Evidence map›Paper›PMID 41207993›Full record

ArticleMolecular neurobiology2025

Heat-Stressed Brains: Epigenetic and Mitochondrial Signatures in Zebrafish.

Ahmet Topal, Selçuk Özdemir, Şeyma Aydın, Ekrem Sulukan, Selim Çomaklı, Elif Dalkılınç, Sinan Gönüllü, Metin Kiliçlioğlu, Meryem Kankaynar, Ufuk Kuşkun and 2 more

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Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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4 · The record

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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

12 authors.

Ahmet TopalDepartment of Basic Sciences, Faculty of Fisheries, Atatürk University, Erzurum, TR-25030, Turkey. ahmet.topal@atauni.edu.tr.
Selçuk ÖzdemirDepartment of Genetic, Faculty of Veterinary Medicine, Atatürk University, Erzurum, Turkey.
Şeyma AydınDepartment of Genetic, Faculty of Veterinary Medicine, Atatürk University, Erzurum, Turkey.
Ekrem SulukanDepartment of Basic Sciences, Faculty of Fisheries, Atatürk University, Erzurum, TR-25030, Turkey.
Selim ÇomaklıDepartment of Pathology, Faculty of Veterinary, Atatürk University, Erzurum, TR-25030, Turkey.
Elif DalkılınçDepartment of Biochemistry, Faculty of Veterinary Medicine, Atatürk University, Erzurum, Turkey.
Sinan GönüllüDepartment of Neurology, Bursa City Hospital, Bursa, Turkey.
Metin KiliçlioğluDepartment of Pathology, Faculty of Veterinary, Atatürk University, Erzurum, TR-25030, Turkey.
Meryem KankaynarDepartment of Nanoscience, Graduate School of Natural and Applied Sciences, Atatürk University, Erzurum, 25030, Turkey.
Ufuk KuşkunThe Central Research Laboratory Application and Research Centre, Ordu University, TR-52200, Ordu, Turkey.
Hamit ÇelikDepartment of Neurology, Private Buhara Hospital, Erzurum, Turkey.
Saltuk Buğrahan CeyhunDepartment of Aquaculture, Faculty of Fisheries, Atatürk University, Erzurum, TR-25030, Turkey. saltuk@atauni.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rising water temperatures due to climate change pose significant risks to aquatic species, particularly during early neurodevelopment. By the end of the century, global temperatures are projected to rise, with similar increases expected in aquatic ecosystems. Here, we investigated the effects of elevated temperatures (28 °C, 31 °C, and 34 °C) on zebrafish (Danio rerio) larvae, focusing on morphology, brain histopathology, oxidative stress, and key molecular pathways. Heat exposure caused a temperature-dependent increase in developmental malformations, reduced survival, and histologically confirmed neurodegeneration. Immunohistochemistry revealed elevated 8-hydroxy-2'-deoxyguanosine (8-OHdG) and 4-hydroxynonenal (4-HNE), indicating oxidative stress in brain tissues. Molecular analyses showed upregulation of epigenetic regulators (dnmt3a, hdac1) with concurrent downregulation of tet1, increased expression of the neuroendocrine stress marker pomca, and unfolded protein response mediators (atf4, xbp1). Mitochondrial genes (cox1 downregulated, cox4 variable) exhibited temperature-dependent changes. Quantitative RT-PCR revealed progressive upregulation of GFAP and Nfl with increasing temperature. Biochemical measurements indicated simultaneous increases in ATP and ROS levels. ELISA analysis showed temperature-dependent elevation of 5-mC, cortisol, norepinephrine, BDNF, IL-6, HSP-70, and TNF-alpha. Together, these findings indicate that heat stress elicits a coordinated response involving oxidative stress, epigenetic remodeling, ER stress, mitochondrial dysfunction, glial activation, and neuronal injury. The results highlight the vulnerability of multiple biological compartments in the developing zebrafish brain and provide mechanistic insight into how rising global temperatures may compromise neurodevelopment in aquatic organisms.

Indexed as

BrainEpigenesis, GeneticHeat-Shock ResponseMitochondriaZebrafishAnimalsLarvaOxidative StressReactive Oxygen SpeciesZebrafish ProteinsReactive Oxygen SpeciesZebrafish ProteinsBrainGlobal warmingOxidative stressTemperature stressZebrafish

Identifiers

PMID41207993

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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.