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胶质血管紧张素原调节转基因大鼠TGR(ASrAOGEN)中的脑血管紧张素II受体。

Glial angiotensinogen regulates brain angiotensin II receptors in transgenic rats TGR(ASrAOGEN).

作者信息

Monti J, Schinke M, Böhm M, Ganten D, Bader M, Bricca G

机构信息

Max Delbrück Center for Molecular Medicine, 13092 Berlin, Germany.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2001 Jan;280(1):R233-40. doi: 10.1152/ajpregu.2001.280.1.R233.

Abstract

TGR(ASrAOGEN)680, a newly developed transgenic rat line with specific downregulation of astroglial synthesis of angiotensinogen, exhibits decreased brain angiotensinogen content associated with a mild diabetes insipidus and lower blood pressure. Autoradiographic experiments were performed on TGR(ASrAOGEN) (TG) and Sprague-Dawley (SD) control rats to quantify AT(1) and AT(2) receptor-binding sites in different brain nuclei and circumventricular organs. Dose-response curves for drinking response to intracerebroventricular injections of ANG II were compared between SD and TG rats. In most of the regions inside the blood-brain barrier [paraventricular nucleus (PVN), piriform cortex, lateral olfactory tract (LOT), and lateral preoptic area (LPO)], AT(1) receptor binding (sensitive to CV-11974) was significantly higher in TG compared with SD. In contrast, in the circumventricular organs investigated [subfornical organ (SFO) and area postrema], AT(1) receptor binding was significantly lower in TG. AT(2) receptors (binding sensitive to PD-123319) were detected at similar levels in the inferior olive (IO) of both strains. Angiotensin-binding sites sensitive to both CV-11974 and PD-123319 were detected in the LPO of SD rats and specifically upregulated in LOT, IO, and most notably PVN and SFO of TG. The dose-response curve for water intake after intracerebroventricular injections showed a higher sensitivity to ANG II of TG (EC(50) = 3.1 ng) compared with SD (EC(50) = 11.2 ng), strongly suggesting that the upregulation of AT(1) receptors inside the blood-brain barrier of TG rats is functional. Finally, we showed that downregulation of angiotensinogen synthesized by astroglial cells differentially regulates angiotensin receptor subtypes inside the brain and in circumventricular organs.

摘要

TGR(ASrAOGEN)680是一种新培育的转基因大鼠品系,其星形胶质细胞合成血管紧张素原的能力特异性下调,表现为脑内血管紧张素原含量降低,伴有轻度尿崩症和血压降低。对TGR(ASrAOGEN)(转基因大鼠)和Sprague-Dawley(SD)对照大鼠进行放射自显影实验,以量化不同脑核和室周器官中的AT(1)和AT(2)受体结合位点。比较了SD大鼠和转基因大鼠对脑室内注射血管紧张素II饮水反应的剂量反应曲线。在血脑屏障内的大多数区域[室旁核(PVN)、梨状皮质、外侧嗅束(LOT)和外侧视前区(LPO)],与SD大鼠相比,转基因大鼠的AT(1)受体结合(对CV-11974敏感)显著更高。相反,在所研究的室周器官[穹窿下器官(SFO)和最后区]中,转基因大鼠的AT(1)受体结合显著更低。在两种品系大鼠的下橄榄核(IO)中,检测到的AT(2)受体(对PD-123319结合敏感)水平相似。在SD大鼠的LPO中检测到对CV-11974和PD-123319均敏感的血管紧张素结合位点,且在转基因大鼠的LOT、IO中特异性上调,在PVN和SFO中上调最为显著。脑室内注射后饮水摄入的剂量反应曲线显示,与SD大鼠(EC(50)=11.2 ng)相比,转基因大鼠对血管紧张素II的敏感性更高(EC(5=3.1 ng),强烈表明转基因大鼠血脑屏障内AT(1)受体的上调具有功能。最后,我们表明星形胶质细胞合成的血管紧张素原下调可差异性调节脑内和室周器官中的血管紧张素受体亚型。

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