Evidence map›Paper›PMID 39346824›Full record

ArticleACS omega2024

Enhancing Cardiomyocyte Resilience to Ischemia-Reperfusion Injury: The Therapeutic Potential of an Indole-Peptide-Tempo Conjugate (IPTC).

Shanshan Hou, Xin Yan, Xiang Gao, Steffen Jockusch, K Michael Gibson, Zhiying Shan, Lanrong Bi

Abstract read
In one paragraph

Article in ACS omega, 2024. 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
–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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

7 authors.

Shanshan HouDepartment of Chemistry, Michigan Technological University, Houghton, Michigan 49931, United States.
Xin YanDepartment of Chemistry, Michigan Technological University, Houghton, Michigan 49931, United States.
Xiang GaoDepartment of Chemistry, Michigan Technological University, Houghton, Michigan 49931, United States.
Steffen JockuschCenter of Photochemical Sciences, Bowling Green State University, Bowling Green, Ohio 43403, United States.ORCID https://orcid.org/0000-0002-4592-5280
K Michael GibsonDepartment of Pharmacotherapy, College of Pharmacy and Pharmaceutical Sciences, Washington State University, Spokane, Washington 99202, United States.
Zhiying ShanDepartment of Kinesiology and Integrative Physiology, Health Research Institute, Michigan Technological University, Houghton, Michigan 49931, United States.ORCID https://orcid.org/0000-0002-9763-205X
Lanrong BiDepartment of Chemistry, Michigan Technological University, Houghton, Michigan 49931, United States.ORCID https://orcid.org/0000-0001-6624-8314

Funding

Contribution of Orexin System to HypertensionR01HL163159 · NHLBI · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI SHAN, ZHIYING · 2022 to 2025
$1.7M
NHLBI NIH HHS R01 HL163159
6 · The paper itself

Abstract

Ischemia/reperfusion (I/R) injury leads to apoptosis and extensive cellular and mitochondrial damage, triggered by the early generation and subsequent accumulation of mitochondrial reactive oxygen species (mtROS). This condition not only contributes to the pathology of I/R injury itself but is also implicated in a variety of other diseases, especially within the cardiovascular domain. Addressing mitochondrial oxidative stress thus emerges as a critical therapeutic target. In this context, our study introduces an indole-peptide-tempo conjugate (IPTC), a compound designed with dual functionalities: antioxidative properties and the ability to modulate autophagy. Our findings reveal that IPTC effectively shields H9C2 cardiomyocytes against hypoxia/reoxygenation (H/R) damage, primarily through counteracting mtROS overproduction linked to impaired mitophagy and mitochondrial dysfunction. We propose that IPTC operates by simultaneously reducing mtROS levels and inducing mitophagy, highlighting its potential as a novel therapeutic strategy for mitigating mitochondrial oxidative damage and, by extension, easing I/R injury and potentially other related cardiovascular conditions.

Identifiers

PMID39346824
PMCPMC11425819

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.