Morris J L, Cunnane T C, Hirst G D
Department of Anatomy and Histology, Centre for Neuroscience, Flinders University of South Australia, Adelaide, Australia.
J Auton Nerv Syst. 1998 Nov 10;73(2-3):115-24. doi: 10.1016/s0165-1838(98)00122-2.
The effects of sympathetic nerve stimulation on different cutaneous arteries were examined in arteries isolated from guinea-pig ears, by measuring membrane potential changes in smooth muscle cells in response to electrical field stimulation. Resting membrane potential (RMP) was similar in proximal (main ear artery) and distal (3rd or 4th branch order) cutaneous arteries (mean -71 mV). Single stimuli evoked excitatory junction potentials (EJPs) in all arteries. The EJPs in proximal arteries were twice the amplitude, and the time constant of EJP decay was almost half the value, compared with distal cutaneous arteries. EJP amplitude was reduced by > 90% by suramin (30 microM) or alpha,beta,methylene-ATP (alpha,beta,m-ATP)(1 microM) in all proximal, and most distal arteries. Residual responses in distal arteries were resistant to tetrodotoxin. The N-type calcium channel blocker, omega-conotoxin GVIA (30 nM), reduced EJP amplitude by 70-100% in both proximal and distal arteries. Successive EJPs evoked by trains of stimuli at 1 to 5 Hz were depressed in amplitude in proximal arteries, but showed facilitation in distal arteries. EJP depression in proximal arteries was reversed to facilitation by the alpha2-adrenoceptor antagonist, yohimbine (30 nM). Trains of stimuli delivered at 10-20 Hz produced summation of EJPs and active membrane responses in 30% of proximal arteries. Active responses were never detected in distal arteries. Slow depolarizations following the EJPs were detected in most arteries after trains of stimuli, and were abolished by prazosin (0.3 microM) or omega-conotoxin GVIA (30 nM). The density of the perivascular plexus of axons innervating proximal arteries, demonstrated with catecholamine fluorescence histochemistry, was twice that in distal cutaneous arteries. These regional differences in sympathetic neurotransmission suggest that cutaneous vasoconstriction in response to thermoregulatory stimuli, which occurs predominantly in distal cutaneous segments, is likely to be qualitatively different from cutaneous vasoconstriction of proximal arteries in response to other physiological stimuli.
通过测量电场刺激后豚鼠耳部分离动脉平滑肌细胞膜电位的变化,研究了交感神经刺激对不同皮肤动脉的影响。近端(主耳动脉)和远端(第3或第4分支级)皮肤动脉的静息膜电位(RMP)相似(平均为-71 mV)。单次刺激在所有动脉中均诱发兴奋性接头电位(EJP)。与远端皮肤动脉相比,近端动脉中EJP的幅度为其两倍,且EJP衰减的时间常数几乎为其一半。在所有近端和大多数远端动脉中,苏拉明(30 μM)或α,β-亚甲基ATP(α,β,m-ATP)(1 μM)可使EJP幅度降低>90%。远端动脉中的残余反应对河豚毒素具有抗性。N型钙通道阻滞剂ω-芋螺毒素GVIA(30 nM)可使近端和远端动脉中的EJP幅度降低70%-100%。以1至5 Hz的刺激串诱发的连续EJP在近端动脉中幅度降低,但在远端动脉中表现为易化。α2-肾上腺素能受体拮抗剂育亨宾(30 nM)可将近端动脉中EJP降低逆转至易化。以10-至20 Hz施加的刺激串在30%的近端动脉中产生EJP总和及主动膜反应。在远端动脉中从未检测到主动反应。刺激串后,在大多数动脉中检测到EJP后的缓慢去极化,且被哌唑嗪(0.3 μM)或ω-芋螺毒素GVIA(30 nM)消除。用儿茶酚胺荧光组织化学法显示,支配近端动脉的轴突血管周围丛的密度是远端皮肤动脉的两倍。交感神经传递的这些区域差异表明,主要发生在远端皮肤节段的对体温调节刺激的皮肤血管收缩,在性质上可能与近端动脉对其他生理刺激的皮肤血管收缩不同。