Pointer Mildred A, Eley Shaleka, Anderson Lauren, Waters Brittany, Royall Brittany, Nichols Sheena, Wells Candace
Julius L. Chambers Biomedical/Biotechnology Research Institute, North Carolina Central University, Durham, North Carolina, USA; Department of Biology; North Carolina Central University, Durham, North Carolina, USA.
Am J Hypertens. 2015 Aug;28(8):1049-55. doi: 10.1093/ajh/hpu255. Epub 2014 Dec 31.
Hypercalciuria is a frequent characteristic of hypertension. In this report we extend our earlier studies investigating the role of renal interstitial fluid calcium (ISF(Ca))(2+) as a link between urinary calcium excretion and blood pressure in the Dahl salt-sensitive (DS) hypertensive model.
Dahl salt-sensitive and salt-resistant (DR) rats were placed on control (0.45%) and high (8%) salt diets to determine if changes in renal cortical and medullary ISF(Ca)(2+)correlated with changes in urinary calcium excretion and blood pressure.
We observed that renal ISFCa(2+) was predicted by urinary calcium excretion (P < 0.05) in DS rats but not DR rats. Renal cortical ISF(Ca)(2+) was negatively associated with blood pressure (P < 0.03) while renal medullary ISF(Ca)(2+) was positively associated with blood pressure in DS rats (P < 0.04). In contrast, neither urinary calcium excretion nor renal ISF(Ca)(2+) was associated with blood pressure in the DR rats under the conditions of this study.
We interpret these findings to suggest that decreased renal cortical ISF(Ca)(2+) plays a role in the increase in blood pressure following a high salt diet in salt hypertension perhaps by mediating renal vasoconstriction; the role of medullary calcium remains to be fully understood. Further studies are needed to determine the mechanism of the altered renal ISF(Ca)(2+) and its role in blood pressure regulation.
高钙尿症是高血压的常见特征。在本报告中,我们扩展了早期研究,以探讨肾间质液钙(ISF(Ca))(2 +)作为达赫盐敏感(DS)高血压模型中尿钙排泄与血压之间联系的作用。
将达赫盐敏感和盐抵抗(DR)大鼠置于对照(0.45%)和高盐(8%)饮食中,以确定肾皮质和髓质ISF(Ca)(2 +)的变化是否与尿钙排泄和血压的变化相关。
我们观察到,DS大鼠的肾ISFCa(2 +)可由尿钙排泄预测(P < 0.05),而DR大鼠则不然。在DS大鼠中,肾皮质ISF(Ca)(2 +)与血压呈负相关(P < 0.03),而肾髓质ISF(Ca)(2 +)与血压呈正相关(P < 0.04)。相比之下,在本研究条件下,DR大鼠的尿钙排泄和肾ISF(Ca)(2 +)均与血压无关。
我们对这些发现的解释是,肾皮质ISF(Ca)(2 +)降低可能通过介导肾血管收缩,在盐敏感性高血压高盐饮食后血压升高过程中起作用;髓质钙的作用仍有待充分了解。需要进一步研究以确定肾ISF(Ca)(2 +)改变的机制及其在血压调节中的作用。