Evidence map›Paper›PMID 26696906›Full record

ArticleFrontiers in physiology2015

Maternal Melatonin Therapy Rescues Prenatal Dexamethasone and Postnatal High-Fat Diet Induced Programmed Hypertension in Male Rat Offspring.

You-Lin Tain, Jiunn-Ming Sheen, Hong-Ren Yu, Chih-Cheng Chen, Mao-Meng Tiao, Chien-Ning Hsu, Yu-Ju Lin, Kuang-Che Kuo, Li-Tung Huang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
11.5field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

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  7. Melatonin and Kidney Health: From Fetal Stage to Later Life.International journal of molecular sciences · 2023
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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

9 authors at 3 institutions in 1 country.

You-Lin TainDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan ; Center for Translational Research in Biomedical Sciences, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Jiunn-Ming SheenDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Hong-Ren YuDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Chih-Cheng ChenDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Mao-Meng TiaoDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Chien-Ning HsuDepartment of Pharmacy, Kaohsiung Chang Gung Memorial Hospital Kaohsiung, Taiwan ; School of Pharmacy, Kaohsiung Medical University Kaohsiung, Taiwan.
Yu-Ju LinDepartment of Obstetrics and Gynecology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Kuang-Che KuoDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan.
Li-Tung HuangDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine Kaohsiung, Taiwan ; Department of Traditional Chinese Medicine, Chang Gung University Linkou, Taiwan.
Chang Gung University · TWKaohsiung Chang Gung Memorial Hospital · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prenatal dexamethasone (DEX) exposure and high-fat (HF) intake are linked to hypertension. We examined whether maternal melatonin therapy prevents programmed hypertension synergistically induced by prenatal DEX plus postnatal HF in adult offspring. We also examined whether DEX and melatonin causes renal programming using next-generation RNA sequencing (NGS) technology. Pregnant Sprague-Dawley rats received intraperitoneal dexamethasone (0.1 mg/kg) or vehicle from gestational day 16 to 22. In the melatonin-treatment groups (M), rats received 0.01% melatonin in drinking water during their entire pregnancy and lactation. Male offspring were assigned to five groups: control, DEX, HF, DEX+HF, and DEX+HF+M. Male offspring in the HF group were fed a HF diet from weaning to 4 months of age. Prenatal DEX and postnatal HF diet synergistically induced programmed hypertension in adult offspring, which melatonin prevented. Maternal melatonin treatment modified over 3000 renal transcripts in the developing offspring kidney. Our NGS data indicate that PPAR signaling and fatty acid metabolism are two significantly regulated pathways. In addition, maternal melatonin therapy elicits longstanding alterations on renal programming, including regulation of the melatonin signaling pathway and upregulation of Agtr1b and Mas1 expression in the renin-angiotensin system (RAS), to protect male offspring against programmed hypertension. Postnatal HF aggravates prenatal DEX induced programmed hypertension in adult offspring, which melatonin prevented. The protective effects of melatonin on programmed hypertension is associated with regulation of the RAS and melatonin receptors. The long-term effects of maternal melatonin therapy on renal transcriptome require further clarification.

Indexed as

fatglucocorticoidhypertensionmelatoninnext generation sequencingrenin-angiotensin system

Identifiers

PMID26696906
PMCPMC4675845
OpenAlexW2202661905

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.