Literature DB >> 24301255

Rosmarinic acid prevents lipid peroxidation and increase in acetylcholinesterase activity in brain of streptozotocin-induced diabetic rats.

Nadia Mushtaq1, Roberta Schmatz, Luciane B Pereira, Mushtaq Ahmad, Naiara Stefanello, Juliano M Vieira, Fátima Abdalla, Marília V Rodrigues, Jucimara Baldissarelli, Luana Paula Pelinson, Diéssica P Dalenogare, Karine Paula Reichert, Eduardo M Dutra, Nádia Mulinacci, Marzia Innocenti, Maria Bellumori, Vera Maria Morsch, Maria Rosa Schetinger.   

Abstract

We investigated the efficacy of rosmarinic acid (RA) in preventing lipid peroxidation and increased activity of acetylcholinesterase (AChE) in the brain of streptozotocin-induced diabetic rats. The animals were divided into six groups (n = 8): control, ethanol, RA 10 mg/kg, diabetic, diabetic/ethanol and diabetic/RA 10 mg/kg. After 21 days of treatment with RA, the cerebral structures (striatum, cortex and hippocampus) were removed for experimental assays. The results demonstrated that the treatment with RA (10 mg/kg) significantly reduced the level of lipid peroxidation in hippocampus (28%), cortex (38%) and striatum (47%) of diabetic rats when compared with the control. In addition, it was found that hyperglycaemia caused significant increased in the activity of AChE in hippocampus (58%), cortex (46%) and striatum (30%) in comparison with the control. On the other hand, the treatment with RA reversed this effect to the level of control after 3 weeks. In conclusion, the present findings showed that treatment with RA prevents the lipid peroxidation and consequently the increase in AChE activity in diabetic rats, demonstrating that this compound can modulate cholinergic neurotransmission and prevent damage oxidative in brain in the diabetic state. Thus, we can suggest that RA could be a promising compound in the complementary therapy in diabetes.
Copyright © 2013 John Wiley & Sons, Ltd.

Entities:  

Keywords:  acetylcholinesterase; diabetes; lipid peroxidation; rosmarinic acid; streptozotocin

Mesh:

Substances:

Year:  2013        PMID: 24301255     DOI: 10.1002/cbf.3014

Source DB:  PubMed          Journal:  Cell Biochem Funct        ISSN: 0263-6484            Impact factor:   3.685


  13 in total

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