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首页> 外文期刊>Life sciences >Leukotriene-induced contraction is mediated by cysteinyl leukotriene receptor CysLT1 in guinea pig fundus but by CysLT1 and CysLT2 in antrum.
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Leukotriene-induced contraction is mediated by cysteinyl leukotriene receptor CysLT1 in guinea pig fundus but by CysLT1 and CysLT2 in antrum.

机译:白三烯诱导的收缩由豚鼠眼底的半胱氨酰白三烯受体CysLT1介导,但在胃窦中由CysLT1和CysLT2介导。

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AIMS: Leukotriene D(4) (LTD(4)) causes contraction of the stomach through unclear receptors. The aim of the present study is to characterize the cysteinyl leukotriene receptor (CysLT) mediating leukotriene-induced muscle contraction in the stomach. MAIN METHODS: We measured contraction of gastric muscle strips isolated from the guinea pig fundus and antrum caused by cysteinyl leukotrienes, including LTC(4), LTD(4) and LTE(4), as well as the dihydroxy leukotriene LTB(4) in vitro. KEY FINDINGS: In both fundic and antral muscle strips, LTC(4) and LTD(4) caused marked whereas LTE(4) caused moderate, concentration-dependent contractions. In contrast, LTB(4) caused only small contraction. The relative potencies for cysteinyl leukotrienes to cause contraction in both fundus and antrum were LTC(4)=LTD(4)>LTE(4). The LTD(4)-induced contraction was not affected by tetrodotoxin or atropine, suggesting that the action is not neurally mediated. The LTD(4)-induced contraction in the fundus was almost abolished by the CysLT(1) selective antagonist montelukast. In contrast, the LTD(4)-induced contraction in the antrum was only partially inhibited by montelukast or the dual CysLT(1) and CysLT(2) antagonist BAY u9773. This antral contraction was almost abolished by the combination of montelukast and BAY u9773, indicating enhancement of inhibition. SIGNIFICANCE: The results of the present study demonstrate that cysteinyl leukotrienes LTC(4), LTD(4) and LTE(4) cause moderate to marked whereas the dihydroxy leukotriene LTB(4) causes small muscle contraction in the stomach in vitro. The leukotriene-induced contraction is mediated by CysLT(1) in fundus but by CysLT(1) and CysLT(2) in antrum.
机译:目的:白三烯D(4)(LTD(4))通过不清楚的受体引起胃部收缩。本研究的目的是表征半胱氨酰白三烯受体(CysLT)介导白三烯诱导的胃部肌肉收缩。主要方法:我们测量了从半胱氨酸白三烯,包括LTC(4),LTD(4)和LTE(4)以及二羟基白三烯LTB(4)引起的豚鼠眼底和胃窦分离出来的胃肌条的收缩。体外。主要发现:在眼底和肛门肌条中,LTC(4)和LTD(4)引起明显收缩,而LTE(4)引起中度,浓度依赖性收缩。相反,LTB(4)仅引起很小的收缩。半胱氨酰白三烯引起眼底和胃窦收缩的相对能力为LTC(4)= LTD(4)> LTE(4)。 LTD(4)诱导的收缩不受河豚毒素或阿托品的影响,表明该作用不是神经介导的。 CysLT(1)选择性拮抗剂孟鲁司特几乎消除了LTD(4)引起的眼底收缩。相比之下,孟鲁司特或双重CysLT(1)和CysLT(2)拮抗剂BAY u9773只能部分抑制LTD(4)诱导的胃窦收缩。孟鲁司特和BAY u9773的结合几乎消除了这种肛门收缩,表明抑制作用增强。意义:本研究的结果表明,半胱氨酰白三烯LTC(4),LTD(4)和LTE(4)引起中度至显着性,而二羟基白三烯LTB(4)导致体外胃中的小肌肉收缩。白三烯诱导的收缩由眼底的CysLT(1)介导,但在胃窦由CysLT(1)和CysLT(2)介导。

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