Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Effects of pioglitazone and metformin on carbohydrate metabolism in experimental models of glucose intolerance

View through CrossRef
The aim of the study was to compare the effects of pioglitazone and metformin on carbohydrate metabolism in diabetic and insulin resistant rats. Male albino rats were randomized into seven groups. The first, control group received high carbohydrate diet. The second, third and fourth groups were fed high fat diets for 6 weeks and either left untreated, or given pioglitazone (2.7 mg/kg/day) or metformin (180 mg/kg/day) in the last 3 weeks. The 5th, 6th, and 7th groups were made diabetic by single intraperitoneal injection of streptozotocin (STZ, 50 mg/kg) on day 15 of the 6-week high fat regimen. They were either left untreated, or given pioglitazone or metformin in the last 3 weeks. High fat diet induced insulin resistance evidenced by increased serum glucose, associated with increase in liver glucose-6-phosphatase and decrease in liver glucose-6-phosphate dehydrogenase and glucokinase activities. No significant difference was observed between rats treated with either pioglitazone or metformin. Both treatments showed significant increase in glucose-6-phosphate dehydrogenase activity by ~20 %, decrease in glucose-6-phosphatase activity by ~25 %, and decreases in liver and kidney glycogen. In diabetic rats, both pioglitazone and metformin decreased elevated serum glucose by ~30 %. Only metformin caused more than 2-fold increase in hepatic glycogen content, and normalized glucose-6-phosphatase activity. Only pioglitazone normalized elevated renal glycogen content and increased glucose-6-phosphate dehydrogenase activity. In conclusion pioglitazone and metformin had comparable effects on estimates of carbohydrate metabolism and insulin sensitivity in insulin resistant rats, but different effects in diabetic rats.
Title: Effects of pioglitazone and metformin on carbohydrate metabolism in experimental models of glucose intolerance
Description:
The aim of the study was to compare the effects of pioglitazone and metformin on carbohydrate metabolism in diabetic and insulin resistant rats.
Male albino rats were randomized into seven groups.
The first, control group received high carbohydrate diet.
The second, third and fourth groups were fed high fat diets for 6 weeks and either left untreated, or given pioglitazone (2.
7 mg/kg/day) or metformin (180 mg/kg/day) in the last 3 weeks.
The 5th, 6th, and 7th groups were made diabetic by single intraperitoneal injection of streptozotocin (STZ, 50 mg/kg) on day 15 of the 6-week high fat regimen.
They were either left untreated, or given pioglitazone or metformin in the last 3 weeks.
High fat diet induced insulin resistance evidenced by increased serum glucose, associated with increase in liver glucose-6-phosphatase and decrease in liver glucose-6-phosphate dehydrogenase and glucokinase activities.
No significant difference was observed between rats treated with either pioglitazone or metformin.
Both treatments showed significant increase in glucose-6-phosphate dehydrogenase activity by ~20 %, decrease in glucose-6-phosphatase activity by ~25 %, and decreases in liver and kidney glycogen.
In diabetic rats, both pioglitazone and metformin decreased elevated serum glucose by ~30 %.
Only metformin caused more than 2-fold increase in hepatic glycogen content, and normalized glucose-6-phosphatase activity.
Only pioglitazone normalized elevated renal glycogen content and increased glucose-6-phosphate dehydrogenase activity.
In conclusion pioglitazone and metformin had comparable effects on estimates of carbohydrate metabolism and insulin sensitivity in insulin resistant rats, but different effects in diabetic rats.

Related Results

SAT031 The Effect Of Metformin On Increasing Glucose Metabolism And Secretion In The Distal Intestine
SAT031 The Effect Of Metformin On Increasing Glucose Metabolism And Secretion In The Distal Intestine
Abstract Disclosure: J. Nam: None. C. Kang: None. J. Oh: None. E. Wang: None. S. Lee: None. J. Hong: None. E. Lee: None. C. Ku: None. Object: Although...
Apoptosis rate and transcriptional response of pancreatic islets exposed to the PPAR gamma agonist Pioglitazone
Apoptosis rate and transcriptional response of pancreatic islets exposed to the PPAR gamma agonist Pioglitazone
Abstract To explore the molecular pathways underlying thiazolidinediones effects on pancreatic islets in conditions mimicking normo- and hyperglycemia, apoptosis rate and...
Abstract 4965: Metformin has an anticancer effect by repressing TWIST/N-cadherin signaling.
Abstract 4965: Metformin has an anticancer effect by repressing TWIST/N-cadherin signaling.
Abstract Introduction and Objective. Metformin, one of the most commonly used medications for treatment of type 2 diabetes, has emerged as a potential anticancer age...
Comparative Toxicological Evaluation of Pioglitazone and Glimepiride in Wistar Rats
Comparative Toxicological Evaluation of Pioglitazone and Glimepiride in Wistar Rats
Introduction: Diabetes mellitus is one of the most common endocrine disorders and affects the body’s ability to produce or effectively utilize insulin. It is ch...

Back to Top