Evidence map›Paper›PMID 41243378›Full record

ArticlePhysiological reports2025

Effects of a novel acetaminophen analog on cardiorespiratory compensatory responses and survival in a male rat model of traumatic hemorrhage.

Miryam M Pando, Kathy L Ryan, Mariam L Calderon, Cassandra M Rodriguez, Brian S Connor, Samantha L Perez, Kevin D Bunker, Chad D Hopkins, Harold G Klemcke, Lonnie E Grantham and 1 more

Abstract read
In one paragraph

Article in Physiological reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Miryam M PandoU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.ORCID 0009-0002-7287-7541
Kathy L RyanU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.
Mariam L CalderonU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.
Cassandra M RodriguezU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.
Brian S ConnorU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.
Samantha L PerezU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.
Kevin D BunkerKalyra Pharmaceuticals, San Diego, California, USA.ORCID 0009-0004-0537-9336
Chad D HopkinsKalyra Pharmaceuticals, San Diego, California, USA.
Harold G KlemckeU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.
Lonnie E GranthamU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.ORCID 0000-0003-2397-2462
Carmen Hinojosa-LabordeU.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, San Antonio, Texas, USA.

Funding

DOD | Combat Casualty Care Research Program (CCCRP) D_007_2017
6 · The paper itself

Abstract

When pain is associated with traumatic hemorrhage, medics must be concerned about secondary effects of analgesics on cardiorespiratory systems. A novel analog of acetaminophen, D-112, was developed to circumvent liver toxicity and improve analgesic efficacy. D-112 causes dose-related inhibition of formalin-induced licking. The objective of this study was to test the effects of D-112 on survival and cardiorespiratory variables following hemorrhage and extremity trauma (ET). We hypothesized that D-112 would significantly change cardiorespiratory responses to HEM and thereby decrease survival. Male rats received either vehicle (lactated Ringer's) or D-112 (50 mg/kg) after conscious hemorrhage of either 37% (n = 10, vehicle and D-112) or 50% (n = 8, vehicle; n = 11, D-112) of blood volume following ET, which consisted of soft tissue injury and fibula fracture. Rats were observed for 4 h after the start of hemorrhage. Neither survival times (37% hemorrhage: p = 0.474; 50% hemorrhage: p = 0.306) nor survival curves (37% hemorrhage: p = 0.146; 50% hemorrhage: p = 0.280) differed between treatments. Mean arterial pressure did not differ between treatments (37% hemorrhage: p = 0.742; 50% hemorrhage: p = 0.521). D-112 transiently elevated minute ventilation (p < 0.001) after both hemorrhages. D-112 does not alter cardiorespiratory responses to the point of depressing survival, suggesting that D-112 could be an appropriate analgesic following traumatic hemorrhage.

Indexed as

AcetaminophenAnalgesics, Non-NarcoticHemorrhageAnimalsBlood PressureDisease Models, AnimalHeart RateMaleRatsRats, Sprague-DawleyAcetaminophenAnalgesics, Non-Narcoticacetaminophenanalgesiahemorrhagepain managementtrauma

Identifiers

PMID41243378
PMCPMC12620408

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LicenceCC BY
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Registered trials

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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.