ReviewRedox biology2025
Peroxiredoxins in central nervous system: implications for chronic pain and anaesthetic-induced neurotoxicity management.
Review in Redox biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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.
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.
Who cites it
4 citing papers in PubMed.
- Article
- 3-Hydroxydehydroleucodin ameliorates neuroinflammation and ischemic brain injury by blocking the TRIM21-PRDX1 interaction.Acta pharmacologica Sinica · 2026Article
- Peroxiredoxin-Mediated Redox Regulation in Neurons: From Neurite Development to Degeneration.Antioxidants (Basel, Switzerland) · 2026Review
- Moonlighting Functions of Mammalian Peroxiredoxins in Cellular Signaling.Antioxidants (Basel, Switzerland) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oxidative stress, an imbalance between the prooxidant-antioxidant system, is regarded as one of the crucial causative pathomechanisms of chronic pain. However, direct scavenging of intracellular reactive oxygen species (ROS) by antioxidants may disrupt normal physiological homeostasis. Peroxiredoxins (Prdxs), a family of ROS-regulating enzymes, have recently aroused growing interest in the broad field of antioxidant research. Six distinct groups of Prdxs (Prdx1-6) have been identified to date. Prdxs are essential for regulating diverse biological processes, including oxidative stress, neuroinflammation, apoptosis, mitochondrial dynamics, endoplasmic reticulum (ER) stress, and synaptic plasticity. Interestingly, the differential expression patterns of Prdxs in central nervous system (CNS) tissues, cell types, and subcellular locations imply specialized functions. This review systematically summarizes the expression patterns of specific Prdxs in tissues and cells of murine and human, as well as the regulatory factors of their enzymatic activities. It also discusses the underlying cellular signaling pathways through which Prdxs participate in several biological processes as well as chronic pain and anaesthetic-induced neurotoxicity. In addition, we summarize the therapeutic potential of Prdxs inducers in CNS disorders based on preclinical studies. A better understanding of these processes can promote the development of novel therapeutic targets for treating chronic pain and anaesthetic-induced neurotoxicity.
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Registered trials
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.