Evidence map›Paper›PMID 30809222›Full record

ArticleFrontiers in immunology2019

Podophyllotoxin and Rutin Modulate M1 (iNOS+) Macrophages and Mitigate Lethal Radiation (LR) Induced Inflammatory Responses in Mice.

Vinod Nadella, Rajiv Ranjan, Balasubramanian Senthilkumaran, S S Y H Qadri, Suresh Pothani, Ajay Kumar Singh, Manju L Gupta, Hridayesh Prakash

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. A derivative of vitamin BScientific reports · 2021
    Article
  5. Flavonoids as Molecules With Anti-Frontiers in microbiology · 2021
    Review
  6. [Research progress on macrophage in radiation induced lung injury].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2020
    Review
  7. Review
  8. Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Vinod NadellaLaboratory of Translational Medicine, School of Life Science, University of Hyderabad, Hyderabad, India.
Rajiv RanjanInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development Organization, New Delhi, India.
Balasubramanian SenthilkumaranDepartment of Animal Biology, School of Life Sciences, University of Hyderabad, Hyderabad, India.
S S Y H QadriNational Institute of Nutrition, Indian Council of Medical Research Hyderabad, Hyderabad, India.
Suresh PothaniNational Animal Resource Facility for Bio-Medical Research, Indian Council of Medical Research Hyderabad, Hyderabad, India.
Ajay Kumar SinghInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development Organization, New Delhi, India.
Manju L GuptaInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development Organization, New Delhi, India.
Hridayesh PrakashLaboratory of Translational Medicine, School of Life Science, University of Hyderabad, Hyderabad, India.
Institute of Nuclear Medicine & Allied Sciences · INUniversity of Hyderabad · INIndian Council of Medical Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accidental exposure to lethal doses of Gamma radiation leads to the systemic inflammatory syndrome which causes mortality. In view of this, management of hemopoietic syndrome by modulating pro-inflammatory response in clinically manageable time period seems to be the most appropriate strategy for encountering radiation induced damage and recovery. As both tissue and peripheral macrophages are critical for the management of radiation induced injuries, we have unraveled the immunomodulatory potential of radioprotective formulation (G-003M) on peripheral macrophages populations in this study. G-003M inhibited lethal radiation induced NO and Th1 effector cytokines in the exposed macrophages indicating its M1 dim polarizing capacity. In similar lines, conditioning of mice with G-003M before lethal irradiation (LR) inhibited LR induced titre of Th1 effector cytokines in both serums as well as in lung, small intestine, and spleen tissue confirming its immunomodulatory potential. G-003M potentially down modulated inflammatory response in LPS induced inflammatory model and enhanced M2 polarization of iNOS+ M1 effector macrophages providing a molecular hint on G-003M mechanism of action on macrophages. These observations revealed that G-003M potentially modulate pro-inflammatory programming of macrophages and mitigate radiation-induced inflammatory stress which is believed to contribute significantly to radioprotective attribute of G-003M. In this study, we demonstrate that Rutin and Podophyllotoxin drive M1

Indexed as

AnimalsCell DifferentiationCells, CulturedCytokinesGamma RaysHumansImmunomodulationMacrophagesMiceMice, Inbred C57BLNitric OxideNitric Oxide Synthase Type IIPodophyllotoxinRadiation InjuriesRutinTh1 CellsCytokinesNitric OxideNitric Oxide Synthase Type IIPodophyllotoxinRutinimmune tolerancemacrophages polarizationradiation syndromeradioprotectionTh1/2 response

Identifiers

PMID30809222
PMCPMC6379314
OpenAlexW2913368179

What OpenQuestion 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 OpenQuestion graph.