Evidence map›Paper›PMID 24646949›Full record

ArticleJournal of lipid research2014

Rohitukine inhibits in vitro adipogenesis arresting mitotic clonal expansion and improves dyslipidemia in vivo.

Salil Varshney, Kripa Shankar, Muheeb Beg, Vishal M Balaramnavar, Sunil Kumar Mishra, Pankaj Jagdale, Shishir Srivastava, Yashpal S Chhonker, Vijai Lakshmi, Bhushan P Chaudhari and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 59 citations in OpenAlex.

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  13. Isobavachalcone fromInternational journal of molecular sciences · 2018
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  14. Article
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  17. Review
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

13 authors at 4 institutions in 1 country.

Salil VarshneyDivision of Pharmacology, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Kripa ShankarDivision of Pharmacology, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Muheeb BegDivision of Pharmacology, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Vishal M BalaramnavarMedicinal and Process Chemistry Division, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Sunil Kumar MishraMedicinal and Process Chemistry Division, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Pankaj JagdaleRegulatory Toxicology Group, Council of Scientific & Industrial Research-Indian Institute of Toxicology Research, Lucknow, Uttar Pradesh 226001, India.
Shishir SrivastavaMedicinal and Process Chemistry Division, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Yashpal S ChhonkerPharmacokinetics and Metabolism Division, Council of Scientific & Industrial Research-Central Drug Research Institute, 10/1, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Vijai LakshmiDepartment of Biochemistry, King George's Medical University, Chowk Area, Lucknow, Uttar Pradesh 226003, India.
Bhushan P ChaudhariRegulatory Toxicology Group, Council of Scientific & Industrial Research-Indian Institute of Toxicology Research, Lucknow, Uttar Pradesh 226001, India.
Rabi Shankar BhattaPharmacokinetics and Metabolism Division, Council of Scientific & Industrial Research-Central Drug Research Institute, 10/1, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Anil Kumar SaxenaMedicinal and Process Chemistry Division, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Anil Nilkanth GaikwadDivision of Pharmacology, Council of Scientific & Industrial Research-Central Drug Research Institute, Sector 10, Jankipuram Extension, Lucknow, Uttar Pradesh 226031, India.
Council of Scientific and Industrial Research · INCentral Drug Research Institute · INIndian Institute of Toxicology Research · INKing George's Medical University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We developed a common feature pharmacophore model using known antiadipogenic compounds (CFPMA). We identified rohitukine, a reported chromone anticancer alkaloid as a potential hit through in silico mapping of the in-house natural product library on CFPMA. Studies were designed to assess the antiadipogenic potential of rohitukine. Rohitukine was isolated from Dysoxylum binacteriferum Hook. to ⬧95% purity. As predicted by CFPMA, rohitukine was indeed found to be an antiadipogenic molecule. Rohitukine inhibited lipid accumulation and adipogenic differentiation in a concentration- and exposure-time-dependent manner in 3T3-L1 and C3H10T1/2 cells. Rohitukine downregulated expression of PPARγ, CCAAT/enhancer binding protein α, adipocyte protein 2 (aP2), FAS, and glucose transporter 4. It also suppressed mRNA expression of LPL, sterol-regulatory element binding protein (SREBP) 1c, FAS, and aP2, the downstream targets of PPARγ. Rohitukine arrests cells in S phase during mitotic clonal expansion. Rohitukine was bioavailable, and 25.7% of orally administered compound reached systemic circulation. We evaluated the effect of rohitukine on dyslipidemia induced by high-fat diet in the hamster model. Rohitukine increased hepatic expression of liver X receptor α and decreased expression of SREBP-2 and associated targets. Rohitukine decreased hepatic and gonadal lipid accumulation and ameliorated dyslipidemia significantly. In summary, our strategy to identify a novel antiadipogenic molecule using CFPMA successfully resulted in identification of rohitukine, which confirmed antiadipogenic activity and also exhibited in vivo antidyslipidemic activity.

Indexed as

3T3-L1 CellsAdipogenesisAnimalsChromonesDyslipidemiasFemaleMaleMesocricetusMiceMitosisPiperidinesS Phase Cell Cycle Checkpoints5,7-dihydroxy-2-methyl-8-(4-(3-hydroxy-1-methyl)-piperidinyl)-4H-1-benzopyran-4-oneChromonesPiperidines3T3-L1C3H10T1/2Dysoxylum binacteriferum Hook. f.S-phase arrest

Identifiers

PMID24646949
PMCPMC4031934
OpenAlexW2132673781

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.