Kawasaki H, Nuki C, Saito A, Takasaki K
Department of Pharmacology, Miyazaki Medical College, Japan.
J Pharmacol Exp Ther. 1990 Jan;252(1):403-9.
The role of calcitonin gene-related peptide (CGRP)-containing nerves in adrenergic vasoconstrictor response to periarterial nerve stimulation (PNS) was investigated in mesenteric vascular beds isolated from rats, which were perfused with Krebs' solution (5 ml/min). In perfused mesenteric vascular beds, PNS (1-12 Hz, for 30 sec) caused a frequency-dependent increase in the perfusion pressure, which was prevented by 50 nM prazosin and abolished by 300 nM tetrodotoxin and 5 microM guanethidine. Bolus infusion of norepinephrine (NE, 0.5 and 1 nmol) also produced a pressor response which was blocked by 50 nM prazosin. In the preparation treated with 500 nM capsaicin for 20 min, pressor responses to PNS of 1 to 8 Hz were potentiated significantly. The pressor responses to NE infusion also were enhanced in both the preparations treated with and without capsaicin. In the capsaicin-untreated preparation contracted by 7 mM methoxamine in the presence of 5 microM guanethidine, PNS (1-12 Hz) caused a frequency-dependent vasodilation, which was abolished by 300 nM tetrodotoxin. However, no vasodilator response to PNS was observed in the preparation treated with capsaicin. In the contracted preparation, bolus infusion of rat CGRP (10 and 100 pmol) produced a marked long-lasting vasodilation which mimicked the PNS-evoked vasodilation, whereas neither bolus infusion of substance P (1 and 10 nmol), neurokinin A (1 and 10 nmol) nor neurokinin B (1 and 10 nmol) produced relaxation. In the preparation labeled with [3H]NE, the PNS (4 Hz)-evoked 3H release was not altered after capsaicin treatment, whereas the pressor response to PNS was potentiated significantly.(ABSTRACT TRUNCATED AT 250 WORDS)
在从大鼠分离的肠系膜血管床中,研究了含降钙素基因相关肽(CGRP)的神经在对动脉周围神经刺激(PNS)的肾上腺素能血管收缩反应中的作用,该血管床用 Krebs 溶液(5 毫升/分钟)灌注。在灌注的肠系膜血管床中,PNS(1 - 12 赫兹,持续 30 秒)导致灌注压呈频率依赖性增加,50 纳摩尔哌唑嗪可阻止这种增加,300 纳摩尔河豚毒素和 5 微摩尔胍乙啶可消除这种增加。静脉推注去甲肾上腺素(NE,0.5 和 1 纳摩尔)也产生升压反应,50 纳摩尔哌唑嗪可阻断该反应。在用 500 纳摩尔辣椒素处理 20 分钟的制剂中,1 至 8 赫兹的 PNS 引起的升压反应显著增强。在用和未用辣椒素处理的制剂中,对 NE 输注的升压反应也增强。在 5 微摩尔胍乙啶存在下由 7 毫摩尔甲氧明收缩的未用辣椒素处理的制剂中,PNS(1 - 12 赫兹)引起频率依赖性血管舒张,300 纳摩尔河豚毒素可消除这种舒张。然而,在用辣椒素处理的制剂中未观察到对 PNS 的血管舒张反应。在收缩的制剂中,静脉推注大鼠 CGRP(10 和 100 皮摩尔)产生明显的持久血管舒张,类似于 PNS 诱发的血管舒张,而静脉推注 P 物质(1 和 10 纳摩尔)、神经激肽 A(1 和 10 纳摩尔)或神经激肽 B(1 和 10 纳摩尔)均未产生舒张作用。在用[3H]NE 标记的制剂中,辣椒素处理后 PNS(4 赫兹)诱发的 3H 释放未改变,而对 PNS 的升压反应显著增强。(摘要截短于 250 字)