Suppr超能文献

正常大鼠在休息时及慢性使用氯沙坦时,双侧穹隆下器官和最后区损伤的心血管反应。

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

机构信息

Department of Veterinary and Biomedical Sciences, University of Minnesota, St Paul, MN 55108, USA.

出版信息

Brain Res. 2009 Dec 11;1302:118-24. doi: 10.1016/j.brainres.2009.09.021. Epub 2009 Sep 16.

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 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.

摘要

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。

相似文献

1
The cardiovascular response of normal rats to dual lesion of the subfornical organ and area postrema at rest and to chronic losartan.
Brain Res. 2009 Dec 11;1302:118-24. doi: 10.1016/j.brainres.2009.09.021. Epub 2009 Sep 16.
2
Role of the subfornical organ in the chronic hypotensive response to losartan in normal rats.
Hypertension. 2003 Mar;41(3):576-82. doi: 10.1161/01.HYP.0000058002.67558.6E. Epub 2003 Feb 17.
3
Subfornical organ lesion attenuates chronic hypotensive effects of losartan in salt-replete rats.
J Renin Angiotensin Aldosterone Syst. 2003 Dec;4(4):207-12. doi: 10.3317/jraas.2003.034.
4
Chronic effects of angiotensin II and at1 receptor antagonists in subfornical organ-lesioned rats.
Clin Exp Pharmacol Physiol. 2005 May-Jun;32(5-6):462-6. doi: 10.1111/j.1440-1681.2005.04212.x.
5
Role of the organum vasculosum of the lamina terminalis for the chronic cardiovascular effects produced by endogenous and exogenous ANG II in conscious rats.
Am J Physiol Regul Integr Comp Physiol. 2010 Dec;299(6):R1564-71. doi: 10.1152/ajpregu.00034.2010. Epub 2010 Sep 22.
6
Hypotensive response to losartan in normal rats. Role of Ang II and the area postrema.
Hypertension. 1996 Mar;27(3 Pt 2):598-606. doi: 10.1161/01.hyp.27.3.598.
7
Subfornical organ differentially modulates baroreflex function in normotensive and two-kidney, one-clip hypertensive rats.
Am J Physiol Regul Integr Comp Physiol. 2008 Sep;295(3):R741-50. doi: 10.1152/ajpregu.00157.2008. Epub 2008 Jul 2.
8
AT receptors in the subfornical organ modulate arterial pressure and the baroreflex in two-kidney, one-clip hypertensive rats.
Am J Physiol Regul Integr Comp Physiol. 2019 Feb 1;316(2):R172-R185. doi: 10.1152/ajpregu.00289.2018. Epub 2019 Jan 9.
9
Median preoptic nucleus and subfornical organ drive renal sympathetic nerve activity via a glutamatergic mechanism within the paraventricular nucleus.
Am J Physiol Regul Integr Comp Physiol. 2012 Feb 15;302(4):R424-32. doi: 10.1152/ajpregu.00403.2011. Epub 2011 Dec 7.
10
Effects of exercise training on SFO-mediated sympathoexcitation during chronic heart failure.
Am J Physiol Heart Circ Physiol. 2014 Jan 1;306(1):H121-31. doi: 10.1152/ajpheart.00534.2013. Epub 2013 Oct 25.

引用本文的文献

1
Apelin acts in the subfornical organ to influence neuronal excitability and cardiovascular function.
J Physiol. 2013 Jul 1;591(13):3421-32. doi: 10.1113/jphysiol.2013.254144. Epub 2013 Apr 29.
2
Role of cGMP and cAMP in the hemodynamic response to intrathecal sildenafil administration.
Clinics (Sao Paulo). 2011;66(8):1407-12. doi: 10.1590/s1807-59322011000800017.

本文引用的文献

1
Baroreceptor reflex modulation by circulating angiotensin II is mediated by AT1 receptors in the nucleus tractus solitarius.
Am J Physiol Regul Integr Comp Physiol. 2007 Dec;293(6):R2267-78. doi: 10.1152/ajpregu.00267.2007. Epub 2007 Sep 12.
2
Circulating angiotensin II and dietary salt: converging signals for neurogenic hypertension.
Curr Hypertens Rep. 2007 Jun;9(3):228-35. doi: 10.1007/s11906-007-0041-3.
3
Cardiovascular effects of angiotensin II in the rostral ventrolateral medulla: the push-pull hypothesis.
Curr Hypertens Rep. 2007 Jun;9(3):222-7. doi: 10.1007/s11906-007-0040-4.
4
ANG II-induced hypertension and the role of the area postrema during normal and increased dietary salt.
Am J Physiol Heart Circ Physiol. 2007 Jan;292(1):H694-700. doi: 10.1152/ajpheart.00998.2005. Epub 2006 Sep 15.
5
Chronic effects of angiotensin II and at1 receptor antagonists in subfornical organ-lesioned rats.
Clin Exp Pharmacol Physiol. 2005 May-Jun;32(5-6):462-6. doi: 10.1111/j.1440-1681.2005.04212.x.
6
Contribution of the subfornical organ to angiotensin II-induced hypertension.
Am J Physiol Heart Circ Physiol. 2005 Feb;288(2):H680-5. doi: 10.1152/ajpheart.00823.2004. Epub 2004 Sep 30.
7
Hypertension caused by angiotensin II infusion involves increased superoxide production in the central nervous system.
Circ Res. 2004 Jul 23;95(2):210-6. doi: 10.1161/01.RES.0000135483.12297.e4. Epub 2004 Jun 10.
8
The role of Ang (1-7) in mediating the chronic hypotensive effects of losartan in normal rats.
J Renin Angiotensin Aldosterone Syst. 2003 Sep;4(3):176-9. doi: 10.3317/jraas.2003.028.
9
Cardiovascular function and circadian patterns in rats after area postrema lesions or prolonged food restriction.
Neurosci Lett. 2003 Oct 16;350(1):46-50. doi: 10.1016/s0304-3940(03)00739-0.
10
Central nervous system blockade by peripheral administration of AT1 receptor blockers.
J Cardiovasc Pharmacol. 2003 Apr;41(4):593-9. doi: 10.1097/00005344-200304000-00012.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验