Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina.
Instituto de Química y Metabolismo del Fármaco (IQUIMEFA), CONICET-Universidad de Buenos Aires, Buenos Aires, Argentina.
Curr Vasc Pharmacol. 2023;21(4):246-256. doi: 10.2174/1570161121666230622121956.
We previously reported that endothelins (ETs) regulate tyrosine hydroxylase (TH) activity and expression in the olfactory bulb (OB) of normotensive and hypertensive animals. Applying an ET receptor type A (ET) antagonist to the brain suggested that endogenous ETs bind to ET receptor type B (ET) to elicit effects.
The aim of the present work was to evaluate the role of central ET stimulation on the regulation of blood pressure (BP) and the catecholaminergic system in the OB of deoxycorticosterone acetate (DOCA)-salt hypertensive rats.
DOCA-salt hypertensive rats were infused for 7 days with cerebrospinal fluid or IRL-1620 (ET receptor agonist) through a cannula placed in the lateral brain ventricle. Systolic BP (SBP) and heart rate were recorded by plethysmography. The expression of TH and its phosphorylated forms in the OB were determined by immunoblotting, TH activity by a radioenzymatic assay, and TH mRNA by quantitative real-time polymerase chain reaction.
Chronic administration of IRL-1620 decreased SBP in hypertensive rats but not in normotensive animals. Furthermore, the blockade of ET receptors also decreased TH-mRNA in DOCA-salt rats, but it did not modify TH activity or protein expression.
These findings suggest that brain ETs through the activation of ET receptors contribute to SBP regulation in DOCA-salt hypertension. However, the catecholaminergic system in the OB does not appear to be conclusively involved although mRNA TH was reduced. Present and previous findings suggest that in this salt-sensitive animal model of hypertension, the OB contributes to chronic BP elevation.
我们之前报道过内皮素(ETs)调节正常血压和高血压动物嗅球(OB)中酪氨酸羟化酶(TH)的活性和表达。将 ET 受体 A(ET)拮抗剂应用于大脑表明,内源性 ET 与 ET 受体 B(ET)结合以产生作用。
本研究旨在评估中枢 ET 刺激对去氧皮质酮醋酸盐(DOCA)-盐高血压大鼠 OB 中血压(BP)和儿茶酚胺能系统调节的作用。
通过放置在侧脑室内的套管,将 DOCA-盐高血压大鼠连续 7 天输注脑脊液或 IRL-1620(ET 受体激动剂)。通过体积描记法记录收缩压(SBP)和心率。通过免疫印迹法测定 OB 中 TH 及其磷酸化形式的表达,通过放射酶测定法测定 TH 活性,通过实时定量聚合酶链反应测定 TH mRNA。
慢性给予 IRL-1620 可降低高血压大鼠但不降低正常血压动物的 SBP。此外,ET 受体阻断也降低了 DOCA-盐大鼠的 TH-mRNA,但并未改变 TH 活性或蛋白表达。
这些发现表明,脑 ET 通过激活 ET 受体有助于 DOCA-盐高血压的 SBP 调节。然而,OB 中的儿茶酚胺能系统似乎没有明确参与,尽管 TH mRNA 减少。目前和以前的研究结果表明,在这种盐敏感的高血压动物模型中,OB 有助于慢性血压升高。