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  • Print ISSN: 1811-9506

  • Online ISSN: 2218-3973

  • Starting year: 2004

  • Current volume: 22

  • Impact Factor (Scopus) : 0.737


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Bioscience Research, volume 22, issue 2 (April-June), 2025

     

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RESEARCH ARTICLE                      BIOSCIENCE RESEARCH, 2025 22(2): 113-118.                     OPEN ACCESS

                                                                                                  

 

Comparative study of oral antidiabetic medications on the Rat Model

 

Patience Nwonu1, Chukwunwike Nwonu2, Bonaventure Obi1, Theophine Akunne1, Chisom Ekeugo1, and Adaobi Ezike1

 

1Department of Pharmacology & Toxicology, Faculty of Pharmaceutical Sciences, University of Nigeria, Nsukka, P.M.B. 410001, Enugu, Enugu State, Nigeria

2Department of Pharmacology & Therapeutics, Faculty of Basic Clinical Sciences, College of Health Sciences, Rev. Fr. Moses Orshio Adasu University, P.M.B. 102343, Makurdi, Benue State, Nigeria         

                        

DOI:

 

Abstract

Introduction: In recent times, comparing the effects of oral antidiabetic agents as monotherapy or in combination in controlling diabetes mellitus and other related complications has become increasingly apparent. The study examined the effects of acarbose (AC), pioglitazone (PGZ), and vildagliptin (VDG) on glycaemic control, as well as on biochemical indices in an alloxan-induced diabetic rat model. Materials and Methods: Adult Wistar rats were induced with diabetes through the alloxan monohydrate (100 mgkg-1; i.v.) administration. Five (5) groups of rats were utilized (n=6); group 1 filled in as the normal control, group 2 filled in as diabetic control group 3, while 4 and 5 were the diabetic experimental groups that got 30 mgkg-1day-1 of AC, PGZ, and VDG. Results: The study analysed the effects of aspartate aminotransferase (AST), agents on blood glucose, low-density lipoprotein (LDL-C), alanine aminotransferase (ALT), high-density lipoprotein, total cholesterol (TC), alanine phosphatase, and triacylglycerol (TAG) activities. In diabetic rats administered AC (P<0.05), the result demonstrated [VDG (P<0.05) and PGZ (P>0.05)] marked decreases in the blood glucose levels. The serum TC, LDL-C, and TAG levels were significant in the AC (P<0.05) and VDG (P<0.05) groups, and were additionally decreased in every treated group, the serum TAG level was insignificantly (P>0.05) diminished in diabetic rats administered PGZ. Likewise, in every single treated group compared with the diabetic control group, ALP, AST, and ALT were significantly (P<0.05) reduced. Conclusion: The administration of AC, PGZ, and VDG displayed significant improvement in the biochemical indices altered during diabetic-related manifestations in the experimental subjects. However, VDG demonstrated superior anti-hyperglycaemic adequacy.

Keywords: Diabetes mellitus, Blood glucose, Alloxan, Lipoproteins, Liver enzymes

 

 

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