Evidence map›Paper›PMID 41874733›Full record

ArticleJournal of bioenergetics and biomembranes2026

Ferulic acid relieves hypoxic damage by inhibiting endoplasmic reticulum stress, oxidative stress, and apoptosis through activating FOXA2-modulated Nrf2/HO-1 pathway in spermatogonial cells.

Weiwei Li, Xiurong Yin, Nan Zhang, Shihao Li, Chengmin Gu

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In one paragraph

Article in Journal of bioenergetics and biomembranes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Weiwei LiDepartment of Reproductive Medicine, Qinhuangdao Maternal and Child Health Hospital, Qinhuangdao, China. wwli531@163.com.
Xiurong YinDepartment of Reproductive Medicine, Qinhuangdao Maternal and Child Health Hospital, Qinhuangdao, China.
Nan ZhangDepartment of Reproductive Medicine, Qinhuangdao Maternal and Child Health Hospital, Qinhuangdao, China.
Shihao LiClinical Laboratory, Qinhuangdao Maternal and Child Health Hospital, Qinhuangdao, China.
Chengmin GuDepartment of Obstetrics, Qinhuangdao Maternal and Child Health Hospital, Qinhuangdao, China. 346032196@qq.com.

Funding

S&T program of Qinhuangdao grant number: 202501A194
6 · The paper itself

Abstract

Male infertility is a global public health problem affecting human development. Ferulic acid (FA) is an important active phenolic substance that has been found to exert a protective effect on male reproductive system. Here we aimed to investigate the effect of FA on hypoxia-induced spermatogenesis damage and explore the underlying mechanisms. Mouse spermatogenic GC-1 spg cells were cultured under hypoxic conditions to establish an in vitro model of spermatogenesis damage. The small interfering RNAs targeting Forkhead Box A2 (FOXA2) were transfected into GC-1 spg cells to construct FOXA2-silencing cells. Cell counting kit-8 (CCK-8) and flow cytometry assays were performed to detect cell viability and apoptosis, respectively. Western blot analysis was conducted to examine the expression levels of related proteins. We found that FA improved the decreased cell viability of GC-1 spg cells under hypoxic conditions. FA attenuated hypoxia-induced endoplasmic reticulum (ER) stress, oxidative stress, and apoptosis in GC-1 spg cells. Both mRNA and protein levels of FOXA2 were reduced after hypoxia induction, which were reversed by FA treatment. Knockdown of FOXA2 reversed the inhibitory effects of FA on ER stress, oxidative stress, and apoptosis in hypoxia-exposed GC-1 spg cells. Furthermore, nuclear factor erythroid 2-related factor 2 (Nrf2) overexpression restored the role of FOXA2 knockdown in FA-treated GC-1 spg cells under hypoxic conditions. Overall, we demonstrated the inhibitory effect of FA on hypoxia-induced ER stress, oxidative stress, and apoptosis in mouse spermatogenic GC-1 spg cells. Furthermore, FOXA2-mediated Nrf2 signaling contributed to the protective effects of FA against hypoxia-induced spermatogenesis damage. These findings suggest that FA may have the potential to ameliorate hypoxia-induced spermatogenesis injury.

Indexed as

ApoptosisCoumaric AcidsEndoplasmic Reticulum StressHepatocyte Nuclear Factor 3-betaNF-E2-Related Factor 2Oxidative StressSpermatogoniaAnimalsCell HypoxiaMaleMiceSignal TransductionCoumaric Acidsferulic acidFoxa2 protein, mouseHepatocyte Nuclear Factor 3-betaNfe2l2 protein, mouseNF-E2-Related Factor 2Ferulic acidFOXA2HypoxiaMale infertilitySpermatogenesis damage

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Registered trials

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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.