Department of Medicine, University of California and Veterans Affairs San Diego Healthcare System, San Diego, 9500 Gilman Drive, La Jolla, California 92093-0838, USA.
Endocrinology. 2010 Oct;151(10):4820-9. doi: 10.1210/en.2009-1454. Epub 2010 Jul 28.
Exaggerated adrenergic activity is associated with human hypertension. The peptide urocortin 2 (Ucn 2) inhibits catecholamine synthesis and secretion from adrenal chromaffin cells in vitro and administration to mammals lowers blood pressure (BP). The chromogranin A-null mouse (Chga-/-) manifests systemic hypertension because of excessive catecholamine secretion from the adrenal and decreased catecholamine storage. In the present study, we investigated whether systemic administration of Ucn 2 could reduce BP and adrenal and plasma levels of catecholamines in vivo. Ucn 2 peptide was administered to freely moving, conscious Chga-/- and wild-type control mice. Telemetry and HPLC measured changes in BP and catecholamine levels, respectively. In both groups of mice, Ucn 2 dose-dependently decreased BP, and this effect was mediated by corticotropin factor-receptor type 2. However, in Chga-/- mice, the maximal percentage decrease of systolic BP from basal systolic BP was 37% compared with only a 23% reduction in wild-type mice (P=0.04). In Chga-/- mice only, Ucn 2 decreased adrenal and plasma levels of catecholamines as well as adrenal levels of tyrosine hydroxylase protein and phosphorylation. In vitro mechanistic studies demonstrated that Ucn 2 reduces both catecholamine secretion and tyrosine hydroxylase promoter activity, suggesting that the exaggerated action of Ucn 2 to reduce BP in the Chga-/- mouse is mediated through inhibition of both catecholamine synthesis and secretion. The data suggest that Ucn 2 may be therapeutically useful in regulating the exaggerated sympathoadrenal function of hyperadrenergic hypertension.
儿茶酚胺活性亢进与人类高血压有关。肽 Ucn2(尿皮质素 2)在体外抑制肾上腺嗜铬细胞瘤儿茶酚胺的合成和分泌,给予哺乳动物可降低血压(BP)。神经颗粒素 A 缺失小鼠(Chga-/-)由于肾上腺儿茶酚胺分泌过多和儿茶酚胺储存减少而表现出系统性高血压。在本研究中,我们研究了 Ucn2 的全身给药是否可以降低体内血压和肾上腺及血浆儿茶酚胺水平。Ucn2 肽被给予自由活动的清醒 Chga-/-和野生型对照小鼠。遥测和 HPLC 分别测量 BP 和儿茶酚胺水平的变化。在两组小鼠中,Ucn2 呈剂量依赖性降低 BP,其作用是通过促肾上腺皮质激素因子受体 2 介导的。然而,在 Chga-/-小鼠中,收缩压从基础收缩压的最大百分比降低为 37%,而野生型小鼠仅降低 23%(P=0.04)。仅在 Chga-/-小鼠中,Ucn2 降低了儿茶酚胺的肾上腺和血浆水平以及酪氨酸羟化酶蛋白和磷酸化的肾上腺水平。体外机制研究表明,Ucn2 降低了儿茶酚胺的分泌和酪氨酸羟化酶启动子活性,这表明 Ucn2 在 Chga-/-小鼠中降低 BP 的夸张作用是通过抑制儿茶酚胺的合成和分泌来介导的。数据表明,Ucn2 可能在调节高儿茶酚胺性高血压的交感肾上腺功能亢进方面具有治疗作用。