FOR 667: Epithelial Mechanisms in Renal Volume Regulation
FOR 667: Epithelial Mechanisms in Renal Volume Regulation
批准号:
16133448
负责人:
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Units
财政年份:
2005
资助国家:
德国
项目状态:
已结题
起止时间:
2004-12-31 至 2016-12-31
中文摘要
肾脏每天过滤1500升血液,并产生180升初级超滤液。超滤液由肾小管形成,直到最终形成1.5升的尿液。肾小管上皮细胞的特殊活动有助于完成肾脏的这一主要任务。在小管中,过滤后的离子和水被重新吸收。此外,许多化合物根据瞬间的需要被运输进和运出,通过循环恢复,或排入尿液。体内的钠和水平衡受到肾脏机制的重要调节,这种机制有助于将血浆渗透压保持在严格的限制范围内,无论饮食中盐和水的摄取量有多大的差异。钠平衡的控制与血压的调节相辅相成。
英文摘要
The kidneys filter a daily input of 1500 liters of blood and produce 180 liters of primary ultrafiltrate. The ultrafiltrate becomes elaborated by the renal tubule until the final formation of 1.5 liters of urine. Specific activities of the tubular epithelium help to perform this major task of the kidney. In the tubule, filtered ions and water are being reabsorbed. In addition, many compounds are transported in- and outwards according to the momentary requirements to be recovered by the circulation, or excreted into the urine. Body sodium and water balance are importantly regulated by renal mechanisms which help to keep plasma osmolality within tight limits irrespective of the wide variations in dietary salt and water uptake. The control of sodium balance and the adjustment of blood pressure depend on each other.
期刊论文(14)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1152/ajprenal.00295.2009
发表时间:
2010
期刊:
American journal of physiology. Renal physiology
影响因子:
--
作者:
[A. Stoessel;N. Himmerkus;M. Bleich;S. Bachmann;F. Theilig]
通讯作者:
A. Stoessel;N. Himmerkus;M. Bleich;S. Bachmann;F. Theilig
DOI:
10.1161/circresaha.115.302882
发表时间:
2014-07
期刊:
Circulation Research
影响因子:
20.1
作者:
[J. Schleifenbaum;M. Kassmann;I. Szijártó;H. Hercule;J. Tano;S. Weinert;Matthias Heidenreich;A. Pathan;Yoland‐Marie Anistan;N. Alenina;N. Rusch;M. Bader;T. Jentsch;M. Gollasch]
通讯作者:
J. Schleifenbaum;M. Kassmann;I. Szijártó;H. Hercule;J. Tano;S. Weinert;Matthias Heidenreich;A. Pathan;Yoland‐Marie Anistan;N. Alenina;N. Rusch;M. Bader;T. Jentsch;M. Gollasch
Group VIA phospholipase A2 is a target for vasopressin signaling in the thick ascending limb.
VIA 组磷脂酶 A2 是粗升肢中加压素信号传导的靶标
DOI:
10.1152/ajprenal.00222.2011
发表时间:
2012
期刊:
American journal of physiology. Renal physiology
影响因子:
--
作者:
[Paliege A, Roeschel T, Neymeyer H, Seidel S, Kahl T, Daigeler A.L, Mutig K, Mrowka R, Ferreri N.R, Wilson B.S, Himmerkus N, Bleich M. , Bachmann S.]
通讯作者:
Bachmann S.
海外基金