Evidence map›Paper›PMID 39356936›Full record

ArticleActa cirurgica brasileira2024

Caffeine mitigates tamoxifen-induced fatty liver in Wistar rats.

Yasin Sezgin, Ejder Saylav Bora, Duygu Burcu Arda, Yiğit Uyanikgil, Oytun Erbaş

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Article in Acta cirurgica brasileira, 2024. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yasin SezginYüzüncü Yıl University - Faculty of Medicine - Clinic of Medical Oncology - Van - Turkey.ORCID http://orcid.org/0000-0003-4122-8389
Ejder Saylav Boraİzmir Katip Çelebi University - Faculty of Medicine - Department of Emergency Medicine - Izmir - Turkey.ORCID http://orcid.org/0000-0002-2448-2337
Duygu Burcu ArdaEge University - Faculty of Medicine - Department of Histology and Embryology - Izmir - Turkey.ORCID http://orcid.org/0000-0002-4384-1323
Yiğit UyanikgilTaksim Research and Training Hospital - Department of Pediatrics - Istanbul - Turkey.ORCID http://orcid.org/0000-0002-4016-0522
Oytun ErbaşDemiroğlu Bilim University - Department of Physiology - Istanbul - Turkey.ORCID http://orcid.org/0000-0001-5427-8428

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTamoxifen, a widely used drug for breast cancer treatment, is associated with adverse effects on the liver, including the development of fatty liver. This study aimed to investigate the potential protective effect of caffeine against tamoxifen-induced fatty liver in Wistar rats.

methodsRats were divided into normal control, tamoxifen + saline, and tamoxifen + caffeine. Plasma samples were assessed for biochemical markers related to oxidative stress, inflammation, liver function, and cell damage. Additionally, liver histopathology was examined to quantify the extent of fatty infiltration.

resultsIn the tamoxifen + saline group, elevated levels of plasma malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-α), alanine aminotransferase (ALT), cytokeratin 18, and soluble ST2 were observed compared to the normal control group, indicating increased oxidative stress, inflammation, and liver injury (p < 0.01). Moreover, histopathological examination revealed a significant increase in fatty infiltration (p < 0.001). However, in the tamoxifen + caffeine group, these markers were markedly reduced (p < 0.05, p < 0.01), and fatty infiltration was significantly mitigated (p < 0.001).

conclusionsThe findings suggest that caffeine administration attenuates tamoxifen-induced fatty liver in rats by ameliorating oxidative stress, inflammation, liver injury, and cell damage. Histopathological evidence further supports the protective role of caffeine. This study highlights the potential of caffeine as a therapeutic intervention to counter tamoxifen-induced hepatic complications, contributing to the optimization of breast cancer treatment strategies.

Indexed as

CaffeineFatty LiverMalondialdehydeOxidative StressRats, WistarTamoxifenAlanine TransaminaseAnimalsAntineoplastic Agents, HormonalBiomarkersDisease Models, AnimalFemaleLiverRatsTumor Necrosis Factor-alphaAlanine TransaminaseAntineoplastic Agents, HormonalBiomarkersCaffeineMalondialdehydeTamoxifenTumor Necrosis Factor-alpha

Identifiers

PMID39356936
PMCPMC11441146

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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.