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T 淋巴细胞介导达尔盐敏感型大鼠的高血压和肾脏损伤。

T lymphocytes mediate hypertension and kidney damage in Dahl salt-sensitive rats.

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2010 Apr;298(4):R1136-42. doi: 10.1152/ajpregu.00298.2009. Epub 2010 Feb 10.

Abstract

This study examined mechanisms by which immune cells participate in the development of hypertension and renal disease in Dahl salt-sensitive (SS) rats. Increasing dietary salt from 0.4% to 4.0% NaCl significantly increased renal infiltration of T lymphocytes from 8.8 +/- 1.2 x 10(5) to 14.4 +/- 2.0 x 10(5) cells/2 kidneys, increased arterial blood pressure from 131 +/- 2 to 165 +/- 6 mmHg, increased albumin excretion rate from 17 +/- 3 to 129 +/- 20 mg/day, and resulted in renal glomerular and tubular damage. Furthermore, renal tissue ANG II was not suppressed in the kidneys of SS rats fed 4.0% NaCl. Administration of the immunosuppressive agent mycophenolate mofetil (MMF; 20 mg.kg(-1).day(-1)) prevented the infiltration of T lymphocytes and attenuated Dahl SS hypertension and renal disease. In contrast to vehicle-treated rats, Dahl SS rats administered MMF demonstrated a suppression of renal tissue ANG II from 163 +/- 26 to 88 +/- 9 pg/g of tissue when fed high salt. Finally, it was demonstrated that the T lymphocytes isolated from the kidney possess renin and angiotensin-converting enzyme activity. These data indicate that infiltrating T cells are capable of participating in the production of ANG II and are associated with increased intrarenal ANG II, hypertension, and renal disease. The suppression of T-cell infiltration decreased intrarenal ANG II and prevented Dahl SS hypertension and kidney damage. As such, infiltrating cells are capable of participating in the established phase of Dahl SS hypertension.

摘要

这项研究旨在探讨免疫细胞参与 Dahl 盐敏感(SS)大鼠高血压和肾脏疾病发展的机制。将饮食中的盐含量从 0.4%增加到 4.0% NaCl,显著增加了 T 淋巴细胞在肾脏中的浸润,从 8.8 +/- 1.2 x 10(5)增加到 14.4 +/- 2.0 x 10(5)细胞/2 个肾脏;显著增加了动脉血压,从 131 +/- 2mmHg 增加到 165 +/- 6mmHg;显著增加了白蛋白排泄率,从 17 +/- 3mg/天增加到 129 +/- 20mg/天;并导致肾脏肾小球和肾小管损伤。此外,在摄入 4.0% NaCl 的 SS 大鼠的肾脏中,肾组织中的 ANG II 并未被抑制。给予免疫抑制药物霉酚酸酯(MMF;20mg.kg(-1).day(-1))可阻止 T 淋巴细胞浸润,并减轻 Dahl SS 高血压和肾脏疾病。与 vehicle 处理的大鼠相比,给予 MMF 的 Dahl SS 大鼠在摄入高盐时,肾脏组织中的 ANG II 从 163 +/- 26pg/g 组织降至 88 +/- 9pg/g 组织。最后,研究表明,从肾脏分离出的 T 淋巴细胞具有肾素和血管紧张素转换酶活性。这些数据表明,浸润的 T 细胞能够参与 ANG II 的产生,并与增加的肾内 ANG II、高血压和肾脏疾病有关。抑制 T 细胞浸润可降低肾内 ANG II,并预防 Dahl SS 高血压和肾脏损伤。因此,浸润细胞能够参与 Dahl SS 高血压的建立阶段。

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Am J Physiol Regul Integr Comp Physiol. 2010 Apr;298(4):R1136-42. doi: 10.1152/ajpregu.00298.2009. Epub 2010 Feb 10.
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