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Making Two Wrongs Right - Case of Using a Patient's Diabetes insipidus to Treat His Heart Failure: Experience with Vasopressin Antagonists from Animal Studies and Clinical Trials

机译:正确犯了两个错误 - 使用患者的糖尿病息肉治疗心力衰竭的情况:血管加压素拮抗剂的经验来自动物研究和临床试验

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摘要

The precise control of body water and solute concentrations is a function of several hormones acting on both the kidneys and circulatory system, with arginine vaso-pressin (AVP) playing a key role in this homeostatic process. Vasopressin, also known as antidiuretic hormone, is secreted from the posterior pituitary in response to signals generated from hypothalamic osmoreceptors when increased plasma osmolality is detected. Neurohormon-al activation in congestive heart failure results in a non-osmotic release of AVP which promotes vasoconstric-tion, water retention, and hyponatremia. Two of the receptor subtypes to which AVP binds, Via and V2, play a role in smooth muscle cell contraction and control the expression of aquaporins in the collecting duct. These receptors have become targets for the medical treatment of heart failure. Research has shown that vasopressin receptor blockers have the ability to favorably alter he-modynamics and stimulate diuresis in animal and human heart failure cases. We describe the case of a patient with central diabetes insipidus whose inability to create vasopressin was utilized to his advantage in the management of his nonischemic cardiomyopathy with heart failure.
机译:人体水和溶质浓度的精确控制是作用于肾脏和循环系统的几种激素的函数,精氨酸血管蛋白(AVP)在此稳态过程中起着关键作用。当检测到增加的血浆渗透压时,血管加压素,也称为抗利尿激素,垂体后垂体分泌,以响应于下丘脑渗透感受体产生的信号。充血性心力衰竭中的神经乳腺激活导致AVP的非渗透性释放,从而促进血管约束,保留水和低钠血症。 AVP通过和V2结合的两个受体亚型在平滑肌细胞收缩中起作用,并控制收集管中水通道蛋白的表达。这些受体已成为心力衰竭治疗的靶标。研究表明,血管加压素受体阻滞剂具有有利地改变HEM动力学并刺激动物和人类心力衰竭病例的利尿作用的能力。我们描述了一个患有中枢性糖尿病的患者,其无法创建加压素的患者在治疗其非缺血性心肌病和心力衰竭的情况下利用了他的优势。

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