Evidence map›Paper›PMID 34876168›Full record

ArticleFluids and barriers of the CNS2021

Lithium administered to pregnant, lactating and neonatal rats: entry into developing brain.

Shene Yi-Shiuan Chiou, Kai Kysenius, Yifan Huang, Mark David Habgood, Liam M Koehn, Fiona Qiu, Peter J Crouch, Swati Varshney, Katherine Ganio, Katarzyna Magdalena Dziegielewska and 1 more

Open access · goldAbstract read
In one paragraph

Article in Fluids and barriers of the CNS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  4. Choroid Plexus Pathophysiology.Annual review of pathology · 2025
    Review
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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

11 authors at 2 institutions in 1 country.

Shene Yi-Shiuan Chiou *Department of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Kai Kysenius *Department of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Yifan HuangDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Mark David HabgoodDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Liam M KoehnDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Fiona QiuDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Peter J CrouchDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Swati VarshneyBio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville, VIC, 3010, Australia.
Katherine GanioDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, 3000, Australia.
Katarzyna Magdalena DziegielewskaDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia.
Norman Ruthven SaundersDepartment of Biochemistry & Pharmacology, University of Melbourne, Parkville, VIC, 3010, Australia. norman.saunders@monash.edu.ORCID http://orcid.org/0000-0001-6660-7639
The University of Melbourne · AUMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLittle is known about the extent of drug entry into developing brain, when administered to pregnant and lactating women. Lithium is commonly prescribed for bipolar disorder. Here we studied transfer of lithium given to dams, into blood, brain and cerebrospinal fluid (CSF) in embryonic and postnatal animals as well as adults.

methodsLithium chloride in a clinically relevant dose (3.2 mg/kg body weight) was injected intraperitoneally into pregnant (E15-18) and lactating dams (birth-P16/17) or directly into postnatal pups (P0-P16/17). Acute treatment involved a single injection; long-term treatment involved twice daily injections for the duration of the experiment. Following terminal anaesthesia blood plasma, CSF and brains were collected. Lithium levels and brain distribution were measured using Laser Ablation Inductively Coupled Plasma-Mass Spectrometry and total lithium levels were confirmed by Inductively Coupled Plasma-Mass Spectrometry.

resultsLithium was detected in blood, CSF and brain of all fetal and postnatal pups following lithium treatment of dams. Its concentration in pups' blood was consistently below that in maternal blood (30-35%) indicating significant protection by the placenta and breast tissue. However, much of the lithium that reached the fetus entered its brain. Levels of lithium in plasma fluctuated in different treatment groups but its concentration in CSF was stable at all ages, in agreement with known stable levels of endogenous ions in CSF. There was no significant increase of lithium transfer into CSF following application of Na

conclusionsInformation obtained on the distribution of lithium in developing brain provides a basis for studying possible deleterious effects on brain development and behaviour in offspring of mothers undergoing lithium therapy.

Indexed as

BloodBrainCerebrospinal FluidMaternal-Fetal ExchangeMilk, HumanAnimalsAnimals, NewbornAnimals, SucklingAntimanic AgentsChoroid PlexusEmbryo, MammalianFemaleLactationLithium ChloridePregnancyRatsAntimanic AgentsLithium ChlorideBipolar-disorder prophylaxisBrain barriersCerebrospinal fluidPlacental transferPostnatalPregnancy

Identifiers

PMID34876168
PMCPMC8650431
OpenAlexW4225764452

What OpenQuestion holds

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LicenceCC BY
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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.