Department of Chemistry, Michigan Sate University, East Lansing, MI 48824, USA.
Auton Neurosci. 2010 Jan 15;152(1-2):11-20. doi: 10.1016/j.autneu.2009.08.008. Epub 2009 Nov 13.
We studied hypertension-associated changes in prejunctional alpha(2) adrenergic receptor (alpha(2)-AR) function using amperometry to monitor in vitro norepinephrine (NE) measured as oxidation currents. Vasoconstriction was measured using video imaging. NE release was induced by electrical stimulation of sympathetic nerves associated with mesenteric arteries (MA) and veins (MV) of sham and DOCA-salt hypertensive rats. NE oxidation currents were larger in DOCA-salt compared to sham MA; there were no differences between currents in sham and DOCA-salt MV. Increases in NE oxidation currents followed a multi-exponential time course in sham MA. In DOCA-salt MA and sham and DOCA-salt MV, the time course was mono-exponential. Yohimbine (alpha(2)-AR antagonist, 1 microM), caused a mono-exponential increase in NE oxidation currents in sham and DOCA-salt MA. Yohimbine increased NE oxidation currents and constrictions more in sham compared to DOCA-salt MA and compared to MV. UK 14,304 (alpha(2)-AR agonist, 1.0 microM), reduced currents less in DOCA-salt MA and sham and DOCA-salt MV compared to sham MA. Prazosin (alpha(1)-AR antagonist, 0.1 microM) did not alter NE oxidation currents. Prazosin inhibited constrictions more in DOCA-salt compared to sham MA and almost completely blocked constrictions in sham and DOCA-salt MV. Prazosin-resistant constrictions in MA were blocked by the P2 receptor antagonist, PPADS (10 microM). Prejunctional alpha(2)-ARs modify NE concentrations near neuroeffector junctions in MA and MV. alpha(2)-AR function is most prominent in MA and is impaired in DOCA-salt MA but not MV. Purinergic transmission predominates in sham MA. NE is the dominant vasoconstrictor in DOCA-salt MA and sham and DOCA-salt MV.
我们使用安培法监测体外去甲肾上腺素(NE)的氧化电流来研究高血压相关的节前α2 肾上腺素能受体(α2-AR)功能变化。使用视频成像测量血管收缩。通过刺激与肠系膜动脉(MA)和静脉(MV)相关的交感神经来诱导 NE 释放。与 sham 相比,DOCA-salt 高血压大鼠的 MA 中 NE 的氧化电流更大;在 sham 和 DOCA-salt MV 中,电流没有差异。在 sham MA 中,NE 氧化电流的增加遵循多指数时间过程。在 DOCA-salt MA 和 sham 和 DOCA-salt MV 中,时间过程是单指数的。育亨宾(α2-AR 拮抗剂,1 μM)导致 sham 和 DOCA-salt MA 中 NE 氧化电流呈单指数增加。育亨宾增加了 sham 与 DOCA-salt MA 相比,以及与 MV 相比,NE 氧化电流和收缩更多。UK 14,304(α2-AR 激动剂,1.0 μM)减少了电流,与 sham MA 相比,在 DOCA-salt MA 和 sham 和 DOCA-salt MV 中更少。哌唑嗪(α1-AR 拮抗剂,0.1 μM)不会改变 NE 氧化电流。与 sham MA 相比,哌唑嗪在 DOCA-salt 中抑制收缩更多,并且几乎完全阻断 sham 和 DOCA-salt MV 中的收缩。MA 中的 P2 受体拮抗剂 PPADS(10 μM)阻断了 Prazosin 抗性收缩。节前α2-AR 可调节 MA 和 MV 中神经效应器接头附近的 NE 浓度。α2-AR 功能在 MA 中最为突出,在 DOCA-salt MA 中受损,但在 MV 中不受损。嘌呤能传递在 sham MA 中占主导地位。NE 是 DOCA-salt MA 和 sham 和 DOCA-salt MV 中主要的血管收缩剂。