Evidence map›Paper›PMID 27306582›Full record

ArticleCNS neuroscience & therapeutics2016

Diurnal Variation of the Peripheral Cholinergic Antiinflammatory Function in Mice.

Bo-Shi Fan, En-Hui Zhang, Ming-He Cheng, Zhao-Tang Wu, Bing Han, Jian-Guang Yu

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2016. 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, 0 citations in OpenAlex.

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

6 authors at 3 institutions in 1 country.

Bo-Shi FanDepartment of Pharmacology, Second Military Medical University, Shanghai, China.
En-Hui ZhangThe 406th Hospital of PLA, Dalian, China.
Ming-He ChengDepartment of Pharmacology, Second Military Medical University, Shanghai, China.
Zhao-Tang WuDepartment of Physiology, Second Military Medical University, Shanghai, China.
Bing HanDepartment of Pharmacy, Minhang Hospital, Fudan University, Shanghai, China.
Jian-Guang YuDepartment of Pharmacology, Second Military Medical University, Shanghai, China.
Second Military Medical University · CN82th Hospital of Pla · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsCholinergic antiinflammatory (CAI) pathway functions importantly in inflammation via α7 nicotinic acetylcholine receptors (α7nAChR). The present work tested circadian rhythm in peripheral CAI activity and validities of CAI activity and glucocorticoids in chronotherapy for lipopolysaccharide (LPS)-induced shock.

methodsVesicular acetylcholine transporter (VAChT) expressed in liver and kidney was examined every 3 h in C57BL/6 mice. Proinflammatory cytokines in serum and survival time in shock were monitored after LPS injection every 3 h. Mifepristone, antagonist of glucocorticoid receptors, and methyllycaconitine (MLA), antagonist of α7nAChR, were administrated before LPS to block antiinflammatory function of endogenous glucocorticoids and acetylcholine.

resultsBoth levels of tumor necrosis factor α, interleukin 1β, and interleukin 6 and mortality exhibited diurnal variations with prominent peaks when LPS was given at 15:00, and the minimum mortality occurred at 00:00. Expression of VAChT increased during resting period. MLA increased serum proinflammatory cytokines slightly, but not affected survival rate. Both differences in cytokines and in survival times between LPS injection at 15:00 and 00:00 were eliminated by mifepristone, but not by MLA.

conclusionPeripheral CAI pathway exerts more powerful antiinflammatory effect during resting period. Glucocorticoids appear to be efficient in chronotherapy for septic shock.

Indexed as

AcetylcholineAconitineAnimalsCircadian RhythmCorticosteroneCytokinesDisease Models, AnimalHormone AntagonistsInflammationKidneyLipopolysaccharidesLiverMiceMice, Inbred C57BLMifepristoneNicotinic AntagonistsAcetylcholineAconitineCorticosteroneCytokinesHormone AntagonistsLipopolysaccharidesmethyllycaconitineMifepristoneNicotinic AntagonistsVesicular Acetylcholine Transport ProteinsCholinergic antiinflammatory pathwayChronotherapyCircadian rhythmGlucocorticoidα7 Nicotinic acetylcholine receptor

Identifiers

PMID27306582
PMCPMC6492785
OpenAlexW2434450821

What OpenQuestion holds

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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.