Research Service, Veterans Affairs Medical Center, Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, PO Box 670575, Cincinnati, OH 45267-0575, USA.
Naunyn Schmiedebergs Arch Pharmacol. 2012 Apr;385(4):437-41. doi: 10.1007/s00210-012-0725-3. Epub 2012 Jan 19.
The rationale for the therapeutic use of dual as opposed to selective endothelin (ET) receptor antagonists stems in part from cross-talk between the ET(A) and ET(B) receptors. However, whether ET(A)-ET(B) receptor cross-talk is present in the cerebral vasculature is difficult to discern since findings of cross-talk contrast even among the few reports available. Thus, this study tested whether ET(A)-ET(B) receptor cross-talk is present in the rat basilar artery. In an in situ cranial window, 0.1 μM sarafotoxin S6c, an ET(B) receptor agonist, relaxed basilar artery basal tone by 54%. ET-1 (3 nM) in the absence and presence of 10 μM BQ123, an ET(A) receptor agonist, induced 13% contraction and 15% relaxation, respectively. In contrast, the 3-nM ET-1 plateau contraction was relaxed by only ∼50% by 3-10 μM BQ123 and 10 μM BQ610, ET(A) receptor antagonists. N(ω)-nitro-L: -arginine, an NO synthase inhibitor, did not enhance contraction to 3 nM ET-1, suggesting that the partial relaxation of the ET-1 plateau contraction did not involve unmasked endothelial ET(B) receptor-mediated relaxation. The ∼50% ET-1 contraction that remained following ET(A) receptor antagonist was relaxed by 3-10 μM BQ788, consistent with an ET(B) receptor-mediated component of contraction. However, 10 μM BQ788 in the absence of prior ET(A) receptor antagonist did not cause relaxation. Subsequent BQ123 addition in the presence of BQ788 completely relaxed the ET-1 contraction. PD145065 (1 μM), an ET(A/B) receptor antagonist, completely relaxed 3-nM ET-1 contracted vessels in both the absence and presence of BQ123. These findings suggest that the inability of ET(A) receptor antagonist to completely relax the ET-1 plateau contraction in rat basilar artery is due to ET(A)-ET(B) receptor cross-talk.
双重而非选择性内皮素(ET)受体拮抗剂的治疗用途的基本原理部分源于 ET(A)和 ET(B)受体之间的串扰。然而,由于甚至在少数可用报告中也存在相互矛盾的发现,因此难以确定脑脉管系统中是否存在 ET(A)-ET(B)受体串扰。因此,本研究测试了 ET(A)-ET(B)受体串扰是否存在于大鼠基底动脉中。在原位颅窗中,0.1μM 沙呋毒素 S6c,一种 ET(B)受体激动剂,使基底动脉基础张力松弛 54%。ET-1(3nM)在不存在和存在 10μM BQ123(一种 ET(A)受体激动剂)的情况下分别诱导 13%收缩和 15%松弛。相比之下,3nM ET-1 平台收缩仅被 3-10μM BQ123 和 10μM BQ610(ET(A)受体拮抗剂)松弛约 50%。NO 合酶抑制剂 N(ω)-硝基-L:-精氨酸没有增强对 3nM ET-1 的收缩,这表明 ET-1 平台收缩的部分松弛不涉及未被掩盖的内皮 ET(B)受体介导的松弛。在 ET(A)受体拮抗剂之后仍然存在的约 50%ET-1 收缩被 3-10μM BQ788 松弛,这与收缩的 ET(B)受体介导成分一致。然而,在没有先前 ET(A)受体拮抗剂的情况下,10μM BQ788 不会引起松弛。随后在存在 BQ788 的情况下加入 BQ123 可完全松弛 ET-1 收缩。PD145065(1μM),一种 ET(A/B)受体拮抗剂,可完全松弛 3nM ET-1 收缩的血管,无论是在没有还是存在 BQ123 的情况下。这些发现表明,ET(A)受体拮抗剂不能完全松弛大鼠基底动脉中 ET-1 平台收缩是由于 ET(A)-ET(B)受体串扰。