Evidence map›Paper›PMID 42543224›Full record

ArticleBirth defects research2026

Maternal and Early Developmental Effects of Perinatal Exposure to Therapeutically Relevant Doses of Common Nonsteroidal Anti-Inflammatory Drugs in Rats.

Sara Tawany Caetano Dos Santos, Reggina Lorena Mellado Castro, Luara Magalhães, Giovanna Ferrari Rosalem, Julia Vitoria Francisco de Aquino, Otávio Galassi Vitale, Livia Trippe Nagaoka, Julia Stein, Beatriz de Matos Manoel, Bárbara Campos Jorge and 1 more

Abstract read
In one paragraph

Article in Birth defects research, 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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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

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

11 authors.

Sara Tawany Caetano Dos SantosDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.
Reggina Lorena Mellado CastroDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0009-0008-2311-3784
Luara MagalhãesDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0009-0004-3742-7830
Giovanna Ferrari RosalemDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.
Julia Vitoria Francisco de AquinoDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0009-0008-5466-6314
Otávio Galassi VitaleDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0009-0009-2558-9185
Livia Trippe NagaokaDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0000-0002-4739-4102
Julia SteinDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0000-0001-8968-7416
Beatriz de Matos ManoelDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0000-0002-3281-6085
Bárbara Campos JorgeDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0000-0001-8754-4876
Arielle Cristina ArenaDepartment of Cellular and Molecular Biology, Institute of Biosciences of Botucatu, UNESP - Paulista State University, Botucatu, São Paulo State, Brazil.ORCID 0000-0002-2373-9399

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2025/02352-9
6 · The paper itself

Abstract

backgroundNonsteroidal anti-inflammatory drugs (NSAIDs) are widely used during pregnancy, yet information on their developmental safety during sensitive perinatal windows remains limited. This study evaluated the maternal and early developmental effects of paracetamol/acetaminophen, aspirin, and nimesulide administered at therapeutically relevant doses during late gestation and lactation.

methodsPregnant Wistar rats were treated daily by oral gavage with paracetamol/acetaminophen (APAP; 126 mg/kg/day), aspirin (ASA; 5.6 mg/kg/day), or nimesulide (NIM; 11 mg/kg/day) from gestational day 15 to postnatal day 22. Maternal clinical parameters, body weight, food and water intake, organ weights, hematological and biochemical markers, and maternal behavior were evaluated. In F1 offspring, early developmental indicators, anogenital distance, sexual maturation endpoints, reproductive organ weights, and hematological parameters were assessed.

resultsExposure to the evaluated NSAIDs produced little evidence of overt maternal toxicity. Maternal body weight, food and water intake, gestational length, and most organ weights remained unchanged. Mild hematological and biochemical alterations were observed, particularly in NIM-treated dams. Maternal behavior was largely preserved, although APAP-treated dams showed reduced latency to initiate pup grooming. In offspring, anogenital distance and female reproductive maturation were unaffected. Male offspring exposed to APAP showed earlier testicular descent, whereas ASA exposure was associated with increased seminal vesicle weight. These findings were isolated and were not associated with a consistent pattern of reproductive alterations.

conclusionPerinatal exposure to therapeutically relevant doses of paracetamol/acetaminophen, aspirin, and nimesulide produced little evidence of overt maternal or developmental toxicity during the evaluated period. Although a limited number of drug-specific findings were identified, they were isolated and did not indicate a consistent pattern of reproductive toxicity. These results contribute to the preclinical safety assessment of NSAID exposure during pregnancy and lactation and support further studies to determine the functional relevance of these early observations.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalPrenatal Exposure Delayed EffectsAcetaminophenAnimalsAnimals, NewbornAspirinBody WeightFemaleLactationMaleMaternal ExposureOrgan SizePregnancyRatsRats, WistarSulfonamidesAcetaminophenAnti-Inflammatory Agents, Non-SteroidalAspirinnimesulideSulfonamidesdevelopmental toxicologymaternal toxicityNSAIDsperinatal exposurepregnancyreproductive development

Identifiers

PMID42543224
PMCPMC13429490

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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.