Back to Search Start Over

Introducing Coffee as a Complementary Agent Beside Metformin Against Type 2 Diabetes

Authors :
Majid Rezaei Tavirani
Masoumeh Farahani
Mostafa Rezaei Tavirani
Zahra Razzaghi
Babak Arjmand
Mahmood Khodadoost
Source :
Research Journal of Pharmacognosy, Vol 11, Iss 3, Pp 31-40 (2024)
Publication Year :
2024
Publisher :
Iranian Society of Pharmacognosy, 2024.

Abstract

Background and objectives: Positive role of coffee consumption on regulation of human blood sugar has been highlighted by researchers. On the other hand, metformin is the common drug against type 2 diabetes. This study aimed to explore possible ways to use coffee as a complementary agent beside metformin or independently versus type 2 diabetes. Methods: Proteomic data about effect of two major compounds of coffee (caffeine and trigonelline) on improvement of diabetic condition was searched and analyzed via protein-protein interaction (PPI) network analysis and gene ontology enrichment. Gene expression profiles of human whole blood of diabetic patients (responsive to metformin) versus control were extracted from GSE83983 which is recorded in Gene Expression Omnibus (GEO) database. After pre-evaluation of data by GEO2R program, the significant differentially expressed genes (DEGs) were assessed via PPI network analysis and regulatory network evaluation. Results: Caffeine and trigonelline effectively regulate the glycolytic processes to fight against diabetic condition. HSP90AA1, TLR4, RELA, ARRB, LRRK2, STAT5B, LYN, and TLR2 genes that are involved in diabetes were affected significantly by metformin. Conclusion: It can be concluded that coffee consumption can improve sugar regulation in diabetes similar to metformin. IT seems that the optimized consumption quantity of coffee can be considered as controller of blood sugar in diabetic patients.

Details

Language :
English
ISSN :
23454458 and 23455977
Volume :
11
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Research Journal of Pharmacognosy
Publication Type :
Academic Journal
Accession number :
edsdoj.9c2881d06b24466e8c1b430e34963a76
Document Type :
article
Full Text :
https://doi.org/10.22127/rjp.2024.418824.2239