Evidence map›Paper›PMID 39997043›Full record

ArticleDiseases (Basel, Switzerland)2025

Ultradiluted

Anirban Roy, Avipsha Sarkar, Asit Kumar Roy, Tanusree Ghorai, Debadatta Nayak, Subhash Kaushik, Satadal Das

Abstract read
In one paragraph

Article in Diseases (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

7 authors.

Anirban RoyVirology Laboratory, DAC Regional Research Institute, 50, Rajendra Chatterjee Road, Kolkata 700035, West Bengal, India.ORCID 0000-0001-9134-6952
Avipsha SarkarVirology Laboratory, DAC Regional Research Institute, 50, Rajendra Chatterjee Road, Kolkata 700035, West Bengal, India.
Asit Kumar RoyDepartment of Environmental Science, University of Calcutta, 35, Ballygunge Circular Road, Kolkata 700019, West Bengal, India.
Tanusree GhoraiVirology Laboratory, DAC Regional Research Institute, 50, Rajendra Chatterjee Road, Kolkata 700035, West Bengal, India.
Debadatta NayakCentral Council of Research in Homeopathy, Institutional Area, Janakpuri, New Delhi 110058, India.
Subhash KaushikCentral Council of Research in Homeopathy, Institutional Area, Janakpuri, New Delhi 110058, India.
Satadal DasVirology Laboratory, DAC Regional Research Institute, 50, Rajendra Chatterjee Road, Kolkata 700035, West Bengal, India.

Funding

Central Council for Research in Homeopathy, Ministry of Ayush, Govt. of India 17-24/2020-21/CCRH/Tech./Coll./DACRRI/Haemoglobin/3995
6 · The paper itself

Abstract

BACKGROUND/

objectivesSARS-CoV-2 provokes acute oxidative stress in the lungs via cytokines, inflammatory mediators, and apoptotic factors, which might cause alveolar injury followed by severe respiratory syndrome during COVID-19 infection. The lack of particular antivirals for SARS-CoV-2 has opened novel avenues of complementary and alternative medicine as a potential remedy. The current study explored the mechanistic role of the ultradiluted formulation of Eupatorium (UDE) against SARS-CoV-2 recombinant S protein-mediated oxidative stress and mitochondriopathy.

methodsCell line and BALB/c mice were used to report that SARS-CoV-2 S protein caused an inflammatory response and subsequent cytokine storm via the NF-κB pathway in the lung along with oxidative damage. Morphological examination was performed using DAPI staining and histology for treated cells and lung tissues of animals, respectively. The molecular mechanism of action of UDE was investigated through qRT-PCR for the genetic expressions of various cytokines, inflammatory, and apoptotic mediators; ELISA, immunofluorescence, immunohistochemistry, and Western blot for the translational expression of the same molecules assayed for genetic expressions; and biochemical assays for various enzymes and ROS.

resultsUDE treatment suppressed the inflammatory cell infiltration and tissue-level oxidative stress and safeguarded mitochondrial integrity from free radical-mediated oxidative damage. Additionally, UDE played a direct role in restoring cellular redox homeostasis and reducing the inflammatory response by suppressing NF-κB, IL-1β, IL-18, caspase-1 expression, and ROS formation. Further, a plausible mechanism of action of UDE against S protein-induced damage was proposed.

conclusionsThis study described a novel therapeutic approach against S protein-mediated hyperinflammation, apoptosis, and oxidative damage. Hence, UDE may be considered as a prospective alternative to combat life-threatening consequences of SARS-CoV-2 infection.

Indexed as

cytokinesmitochondriaoxidative stressROSSARS-CoV-2S protein

Identifiers

PMID39997043
PMCPMC11854276

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.