Raevskaia O S, Fedoseeva O V
Farmakol Toksikol. 1988 Sep-Oct;51(5):23-7.
In unanesthetized rabbits intraventricular and intravenous administration of angiotensin II resulted in a decrease of the somatosensory evoked potential amplitude in response to nociceptive electrodental stimulation but not nociceptive electrocutaneous stimulation. Saralasin administered intraventricularly abolished the effect of angiotensin II. Naloxone injected by the same route increased the evoked potential amplitude in response to electrodental but not to electrocutaneous stimulation and also reversed the analgesic effect of angiotensin II. The selectivity of the antinociceptive effect of angiotensin II is probably due to the presence of different specific peptide pain mechanisms of varying origin.
在未麻醉的家兔中,脑室内和静脉内给予血管紧张素II会导致对伤害性牙髓电刺激的体感诱发电位幅度降低,但对伤害性皮肤电刺激则无此作用。脑室内给予沙拉新可消除血管紧张素II的作用。经相同途径注射纳洛酮可增加对牙髓电刺激而非皮肤电刺激的诱发电位幅度,并且还可逆转血管紧张素II的镇痛作用。血管紧张素II抗伤害感受作用的选择性可能是由于存在不同来源的特定肽类疼痛机制。