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血管紧张素原的中枢性耗竭与终板血管器和室旁核中血管紧张素II 1型受体的升高有关。

Central depletion of angiotensinogen is associated with elevated AT1 receptors in the SFO and PVN.

作者信息

Kasper Sherry O, Ferrario Carlos M, Ganten Detlev, Diz Debra I

机构信息

The Hypertension and Vascular Disease Center and Physiology/Pharmacology Department, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1032, USA.

出版信息

Neurotox Res. 2004;6(4):259-65. doi: 10.1007/BF03033436.

Abstract

The brain renin-angiotensin system (RAS) is important in fluid balance and blood pressure regulation. In this study, we compared angiotensin (Ang) receptor density in the subfornical organ (SFO) and paraventricular nucleus (PVN) of a) brain angiotensinogen deficient rats (ASrAogen); b) those with high levels of brain Ang II [(mRen2)27]; c) Hannover Sprague Dawley (SD) rats at 48 and 68 wks of age. Since there was no difference between the two ages in any of the three strains, the data from the 48 and 68 wk time points were combined. There was a significantly higher level of AT1 receptors in the SFO and PVN of ASrAogen animals compared to both the SD and (mRen2)27 rats. This suggests that the brain RAS is important in regulating receptor density and that the differences may be explained by lower levels of the peptide locally. These higher levels of receptors suggest that the ASrAogen animals in adulthood and early aging would be more sensitive to either circulating or endogenous brain Ang II than the SD animals of similar age. In contrast, the similar receptor density in the (mRen2)27 and SD rats suggest that previous reports of reduced responses in the (mRen2)27 rats may result from differences in post receptor mechanisms such as intracellular signaling. Moreover, our data reveal that functional assessments are necessary in addition to receptor density levels to understand the consequences of long-term alterations in brain tissue peptides.

摘要

脑肾素-血管紧张素系统(RAS)在体液平衡和血压调节中起重要作用。在本研究中,我们比较了以下三组动物穹窿下器(SFO)和室旁核(PVN)中血管紧张素(Ang)受体密度:a)脑内血管紧张素原缺乏的大鼠(ASrAogen);b)脑内Ang II水平高的大鼠[(mRen2)27];c)48周龄和68周龄的汉诺威斯普拉格-道利(SD)大鼠。由于在这三个品系中两个年龄组之间均无差异,因此将48周和68周时间点的数据合并。与SD大鼠和(mRen2)27大鼠相比,ASrAogen动物的SFO和PVN中AT1受体水平显著更高。这表明脑RAS在调节受体密度中起重要作用,且差异可能是由于局部肽水平较低所致。这些较高的受体水平表明,成年期和衰老早期的ASrAogen动物比相似年龄的SD动物对循环或内源性脑Ang II更敏感。相比之下,(mRen2)27大鼠和SD大鼠中相似的受体密度表明,先前关于(mRen2)27大鼠反应降低的报道可能是由于受体后机制(如细胞内信号传导)的差异所致。此外,我们的数据表明,除了受体密度水平外,还需要进行功能评估以了解脑组织肽长期改变的后果。

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