Type 2 diabetes is caused by insulin resistance coupled with an inability to produce enough insulin to control blood glucose, and thiazolidinediones (TZDs) are the only current antidiabetic agents that function primarily by increasing insulin sensitivity. However, despite clear benefits in glycemic control, this class of drugs has recently fallen into disuse due to concerns over side effects and adverse events. Here we review the clinical data and attempt to balance the benefits and risks of TZD therapy. We also examine potential mechanisms of action for the beneficial and harmful effects of TZDs, mainly via agonism of the nuclear receptor PPARγ. Based on critical appraisal of both preclinical and clinical studies, we discuss the prospect o...
Peroxisome proliferator-activated receptor (PPAR) is involved in the pathology of numerous diseases ...
Thiazolidinediones (TZDs) are PPARγ ligands and the newest class of agents in routine clinical pract...
G Protein-coupled receptor 120 (GPR120; fatty acid receptor 4, FFAR4) and PPARγ agonists both lead t...
Type 2 diabetes is caused by insulin resistance coupled with an inability to produce enough insulin ...
The incidence of type 2 diabetes mellitus (T2DM) is increasing, caused by our growingly obese popula...
ABSTRACTThe incidence of type 2 (T2D) diabetes and other chronic conditions associated with insulin ...
Thiazolidinediones (TZDs), such as rosiglitazone and pioglitazone, are peroxisome proliferator-activ...
AbstractThiazolidinedione (TZD) is a powerful insulin sensitizer in the treatment of type 2 diabetes...
Thiazolidinediones, which are being developed for the treatment of insulin resistance and type 2 dia...
Abstract: Insulin sensitizing thiazolidinediones (TZDs) are generally considered to work as agonists...
Glitazones or thiazolidinediones (TZDs) are a class of oral insulin sensitizing agents. They act on ...
The thiazolidinediones (TZDs; see Fig. 1) are peroxisome proliferator–activated receptor (PPAR) ago...
Although peroxisome proliferator-activated receptor gamma (PPARγ) agonists such as thiazolidinedione...
Thiazolidinediones (TZDs), such as rosiglitazone and pioglitazone, are peroxisome proliferator-activ...
Peroxisome proliferator-activated receptor (PPAR) is involved in the pathology of numerous diseases ...
Peroxisome proliferator-activated receptor (PPAR) is involved in the pathology of numerous diseases ...
Thiazolidinediones (TZDs) are PPARγ ligands and the newest class of agents in routine clinical pract...
G Protein-coupled receptor 120 (GPR120; fatty acid receptor 4, FFAR4) and PPARγ agonists both lead t...
Type 2 diabetes is caused by insulin resistance coupled with an inability to produce enough insulin ...
The incidence of type 2 diabetes mellitus (T2DM) is increasing, caused by our growingly obese popula...
ABSTRACTThe incidence of type 2 (T2D) diabetes and other chronic conditions associated with insulin ...
Thiazolidinediones (TZDs), such as rosiglitazone and pioglitazone, are peroxisome proliferator-activ...
AbstractThiazolidinedione (TZD) is a powerful insulin sensitizer in the treatment of type 2 diabetes...
Thiazolidinediones, which are being developed for the treatment of insulin resistance and type 2 dia...
Abstract: Insulin sensitizing thiazolidinediones (TZDs) are generally considered to work as agonists...
Glitazones or thiazolidinediones (TZDs) are a class of oral insulin sensitizing agents. They act on ...
The thiazolidinediones (TZDs; see Fig. 1) are peroxisome proliferator–activated receptor (PPAR) ago...
Although peroxisome proliferator-activated receptor gamma (PPARγ) agonists such as thiazolidinedione...
Thiazolidinediones (TZDs), such as rosiglitazone and pioglitazone, are peroxisome proliferator-activ...
Peroxisome proliferator-activated receptor (PPAR) is involved in the pathology of numerous diseases ...
Peroxisome proliferator-activated receptor (PPAR) is involved in the pathology of numerous diseases ...
Thiazolidinediones (TZDs) are PPARγ ligands and the newest class of agents in routine clinical pract...
G Protein-coupled receptor 120 (GPR120; fatty acid receptor 4, FFAR4) and PPARγ agonists both lead t...