Evidence map›Paper›PMID 30123446›Full record

ArticleMolecular autism2018

Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation.

Weiguo Xie, Xiaohu Ge, Ling Li, Athena Yao, Xiaoyan Wang, Min Li, Xiang Gong, Zhigang Chu, Zhe Lu, Xiaodong Huang and 6 more

Open access · goldAbstract read
In one paragraph

Article in Molecular autism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 10% of its field
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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

Weiguo Xie *1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.
Xiaohu Ge *SALIAI Stem Cell Institute of Guangdong, Guangzhou SALIAI Stem Cell Science and Technology Co. LTD, Guangzhou, 510055 People's Republic of China.
Ling Li *3Department of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, 570206 People's Republic of China.
Athena Yao1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.
Xiaoyan WangSALIAI Stem Cell Institute of Guangdong, Guangzhou SALIAI Stem Cell Science and Technology Co. LTD, Guangzhou, 510055 People's Republic of China.
Min Li1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.
Xiang Gong1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.
Zhigang Chu1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.
Zhe Lu3Department of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, 570206 People's Republic of China.
Xiaodong Huang1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.
Yun Jiao3Department of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, 570206 People's Republic of China.
Yifei WangSALIAI Stem Cell Institute of Guangdong, Guangzhou SALIAI Stem Cell Science and Technology Co. LTD, Guangzhou, 510055 People's Republic of China.
Meifang Xiao3Department of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, 570206 People's Republic of China.
Haijia ChenSALIAI Stem Cell Institute of Guangdong, Guangzhou SALIAI Stem Cell Science and Technology Co. LTD, Guangzhou, 510055 People's Republic of China.
Wei Xiang3Department of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, 570206 People's Republic of China.
Paul Yao1Institute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, 430060 People's Republic of China.ORCID 0000-0001-9407-0779
Hainan Maternal and Child Health Hospital · CNTongren Hospital · CNCell Technology (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recent literatures indicate that maternal hormone exposure is a risk factor for autism spectrum disorder (ASD). We hypothesize that prenatal progestin exposure may counteract the neuroprotective effect of estrogen and contribute to ASD development, and we aim to develop a method to ameliorate prenatal progestin exposure-induced autism-like behavior. Methods: Experiment 1: Prenatal progestin exposure-induced offspring are treated with resveratrol (RSV) through either prenatal or postnatal exposure and then used for autism-like behavior testing and other biomedical analyses. Experiment 2: Prenatal norethindrone (NET) exposure-induced offspring are treated with ERβ knockdown lentivirus together with RSV for further testing. Experiment 3: Pregnant dams are treated with prenatal NET exposure together with RSV, and the offspring are used for further testing. Results: Eight kinds of clinically relevant progestins were used for prenatal exposure in pregnant dams, and the offspring showed decreased ERβ expression in the amygdala with autism-like behavior. Oral administration of either postnatal or prenatal RSV treatment significantly reversed this effect with ERβ activation and ameliorated autism-like behavior. Further investigation showed that RSV activates ERβ and its target genes by demethylation of DNA and histone on the ERβ promoter, and then minimizes progestin-induced oxidative stress as well as the dysfunction of mitochondria and lipid metabolism in the brain, subsequently ameliorating autism-like behavior. Conclusions: We conclude that resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation. Our data suggest that prenatal progestin exposure is a strong risk factor for autism-like behavior. Many potential clinical progestin applications, including oral contraceptive pills, preterm birth drugs, and progestin-contaminated drinking water or seafood, may be risk factors for ASD. In addition, RSV may be a good candidate for clinically rescuing or preventing ASD symptoms in humans, while high doses of resveratrol used in the animals may be a potential limitation for human application.

Indexed as

Autistic DisorderAmygdalaAnimalsBehavior, AnimalCells, CulturedDisease Models, AnimalEstrogen Receptor betaFemaleMaleNeuronsNorethindronePregnancyPrenatal Exposure Delayed EffectsProgestinsRats, Sprague-DawleyResveratrolEstrogen Receptor betaNorethindroneProgestinsResveratrolRNA, MessengerAutism spectrum disorderEstrogen receptor βLipid metabolismMitochondriaOxidative stressProgestinResveratrol

Identifiers

PMID30123446
PMCPMC6090838
OpenAlexW2886045558

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.