Fu Liang-Wu, Guo Zhi-Ling, Longhurst John C
Department of Medicine, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA.
J Physiol. 2008 Jul 1;586(13):3287-300. doi: 10.1113/jphysiol.2007.148106. Epub 2008 May 15.
Myocardial ischaemia activates blood platelets, which in turn stimulate cardiac sympathetic afferents, leading to chest pain and sympathoexcitatory reflex cardiovascular responses. Previous studies have shown that activated platelets stimulate ischaemically sensitive cardiac sympathetic afferents, and that thromboxane A(2) (TxA(2)) is one of the mediators released from activated platelets during myocardial ischaemia. The present study tested the hypothesis that endogenous TxA(2) stimulates cardiac afferents during ischaemia through direct activation of TxA(2) (TP) receptors coupled with the phospholipase C-protein kinase C (PLC-PKC) cellular pathway. Nerve activity of single unit cardiac sympathetic afferents was recorded from the left sympathetic chain or rami communicantes (T(2)-T(5)) in anaesthetized cats. Single fields of 39 afferents (conduction velocity = 0.27-3.65 m s(-1)) were identified in the left or right ventricle initially with mechanical stimulation and confirmed with a stimulating electrode. Five minutes of myocardial ischaemia stimulated all 39 cardiac afferents (8 Adelta-, 31 C-fibres) and the responses of these 39 afferents to chemical stimuli were further studied in the following four protocols. In the first protocol, 2.5, 5 and 10 microg of the TxA(2) mimetic, U46619, injected into the left atrium (LA), stimulated seven ischaemically sensitive cardiac afferents in a dose-dependent manner. Second, BM13,177, a selective TxA(2) receptor antagonist, abolished the responses of six afferents to 5 microg of U46619 injected into the left atrium and attenuated the ischaemia-related increase in activity of seven other afferents by 44%. In contrast, cardiac afferents, in the absence of TP receptor blockade responded consistently to repeated administration of U46619 (n = 6) and to recurrent myocardial ischaemia (n = 7). In the fourth protocol, administration of PKC-(19-36), a selective PKC inhibitor, attenuated the responses of six other cardiac afferents to U46619 by 38%. Finally, using an immunohistochemical staining approach, we observed that TP receptors were expressed in cardiac sensory neurons in thoracic dorsal root ganglia. Taken together, these data indicate that endogenous TxA(2) contributes to the activation of cardiac afferents during myocardial ischaemia through direct stimulation of TP receptors probably located in the cardiac sensory nervous system and that the stimulating effect of TxA(2) on cardiac afferents is dependent, at least in part, upon the PLC-PKC cellular pathway.
心肌缺血会激活血小板,而血小板又会刺激心脏交感传入神经,导致胸痛和交感神经兴奋反射性心血管反应。先前的研究表明,活化的血小板会刺激对缺血敏感的心脏交感传入神经,并且血栓素A2(TxA2)是心肌缺血期间活化血小板释放的介质之一。本研究检验了以下假设:内源性TxA2在缺血期间通过直接激活与磷脂酶C - 蛋白激酶C(PLC - PKC)细胞途径偶联的TxA2(TP)受体来刺激心脏传入神经。在麻醉猫的左交感神经链或交通支(T2 - T5)记录单个心脏交感传入神经的神经活动。最初通过机械刺激在左心室或右心室识别出39个传入神经的单个区域(传导速度 = 0.27 - 3.65 m s-1),并用刺激电极进行确认。五分钟的心肌缺血刺激了所有39个心脏传入神经(8个Aδ纤维、31个C纤维),并在以下四个实验方案中进一步研究了这39个传入神经对化学刺激的反应。在第一个实验方案中,将2.5、5和10微克TxA2模拟物U46619注入左心房(LA),以剂量依赖方式刺激了7个对缺血敏感的心脏传入神经。其次,选择性TxA2受体拮抗剂BM13,177消除了6个传入神经对注入左心房的5微克U46619的反应,并使其他7个传入神经的缺血相关活动增加减弱了44%。相比之下,在没有TP受体阻断的情况下,心脏传入神经对重复给予U46619(n = 6)和复发性心肌缺血(n = 7)持续有反应。在第四个实验方案中,给予选择性PKC抑制剂PKC - (19 - 36)使另外6个心脏传入神经对U46619的反应减弱了38%。最后,使用免疫组织化学染色方法,我们观察到TP受体在胸段背根神经节的心脏感觉神经元中表达。综上所述,这些数据表明内源性TxA2可能通过直接刺激可能位于心脏感觉神经系统的TP受体,在心肌缺血期间促成心脏传入神经的激活,并且TxA2对心脏传入神经的刺激作用至少部分依赖于PLC - PKC细胞途径。