Harty H R, Thornbury K D, McHale N G
School of Biomedical Science, Queen's University of Belfast.
Microvasc Res. 1993 Nov;46(3):310-9. doi: 10.1006/mvre.1993.1055.
Spontaneous isometric contractions were measured in rings of sheep mesenteric lymphatics. Field stimulation at short pulse widths increased the frequency of spontaneous contractions and this response was blocked by 10(-7) M tetrodotoxin. The alpha-antagonists phentolamine, prazosin, and yohimbine failed to block the excitatory response in a dose of 10(-6) M. Exogenous noradrenaline (10(-6) M) increased the frequency and force of spontaneous contractions and this effect was blocked by a 10(-6) M phentolamine. Atropine 10(-6) M failed to block the excitatory response to field stimulation. alpha beta-methylene ATP caused an intense transient excitatory effect followed by recovery to a frequency level just above that of control but the excitatory effect of field stimulation was not blocked in these desensitized vessels. When vessels were exposed to a mixture of 10(-4) M noradrenaline and 10(-5) M phentolamine field stimulation did not further increase the frequency of spontaneous contractions. These results demonstrate that the innervation of sheep mesenteric lymphatics is different from that of bovine mesenteric lymphatics. The identity of the transmitter is as yet unknown but it does not appear to be ATP nor is it noradrenaline acting on postsynaptic alpha-receptors.
在羊肠系膜淋巴管环中测量自发性等长收缩。短脉冲宽度的场刺激增加了自发性收缩的频率,并且这种反应被10^(-7)M的河豚毒素阻断。α-拮抗剂酚妥拉明、哌唑嗪和育亨宾在10^(-6)M的剂量下未能阻断兴奋反应。外源性去甲肾上腺素(10^(-6)M)增加了自发性收缩的频率和力量,并且这种效应被10^(-6)M的酚妥拉明阻断。10^(-6)M的阿托品未能阻断对场刺激的兴奋反应。α,β-亚甲基ATP引起强烈的短暂兴奋效应,随后恢复到略高于对照频率的水平,但在这些脱敏血管中场刺激的兴奋效应未被阻断。当血管暴露于10^(-4)M去甲肾上腺素和10^(-5)M酚妥拉明的混合物中时,场刺激不再进一步增加自发性收缩的频率。这些结果表明,羊肠系膜淋巴管的神经支配与牛肠系膜淋巴管不同。神经递质的身份尚不清楚,但它似乎不是ATP,也不是作用于突触后α受体的去甲肾上腺素。