Back to Search Start Over

Combination of Metformin and Magnesium Citrate Reduces TNF-α, NF-κB p65, IL-6, CD4, and MMP-9 Expressions in Diabetic Model Rats

Authors :
Rachmi Fauziah Rahayu
Adi Prayitno
Bambang Purwanto
Widiastuti Soewondo
Ida Nurwati
Eti Poncorini Pamungkasari
Paramasari Dirgahayu
Source :
Indonesian Biomedical Journal, Vol 16, Iss 6, Pp 546-52 (2024)
Publication Year :
2024
Publisher :
Secretariat of The Indonesian Biomedical Journal, 2024.

Abstract

BACKGROUND: Diabetes, which causes various complications, involves pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), nuclear factor kappa B p65 (NF-κB p65), interleukin-6 (IL-6), cluster of differentiation 4 (CD4), and matrix metalloproteinase-9 (MMP-9). Magnesium has demonstrated anti-diabetic properties, but its anti-inflammatory effects in preventing cardiovascular complications remain unclear. This study aimed to evaluate the anti-inflammatory effects of magnesium citrate, alone and in combination with metformin, by measuring TNF-α, NF-κB p65, IL-6, CD4, and MMP-9 expression in diabetic model rats. METHODS: Thirty male Wistar rats were divided into five groups: normal control, diabetes control, metformin (treated with 9 mg/200 g/day metformin), magnesium citrate (treated with 3.6 mg/200 g/day magnesium citrate), and combination therapy (treated with 4.5 mg/200 g/day metformin + 1.8 mg/200 g/day magnesium citrate). Diabetes was induced in all groups except the normal control group using streptozotocin (STZ) and nicotinamide (NA). TNF-α, NF-κB p65, IL-6, CD4, and MMP-9 expression levels were measured using enzyme-linked immunosorbent assay (ELISA). RESULTS: Significant differences in TNF-α, NF-κB p65, IL-6, CD4, and MMP-9 expression levels were observed across all groups (p

Subjects

Subjects :
Medicine (General)
R5-920

Details

Language :
English
ISSN :
20853297 and 23559179
Volume :
16
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Indonesian Biomedical Journal
Publication Type :
Academic Journal
Accession number :
edsdoj.52a15a2d7e4700b4844eab24a7b192
Document Type :
article
Full Text :
https://doi.org/10.18585/inabj.v16i6.3360