Curcumin restores diabetes induced neurochemical changes in the brain stem of Wistar rats

Eur J Pharmacol. 2013 Feb 28;702(1-3):323-31. doi: 10.1016/j.ejphar.2013.01.012. Epub 2013 Feb 1.

Abstract

Diabetes mellitus, when poorly controlled, leads to debilitating central nervous system (CNS) complications including cognitive deficits, somatosensory and motor dysfunction. The present study investigated curcumin's potential in modulating diabetes induced neurochemical changes in brainstem. Expression analysis of cholinergic, insulin receptor and GLUT-3 in the brainstem of streptozotocin (STZ) induced diabetic rats were studied. Radioreceptor binding assays, gene expression studies and immunohistochemical analysis were done in the brainstem of male Wistar rats. Our result showed that Bmax of total muscarinic and muscarinic M3 receptors were increased and muscarinic M1 receptor was decreased in diabetic rats compared to control. mRNA level of muscarinic M3, α7-nicotinic acetylcholine, insulin receptors, acetylcholine esterase, choline acetyltransferase and GLUT-3 significantly increased and M1 receptor decreased in the brainstem of diabetic rats. Curcumin and insulin treatment restored the alterations and maintained all parameters to near control. The results show that diabetes is associated with significant reduction in brainstem function coupled with altered cholinergic, insulin receptor and GLUT-3 gene expression. The present study indicates beneficial effect of curcumin in diabetic rats by regulating the cholinergic, insulin receptor and GLUT-3 in the brainstem similar to the responses obtained with insulin therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / genetics
  • Animals
  • Brain Stem / drug effects*
  • Brain Stem / metabolism
  • Choline O-Acetyltransferase / genetics
  • Curcumin / pharmacology*
  • Diabetes Mellitus, Experimental / metabolism*
  • Gene Expression Regulation / drug effects
  • Glucose Transporter Type 3 / genetics
  • Male
  • Neuroprotective Agents / pharmacology*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptor, Insulin / genetics
  • Receptors, Muscarinic / metabolism
  • alpha7 Nicotinic Acetylcholine Receptor / metabolism

Substances

  • Glucose Transporter Type 3
  • Neuroprotective Agents
  • RNA, Messenger
  • Receptors, Muscarinic
  • Slc2a3 protein, rat
  • alpha7 Nicotinic Acetylcholine Receptor
  • Choline O-Acetyltransferase
  • Receptor, Insulin
  • Acetylcholinesterase
  • Curcumin