Evidence map›Paper›PMID 38350434›Full record

ArticleKidney & blood pressure research2024

Hemodynamic Renal Reserve Response in Conscious Normotensive and Hypertensive Mice.

Minh H Tran, Catherine Y Liu, Muhammad Usman Naeem, Colby L Parris, Lei Wang

Open access · goldAbstract read
In one paragraph

Article in Kidney & blood pressure research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 97% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 0 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Minh H TranDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida, USA.
Catherine Y LiuDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida, USA.
Muhammad Usman NaeemDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida, USA.
Colby L ParrisDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida, USA.
Lei WangDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida, USA.
University of South Florida · USFlorida College · US

Funding

Tubuloglomerular feedback response in AKI to CKD transitionR01DK134028 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI LIU, RUISHENG · 2022 to 2025
$2.6M
Macula densa NOS1 and transplanted renal graft functionR01DK122050 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI WANG, LEI · 2020 to 2024
$1.6M
Protection of donor kidneys with synchronization modulation electric field (SMEF)R42DK130764 · NIDDK · WR BIOTECH, LLC · PI CHEN, WEI, LIU, RUISHENG · 2022 to 2023
$1.6M
Protection of donor kidneys with synchronization modulation electric field (SMEF)R41DK130764 · NIDDK · WR BIOTECH, LLC · PI CHEN, WEI, LIU, RUISHENG · 2021 to 2021
$251k
NIDDK NIH HHS R01 DK122050NIDDK NIH HHS R01 DK134028NIDDK NIH HHS R41 DK130764NIDDK NIH HHS R42 DK130764
6 · The paper itself

Abstract

introductionRenal 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.

methodsWe 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.

resultsThe 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.

conclusionPerforming 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.

Indexed as

HypertensionKidneyAnimalsBlood PressureConsciousnessDisease Models, AnimalHemodynamicsMaleMiceAcute volume expansionConsciousHypertensionRenal functional reserveSodium excretion

Identifiers

PMID38350434
PMCPMC11042998
OpenAlexW4391771455

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.