Evidence map›Paper›PMID 36558918›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

Natural Compounds of

Md Mamunur Rashid, Md Atiar Rahman, Md Shahidul Islam, Md Amjad Hossen, A M Abu Ahmed, Mirola Afroze, Alaa H Habib, Manal M S Mansoury, Hend F Alharbi, Reham M Algheshairy and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Correction: Rashid et al. Natural Compounds ofPharmaceuticals (Basel, Switzerland) · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 3 countries.

Md Mamunur RashidDepartment of Biochemistry and Molecular Biology, University of Chittagong, Chittagong 4331, Bangladesh.
Md Atiar RahmanDepartment of Biochemistry and Molecular Biology, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0002-4902-8923
Md Shahidul IslamDepartment of Biochemistry and Molecular Biology, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0003-1297-5895
Md Amjad HossenDepartment of Pharmacy, Faculty of Science and Engineering, International Islamic University Chittagong, Chittagong 4318, Bangladesh.ORCID 0000-0003-2850-1635
A M Abu AhmedDepartment of Genetic Engineering and Biotechnology, University of Chittagong, Chittagong 4331, Bangladesh.
Mirola AfrozeBangladesh Reference Institute for Chemical Measurements (BRiCM), Dr. Qudrat-e-Khuda Road (Laboratory Road), Dhanmondi, Dhaka 1205, Bangladesh.
Alaa H HabibDepartment of Physiology, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-9198-7714
Manal M S MansouryDepartment of Physiology, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Hend F AlharbiDepartment of Food Science and Human Nutrition, College of Agriculture and Veterinary Medicine, Qassim University, Buraydah 51452, Saudi Arabia.ORCID 0000-0003-2280-9225
Reham M AlgheshairyDepartment of Food Science and Human Nutrition, College of Agriculture and Veterinary Medicine, Qassim University, Buraydah 51452, Saudi Arabia.ORCID 0000-0002-9934-0691
Walla AlelwaniDepartment of Biochemistry, Collage of Science, University of Jeddah, Jeddah 80203, Saudi Arabia.
Afnan M AlnajeebiDepartment of Biochemistry, Collage of Science, University of Jeddah, Jeddah 80203, Saudi Arabia.ORCID 0000-0002-5670-1688
Jitbanjong TangpongSchool of Allied Health Sciences, Walailak University, Nakhon Si Thammarat 80160, Thailand.
Srabonti SahaDepartment of Biochemistry and Molecular Biology, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0002-8844-345X
Alaa QadhiClinical Nutrition Department, Faculty of Applied Medical Sciences, Umm Al-Qura University, P.O. Box 715, Makkah 21955, Saudi Arabia.
Wedad AzharClinical Nutrition Department, Faculty of Applied Medical Sciences, Umm Al-Qura University, P.O. Box 715, Makkah 21955, Saudi Arabia.
University of Chittagong · BDKing Abdulaziz University · SAQassim University · SAUmm al-Qura University · SAUniversity of Jeddah · SABangladesh Reference Institute for Chemical MeasurementsInternational Islamic University Chittagong · BDWalailak University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural biometabolites of plants have been reported to be useful in chronic diseases including diabetes and associated complications. This research is aimed to investigate how the biometabolites of Lasia spinosa methanol stem (MEXLS) extract ameliorative diabetes and diabetes-related complications. MEXLS was examined for in vitro antioxidant and in vivo antidiabetic effects in a streptozotocin-induced diabetes model, and its chemical profiling was done by gas chromatography-mass spectrometry analysis. The results were verified by histopathological examination and in silico ligand-receptor interaction of characterized natural biometabolites with antidiabetic receptor proteins AMPK (PDB ID: 4CFH); PPARγ (PDB ID: 3G9E); and mammalian α-amylase center (PDB ID: 1PPI). The MEXLS was found to show a remarkable α-amylase inhibition (47.45%), strong antioxidant action, and significant (p < 0.05) decrease in blood glucose level, serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), low-density lipoprotein (LDL), urea, uric acid, creatinine, total cholesterol, triglyceride (TG), liver glycogen, creatinine kinase (CK-MB), and lactate dehydrogenase (LDH) and increase in serum insulin, glucose tolerance, and high-density lipoprotein (HDL). Rat’s pancreas and kidney tissues were found to be partially recovered in histopathological analyses. Methyl α-d-galactopyranoside displayed the highest binding affinity with AMPK (docking score, −5.764), PPARγ (docking score, −5.218), and 1PPI (docking score, −5.615) receptors. Data suggest that the MEXLS may be an exciting source to potentiate antidiabetic activities affirming a cell-line study.

Indexed as

AMPKdiabetes mellitusLasia spinosaMethyl α-d-galactopyranosidemethyl α-d-glucopyranosidePPARγ

Identifiers

PMID36558918
PMCPMC9781412
OpenAlexW4310187872

What OpenQuestion holds

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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.