Ishihara Y, Sheller J
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232.
J Lipid Mediat. 1993 May;7(1):47-56.
The effects of leukotrienes (LT) C4, LTD4, LTE4 and LTB4 on the development of isometric tension by sheep airway smooth muscle were determined in a tissue bath. LTE4 (1.5 x 10(-7) M) had no contractile effect. LTB4 contracted only lung parenchymal strips. LTC4 (8 x 10(-8) M) and LTD4 (1.1 x 10(-7) M) caused contractions in trachea, bronchi and lung parenchyma that developed slowly and persisted. The tracheal contractions caused by LTD4 and ACh were potentiated approx. 30% by the cyclooxygenase inhibitor meclofenamate (10(-6) M). Meclofenamate had no effect on leukotriene induced contractions in bronchi or lung parenchymal strips. The bronchodilator prostaglandins PGI2 and PGE2 were released from sheep trachea at rest and after contraction by LTD4. Inhibition of their release by meclofenamate may explain the potentiation of LTD4 contractions by meclofenamate. In vitro, LTD4 and LTC4 have potent contractile effects on sheep airway smooth muscle that are not mediated by the secondary release of constrictor cyclooxygenase products. These leukotrienes may play a substantial role in the pathogenesis of allergen and endotoxin induced lung mechanics changes in sheep.
在组织浴中测定了白三烯(LT)C4、LTD4、LTE4和LTB4对绵羊气道平滑肌等长张力发展的影响。LTE4(1.5×10⁻⁷ M)无收缩作用。LTB4仅使肺实质条收缩。LTC4(8×10⁻⁸ M)和LTD4(1.1×10⁻⁷ M)引起气管、支气管和肺实质缓慢发展并持续的收缩。LTD4和乙酰胆碱(ACh)引起的气管收缩被环氧合酶抑制剂甲氯芬那酸(10⁻⁶ M)增强约30%。甲氯芬那酸对支气管或肺实质条中白三烯诱导的收缩无作用。支气管扩张剂前列腺素PGI2和PGE2在绵羊气管静止时以及被LTD4收缩后释放。甲氯芬那酸对其释放的抑制可能解释了甲氯芬那酸对LTD4收缩的增强作用。在体外,LTD4和LTC4对绵羊气道平滑肌有强大的收缩作用,并非由收缩性环氧合酶产物的二次释放介导。这些白三烯可能在变应原和内毒素诱导的绵羊肺力学变化的发病机制中起重要作用。