Sahai A, Weiser S J, Ganguly P K
Division of Cardiovascular Sciences, St Boniface General Hospital Research Centre, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
Angiology. 1993 Oct;44(10):769-75. doi: 10.1177/000331979304401002.
The authors have previously shown that atrial natriuretic peptide (ANP) mediates its cellular effects in part by changes in Ca2+ homeostasis in kidney cortex and that Ca2+ + Mg2+ ATPase is linked to ANP receptors, being reciprocally modulated by the guanylate cyclase system. The present study was designed to examine the status of this coupling in diabetes-induced congestive heart failure and the effect of its alterations on the functional integrity of the renal cell. Ca2+ + Mg2+ ATPase and guanylate cyclase were tested in hypertensive-diabetic rats (D + H), which develop congestive heart failure (CHF) at ten weeks following streptozotocin (65 mg/kg) injection and abdominal aortic constriction. The ATPase activity was measured by the release of 32P from [gamma-32P]ATP in the medium. While the guanylate cyclase activity was decreased very rapidly in the hypertensive-diabetic group, the sensitivity of the Ca2+ pump to ANP was increased at an early stage (three weeks) and decreased at a late stage (ten weeks) of CHF. The authors conclude that a defect in coupling between the Ca2+ pump and the ANP-receptor system as observed in the D + H group may contribute to the development of nephropathy and CHF.
作者们先前已表明,心房利钠肽(ANP)部分通过肾皮质中Ca2+ 稳态的变化介导其细胞效应,并且Ca2+ + Mg2+ ATP酶与ANP受体相关联,受鸟苷酸环化酶系统的反向调节。本研究旨在检查糖尿病诱发的充血性心力衰竭中这种偶联的状态,以及其改变对肾细胞功能完整性的影响。在高血压糖尿病大鼠(D + H)中检测Ca2+ + Mg2+ ATP酶和鸟苷酸环化酶,这些大鼠在注射链脲佐菌素(65 mg/kg)和腹主动脉缩窄后十周会发生充血性心力衰竭(CHF)。通过培养基中[γ-32P]ATP释放32P来测量ATP酶活性。虽然高血压糖尿病组中鸟苷酸环化酶活性迅速降低,但在CHF的早期阶段(三周)Ca2+ 泵对ANP的敏感性增加,而在晚期阶段(十周)降低。作者得出结论,在D + H组中观察到的Ca2+ 泵与ANP受体系统之间偶联的缺陷可能导致肾病和CHF的发展。