The Anti-Diabetic, Lipidemic, And Pro-Inflammatory Effects of oral hypoglycemic on T2DM Obese Patients

Background: Diabetes complications are the primary causes of DM morbidity and mortality. Objectives: comparing the anti-diabetic, lipidemic, and pro-inflammatory effects of metformin and glibenclamide in treating T2DM-obese patients, suggesting a probable novel mode of action and providing a more comprehensive understanding of T2DM pathophysiology for future therapeutic application. The effect of the adipocytokines and pro-inflammatory cytokines in T2DM was also investigated. Patients and methods: 150 subjects were allocated into five equal groups (n=30): the normal, the obese control, the obese diabetic control, the obese diabetic treated with 500 mg metformin twice daily, and the obese diabetic glibenclamide-treated, receiving 5 mg glibenclamide once daily. The blood samples were collected after six months of treatment. Results and conclusion: Metformin improved BMI, FSG, glycosylated hemoglobin, total cholesterol, and triglycerides, but it raised low-density lipoproteins and lowered high-density lipoproteins. The glibenclamide treatment significantly improved fasting insulin and C-peptide serum levels with subsequent better homeostatic model assessment for insulin resistance, but it increased BMI, TC, and TG. Visfatin and Retinol binding protein-4 showed less improvement in the glibenclamide than in the metformin-treated obese diabetic patients. In contrast, resistin decreased with glibenclamide treatment compared to metformin. The IL-1β expression was higher in the obese diabetic control and declined in the glibenclamide-treated obese diabetic patients while, IL-6, TNF-α, and IFN-γ expression decreased in metformin-treated obese diabetic patients than in glibenclamide ones. Our results also demonstrated a high positive correlation between the adipocytokines, visfatin, resistin, and RBP4 and the pro-inflammatory, cytokines IL-1β, IL-6, TNF-α and IFN-γ. From those results, treatment with metformin is recommended in the cases of obesity, inflammation, hypercholesterolemia, and hypertriglyceridemia. In addition, treatment with glibenclamide is recommended in the cases of insulin resistance and dyslipidemia.

Authors

Institutions

Publication Details

Journal
Egyptian Journal of Chemistry
Published
2024-09-09
DOI
https://doi.org/10.21608/ejchem.2024.310327.10156
Primary Topic
Diabetes Management and Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Anti-Diabetic, Lipidemic, And Pro-Inflammatory Effects of oral hypoglycemic on T2DM Obese Patients

Mohammed Abdel‐Gabbar, Ayman M. Abdel‐Aziz, Hader I. Sakr, Naglaa Hamdy et al.
Egyptian Journal of Chemistry
Diabetes Management and Research
article

The Anti-Diabetic, Lipidemic, And Pro-Inflammatory Effects of oral hypoglycemic on T2DM Obese Patients

Mohammed Abdel‐Gabbar, Ayman M. Abdel‐Aziz, Hader I. Sakr, Naglaa Hamdy, Mohamed Kandeal, S. Gaber, Osama Ahmed
article en

Abstract

Background: Diabetes complications are the primary causes of DM morbidity and mortality. Objectives: comparing the anti-diabetic, lipidemic, and pro-inflammatory effects of metformin and glibenclamide in treating T2DM-obese patients, suggesting a probable novel mode of action and providing a more comprehensive understanding of T2DM pathophysiology for future therapeutic application. The effect of the adipocytokines and pro-inflammatory cytokines in T2DM was also investigated. Patients and methods: 150 subjects were allocated into five equal groups (n=30): the normal, the obese control, the obese diabetic control, the obese diabetic treated with 500 mg metformin twice daily, and the obese diabetic glibenclamide-treated, receiving 5 mg glibenclamide once daily. The blood samples were collected after six months of treatment. Results and conclusion: Metformin improved BMI, FSG, glycosylated hemoglobin, total cholesterol, and triglycerides, but it raised low-density lipoproteins and lowered high-density lipoproteins. The glibenclamide treatment significantly improved fasting insulin and C-peptide serum levels with subsequent better homeostatic model assessment for insulin resistance, but it increased BMI, TC, and TG. Visfatin and Retinol binding protein-4 showed less improvement in the glibenclamide than in the metformin-treated obese diabetic patients. In contrast, resistin decreased with glibenclamide treatment compared to metformin. The IL-1β expression was higher in the obese diabetic control and declined in the glibenclamide-treated obese diabetic patients while, IL-6, TNF-α, and IFN-γ expression decreased in metformin-treated obese diabetic patients than in glibenclamide ones. Our results also demonstrated a high positive correlation between the adipocytokines, visfatin, resistin, and RBP4 and the pro-inflammatory, cytokines IL-1β, IL-6, TNF-α and IFN-γ. From those results, treatment with metformin is recommended in the cases of obesity, inflammation, hypercholesterolemia, and hypertriglyceridemia. In addition, treatment with glibenclamide is recommended in the cases of insulin resistance and dyslipidemia.

Egyptian Journal of ChemistryVol. 0(0)
Beni-Suef University (EG), Seva Mandir (IN), Fayoum University (EG)
Good health and well-being
Openalex Percentile: Top 77%
Diabetes Management and Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.