Jeanneton O, Delvaux M, Botella A, Frexinos J, Bueno L
Department of Pharmacology, INRA, Toulouse, France.
J Pharmacol Exp Ther. 1993 Oct;267(1):31-7.
This study was designed to evaluate the effect of platelet-activating factor (PAF) on isolated smooth muscle cells from guinea pig ileum circular layer, to characterize the PAF receptors involved in this effect and to determine the intracellular pathways triggered by PAF. Cells dispersed by enzymatic digestion were incubated for 30 sec in the presence of PAF and fixed by glutaraldehyde. When inhibitors or antagonists were tested, cells were preincubated with them for 1 min. Then PAF was added for 30 sec, and the cells were fixed. Contraction was assessed by measuring the length of 50 cells and was expressed as the percentage decrease in cell length from controls. The relaxing effect of inhibitors was expressed as the percentage of the maximal contraction observed in their absence. PAF induced a cell contraction in a concentration-dependent manner. Maximal contraction (24.2 +/- 4.2%) was obtained for a PAF concentration of 10 nM (EC50 = 10 pM). PAF-induced contraction was inhibited by the PAF receptor antagonists BN52021, L659.989 and SR27417. Contraction induced by 10 nM PAF was inhibited when cells were incubated in Ca(++)-free medium with or without 2 mM EGTA or in a 1 mM Ca++ medium to which 100 nM nifedipine was added. When cells were preincubated with concentrations ranging from 0.01 pM to 10 microM of relaxing agents (vasoactive intestinal polypeptide, forskolin, 8 Bromo cAMP) known to increase the intracellular level of cAMP, PAF-induced contraction was inhibited. Moreover, when cells were preincubated with pertussis toxin (200 ng/ml) or cholera toxin (8.4 ng/ml), contraction induced by PAF was also inhibited.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在评估血小板活化因子(PAF)对豚鼠回肠环形肌层分离的平滑肌细胞的作用,鉴定参与此作用的PAF受体,并确定PAF触发的细胞内信号通路。经酶消化分散的细胞在PAF存在下孵育30秒,然后用戊二醛固定。当测试抑制剂或拮抗剂时,细胞先与它们预孵育1分钟。然后加入PAF 30秒,再固定细胞。通过测量50个细胞的长度评估收缩情况,并表示为细胞长度相对于对照的减少百分比。抑制剂的舒张作用表示为在无抑制剂时观察到的最大收缩的百分比。PAF以浓度依赖性方式诱导细胞收缩。PAF浓度为10 nM时获得最大收缩(24.2±4.2%)(EC50 = 10 pM)。PAF诱导的收缩被PAF受体拮抗剂BN52021、L659.989和SR27417抑制。当细胞在含或不含2 mM乙二醇双四乙酸(EGTA)的无钙培养基中孵育,或在加入100 nM硝苯地平的1 mM钙培养基中孵育时,10 nM PAF诱导的收缩受到抑制。当细胞用浓度范围为0.01 pM至10 μM的已知可增加细胞内cAMP水平的舒张剂(血管活性肠肽、福斯可林、8-溴腺苷-3',5'-环化一磷酸)预孵育时,PAF诱导的收缩受到抑制。此外,当细胞用百日咳毒素(200 ng/ml)或霍乱毒素(8.4 ng/ml)预孵育时,PAF诱导的收缩也受到抑制。(摘要截短于250字)