Evidence map›Paper›PMID 41789243›Full record

ArticleAnnals of medicine and surgery (2012)2026

Antihyperglycemic and antioxidant potential of

Antonia R Lyngdoh, Sumira Malik, Ankita Dey, Caster Marbaniang, Ridashisha Rymbai, Nayan Talukdar, Shailendra Thapliyal, Sarvesh Rustagi, Ravi Kumar Deshwal, Surya Bhan and 1 more

Abstract read
In one paragraph

Article in Annals of medicine and surgery (2012), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Antonia R LyngdohBiochemistry Department, North Eastern Hill University, Shillong, Meghalaya, India.
Sumira MalikAmity Institute of Biotechnology, Amity University Jharkhand, Ranchi, India.
Ankita DeyUniversity Centre for Research and Development University of Biotechnology, Chandigarh University, Gharuan Mohali, Punjab, India.
Caster MarbaniangUniversity Centre for Research and Development University of Biotechnology, Chandigarh University, Gharuan Mohali, Punjab, India.
Ridashisha RymbaiUniversity Centre for Research and Development University of Biotechnology, Chandigarh University, Gharuan Mohali, Punjab, India.
Nayan TalukdarProgram of Biotechnology, Faculty of Science, Assam down town University, Guwahati, Assam, India.
Shailendra ThapliyalSchool of Agriculture, Uttaranchal University, Dehradun, Uttarakhand, India.
Sarvesh RustagiDepartment of Food Technology, School of Agriculture, Maya Devi University, Dehradun, Uttrakhand, India.
Ravi Kumar DeshwalInstitute of Bioscience and Technology, Shri Ramswaroop Memorial University, Lucknow-Deva Road, Uttar Pradesh, India.
Surya BhanBiochemistry Department, North Eastern Hill University, Shillong, Meghalaya, India.
Jutishna BoraAmity Institute of Biotechnology, Amity University Jharkhand, Ranchi, India.ORCID https://orcid.org/0000-0003-2390-9244

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: The research aimed to access the antihyperglycemic and antioxidant properties of the methanolic extract of Objective: The objective aims to examine the effects of MECC on fasting blood glucose (FBG), glucose tolerance, antioxidant enzyme activity, lipid peroxidation, and histopathological alterations in the liver and kidneys of diabetic mice. Method: Male Swiss albino mice were categorized into normal untreated control, diabetic untreated control, and diabetic + ascorbic acid-treated, diabetic + MECC treated (350 mg/kg body weight [b.w.]). Diabetes was induced using STZ, and the effects of MECC were assessed through FBG, intraperitoneal glucose tolerance tests, and measurement of oxidative stress markers such as thiobarbituric acid reactive Substances (TBARS), superoxide dismutase (SOD), and catalase (CAT). Histopathological analysis of kidney and liver tissues was performed to evaluate tissue damage and recovery. Results: MECC treatment at 350 mg/kg b.w. significantly decreased the FBG levels in diabetic control mice, with effects comparable to standard antihyperglycemic drugs like metformin and glibenclamide. Glucose tolerance was notably improved, and oxidative stress markers, including TBARS, were normalized in treated groups. Antioxidant enzyme activity (SOD and CAT) was restored in the liver and kidneys. Histopathological analysis revealed substantial recovery of tissue architecture, with nearly normal glomeruli and hepatocytes in diabetic-MECC-treated mice, indicating protection against diabetes-induced damage. Conclusion: MECC demonstrated potent antihyperglycemic, antioxidant, and tissue-protective effects in diabetic mice, suggesting its capability as a treatment option for diabetes management. Further evaluation is needed to investigate its potential clinical uses.

Indexed as

antioxidantCurcuma caesiamethanolic extract of Curcuma caesiaoxidative stress

Identifiers

PMID41789243
PMCPMC12959782

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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.