Saban M R, Saban R, Bjorling D E
Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, USA.
Br J Urol. 1997 Nov;80(5):742-7. doi: 10.1046/j.1464-410x.1997.00415.x.
To investigate the release of inflammatory mediators by the urinary bladder in response to exposure to pro-inflammatory peptides.
Isolated guinea pig urinary bladder was incubated with 10 mumol/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) E2, PGF2 alpha and leukotriene B4 (LTB4) was determined during 0-5, 5-30 and 30-120 min after addition.
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 PGE2 between 0 and 30 min, and only VIP failed to stimulate the release of PGF2 alpha within 5 min of exposure. Substance P, NKA, VIP and BK stimulated the release of LTB4 and this required > 5 min of exposure.
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.
研究膀胱在暴露于促炎肽时炎症介质的释放情况。
将分离的豚鼠膀胱分别与10 μmol/L的P物质(SP)、神经激肽A(NKA)、降钙素基因相关肽(CGRP)、血管活性肠肽(VIP)、醋酸奥曲肽(生长抑素长效类似物,SOM)或缓激肽(BK)孵育,并在添加后0 - 5、5 - 30和30 - 120分钟期间测定组胺、前列腺素(PG)E2、PGF2α和白三烯B4(LTB4)的释放量。
P物质、NKA、VIP和BK刺激组胺释放,而CGRP和SOM将释放抑制至自发释放率以下。除CGRP和SOM外,所有肽在0至30分钟内刺激PGE2释放,且仅VIP在暴露5分钟内未刺激PGF2α释放。P物质、NKA、VIP和BK刺激LTB4释放,且这需要>5分钟的暴露时间。
这些结果表明,所评估的肽诱导组胺的即刻和短暂释放以及环氧化酶的激活,并延迟5 - 脂氧合酶的激活。这些作用可能直接调节这些肽在膀胱炎发病机制中的参与情况。