Back to Search
Start Over
PAMAM G4 dendrimers lower high glucose but do not improve reduced survival in diabetic rats.
- Source :
-
International journal of pharmaceutics [Int J Pharm] 2008 Nov 19; Vol. 364 (1), pp. 142-9. Date of Electronic Publication: 2008 Aug 09. - Publication Year :
- 2008
-
Abstract
- For nearly a decade poly(amidoamine) (PAMAM) dendrimers G4 were claimed unnegligible cytotoxic agents. Here we monitored whether in vivo cytotoxic effect of PAMAM G4 (0.5 micromol kg(-1) day(-1)) may be compromised by its ameliorating effect on severe hyperglycaemia in chronic streptozotocin-diabetic Wistar rats. PAMAM G4 significantly reduced the 60-day overall survival in long-term experimental diabetes: treated animals were 6.7 times more likely to die than control animals (p<0.025). PAMAM G4 significantly reduced numerous biochemical parameters in blood, including glucose, glycated haemoglobin or protein oxidation, cholesterol and triglycerides, but apparently unchanged plasma insulin peptide C. Terminal blood glucose in PAMAM-treated animals was significantly higher in survivors, pointing to the possible preventive role of glycation in reducing of PAMAM G4 cytotoxicity. Our results provide the first in vivo evidence that PAMAM G4 is able to lower plasma glucose and suppress long-term markers of diabetic hyperglycaemia. Nevertheless, this beneficial influence cannot override PAMAM G4 cytotoxic effects in the increased mortality of streptozotocin-diabetic rats.
- Subjects :
- Animals
Body Weight drug effects
Dendrimers chemistry
Diabetes Mellitus, Experimental blood
Diabetes Mellitus, Experimental mortality
Erythrocytes metabolism
Glycation End Products, Advanced metabolism
Hemolysis
Hypoglycemic Agents chemistry
Indicators and Reagents
Male
Nylons chemistry
Pilot Projects
Rats
Rats, Wistar
Survival Analysis
Blood Glucose metabolism
Dendrimers pharmacology
Diabetes Mellitus, Experimental drug therapy
Hypoglycemic Agents pharmacology
Nylons pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0378-5173
- Volume :
- 364
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- International journal of pharmaceutics
- Publication Type :
- Academic Journal
- Accession number :
- 18761397
- Full Text :
- https://doi.org/10.1016/j.ijpharm.2008.08.001