Evidence map›Paper›PMID 36366849›Full record

ArticleCurrent topics in medicinal chemistry2022

Co-administration of

Neha Sharma, Anand Kar, Sunanda Panda, Dhananjay Yadav

Abstract read
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In one paragraph

Article in Current topics in medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 2 countries.

Neha SharmaSchool of Life Sciences, Devi Ahilya University, Khandwa Road, Indore, 452017, India.
Anand KarSchool of Life Sciences, Devi Ahilya University, Khandwa Road, Indore, 452017, India.
Sunanda PandaSchool of Life Sciences, Devi Ahilya University, Khandwa Road, Indore, 452017, India.
Dhananjay YadavDepartment of Life Sciences, Yeungnam University, Gyeongsan, 38541, South Korea.
Devi Ahilya Vishwavidyalaya · INYeungnam University · KR

Funding

University Grants Commission, New Delhi F-4-3/2006, BSR/5-26/2007
6 · The paper itself

Abstract

backgroundDiabetes mellitus (DM) is a well-known global metabolic disorder. For its treatment, glibenclamide (GLB) is very often prescribed. However, herbal drugs are considered effective and better alternatives due to their low risk of side effects. This study was conducted to determine the combined effects of GLB and Pterocarpus marsupium (PM, a commonly available Indian herb) extract for the effective and safe treatment of hyperglycemia in the mouse model.

methodsHealthy adult male mice were distributed into five groups (n=7 in each group). Group I acted as the control, whereas groups II, III, IV, and V were considered experimental groups which received a single dosage (150 mg/kg body weight) of alloxan (ALX) intraperitoneally (i.p.). In addition, groups III, IV, and V received a pre-standardized dose of GLB (500 μg/kg body weight), PM extract (150 mg/kg body weight), and GLB+PM, respectively, at the same doses as used in individual treatment, after the seventh day of ALX administration for 15 days and the alterations in different DM related parameters were evaluated.

resultsALX-induced hyperglycemia and other adverse effects were nearly normalized by GLB and PM co-treatment as evidenced by marked suppression in glucose, triglyceride, total-cholesterol, lipid-peroxidation, and lipid-hydroperoxides with an increase in antioxidants status and liver glycogen content. The positive effects were more pronounced when both GLB and PM were given, as compared to that of either of the drugs, administered alone. Liver ultra-structure, analyzed through histology and transmission electron microscopy revealed normalization of the ALX-induced damaged hepatocytes. The presence of epicatechin, the major phytoconstituent of the PM extract, as confirmed by high-performance liquid chromatography (HPLC), is responsible for its antioxidative and glucose-lowering activities.

conclusionThese findings reveal that PM, along with GLB, exhibits synergistic and better effects than the individual drug in regulating hyperglycemia and associated changes in alloxan-induced mice.

Indexed as

Diabetes Mellitus, ExperimentalHyperglycemiaAlloxanAnimalsAntioxidantsBlood GlucoseBody WeightGlucoseGlyburideHypoglycemic AgentsLipidsMaleMicePhytotherapyPlant ExtractsPterygotaAlloxanAntioxidantsBlood GlucoseGlucoseGlyburideHypoglycemic AgentsLipidsPlant ExtractsAntioxidantsDiabetes mellitusGlibenclamide.HistopathologyOxidative stressPterocarpus marsupium

Identifiers

PMID36366849
OpenAlexW4308772236

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.