Relative potency of protease inhibitors on glucose-insulin homeostasis, hemoglobin and glycosylated hemoglobin in normal rats

2009 
The present study has been carried out to investiga te the relative potency of protease inhibitors (indinavir, ritonavir and atazanavir) on glucose-insulin homeostasis, hemoglobin and glycosylated hemoglobin in normal rats following oral administration for a period of 30 days. The effects of protease inhibi tors were compared with normal control rats. Blood samples were collected from retro orbit al puncture and the parameters observed are blood glucose, insulin, total hemoglob in, glycosylated hemoglobin and body weight. The insulin resistance index and percent be ta cell function were determined by homeostasis model assessment (HOMA-1 and HOMA-2) models. Percent insulin sensitivity was determined by HOMA-2 model. Indinavir and ritonavir were significantly (p<0.05) elevated the blood glucose, insulin, insul in resistance index and glycosylated hemoglobin values and decreased the total hemoglobin, beta cell function, insulin sensitivity and body weights when compared to control rats. The alterations associated with indinavir are more compared to ritonavir treat ed rats. Atazanavir has not shown any significant effect on any parameter when compared t o control rats, except increase in body weight. From this study we conclude that gluco se-insulin homeostasis disorders associated with protease inhibitors are not a class specific, but are drug specific. Thus, it can be concluded that atazanavir is having safe pro file compared to indinavir and ritonavir with respect to glucose-insulin homeostas is. Indinavir and ritonavir are having potent tendency to alter the glucose homeostasis an d insulin profile to produce the events related to type 2 diabetes. So care should be taken when the indinavir and ritonavir are prescribed for their clinical benefit in diabetic p atients.
    • Correction
    • Source
    • Cite
    • Save
    • Machine Reading By IdeaReader
    1
    References
    0
    Citations
    NaN
    KQI
    []