Evidence map›Paper›PMID 34414905›Full record

ArticleIndian journal of pharmacology

Natural product topical therapy in mitigating imiquimod-induced psoriasis-like skin inflammation-underscoring the anti-psoriatic potential of Nimbolide.

Nilesh Barku More, Nivya Sharma, Gauthami Pulivendala, Swarna Bale, Chandraiah Godugu

Abstract read
In one paragraph

Article in Indian journal of pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. The Essential Oil Derived fromMolecules (Basel, Switzerland) · 2022
    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

5 authors.

Nilesh Barku MoreDepartment of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Nivya SharmaDepartment of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Gauthami PulivendalaDepartment of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Swarna BaleDepartment of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Chandraiah GoduguDepartment of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPsoriasis is a chronic inflammatory dermatological disorder having complex pathophysiology with autoimmune and genetic factors being the major players. Despite the availability of a gamut of therapeutic strategies, systemic toxicity, poor efficacy, and treatment tolerance due to genetic variability among patients remain the major challenges. This calls for effective intervention with the superior pharmacological profile. Nimbolide (NIM), a major limonoid is an active chemical constituent found in the leaves of the Indian Neem tree, Azadirachta indica. It has gained immense limelight in the past decades for the treatment of various diseases owing to its anti-proliferative, anti-inflammatory, and anti-cancer potentials.

objectiveThe present study was centered around evaluating the anti-psoriatic effect of NIM in the experimental model of Imiquimod (IMQ)-induced psoriasis-like inflammation model. MATERIALS AND

methodsApplication of IMQ topically on the dorsum of Balb/c mice from day 0-6 prompted psoriasis-like inflammatory symptoms. Treatment groups included topical administration of NIM incorporated carbopol gel formulation and NIM free drug given through subcutaneous route. Protein expression studies such as immunohistochemistry, Western blotting, and ELISA were employed.

resultsIt was clearly observed from our results that NIM significantly ameliorated the expression of inflammatory and proliferation mediators. Further, NIM in the treatment groups significantly improved classic Psoriasis Area Severity Index scoring when compared to IMQ administered group.

conclusionIt is noteworthy that NIM showed a predominant therapeutic effect as compared to other treatment group. To recapitulate, NIM has shown promising activity as an anti-psoriatic agent by remarkably ameliorating inflammation and associated proliferation.

Indexed as

Administration, TopicalAnimalsBiological ProductsDisease Models, AnimalImiquimodIntercellular Adhesion Molecule-1LimoninsMiceMice, Inbred BALB CNF-kappa BPsoriasisSeverity of Illness IndexBiological ProductsImiquimodIntercellular Adhesion Molecule-1LimoninsNF-kappa BnimbolideAnti-inflammatoryImiquimodNimbolidepsoriasistopical therapy

Identifiers

PMID34414905
PMCPMC8411965

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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.