Evidence map›Paper›PMID 37092117›Full record

ArticleRPS pharmacy and pharmacology reports2023

LP342, a novel histone deacetylase inhibitor, decreases nitro-oxidative stress, mitochondrial dysfunction and hepatic ischaemia/reperfusion injury in mice.

Devadoss J Samuvel, Yasodha Krishnasamy, Li Li, John J Lemasters, C James Chou, Zhi Zhong

Open access · hybridAbstract read
In one paragraph

Article in RPS pharmacy and pharmacology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 8 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

6 authors at 1 institution in 1 country.

Devadoss J SamuvelDepartment of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.
Yasodha KrishnasamyDepartment of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.
Li LiDepartment of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.
John J LemastersDepartment of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.
C James ChouDepartment of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.
Zhi ZhongDepartment of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.ORCID https://orcid.org/0000-0002-2377-0070
Medical University of South Carolina · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Jian Ouyang · 2009 to 2026
$42.7M
SOUTH CAROLINA COBRE IN OXIDANTS, REDOX BALANCE AND STRESS SIGNALINGP20GM103542 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI TEW, KENNETH D. · 2012 to 2020
$20.2M
The role of SMAD1 and SATB2 in colon patterningP20GM130457 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Hailong Zhang · 2020 to 2026
$18.7M
Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DON C. ROCKEY · 2020 to 2026
$8.8M
South Carolina COBRE in Oxidants, Redox Balance and Stress SignalingP30GM140964 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI EBLEN, SCOTT T · 2021 to 2025
$6.4M
Mitochondrial depolarization, mitophagy, and mitochondrial DAMPs in ALDR01AA025379 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ZHI ZHONG · 2018 to 2026
$3.8M
Mechanisms of Mitochondrial Iron Uptake: New Therapeutic Targets in HepatotoxicityR01DK119523 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LEMASTERS, JOHN J, NIEMINEN, ANNA-LIISA · 2021 to 2024
$1.8M
Confocal/Multiphoton Microscope UpgradeS10OD018113 · OD · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LEMASTERS, JOHN J · 2015 to 2015
$570k
Treatment of liver fibrosis with oral hepatic stable and non-genotoxic HDAC inhibitorsR41DK130707 · NIDDK · LYDEX PHARMACEUTICALS, LLC · PI CHOU, CHUNG-JEN JAMES, ZHONG, ZHI · 2021 to 2021
$350k
Next generation HDAC inhibitors with superior potency, selectivity, and pharmacokinetic profiles for the treatment of liver ischemia-reperfusion injuryR41DK120247 · NIDDK · LYDEX PHARMACEUTICALS, LLC · PI CHOU, CHUNG-JEN JAMES, ZHONG, ZHI · 2019 to 2019
$295k
NCI NIH HHS P30 CA138313NIAAA NIH HHS R01 AA025379NIDDK NIH HHS P30 DK123704NIDDK NIH HHS R01 DK119523NIDDK NIH HHS R41 DK120247NIDDK NIH HHS R41 DK130707NIGMS NIH HHS P20 GM103542NIGMS NIH HHS P20 GM130457NIGMS NIH HHS P30 GM140964NIH HHS S10 OD018113
6 · The paper itself

Abstract

Objectives: Some histone deacetylase (HDAC) isoforms contribute to ischaemia/reperfusion (IR) injury (IRI). Here, we examined whether LP342, the lead candidate of a new generation of hydrazide-based HDAC inhibitors (HDACi), decreases hepatic IRI. Methods: IR was induced by clamping blood vessels to ~70% of the livers of mice for 1 h. Key findings: At 6 h after reperfusion, ALT markedly increased, and wide-spread necrosis, leukocyte infiltration, and apoptosis occurred. LP342 treatment (1 mg/kg, ip) at 20 h or 1 h before ischaemia markedly decreased IRI whereas LP342 treatment upon reperfusion was marginally protective. Nitro-oxidative stress, c-Jun- Conclusions: This novel HDACi protects against IRI most likely by epigenetic upregulation of antioxidant proteins and post-translational modifications of NFκB thus inhibiting iNOS expression and inflammatory responses.

Indexed as

c-Jun-N-terminal kinasehistone deacetylaseischaemia/reperfusion injurylivermitochondrial depolarisationnitro-oxidative stress

Identifiers

PMID37092117
PMCPMC10114105
OpenAlexW4362555557

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.