Evidence map›Paper›PMID 42375251›Full record

ArticleOpen veterinary journal2026

Effects of nanocurcumin administration on malondialdehyde and estrogen levels in mice exposed to noise-induced stress.

Viski Fitri Hendrawan, Qatrinnada Hazimah, Tiara Widyaputri, Galuh Chandra Agustina, Dwi Rahmawati, Ertika Fitri Lisnanti

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Article in Open veterinary journal, 2026. 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Viski Fitri HendrawanDepartment of Veterinary Reproduction, Faculty of Veterinary Medicine, Universitas Brawijaya, Jakarta, Indonesia.
Qatrinnada HazimahFaculty of Veterinary Medicine, Universitas Brawijaya, Malang, Indonesia.
Tiara WidyaputriVeterinary Clinical Pathology and Laboratory Animal Laboratory, Faculty of Veterinary Medicine, Universitas Brawijaya, Malang, Indonesia.
Galuh Chandra AgustinaDepartment of Veterinary Physiology, Faculty of Veterinary Medicine, Universitas Brawijaya, Malang, Indonesia.
Dwi RahmawatiDepartment of Orthodontics, Faculty of Dentistry, Universitas Brawijaya, Malang, Indonesia.
Ertika Fitri LisnantiProgram of Animal Husbandry, Faculty of Agriculture, Universitas Islam Kediri, Kediri, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: During pregnancy, noise stress has been associated with the activation of the hypothalamic-pituitary-adrenal axis and increased oxidative stress, which can disrupt hormonal balance and adversely affect pregnancy outcomes. Malondialdehyde (MDA) is a key biomarker of lipid peroxidation, whereas estrogen plays a critical role in maintaining gestational homeostasis. Excess oxidative stress and hormonal imbalance may impair fetal development. Nanocurcumin, a curcumin nanoparticle formulation, exhibits enhanced antioxidant and anti-inflammatory properties compared with conventional curcumin and may offer protective effects against pregnancy-related oxidative damage. Aim: This study aimed to evaluate the effects of nanocurcumin on MDA and estrogen levels in pregnant mice exposed to noise-induced stress, contributing to Sustainable Development Goals Methods: An experimental study was conducted using 25 pregnant BALB/c mice randomly divided into five groups: K(-): untreated control, K(+): exposed to 135 dB noise for 40 minutes, P1, P2, and P3: exposed to noise and treated with nanocurcumin at 14, 21, and 24.5 mg/kg body weight, respectively. An electric siren was placed inside a soundproof chamber to deliver noise, and the 135 dB intensity was calibrated using a precision digital decibel meter (Benetech GM1356). Oral treatment was administered from gestational day (GD) 6 to gestational day 18. Serum MDA and estrogen levels were measured using an enzyme-linked immunosorbent assay. Data were analyzed using one-way analysis of variance followed by Tukey's honest significant difference post hoc test ( Results: Noise exposure numerically increased both MDA and estrogen levels, although not all differences reached statistical significance. However, nanocurcumin administration significantly reduced both parameters in a dose-dependent manner. The highest dose (24.5 mg/kg BW, P3 group) resulted in a 40.87% reduction in MDA and a 22.88% reduction in estrogen compared to K(+), with values approaching those in the untreated control. Conclusion: Nanocurcumin has potential as a protective agent against noise-induced oxidative stress and hormonal disturbances during pregnancy. To confirm translational relevance, future research should focus on elucidating underlying molecular mechanisms and evaluating fetal outcomes.

Indexed as

AntioxidantsCurcuminEstrogensMalondialdehydeNoiseOxidative StressAnimalsFemaleMiceMice, Inbred BALB CNanoparticlesPregnancyRandom AllocationAntioxidantsCurcuminEstrogensMalondialdehydenanocurcuminEstrogenGood Health and Well-beingMalondialdehydeNoisePregnant mice

Identifiers

PMID42375251
PMCPMC13314144

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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.