VIP and BK stimulated the release of LTB
4
and this required >5 min of exposure.
Conclusion
These results indicate that the peptides evaluated induce an immediate and transient release of histamine and activation of cyclooxygenase and delayed activation of 5‐lipoxygenase. These actions may directly regulate the participation of these peptides in the pathogenesis of cystitis.
Title: Kinetics of peptide‐induced release of inflammatory mediators by the urinary bladder
Description:
Objective
To investigate the release of inflammatory mediators by the urinary bladder in response to exposure to pro‐inflammatory peptides.
Materials and methods
Isolated guinea pig urinary bladder was incubated with 10 &mgr;mol/L each of substance P (SP), neurokinin A (NKA), calcitonin gene‐related peptide (CGRP), vasoactive intestinal peptide (VIP), octreotide acetate (a long‐acting analogue of somatostatin, SOM), or bradykinin (BK), and the release of histamine, prostaglandin (PG) E
2
, PGF
2
&agr;
and leukotriene B
4
(LTB
4
) was determined during 0–5, 5–30 and 30–120 min after addition.
Results
Substance P, NKA, VIP and BK stimulated the release of histamine, while CGRP and SOM suppressed the release to below the spontaneous rates.
All peptides, except CGRP and SOM, stimulated the release of PGE
2
between 0 and 30 min, and only VIP failed to stimulate the release of PGF
2
&agr;
within 5 min of exposure.
Substance P, NKA, VIP and BK stimulated the release of LTB
4
and this required >5 min of exposure.
Conclusion
These results indicate that the peptides evaluated induce an immediate and transient release of histamine and activation of cyclooxygenase and delayed activation of 5‐lipoxygenase.
These actions may directly regulate the participation of these peptides in the pathogenesis of cystitis.
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