Department of Veterinary and Biomedical Sciences, University of Minnesota, St Paul, MN 55108, USA.
Brain Res. 2009 Dec 11;1302:118-24. doi: 10.1016/j.brainres.2009.09.021. Epub 2009 Sep 16.
The subfornical organ (SFO) and the area postrema (AP), two of the sensory circumventricular organs (CVO), are known to play a role in the chronic central control of blood pressure. In previous studies in which these regions were independently lesioned, the chronic hypotensive effects of the AT(1) receptor blocker losartan (10 mg/kg/day) were attenuated by ~15 mm Hg. In the present study, we sought to investigate the effect of concurrent lesion of both the SFO and the AP on the cardiovascular effects of chronic losartan infusion in order to test the hypothesis that a greater attenuation of the hypotensive effects of losartan would be observed in rats with dual lesions. To do so, arterial pressure and heart rate responses to 10-day infusion of losartan were compared in sham rats and those with dual lesions of the AP and SFO. Two important findings resulted from this study. First, dual lesion rats exhibited a sustained and significant decrease in resting blood pressure (83+/-1 mm Hg vs. 104+/-1 mm Hg, respectively) and heart rate (356+/-3 bpm vs. 398+/-6 bpm, respectively) compared to sham animals. Secondly, rats with concurrent lesion of both the AP and the SFO demonstrated a significantly attenuated response to losartan compared to sham animals but showed no greater attenuation of losartan's chronic hypotensive effects than animals with lesion of either the SFO or the AP (approximately 15 mm Hg). Although these results do not support the stated hypothesis, they do suggest redundancy and compensatory roles of the AP and SFO in basal cardiovascular control.
神经内分泌器官(SFO)和最后区(AP),两个感觉室周器官(CVO),已知在血压的慢性中枢控制中发挥作用。在这些区域被独立破坏的先前研究中,AT(1)受体阻滞剂氯沙坦(10mg / kg /天)的慢性降压作用被削弱了约 15mmHg。在本研究中,我们试图研究同时破坏 SFO 和 AP 对慢性氯沙坦输注的心血管作用的影响,以检验以下假设:在具有双重损伤的大鼠中,氯沙坦的降压作用会观察到更大的衰减。为此,比较了假手术大鼠和 AP 和 SFO 双重损伤大鼠对 10 天氯沙坦输注的动脉压和心率反应。这项研究产生了两个重要发现。首先,与假手术动物相比,双重损伤大鼠的静息血压(分别为 83 +/- 1mmHg 和 104 +/- 1mmHg)和心率(分别为 356 +/- 3bpm 和 398 +/- 6bpm)持续且显著降低。其次,与假手术动物相比,同时损伤 AP 和 SFO 的大鼠对氯沙坦的反应明显减弱,但与 SFO 或 AP 损伤的大鼠相比,氯沙坦的慢性降压作用没有更大的衰减(约 15mmHg)。尽管这些结果不支持所述假设,但它们确实表明 AP 和 SFO 在基础心血管控制中具有冗余和代偿作用。