Baan J, Chang P C, Vermeij P, Pfaffendorf M, van Zwieten P A
Department of Nephrology, Leiden University Medical Centre, The Netherlands.
J Hypertens. 1999 Feb;17(2):229-35. doi: 10.1097/00004872-199917020-00007.
Sodium depletion stimulates the renin-angiotensin and sympathetic nervous systems, which may affect the role of each of these systems in the regulation of vascular tone. We investigated the influence of sodium depletion on the roles of the angiotensin II type 1 receptor and the alpha1- and alpha2-adrenergic receptors, and on nitric oxide generation, in the regulation of human forearm vascular tone.
We studied the effects of the angiotensin II type 1 receptor antagonist losartan (0.1-3 microg/kg per min), angiotensin II (0.01-10 ng/kg per min), the alpha1- and alpha2-adrenoceptor antagonists doxazosin (3-100 ng/kg per min) and yohimbine (0.5-4 microg/kg per min) and the nitric oxide synthase inhibitor N(G)-monomethyl-L-arginine (L-NMMA; 7.5-60 microg/kg per min) on forearm blood flow in control subjects (n = 12) and sodium-depleted subjects (n = 11). Sodium depletion was achieved by 3 days of pretreatment with 40 mg furosemide twice a day and a sodium-restricted diet. Forearm blood flow was measured by venous occlusion plethysmography.
Sodium depletion resulted in activation of the renin-angiotensin and sympathetic nervous systems, as indicated by increased levels of plasma renin, aldosterone and heart rate (P < 0.05). Blood pressure remained unchanged. Losartan at the highest dose increased forearm blood flow in the sodium-depleted group by 42 +/- 9%, but had no effect in controls (P < 0.05). Both doxazosin and yohimbine caused an increased vasodilatory effect in the sodium-depleted versus the control group (228 +/- 42 versus 83 +/- 13% and 192 +/- 24 versus 95 +/- 8%, respectively; P < 0.05). The constrictor effects by angiotensin II and L-NMMA of -65 +/- 6% and -79 +/- 4%, respectively, in controls were unchanged by sodium depletion.
In sodium-depleted subjects, endogenous angiotensin II appears to play a role in the regulation of forearm vascular tone, in contrast to sodium-replete conditions. Furthermore, in these subjects the role of alpha1- and alpha2-adrenoceptors in the regulation of forearm vascular tone was enhanced compared with control conditions. Neither the forearm vascular effects of exogenously infused angiotensin II nor those of baseline nitric oxide production were influenced by sodium depletion.
钠缺乏会刺激肾素 - 血管紧张素系统和交感神经系统,这可能会影响这些系统在血管张力调节中的各自作用。我们研究了钠缺乏对血管紧张素II 1型受体、α1和α2肾上腺素能受体的作用以及一氧化氮生成在人前臂血管张力调节中的影响。
我们研究了血管紧张素II 1型受体拮抗剂氯沙坦(0.1 - 3微克/千克每分钟)、血管紧张素II(0.01 - 10纳克/千克每分钟)、α1和α2肾上腺素能受体拮抗剂多沙唑嗪(3 - 100纳克/千克每分钟)和育亨宾(0.5 - 4微克/千克每分钟)以及一氧化氮合酶抑制剂N(G)-单甲基-L-精氨酸(L-NMMA;7.5 - 60微克/千克每分钟)对对照组(n = 12)和钠缺乏组(n = 11)受试者前臂血流量的影响。通过每天两次服用40毫克呋塞米并限制钠摄入的饮食进行3天预处理来实现钠缺乏。通过静脉阻断体积描记法测量前臂血流量。
钠缺乏导致肾素 - 血管紧张素系统和交感神经系统激活,表现为血浆肾素、醛固酮水平和心率升高(P < 0.05)。血压保持不变。最高剂量的氯沙坦使钠缺乏组的前臂血流量增加了42±9%,但对对照组无影响(P < 0.05)。多沙唑嗪和育亨宾在钠缺乏组比对照组均引起更强的血管舒张作用(分别为228±42%对83±13%和192±24%对95±8%;P < 0.05)。对照组中血管紧张素II和L-NMMA分别引起的收缩作用-65±6%和-79±4%,在钠缺乏时未改变。
与钠充足的情况相比,在钠缺乏的受试者中,内源性血管紧张素II似乎在前臂血管张力调节中起作用。此外,与对照情况相比,在这些受试者中α1和α2肾上腺素能受体在前臂血管张力调节中的作用增强。外源性输注血管紧张素II的前臂血管效应以及基线一氧化氮生成的效应均不受钠缺乏的影响。