Wittmann G, Weinerowski P, Simmet T, Peskar B A
Department of Pharmacology and Toxicology, Ruhr-Universität Bochum, Federal Republic of Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Nov;338(5):577-81. doi: 10.1007/BF00179333.
The effects of muscarinic receptor stimulation by infusions of methacholine (6.25 x 10(-8) mol/min or 1.9 x 10(-7) mol/min) into isolated perfused, spontaneously beating sensitized guinea-pig hearts on the anaphylactic release of cysteinyl-leukotrienes (LT) and thromboxane (TX) B2 were investigated. Methacholine increased coronary flow and decreased heart rate under basal conditions. Furthermore, infusions of methacholine (1.9 x 10(-7) mol/min) significantly increased the anaphylactic release of TXB2 as well as of immunoreactive cysteinyl-LT, which were demonstrated by reversed phase high pressure liquid chromatography to consist of a mixture of LTC4, LTD4 and LTE4. Infusions of atropine (1.3 x 10(-7) mol/min) alone did not significantly affect coronary flow and heart rate prior to ovalbumin injection nor anaphylactic release of cysteinyl-LT. The anaphylactic release of TXB2 was, however, significantly decreased in the presence of atropine. Atropine (1.3 x 10(-7) mol/min) infused in addition to methacholine (1.9 x 10(-7) mol/min) abolished the effects of the muscarinic receptor agonist on spontaneous heart rate and significantly antagonized the increase in coronary flow prior to ovalbumin injection. Similarly, the simultaneous infusion of atropine abolished the effects of methacholine on the anaphylactic release of TXB2 and cysteinyl-LT. After antigen challenge hearts infused with methacholine, atropine or the combination of both drugs did not exhibit any differences with respect to anaphylactic changes of heart rate or the time course of anaphylactic coronary flow reduction. Thus, in the isolated perfused anaphylactic guinea-pig heart, muscarinic receptor stimulation significantly enhanced the release of the arachidonic acid-derived mediators TXB2 and cysteinyl-LT.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了向离体灌注、自发搏动的致敏豚鼠心脏中输注乙酰甲胆碱(6.25×10⁻⁸摩尔/分钟或1.9×10⁻⁷摩尔/分钟)对毒蕈碱受体的刺激作用,以及对胱氨酰白三烯(LT)和血栓素(TX)B2过敏释放的影响。在基础条件下,乙酰甲胆碱增加冠脉流量并降低心率。此外,输注乙酰甲胆碱(1.9×10⁻⁷摩尔/分钟)显著增加TXB2以及免疫反应性胱氨酰-LT的过敏释放,反相高压液相色谱显示其由LTC4、LTD4和LTE4的混合物组成。单独输注阿托品(1.3×10⁻⁷摩尔/分钟)在注射卵清蛋白之前对冠脉流量和心率以及胱氨酰-LT的过敏释放没有显著影响。然而,在阿托品存在的情况下,TXB2的过敏释放显著降低。除乙酰甲胆碱(1.9×10⁻⁷摩尔/分钟)外输注阿托品(1.3×10⁻⁷摩尔/分钟)消除了毒蕈碱受体激动剂对自发心率的影响,并显著拮抗了注射卵清蛋白之前冠脉流量的增加。同样,同时输注阿托品消除了乙酰甲胆碱对TXB2和胱氨酰-LT过敏释放的影响。抗原激发后,输注乙酰甲胆碱、阿托品或两种药物组合的心脏在心率过敏变化或过敏冠脉流量减少的时间进程方面没有表现出任何差异。因此,在离体灌注的过敏豚鼠心脏中,毒蕈碱受体刺激显著增强了花生四烯酸衍生介质TXB2和胱氨酰-LT的释放。(摘要截短至250字)