Evidence map›Paper›PMID 35478935›Full record

ArticleDrug design, development and therapy2022

Analagesic and Anti-Inflammatory Potentials of a Less Ulcerogenic Thiadiazinethione Derivative in Animal Models: Biochemical and Histochemical Correlates.

Khista Rahman, Gowhar Ali, Rasool Khan, Imad Khan, Izaz Ali, Osama F Mosa, Alshebli Ahmed, Muhammad Ayaz, Asif Nawaz, H C Ananda Murthy

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. 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
1.4field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

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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

10 authors at 6 institutions in 6 countries.

Khista RahmanDepartment of Pharmacy, University of Peshawar, Peshawar, Pakistan.
Gowhar AliDepartment of Pharmacy, University of Peshawar, Peshawar, Pakistan.ORCID 0000-0002-9749-0645
Rasool KhanInstitute of Chemistry Sciences, University of Peshawar, Peshawar, Pakistan.
Imad KhanInstitute of Chemistry Sciences, University of Peshawar, Peshawar, Pakistan.
Izaz AliDepartment of Pharmacy, University of Peshawar, Peshawar, Pakistan.
Osama F MosaPublic Health Department,Health Sciences College at Lieth, Umm Al Qura University, Makkah, Kingdom of Saudi Arabia.
Alshebli AhmedPublic Health Department,Health Sciences College at Lieth, Umm Al Qura University, Makkah, Kingdom of Saudi Arabia.ORCID 0000-0001-8083-9145
Muhammad AyazDepartment of Pharmacy, Faculty of Biological Sciences, University of Malakand, Chakdara, 18000, Dir (L), KP, Pakistan.ORCID 0000-0002-4299-2445
Asif NawazDepartment of Pharmacy, Faculty of Biological Sciences, University of Malakand, Chakdara, 18000, Dir (L), KP, Pakistan.
H C Ananda MurthyDepartment of Applied Chemistry, School of Applied Natural Science, Adama Science and Technology University, Adama, Ethiopia.ORCID 0000-0002-2361-086X
University of Peshawar · PKUniversity of Malakand · PKAdama Science and Technology University · ETNorthwestern University · USUmm al-Qura University · SAUniversity of Khartoum · SD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Gastric ulcer induced by NSAIDs is the major medical concern and researchers are utilizing several approaches to combat this medical issue. In the current study, we investigated the efficacy of thiadiazinethione derivative (2,2'(2-thioxo-1,3,5-thiadiazinane-3,5-diyl) diacetic acid, as new less ulcerogenic compound. Methods: 2,2'(2-thioxo-1,3,5-thiadiazinane-3,5-diyl) diacetic acid was evaluated using standard animal models including hot plate, writhing test and formalin induced nociceptive models. Anti-inflammatory activity was assessed via carrageenan-induced paw oedema model. Involvement of opioidergic nociceptive mechanism was confirmed via naloxone administration in hot plat assay. The gastro-ulcerogenic potential of test and standard compounds were evaluated via NSAID-induced pyloric ligation model followed by standard histopathological and biochemical analysis. Results: In acetic acid-induced writhing test, our compound significantly reduced abdominal constrictions at the tested doses of 15 ( Conclusion: Our findings suggests that our test compound has desirable anti-nociceptive and anti-inflammatory potentials with less propensity to cause gastric ulcer.

Indexed as

Stomach UlcerTramadolAnalgesicsAnimalsAnti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalAspirinCarrageenanEdemaFormaldehydeNaloxoneUlcerAnalgesicsAnti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalAspirinCarrageenanFormaldehydeNaloxoneTramadolgastric ulcerhot plateinflammationnociceptionNSAIDs

Identifiers

PMID35478935
PMCPMC9037714
OpenAlexW4224272823

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.