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The Pseudomonas aeruginosa quorum-sensing signal molecule, N-(3-oxododecanoyl)-L-homoserine lactone, inhibits porcine arterial smooth muscle contraction

机译:铜绿假单胞菌群体感应信号分子N-(3-氧十二烷酰)-L-高丝氨酸内酯可抑制猪动脉平滑肌收缩

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摘要

The Pseudomonas aeruginosa quorum sensing molecule N-(3-oxododecanoyl)-L-homoserine lactone (OdDHL) has been shown to suppress cytokine production in macrophages. We have examined the effect of OdDHL and related compounds on constrictor tone of porcine blood vessels. OdDHL (1–30 μM) caused a concentration-dependent inhibition of U46619-induced contractions of the coronary artery through a largely endothelium-independent mechanism, but was markedly less effective in the pulmonary artery. Quantitively similar effects to those produced by OdDHL were observed with N-(3-oxododecanoyl)-L-homocysteine thiolactone, a thiolactone derivative, while N-3-oxododecanamide, a lactone-free acyl analogue, possessed 1/3rd the potency as a vasorelaxant. Neither N-butanoyl-L-homoserine lactone nor L-homoserine lactone (up to 30 μM) were active. Our findings indicate that OdDHL inhibits vasoconstrictor tone of both pulmonary and coronary blood vessels from the pig. The vasorelaxant action of OdDHL appears to be primarily determined by the N-acyl chain length, with a minor contribution by the homoserine lactone moiety.
机译:铜绿假单胞菌群体感应分子N-(3-oxododecanoyl)-L-高丝氨酸内酯(OdDHL)已显示可抑制巨噬细胞中细胞因子的产生。我们检查了OdDHL和相关化合物对猪血管收缩压的影响。 OdDHL(1–30μm)通过很大程度上不依赖内皮的机制引起了浓度依赖性抑制U46619诱导的冠状动脉收缩,但在肺动脉中效果明显较差。 N-(3-oxododecanoyl)-L-homocysteine thiolactone,一种硫代内酯衍生物,与OdDHL产生的效果在数量上相似,而N-oxododecanamide,一种无内酯的酰基类似物,具有1/3的效价。血管舒张药。 N-丁酰-L-高丝氨酸内酯和L-高丝氨酸内酯(最高30μm)均无活性。我们的发现表明,OdDHL抑制了猪肺和冠状血管的血管收缩张力。 OdDHL的血管舒张作用似乎主要由N-酰基链长决定,而高丝氨酸内酯部分的贡献很小。

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