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人嗜酸性粒细胞的激活方式对豚鼠气管平滑肌收缩的影响。

Effect of mode of activation of human eosinophils on tracheal smooth muscle contraction in guinea pigs.

作者信息

Strek M E, White S R, Hsiue T R, Kulp G V, Williams F S, Leff A R

机构信息

Department of Medicine, University of Chicago, Illinois 60637.

出版信息

Am J Physiol. 1993 May;264(5 Pt 1):L475-81. doi: 10.1152/ajplung.1993.264.5.L475.

Abstract

We studied the relationship between mode of activation of isolated human eosinophils and in situ responsiveness in isolated tracheal smooth muscle (TSM) of guinea pigs. Human peripheral blood eosinophils were activated with either 10(-7) M phorbol myristate acetate (PMA) or 10(-6) M formyl-methionyl-leucyl-phenylalanine (fMLP) + 5 micrograms/ml cytochalasin B (CYB), and activation was confirmed by measurement of eosinophil peroxidase (EPO) secretion by kinetic assay. EPO secretion was similar after activation with fMLP+CYB (10.2 +/- 3.2% of total eosinophil content) and PMA (10.0 +/- 2.8% of total content; P = NS). Topical application of 6 x 10(6) eosinophils/cm2 activated with fMLP+CYB to the TSM segment caused 0.51 +/- 0.14 g/cm active tension (AT) in five preparations (P < 0.03 vs. baseline); cells activated with PMA caused no contractile response (0.04 +/- 0.03 g/cm AT, P = NS vs. baseline). Both PMA- and fMLP+CYB-activated cells caused augmentation of muscarinic responsiveness of guinea pig trachealis. The dose of intravenous acetylcholine required to cause a threshold response (ED0.3) was -7.3 +/- 0.1 log mol/kg at baseline vs. -8.7 +/- 0.5 log mol/kg after treatment with fMLP+CYB-activated eosinophils (P = 0.05) and -6.9 +/- 0.1 log mol/kg at baseline vs. -7.5 +/- 0.1 log mol/kg after PMA-activated cells (P < 0.01). Both AT and augmented muscarinic responsiveness were blocked by pretreating the eosinophils with 200 microM A-63162, an inhibitor of 5-lipoxygenase, before activation with fMLP+CYB. We demonstrate that eosinophils activated comparably (as assessed by EPO secretion) cause augmented muscarinic responsiveness and/or direct contraction of guinea pig TSM through secretion of a product of the 5-lipoxygenase pathway.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了分离的人嗜酸性粒细胞的激活模式与豚鼠离体气管平滑肌(TSM)原位反应性之间的关系。用10⁻⁷ M佛波酯肉豆蔻酸乙酸酯(PMA)或10⁻⁶ M甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)+5微克/毫升细胞松弛素B(CYB)激活人外周血嗜酸性粒细胞,并通过动力学测定法测量嗜酸性粒细胞过氧化物酶(EPO)分泌来确认激活情况。用fMLP+CYB激活后EPO分泌(占嗜酸性粒细胞总含量的10.2±3.2%)与用PMA激活后(占总含量的10.0±2.8%;P=无显著性差异)相似。将6×10⁶个用fMLP+CYB激活的嗜酸性粒细胞/平方厘米局部应用于TSM段,在五个标本中引起0.51±0.14克/厘米的主动张力(AT)(与基线相比,P<0.03);用PMA激活的细胞未引起收缩反应(0.04±0.03克/厘米AT,与基线相比,P=无显著性差异)。PMA和fMLP+CYB激活的细胞均导致豚鼠气管平滑肌毒蕈碱反应性增强。引起阈值反应(ED0.3)所需的静脉注射乙酰胆碱剂量在基线时为-7.3±0.1对数摩尔/千克,在用fMLP+CYB激活的嗜酸性粒细胞处理后为-8.7±0.5对数摩尔/千克(P=0.05),在基线时为-6.9±0.1对数摩尔/千克,在用PMA激活的细胞处理后为-7.5±0.1对数摩尔/千克(P<0.01)。在用fMLP+CYB激活之前,用200微摩尔A-63162(一种5-脂氧合酶抑制剂)预处理嗜酸性粒细胞,可阻断AT和增强的毒蕈碱反应性。我们证明,以相似方式激活的嗜酸性粒细胞(通过EPO分泌评估)通过分泌5-脂氧合酶途径的产物,导致豚鼠TSM毒蕈碱反应性增强和/或直接收缩。(摘要截短至250字)

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