Huang B S, Sancho J M, Garcia-Robles R, Leenen F H
University of Ottawa, Heart Institute, Ontario, Canada.
Hypertension. 1997 Jun;29(6):1291-5. doi: 10.1161/01.hyp.29.6.1291.
We recorded changes in arterial blood pressure, heart rate, and renal sympathetic nerve activity in response to intracerebroventricular injection of bovine hypothalamic/hypophysary inhibitory factor and ouabain in conscious Wistar rats. Ouabain at 0.3 to 0.6 microgram caused dose-related increases in blood pressure, heart rate, and nerve activity (peak increases: 19 +/- 2 mm Hg, 42 +/- 4 beats per minute, and 48 +/- 4%, respectively; P < .05 versus basal). These responses were all blocked by central antibody Fab fragments, which bind ouabain and related steroids with high affinity. The inhibitory factor significantly increased blood pressure but decreased heart rate and nerve activity. Dose-dependent increases in blood pressure as well as heart rate and nerve activity were observed when the inhibitory factor was injected after intravenous injection of the vasopressin antagonist D-(CH2)5Tyr-(Me)AVP. Central Fab fragments, however, did not affect these responses. Both ouabain and the inhibitory factor inhibited Na+,K+-ATPase activity in vitro. Fab fragments blocked this inhibition by ouabain but not by the inhibitory factor. These data indicate that the ouabainlike sympathoexcitatory effect of this factor is masked probably by a potent central effect on vasopressin release. In contrast to rat brain "ouabain," this factor does not exhibit a high affinity for the Fab fragments, supporting the previous finding that this compound is structurally a nonouabain Na+,K+-ATPase inhibitor.
我们记录了清醒Wistar大鼠脑室内注射牛下丘脑/垂体抑制因子和哇巴因后动脉血压、心率和肾交感神经活动的变化。0.3至0.6微克的哇巴因引起血压、心率和神经活动呈剂量相关增加(峰值增加分别为:19±2毫米汞柱、42±4次/分钟和48±4%;与基础值相比P<0.05)。这些反应均被能与哇巴因及相关类固醇高亲和力结合的中枢抗体Fab片段阻断。抑制因子显著升高血压,但降低心率和神经活动。静脉注射血管加压素拮抗剂D-(CH2)5Tyr-(Me)AVP后再注射抑制因子时,观察到血压以及心率和神经活动呈剂量依赖性增加。然而,中枢Fab片段不影响这些反应。哇巴因和抑制因子在体外均抑制Na+,K+-ATP酶活性。Fab片段阻断哇巴因的这种抑制作用,但不阻断抑制因子的抑制作用。这些数据表明,该因子类似哇巴因的交感神经兴奋作用可能被其对血管加压素释放的强大中枢作用所掩盖。与大鼠脑“哇巴因”不同,该因子对Fab片段不具有高亲和力,支持了之前的发现,即该化合物在结构上是一种非哇巴因类Na+,K+-ATP酶抑制剂。