Figueroa Xavier F, Paul David L, Simon Alexander M, Goodenough Daniel A, Day Kathy H, Damon David N, Duling Brian R
Dept of Molecular Physiology and Biological Physics, University of Virginia Health Sciences Center, PO Box 800736, Charlottesville, Va 22908-0736, USA.
Circ Res. 2003 Apr 18;92(7):793-800. doi: 10.1161/01.RES.0000065918.90271.9A. Epub 2003 Mar 13.
When a short segment of arteriole is stimulated, vasomotor responses spread bidirectionally along the vessel axis purportedly via gap junctions. We used connexin40 knockout (Cx40-/-) mice to study vasomotor responses induced by 10-second trains of electrical stimulation (30 Hz, 1 ms, 30 to 50 V) in 2nd or 3rd order arterioles of the cremaster muscle. Measurements were made at the stimulation site (local) and at conducted sites (500, 1000, and 2000 microm upstream). In wild-type (Cx40+/+) animals, electrical stimulation evoked a local vasoconstriction and a conducted vasodilation that spread very rapidly along the vessel length without detectable decay. In Cx40-/- mice, the conducted dilation was converted into either vasoconstriction or a slowly developing vasodilation that decayed along the vessel length. Tetrodotoxin (TTX, 1 micromol/L) had no effect on the local vasoconstriction in either Cx40+/+ or Cx40-/- mice, but enhanced the conducted vasodilation in Cx40+/+ animals. In Cx40-/- mice, TTX abolished the conducted vasoconstriction when present and revealed a small vasodilation that decayed with distance. In the group of Cx40-/- mice in which electrical stimulation elicited a conducted vasodilation, TTX had no effect. Immunocytochemistry revealed Cx40 only in the endothelial layer of arterioles from Cx40+/+ mice and complete elimination of this connexin in the Cx40-/- animals. These results indicate that focal current stimulation causes vasoconstriction by a combination of perivascular nerve stimulation and smooth muscle activation. Moreover, electrical stimulation activates a nonneuronal, Cx40-dependent vasodilator response that spreads along the vessel length without decay.
当一小段小动脉受到刺激时,血管运动反应据推测通过缝隙连接沿血管轴双向传播。我们使用连接蛋白40基因敲除(Cx40-/-)小鼠来研究在提睾肌二级或三级小动脉中由10秒的电刺激序列(30赫兹,1毫秒,30至50伏)诱导的血管运动反应。在刺激部位(局部)和传导部位(上游500、1000和2000微米处)进行测量。在野生型(Cx40+/+)动物中,电刺激引起局部血管收缩和传导性血管舒张,后者沿血管长度迅速传播且无明显衰减。在Cx40-/-小鼠中,传导性舒张转变为血管收缩或沿血管长度衰减的缓慢发展的血管舒张。河豚毒素(TTX,1微摩尔/升)对Cx40+/+或Cx40-/-小鼠的局部血管收缩均无影响,但增强了Cx40+/+动物的传导性血管舒张。在Cx40-/-小鼠中,TTX在存在时消除了传导性血管收缩,并揭示出一种随距离衰减的小血管舒张。在电刺激引起传导性血管舒张的Cx40-/-小鼠组中,TTX无作用。免疫细胞化学显示Cx40仅存在于Cx40+/+小鼠小动脉的内皮细胞层中,而在Cx40-/-动物中该连接蛋白完全缺失。这些结果表明,局部电流刺激通过血管周围神经刺激和平滑肌激活的组合导致血管收缩。此外,电刺激激活了一种非神经元的、依赖Cx40的血管舒张反应,该反应沿血管长度传播而不衰减。