Yashon D, Blocker D, Brown R J, Hunt W E
Surg Neurol. 1975 Jun;3(6):295-300.
The importance of autacoidal substances in the genesis of cerebral vascular constriction and spasm is an unresolved issue. Comparative vasoactivity of 5-hydroxytryptamine (5HT) and norepinephrine (NE) on the human basilar artery was quantitatively assessed in vitro. 5HT was decidedly more vasoactive in this preparation. Three patterns of vasoactivity were noted with 5HT. Type I was an immediate sustained increase in tension lasting more than 30 minutes. Average increase in tension was 2988 mg (range 120-8600). Type II consisted of a sharp immediate increase in tension to average 1555 mg (range 240-4500) followed by gradual dissipation to base-line levels within 15 minutes. Type III pattern was a lesser immediate increase (372 mg; range 100-850) and more rapid dissipation over ten minutes. NE-induced Type I and Type III activity was present in only six of 20 segments. This study demonstrates that 5HT is vasoactive in human cerebral arteries. Type I sustained contractions may possibly be implicated in spasm. It is hypothesized that such autacoid-induced contraction may contribute to vascular wall ischemia, necrosis, and irreversible constriction as seen in human vasospasm.
自体活性物质在脑血管收缩和痉挛发生过程中的重要性是一个尚未解决的问题。在体外定量评估了5-羟色胺(5HT)和去甲肾上腺素(NE)对人基底动脉的血管活性比较。在该制剂中,5HT的血管活性明显更强。观察到5HT有三种血管活性模式。I型是张力立即持续增加,持续超过30分钟。张力平均增加2988毫克(范围120 - 8600)。II型包括张力立即急剧增加至平均1555毫克(范围240 - 4500),随后在15分钟内逐渐消散至基线水平。III型模式是立即增加较少(372毫克;范围100 - 850),并在十分钟内更快消散。在20个节段中,NE诱导的I型和III型活性仅在6个节段中出现。本研究表明5HT在人脑血管中具有血管活性。I型持续收缩可能与痉挛有关。据推测,这种自体活性物质诱导的收缩可能导致血管壁缺血、坏死以及如人类血管痉挛中所见的不可逆收缩。