Literature DB >> 33553033

Investigation of the synergistic effect of glimepiride and rosuvastatin on alloxan-induced diabetic rat.

Debashish Mondol1, Md Nahinul Islam1, Sonchita Biswas1, Protic Jodder1, Samiron Sana1, Md Abu Saleh2, Md Rafiqul Islam1.   

Abstract

PURPOSE: Diabetes mellitus is characterized by having a multitude of life-threatening secondary complications, particularly dyslipidemia, which ultimately leads to the development of comorbid diseases, such as cardiovascular diseases. This research work was designed to investigate the synergistic effect of glimepiride (1 mg/kg b.w.) and rosuvastatin (10 mg /kg b.w.) on alloxan-induced diabetic rats having dyslipidemia.
METHODS: Diabetes was induced by injecting alloxan (120 mg/kg b.w.) intraperitoneally. The experiment was conducted to determine the level of blood glucose, HbA1c, lipid profile, and body weight variation of rats.
RESULTS: This study's outcomes suggested that the combination therapy showed more statistically significant effect on blood glucose level, HbA1c level, lipid profile, and body weight variation than any single therapy. While the glimepiride monotherapy showed a statistically considerable effect on blood glucose level, HbA1c level, and body weight variation, the rosuvastatin treated group gave statistically non-significant effect on these parameters except body weight variation, which was found as downward trend. In addition, the rosuvastatin treated group showed a healthy lipid profile compared to glimepiride treated group.
CONCLUSIONS: Concluding the results of this study, it can be said that the treatment of glimepiride in combination with rosuvastatin may be more efficacious than monotherapy for preventing diabetes in rats with dyslipidemia. © Springer Nature Switzerland AG 2020.

Entities:  

Keywords:  Alloxan; Cardiovascular disease; Combination therapy; Diabetes; Dyslipidemia; Hyperglycemia

Year:  2020        PMID: 33553033      PMCID: PMC7843842          DOI: 10.1007/s40200-020-00662-6

Source DB:  PubMed          Journal:  J Diabetes Metab Disord        ISSN: 2251-6581


  38 in total

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