Hemodynamic Renal Reserve Response in Conscious Normotensive and Hypertensive Mice.

IF 2.3 4区 医学 Q2 PERIPHERAL VASCULAR DISEASE
Kidney & blood pressure research Pub Date : 2024-01-01 Epub Date: 2024-02-13 DOI:10.1159/000537806
Minh H Tran, Catherine Y Liu, Muhammad Usman Naeem, Colby L Parris, Lei Wang
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Abstract

Introduction: Renal function may be compromised following recovery from kidney insults. Renal functional reserve (RFR) is a measure of the difference between the kidney's maximum capacity and its baseline function, which helps identify any areas of the kidney with compromised function. Usually, RFR is evaluated using acute volume expansion (AVE), but this is typically done in anesthetized animals, which may not accurately represent the kidney's complete functional capacity. In this study, we have introduced a novel method that enables AVE to be conducted in conscious mice.

Methods: We have implemented this innovative approach in two animal models representing either intact or impaired renal function, specifically utilizing a lower nephron hypertensive model. Mice were implanted with radio-transmitters for mean artery blood pressure (MAP) monitoring during the experiment. After recovery, half of the mice were induced hypertension by right kidney nephrectomy combined with the ligation of the upper branch of the left kidney. For the AVE, a volume equivalent to 5% of the mouse's body weight was administered via intravenous (IV) or intraperitoneal bolus injection. Subsequently, the mice were individually housed in cages covered with plastic wrap. Urine was collected every hour for a total of 3 h for the measurement of urine and sodium excretion.

Results: The MAPs for all normotensive mice were consistent throughout the AVE, but it increased 5-16 mm Hg in the hypertensive mice upon AVE. Remarkably, conscious mice exhibited a significantly stronger response to IV-administered AVE when compared to anesthetized mice. This response was evident in the increase in urinary flow, which was approximately 170% and 145% higher in conscious normotensive and hypertensive mice, respectively, compared to their respective baselines. In contrast, anesthetized normotensive and hypertensive mice showed only around a 130% and 100% increase in urinary flow, respectively. Additionally, upon AVE, conscious normotensive mice excreted approximately 47% more sodium than conscious hypertensive mice. In contrast, anesthetized normotensive mice excreted only about 30% more sodium than their anesthetized hypertensive counterparts.

Conclusion: Performing a kidney stress test with a significant solution load in conscious mice seems to be a superior method for evaluating RFR compared to conducting the test under anesthesia. Assessing kidney clearance while the mice are conscious has the potential to enhance the precision of diagnosing and predicting both acute and chronic kidney diseases.

意识正常和高血压小鼠的血流动力学肾储备反应
引言 肾脏损伤恢复后,其功能可能会受到损害。肾功能储备(RFR)是对肾脏最大容量与其基线功能之间差值的测量,有助于确定肾脏功能受损的任何区域。通常,RFR 是通过急性容量扩张(AVE)来评估的,但这通常是在麻醉动物体内进行的,可能无法准确代表肾脏的全部功能。在本研究中,我们引入了一种新方法,可在有意识的小鼠体内进行 AVE。方法 我们在代表肾功能完好或受损的两种动物模型中采用了这种创新方法,特别是利用了下肾小球高血压模型。实验过程中,小鼠体内植入无线电发射器,用于监测平均动脉血压(MAP)。恢复后,一半小鼠通过右肾肾切除术和左肾上分支结扎术诱发高血压。对于 AVE,通过静脉注射或腹膜内注射相当于小鼠体重 5%的剂量。随后,将小鼠单独饲养在笼子里,笼子上覆盖保鲜膜。每小时收集一次尿液,共收集 3 小时,以测量尿液和钠的排泄量。结果 所有正常血压小鼠的血压在整个 AVE 期间保持一致,但高血压小鼠的血压在 AVE 期间增加了 5-16mmHg。值得注意的是,与麻醉小鼠相比,清醒小鼠对静脉注射 AVE 的反应明显更强。这种反应明显表现在尿流的增加上,与各自的基线相比,清醒的正常血压小鼠和高血压小鼠的尿流分别增加了约 170% 和 145%。相比之下,麻醉后的正常血压小鼠和高血压小鼠的尿流分别只增加了约 130% 和 100%。此外,在 AVE 作用下,意识正常的高血压小鼠排出的钠比意识正常的高血压小鼠多出约 47%。相比之下,麻醉后的正常血压小鼠排出的钠只比麻醉后的高血压小鼠多出约 30%。结论 与在麻醉状态下进行测试相比,在有意识的小鼠体内进行带有大量溶液负荷的肾脏压力测试似乎是一种更优越的 RFR 评估方法。在小鼠有意识的情况下评估肾脏清除率有可能提高诊断和预测急性和慢性肾脏疾病的准确性。
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来源期刊
Kidney & blood pressure research
Kidney & blood pressure research 医学-泌尿学与肾脏学
CiteScore
4.80
自引率
3.60%
发文量
61
审稿时长
6-12 weeks
期刊介绍: This journal comprises both clinical and basic studies at the interface of nephrology, hypertension and cardiovascular research. The topics to be covered include the structural organization and biochemistry of the normal and diseased kidney, the molecular biology of transporters, the physiology and pathophysiology of glomerular filtration and tubular transport, endothelial and vascular smooth muscle cell function and blood pressure control, as well as water, electrolyte and mineral metabolism. Also discussed are the (patho)physiology and (patho) biochemistry of renal hormones, the molecular biology, genetics and clinical course of renal disease and hypertension, the renal elimination, action and clinical use of drugs, as well as dialysis and transplantation. Featuring peer-reviewed original papers, editorials translating basic science into patient-oriented research and disease, in depth reviews, and regular special topic sections, ''Kidney & Blood Pressure Research'' is an important source of information for researchers in nephrology and cardiovascular medicine.
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