Evidence map›Paper›PMID 28477089›Full record

ArticlePsychopharmacology2017

The phosphodiesterase-4 inhibitor roflumilast decreases ethanol consumption in C57BL/6J mice.

Xin Liu, Pi-Da Hao, Ming-Feng Yang, Jing-Yi Sun, Lei-Lei Mao, Cun-Dong Fan, Zong-Yong Zhang, Da-Wei Li, Xiao-Yi Yang, Bao-Liang Sun and 1 more

Abstract read
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In one paragraph

Article in Psychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. 3D-QSAR Studies on High-affinity Phosphodiestera.Current medicinal chemistry · 2025
    Article
  3. PET imaging in rat brain shows opposite effects of acute and chronic alcohol exposure on phosphodiesterase-4B, an indirect biomarker of cAMP activity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  4. Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2024
    Article
  5. Article
  6. Review
  7. Novel medications for problematic alcohol use.The Journal of clinical investigation · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Neuroimmune signaling in alcohol use disorder.Pharmacology, biochemistry, and behavior · 2019
    Review
  20. Article
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 1 institution in 1 country.

Xin LiuKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Pi-Da HaoKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Ming-Feng YangKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Jing-Yi SunKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Lei-Lei MaoKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Cun-Dong FanKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Zong-Yong ZhangKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Da-Wei LiKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China.
Xiao-Yi YangKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China. xyyang@tsmc.edu.cn.
Bao-Liang SunKey Lab of Cerebral Microcirculation in Universities of Shandong, Institute of Neurological Disorders, Taishan Medical University, Taian, Shandong, 271000, China. blsun@tsmc.edu.cn.
Han-Ting ZhangInstitute of Pharmacology, Taishan Medical University, Taian, Shandong, 271016, China. hzhang@hsc.wvu.edu.
Taishan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleAlcohol use disorders have become one of the most damaging psychiatric disorders in the world; however, there are no ideal treatments in clinic. Phosphodiesterase-4 (PDE4), an enzyme that specifically hydrolyzes intracellular cyclic AMP (cAMP), has been involved in alcohol use disorders. Roflumilast is the first PDE4 inhibitor approved for treatment of chronic obstructive pulmonary diseases in clinic. It was of particular interest to researchers to determine whether roflumilast altered ethanol consumption.

objectivesThe present study tried to determine the effects of roflumilast on ethanol intake and preference.

methodsWe used the two-bottle choice paradigm to assess ethanol intake and preference in C57BL/6J mice treated with roflumilast (1, 3, or 10 mg/kg) or rolipram (0.5 mg/kg; positive control). The effect of roflumilast was verified using the ethanol drinking-in-dark (DID) test. Locomotor activity was examined using the open-field test. Intake of sucrose or quinine was also tested to determine whether natural reward preference and aversive stimuli were involved in the effect of PDE4 inhibitors.

resultsSimilar to rolipram, roflumilast decreased ethanol intake and preference in two-bottle choice and DID tests in a dose-dependent manner, with significant changes at the dose of 10 mg/kg; in contrast, roflumilast did not affect sucrose or quinine drinking, although it decreased locomotor activity at the high dose within 3 h of treatment.

conclusionsThese data provide novel demonstration for the effect of roflumilast on ethanol consumption and suggest that roflumilast may be beneficial for treatment of alcoholism.

Indexed as

Alcohol DrinkingAminopyridinesAnimalsBenzamidesCyclic Nucleotide Phosphodiesterases, Type 4CyclopropanesEthanolMaleMiceMice, Inbred C57BLMotor ActivityPhosphodiesterase 4 InhibitorsRolipramAminopyridinesBenzamidesCyclic Nucleotide Phosphodiesterases, Type 4CyclopropanesEthanolPhosphodiesterase 4 InhibitorsRoflumilastRolipramC57BL/6J micecAMP signalingEthanol consumptionPhosphodiesterase-4 (PDE4)Roflumilast

Identifiers

PMID28477089
OpenAlexW2610372929

What OpenQuestion holds

Textmetadata
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.