Cox B F, Hay M, Bishop V S
Department of Pharmacology, University of Texas Health Science Center, San Antonio 78284-7764.
Am J Physiol. 1990 Jun;258(6 Pt 2):H1943-6. doi: 10.1152/ajpheart.1990.258.6.H1943.
Intravenous infusion of arginine vasopressin (AVP) has been shown to enhance baroreflex sensitivity, and this enhancement is dependent on the integrity of the area postrema. However, previous studies did not differentiate a role for cell bodies in the area postrema vs. the dense network of fibers located in and around the lateral and ventral margins of this circumventricular organ. In the present study, baroreflex function was assessed in conscious rabbits by examining heart rate after ramp infusions of phenylephrine (PE) and AVP. The subsequent day, the excitotoxin kainic acid was injected (30 nl initially, with five 15-nl supplemental injections of a 1 ng/nl solution over 1 h) into the area postrema, thus selectively destroying cell bodies. After an 8-day recovery period, baroreflex function was again assessed. The bradycardic response to graded infusion of PE (slope = -2.29 +/- 0.30) was not significantly different after selective lesions of area postrema neurons (slope = -1.88 +/- 0.49). In contrast, the previously enhanced bradycardic response to infusion of AVP (slope = -5.76 +/- 1.02) was significantly attenuated (slope = -2.31 +/- 0.21) to levels similar to that seen with infusion of PE. Thus selective chemical lesions of area postrema neurons block vasopressin-induced enhancement of the baroreflex.
静脉输注精氨酸加压素(AVP)已被证明可增强压力感受性反射敏感性,且这种增强依赖于最后区的完整性。然而,先前的研究并未区分最后区的细胞体与位于这个脑室周器官外侧和腹侧边缘及其周围的密集纤维网络所起的作用。在本研究中,通过在静脉输注去氧肾上腺素(PE)和AVP后检查心率,对清醒家兔的压力感受性反射功能进行评估。在随后的一天,将兴奋性毒素 kainic 酸(最初注射 30 nl,并在 1 小时内分五次补充注射 15 nl、浓度为 1 ng/nl 的溶液)注射到最后区,从而选择性地破坏细胞体。经过 8 天的恢复期后,再次评估压力感受性反射功能。在选择性损毁最后区神经元后,对分级输注 PE 的心动过缓反应(斜率 = -2.29 ± 0.30)与损毁前(斜率 = -1.88 ± 0.49)无显著差异。相比之下,先前增强的对输注 AVP 的心动过缓反应(斜率 = -5.76 ± 1.02)显著减弱(斜率 = -2.31 ± 0.21),降至与输注 PE 时相似的水平。因此,最后区神经元的选择性化学损毁可阻断血管加压素诱导的压力感受性反射增强。