Evidence map›Paper›PMID 35056980›Full record

ArticlePharmaceutics2021

A Kidney-Targeted Nanoparticle to Augment Renal Lymphatic Density Decreases Blood Pressure in Hypertensive Mice.

Bethany L Goodlett, Chang Sun Kang, Eunsoo Yoo, Shobana Navaneethabalakrishnan, Dakshnapriya Balasubbramanian, Sydney E Love, Braden M Sims, Daniela L Avilez, Winter Tate, Delilah R Chavez and 5 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 25 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

15 authors at 1 institution in 1 country.

Bethany L GoodlettDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Chang Sun KangDepartment of Pharmaceutical Sciences, College of Pharmacy, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0003-4541-0057
Eunsoo YooDepartment of Pharmaceutical Sciences, College of Pharmacy, Texas A&M University, College Station, TX 77843, USA.
Shobana NavaneethabalakrishnanDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Dakshnapriya BalasubbramanianDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Sydney E LoveDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Braden M SimsDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Daniela L AvilezDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Winter TateDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Delilah R ChavezDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Gaurav BaranwalDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.ORCID 0000-0002-0148-6650
Mary B NabityDepartment of Veterinary Pathobiology, College of Veterinary Medicine & Biomedical Science, Texas A&M University, College Station, TX 77843, USA.
Joseph M RutkowskiDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Dongin KimDepartment of Pharmaceutical Sciences, College of Pharmacy, Texas A&M University, College Station, TX 77843, USA.
Brett M MitchellDepartment of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.ORCID 0000-0002-2575-8761
Texas A&M University · US

Funding

Lymphatics and lymphangiogenesis in kidney function and inflammationR01DK119497 · NIDDK · TEXAS A&M UNIVERSITY · PI RUTKOWSKI, JOSEPH MICHAEL · 2020 to 2024
$2.1M
NIDDK NIH HHS R01 DK119497NIH HHS DK119497NIH HHS RO1 DK120493Texas A&M University Triads for Transformation
6 · The paper itself

Abstract

Chronic interstitial inflammation and renal infiltration of activated immune cells play an integral role in hypertension. Lymphatics regulate inflammation through clearance of immune cells and excess interstitial fluid. Previously, we demonstrated increasing renal lymphangiogenesis prevents hypertension in mice. We hypothesized that targeted nanoparticle delivery of vascular endothelial growth factor-C (VEGF-C) to the kidney would induce renal lymphangiogenesis, lowering blood pressure in hypertensive mice. A kidney-targeting nanoparticle was loaded with a VEGF receptor-3-specific form of VEGF-C and injected into mice with angiotensin II-induced hypertension or LNAME-induced hypertension every 3 days. Nanoparticle-treated mice exhibited increased renal lymphatic vessel density and width compared to hypertensive mice injected with VEGF-C alone. Nanoparticle-treated mice exhibited decreased systolic blood pressure, decreased pro-inflammatory renal immune cells, and increased urinary fractional excretion of sodium. Our findings demonstrate that pharmacologically expanding renal lymphatics decreases blood pressure and is associated with favorable alterations in renal immune cells and increased sodium excretion.

Indexed as

hypertensionimmunityinflammationkidneylymphatics

Identifiers

PMID35056980
PMCPMC8780399
OpenAlexW4206826319

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.