Hydrogenology
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Hydrogen suppresses oxidative stress by inhibiting the p38 MAPK signaling pathway in preeclampsia

Guo L, Liu M, Duan T. · Adv Clin Exp Med. 2023;32(3):357–367.

PreclinicalOther formsPublished 2023Source checked
Study record, not medical adviceThis record reports what the source states. It is not medical advice and does not establish that molecular hydrogen is effective, safe or appropriate for any person.
Quick summary

Study at a glance

Evidence type

Preclinical

Population or model

Pregnant Sprague-Dawley rats in an L-NAME preeclampsia model.

Intervention and dose

Hydrogen-rich saline in the L-NAME intervention arms, with a p38 inhibitor in one additional arm. · L-NAME was delivered in hydrogen-rich saline; the full article describes preparation and arm-specific dosing.

Duration

Late-gestation experimental protocol.

Reported result

The hydrogen-rich-saline arm had lower proteinuria and several placental oxidative, inflammatory and p38-pathway measures than the L-NAME model arm.

Main limitation

Animal-model evidence only; the inhibitor arm is a mechanistic co-intervention and does not establish clinical benefit.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Randomized controlled rat study

Research topic

Women’s health

Administration form

Other forms

Study result signal

Positive preclinical signal with mechanistic co-intervention.

Outcome type

Physiological, tissue and biomarker outcomes in a rat model.

Reported in the source

Methods

Population or model

Pregnant Sprague-Dawley rats in an L-NAME preeclampsia model.

Sample

Five experimental groups; group sizes were checked in the full methods.

Duration

Late-gestation experimental protocol.

Intervention

Hydrogen-rich saline in the L-NAME intervention arms, with a p38 inhibitor in one additional arm.

Hydrogen form

H₂ dissolved in saline.

Dose or H₂ specification

L-NAME was delivered in hydrogen-rich saline; the full article describes preparation and arm-specific dosing.

Comparator

Non-pregnant, normal-pregnancy and L-NAME saline controls.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Blood pressure, proteinuria, placental oxidative and inflammatory markers and p38 MAPK expression.

Reported result

The hydrogen-rich-saline arm had lower proteinuria and several placental oxidative, inflammatory and p38-pathway measures than the L-NAME model arm.

Extraction completeness

The full article methods, intervention, outcomes, positive and null findings, funding and conflict statements were checked.

A reported association, difference or mechanism is not automatically a clinical benefit.

Interpretation limits

Limitations and applicability

Main methodological cautions

Animal-model evidence only; the inhibitor arm is a mechanistic co-intervention and does not establish clinical benefit.

Applies directly to

The reported L-NAME rat model only.

Preliminary appraisal framework

SYRCLE animal-study tool — preliminary

Preliminary risk-of-bias status

Some concerns

Appraisal rationale

Randomization was reported, but concealment and assessor blinding were not established and several outcomes were analyzed.

Appraisal domains

Sequence generation checked where reported · Allocation concealment generally unclear · Personnel blinding generally unclear · Outcome-assessor blinding generally unclear · No prospectively registered analysis plan identified

No single-study GRADE certainty rating is assigned. Read how records and evidence assessments are prepared.

Sources and status

Sources and record status

Identifiers

PMID: 36330842 · DOI: 10.17219/acem/154623

Publisher access

A free publisher or repository full article was checked.

Extraction basis

Publisher or repository full article and bibliographic record; checked 10 August 2026.

Last reviewed

10 August 2026

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