Evidence map›Paper›PMID 34852633›Full record

ArticleHypertension (Dallas, Tex. : 1979)2022

Nalfurafine, a G-Protein-Biased KOR (Kappa Opioid Receptor) Agonist, Enhances the Diuretic Response and Limits Electrolyte Losses to Standard-of-Care Diuretics.

Jacob K Meariman, Jane C Sutphen, Juan Gao, Daniel R Kapusta

Open access · bronzeAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

4 authors at 1 institution in 1 country.

Jacob K MearimanDepartment of Pharmacology and Experimental Therapeutics (J.K.M., J.C.S., J.G., D.R.K.), Louisiana State University Health Sciences Center, 1901 Perdido St, New Orleans, LA.
Jane C SutphenDepartment of Pharmacology and Experimental Therapeutics (J.K.M., J.C.S., J.G., D.R.K.), Louisiana State University Health Sciences Center, 1901 Perdido St, New Orleans, LA.
Juan GaoDepartment of Pharmacology and Experimental Therapeutics (J.K.M., J.C.S., J.G., D.R.K.), Louisiana State University Health Sciences Center, 1901 Perdido St, New Orleans, LA.
Daniel R KapustaDepartment of Pharmacology and Experimental Therapeutics (J.K.M., J.C.S., J.G., D.R.K.), Louisiana State University Health Sciences Center, 1901 Perdido St, New Orleans, LA.ORCID 0000-0002-7593-6984
Louisiana State University Health Sciences Center New Orleans · US

Funding

Vascular and Cardiac Function Core - "Mentoring in Cardiovascular BiologyP30GM106392 · NIGMS · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2014 to 2018
$5.5M
NIGMS NIH HHS P30 GM106392
6 · The paper itself

Abstract

Nalfurafine is a G-protein-biased KOR (kappa opioid receptor) agonist that produces analgesia and lacks central nervous system adverse effects. Here, we examined the cardiovascular and renal responses to intravenous and oral nalfurafine alone and in combination with furosemide, hydrochlorothiazide, or amiloride. We hypothesized that nalfurafine, given its distinct mechanism of vasopressin inhibition, would increase urine output to these diuretics and limit electrolyte loss. Following catheterization, conscious Sprague-Dawley rats received an isotonic saline infusion and were then administered an intravenous bolus of nalfurafine, a diuretic, or a combination. Mean arterial pressure, heart rate, and urine output were recorded for 90 minutes. In another study, rats were placed in metabolic cages and administered drug in an oral volume load. Hourly urine samples were then collected for 5 hours. Intravenous and oral nalfurafine produced a marked diuresis, antinatriuresis, antikaliuresis, and a decrease in mean arterial pressure. Compared with diuretic treatment alone, intravenous coadministration with nalfurafine significantly increased urine output to furosemide and hydrochlorothiazide and decreased sodium and potassium excretion. Notably, mean arterial pressure was reduced with nalfurafine/diuretic combination therapy compared to diuretics alone. Similarly, oral coadministration of nalfurafine significantly increased urine output to hydrochlorothiazide and decreased sodium and potassium excretion, whereas combination with furosemide only limited the amount of sodium excreted. Further, both intravenous and oral coadministration of nalfurafine enhanced the diuresis to amiloride and decreased sodium excretion. Together, these findings demonstrate that nalfurafine enhances the diuresis to standard-of-care diuretics without causing an excessive loss of electrolytes, offering a new approach to treat several cardiovascular conditions.

Indexed as

Analgesics, OpioidAnimalsDiuresisDiureticsFurosemideHydrochlorothiazideKidneyMaleMorphinansRatsRats, Sprague-DawleyReceptors, Opioid, kappaSpiro CompoundsAnalgesics, OpioidDiureticsFurosemideHydrochlorothiazideMorphinansReceptors, Opioid, kappaSpiro CompoundsTRK 820diuresisfurosemidehydrochlorothiazideratsreceptor, opioid, kappa

Identifiers

PMID34852633
PMCPMC8755620
OpenAlexW3216606238

What OpenQuestion holds

Textmetadata
LicenceTDM
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.