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炎症诱导猫食管下括约肌环形肌中花生四烯酸代谢的变化。

Inflammation induced changes in arachidonic acid metabolism in cat LES circular muscle.

作者信息

Cheng Ling, Cao Weibiao, Behar Jose, Biancani Piero, Harnett Karen M

机构信息

G.I. Motility Research Laboratory, Rhode Island Hospital and Brown Univ., 55 Claverick St., Room 333, Providence RI 02903, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2005 Apr;288(4):G787-97. doi: 10.1152/ajpgi.00327.2004. Epub 2004 Nov 18.

Abstract

Myogenic lower esophageal sphincter (LES) tone is maintained by arachidonic acid metabolites, such as PGF(2alpha) and thromboxane A(2)/B(2). Experimental esophagitis in cat reduces LES in vivo pressure and in vitro tone. Because IL-1beta may mediate esophagitis-associated reduction in ACh release in esophagus, we examined whether IL-1beta may also play a role in esophagitis-induced reduction of LES tone. A cat model of experimental esophagitis was obtained by repeated esophageal perfusion with HCl (Biancani P, Barwick K, Selling J, and McCallum R. Gastreonterology 87: 8-16, 1984 and Sohn UD, Harnett KM, Cao W, Rich H, Kim N, Behar J, and Biancani P. J Pharmacol Exp Ther 283: 1293-1304, 1997.). LES circular muscle strips were examined in muscle chambers as previously described (Biancani P, Billett G, Hillemeier C, Nissenshon M, Rhim BY, Sweczack S, and Behar J. Gastroenterology 103: 1199-1206, 1992). Levels of inflammatory mediators were measured. IL-1beta levels were higher in esophagitis than in normal LES. IL-1beta reduced normal LES tone, and the reduction was reversed by catalase, suggesting a role of H(2)O(2). This was confirmed by IL-1beta-induced production of H(2)O(2) in normal LES and elevated H(2)O(2) levels in esophagitis. H(2)O(2) by itself is sufficient to explain the changes that occur in the muscle, reducing its ability to contract. H(2)O(2) increased PGE(2) in normal LES, and PGE(2) levels were elevated in esophagitis LES, whereas PGF(2alpha) levels were unchanged. H(2)O(2) also increased levels of 8-isoprostanes, stable prostaglandin-like compounds formed by free radical-induced peroxidation of arachidonic acid, and 8-isoprostane levels were elevated in esophagitis. The PGF(2alpha) analog 8-iso-PGF(2alpha) caused little contraction of LES strips but reduced PGF(2alpha) binding and contraction of normal LES. In esophagitis, PGF(2alpha) binding and contraction were reduced in LES, suggesting that isoprostanes may contribute to reduction in tone in esophagitis. The data suggest that, in esophagitis, IL-1beta causes production of H(2)O(2). H(2)O(2) increases PGE(2), which relaxes the LES, and 8-iso-F(2alpha), which blocks PGF(2alpha)-mediated contraction.

摘要

肌源性下食管括约肌(LES)张力由花生四烯酸代谢产物维持,如前列腺素F2α(PGF2α)和血栓素A2/ B2。猫实验性食管炎可降低LES的体内压力和体外张力。由于白细胞介素-1β(IL-1β)可能介导食管炎相关的食管乙酰胆碱释放减少,我们研究了IL-1β是否也在食管炎诱导的LES张力降低中起作用。通过用盐酸反复食管灌注获得猫实验性食管炎模型(Biancani P,Barwick K,Selling J和McCallum R. Gastroenterology 87:8 - 16,1984以及Sohn UD,Harnett KM,Cao W,Rich H,Kim N,Behar J和Biancani P. J Pharmacol Exp Ther 283:1293 - 1304,1997)。如先前所述(Biancani P,Billett G,Hillemeier C,Nissenshon M,Rhim BY,Sweczack S和Behar J. Gastroenterology 103:1199 - 1206,1992)在肌肉腔中检查LES环形肌条。测量炎症介质水平。食管炎中IL-1β水平高于正常LES。IL-1β降低正常LES张力,而过氧化氢酶可逆转这种降低,提示过氧化氢(H2O2)起作用。这在正常LES中由IL-1β诱导的H2O2产生以及食管炎中升高的H2O2水平得到证实。H2O2本身足以解释肌肉中发生的变化,降低其收缩能力。H2O2增加正常LES中的前列腺素E2(PGE2),食管炎LES中PGE2水平升高,而PGF2α水平不变。H2O2还增加8-异前列腺素水平,8-异前列腺素是由花生四烯酸自由基诱导过氧化形成的稳定前列腺素样化合物,食管炎中8-异前列腺素水平升高。PGF2α类似物8-异-PGF2α引起LES条带收缩很少,但减少正常LES中PGF2α的结合和收缩。在食管炎中,LES中PGF2α的结合和收缩减少,提示异前列腺素可能导致食管炎中张力降低。数据表明,在食管炎中,IL-1β导致H2O2产生。H2O2增加PGE2,使LES松弛,增加8-异-F2α,阻断PGF2α介导的收缩。

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