The cardiovascular response of normal rats to dual lesion of the subfornical organ and area postrema at rest and to chronic losartan

• Published in: Brain research 2009-12, Vol.1302, p.118-124
• Main Authors: Collister, John P, Nahey, David B
• Format: Article
• Language: English
• Subjects: Angiotensin II Type 1 Receptor Blockers - pharmacology; Angiotensins - metabolism; Animals; Area postrema; Area Postrema - drug effects; Area Postrema - physiology; Blood Pressure - drug effects; Blood Pressure - physiology; Cardiovascular Physiological Phenomena - drug effects; Denervation; Drug Administration Schedule; Heart Rate - drug effects; Heart Rate - physiology; Hypertension; Hypotension - etiology; Hypotension - physiopathology; Losartan; Losartan - pharmacology; Male; Neurology; Rats; Rats, Sprague-Dawley; Receptor, Angiotensin, Type 1 - drug effects; Receptor, Angiotensin, Type 1 - metabolism; Rest - physiology; Subfornical organ; Subfornical Organ - drug effects; Subfornical Organ - physiology
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/j.brainres.2009.09.021

Abstract 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 AT1 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 (∼ 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.