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首页> 外文期刊>Archives of dermatological research. >Substance P- and antigen-induced release of leukotriene B4, prostaglandin D2 and histamine from guinea pig skin by different mechanisms in vitro.
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Substance P- and antigen-induced release of leukotriene B4, prostaglandin D2 and histamine from guinea pig skin by different mechanisms in vitro.

机译:P物质和抗原诱导豚鼠皮肤中白三烯B4,前列腺素D2和组胺的释放通过不同的机制在体外。

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摘要

Substance P (SP) induces increased vascular permeability, vasodilatation and granulocyte infiltration upon intradermal injection. Studies with antagonists and mast cell-deficient mice have suggested that granulocyte infiltration in response SP is mediated by leukotriene (LT) B4 derived from mast cells. However, the release of LTB4 has not been detected using mast cells isolated from human skin. Here we report the release of LTB4, prostaglandin (PG) D2 and histamine from guinea pig skin tissue in response to SP. The release of these agents occurred in a dose-dependent manner over a concentration range of SP from 1 x 10(-6) to 3 x 10(-4) M. No detectable PGE2 was released at any concentration up to 3 x 10(-4) M SP. The kinetics of histamine release induced in response to SP was more rapid than that induced by antigen. By comparison, SP-induced and antigen-induced release of LTB4 and PGD2 were similar, but slower than the histamine release. In the absence of extracellular Ca2+, release of histamine and PGD2 in response to SP was partially impaired, but to a lesser extent than that induced by antigen. On the other hand, LTB4 release in response to both SP and antigen was abolished under the same conditions. These results indicate that SP induces the release of LTB4, as well as histamine and PGD2, in the skin most likely from mast cells by a mechanism which may be different from that of mediator release in response to antigen.
机译:皮内注射后,P(SP)物质诱导增加的血管通透性,血管舒张作用和粒细胞浸润。对拮抗剂和肥大细胞缺乏小鼠的研究表明,反应性SP中的粒细胞浸润是由肥大细胞衍生的白三烯(LT)B4介导的。然而,尚未使用从人皮肤分离的肥大细胞检测到LTB4的释放。在这里我们报告响应SP从豚鼠皮肤组织释放LTB4,前列腺素(PG)D2和组胺。这些试剂的释放在1 x 10(-6)至3 x 10(-4)M的SP浓度范围内以剂量依赖性方式发生。在任何浓度高达3 x 10(P)的情况下均未释放出可检测到的PGE2。 -4)M SP。 SP诱导的组胺释放动力学比抗原诱导的动力学更快。相比之下,SP诱导和抗原诱导的LTB4和PGD2释放相似,但比组胺释放慢。在不存在细胞外Ca2 +的情况下,响应SP的组胺和PGD2的释放会部分受损,但程度要小于抗原诱导的释放。另一方面,在相同条件下消除了响应SP和抗原的LTB4释放。这些结果表明SP通过可能不同于肥大细胞响应抗原的介质释放的机制,诱导了肥大细胞中皮肤中LTB4以及组胺和PGD2的释放。

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