Cheng Man, Lee Susanna S T, Cheung Wing-Tai
Department of Biochemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.
Eur J Pharmacol. 2007 Feb 28;557(2-3):204-11. doi: 10.1016/j.ejphar.2006.11.035. Epub 2006 Nov 25.
Angiotensin and endothelin are vasoactive peptides with neuromodulatory effect, however their interactions in facilitating neurotransmission are largely unknown. In the present study, effort was made to examine how endothelin 1 modulates angiotensin II-potentiated purinergic neurotransmission in prostatic rat vas deferens. Both peptides facilitated field-stimulated muscle contraction in a concentration-dependent manner with Kd values of 16.97+/-6.47 and 2.46+/-0.83 nM for angiotensin II and endothelin 1, respectively. Hill plot analysis gave Hill constants of 0.91+/-0.15 and 0.97+/-0.26 for angiotensin II and endothelin 1, respectively. Correlation analysis indicated that the extent of potentiation by angiotensin II, but not endothelin 1, was proportional to the basal field-stimulated muscle contraction. In the presence of low concentrations of endothelin 1 (< or = 3 nM), angiotensin II-potentiated field-stimulated contraction was further enhanced by endothelin. However, in the presence of high concentrations of endothelin 1 (> or = 10 nM), a much increased basal field-stimulated contraction was observed, and the addition of angiotensin II did not elicit any further enhancement in the contractile response. Intriguingly, after prolonged exposure of prostatic rat vas deferens to a high concentration of endothelin 1, the addition of angiotensin II induced a refractory response to field-stimulation. Taken together, our result indicated that endothelin 1 augmented angiotensin II-facilitated purinergic neurotransmission in prostatic rat vas deferens at low concentrations, but inhibited gradually at high concentrations.
血管紧张素和内皮素是具有神经调节作用的血管活性肽,然而它们在促进神经传递方面的相互作用在很大程度上尚不清楚。在本研究中,我们致力于研究内皮素-1如何调节前列腺大鼠输精管中血管紧张素II增强的嘌呤能神经传递。两种肽均以浓度依赖性方式促进电场刺激的肌肉收缩,血管紧张素II和内皮素-1的Kd值分别为16.97±6.47和2.46±0.83 nM。希尔图分析得出血管紧张素II和内皮素-1的希尔常数分别为0.91±0.15和0.97±0.26。相关性分析表明,血管紧张素II而非内皮素-1的增强程度与基础电场刺激的肌肉收缩成正比。在低浓度内皮素-1(≤3 nM)存在的情况下,内皮素可进一步增强血管紧张素II增强的电场刺激收缩。然而,在高浓度内皮素-1(≥10 nM)存在的情况下,观察到基础电场刺激收缩大幅增加,添加血管紧张素II并未引起收缩反应的进一步增强。有趣的是,在前列腺大鼠输精管长时间暴露于高浓度内皮素-1后,添加血管紧张素II会诱导对电场刺激的不应性反应。综上所述,我们的结果表明,内皮素-1在低浓度时增强了前列腺大鼠输精管中血管紧张素II促进的嘌呤能神经传递,但在高浓度时逐渐抑制。