Evidence map›Paper›PMID 41915179›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2026

Immunomodulatory and locomotor regulations via Diosgenin treatment in lipopolysaccharide-induced chronic fatigue syndrome (CFS)/ depressive despair symptom: an in vivo assessment.

Rahul Lotan Shirole, Mohan Rajendra Khalane, Vijayeta Pralhad Nage, Nitin Lotan Shirole, Sushil Vilas Chawre, Abdulrhman Alsayari, Shadma Wahab, Adrija Bhunia, Digvijay Kailas Patil

Abstract read
PubMed Publisher
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

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

9 authors.

Rahul Lotan ShiroleDepartment of Pharmacology, DCS's A. R. A. College of Pharmacy, Dhule, Maharashtra, 424005, India.
Mohan Rajendra KhalaneDepartment of Pharmacology, DCS's A. R. A. College of Pharmacy, Dhule, Maharashtra, 424005, India.
Vijayeta Pralhad NageDepartment of Kayachikitsa, Government Ayurvedic College, Nagpur, Maharashtra, 440024, India.
Nitin Lotan ShiroleDepartment of Pharmaceutical Chemistry, DCS's A. R. A. College of Pharmacy, Dhule, Maharashtra, 424005, India.
Sushil Vilas ChawreDepartment of Kayachikitsa, Government Ayurvedic College, Nagpur, Maharashtra, 440024, India.
Abdulrhman AlsayariDepartment of Pharmacognosy, College of Pharmacy, King Khalid University, Abha, 62529, Saudi Arabia.
Shadma WahabDepartment of Pharmacognosy, College of Pharmacy, King Khalid University, Abha, 62529, Saudi Arabia.
Adrija BhuniaDepartment of Pharmaceutics, Yenepoya Pharmacy College & Research Centre, Yenepoya (Deemed to Be University), Mangalore, Karnataka, 575018, India. adrija@yenepoya.edu.in.
Digvijay Kailas PatilDepartment of Pharmacology, DCS's A. R. A. College of Pharmacy, Dhule, Maharashtra, 424005, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diosgenin is one of the several bioactive chemicals found in fenugreek. In traditional Chinese medicine and modern pharmacological studies, it is useful as anti-cancer, antiviral, anti-inflammatory, and hepatoprotective agents. However, studies investigating its role against antigen-induced neuroinflammation, providing new insights at cellular levels in its pharmacological potential, have not been completely investigated yet. Diosgenin was tested against lipopolysaccharide (LPS)-induced neuroinflammation in mice using forced swim test, tail suspension test, thermal hyperalgesia, locomotor activity, and grip strength on day 19. Brain homogenate was analyzed for estimation of reduced glutathione, superoxide dismutase (SOD), catalase (CAT), lipid peroxidation, total nitric oxide, and TNF-α levels. Pre-treatment with Diosgenin 10, 20, and 40 mg/kg, i.p. for 21 days showed a significant reduction in immobility duration and improved anxiety-like behavior. Diosgenin further reduced LPS-induced increased nitrosative and oxidative stress, evidenced by increased nitrite levels, lipid peroxidation, and reduced activity of antioxidant enzymes (CAT, SOD, and reduced glutathione), as well as amplified levels of tumor necrosis factor-α, which were associated with behavioral abnormalities. The current research indicates that Diosgenin has a protective role against LPS-induced chronic fatigue syndrome, suggesting that it could be a potent treatment option for the disease.

Indexed as

Anti-Inflammatory AgentsDepressionDiosgeninFatigue Syndrome, ChronicImmunologic FactorsLocomotionAnimalsBehavior, AnimalBrainDisease Models, AnimalLipid PeroxidationLipopolysaccharidesMaleMiceNitric OxideOxidative StressAnti-Inflammatory AgentsDiosgeninImmunologic FactorsLipopolysaccharidesNitric OxideTumor Necrosis Factor-alphaChronic fatigue syndromeDepressionDiosgeninExperimental pharmacologyInflammationNatural medicine

Identifiers

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.