Article

A short-term diabetes induced changes of catecholamines and p38-MAPK in discrete areas of rat brain.

Department of Surgery, Drexel University College of Medicine, MS 413, 245 N. 15th Street, Philadelphia, PA, 19102, USA.
Life Sciences (impact factor: 2.53). 09/2005; 77(15):1825-35. DOI:10.1016/j.lfs.2004.12.038 pp.1825-35
Source: PubMed

ABSTRACT Chronic diabetes is associated with the alteration of second messengers and CNS disorders. We have recently identified that protein kinases (CaMKII and PKC-alpha) and brain neurotransmitters are altered during diabetes as well as in hyperglycemic and acidotic conditions. In this study, we investigated the effects of acute diabetes on the levels of dopamine (DA), norepinephrine (NE), epinephrine (E) and p38-Mitogen-Activated Protein Kinase (p38-MAPK) in striatum (ST), hippocampus (HC), hypothalamus (HT), midbrain (MB), pons medulla (PM), cerebellum (CB) and cerebral cortex (CCX). Alloxan (45 mg/kg) diabetic untreated rats that showed hyperglycemia (>260 mg%), revealed significant increases of DA level in ST (1.5 fold), HC (2.2 fold) and PM (2.0 fold) and the E level also found to be increased significantly in HT (2.4 fold), whereas the NE level was decreased in CB (0.5 fold), after 7 days of diabetes. Immunoblotting study of p38-MAPK expression under identical conditions showed significant alterations in ST, HC, HT and PM (p<0.05) correlated with the changes of catecholamines (DA and E). On the other hand, the above changes were reversed in insulin-treated diabetic rats maintained under normal glucose level (80 -110 mg %). These results suggest that p38-MAPK may regulate the rate of either the synthesis or release of DA and E in corresponding brain areas, but not NE, under these conditions.

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Keywords

acute diabetes
 
brain neurotransmitters
 
Chronic diabetes
 
CNS disorders
 
corresponding brain areas
 
DA level
 
dopamine
 
E level
 
epinephrine
 
Immunoblotting study
 
insulin-treated diabetic rats
 
NE level
 
norepinephrine
 
normal glucose level
 
p38-Mitogen-Activated Protein Kinase
 
pons medulla
 
protein kinases
 
second messengers
 
showed hyperglycemia
 
significant alterations