Esmaeil Akbari - Department of Physiology and Pharmacology, Psychia try and Behavioral Sciences Research Center, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Nima Naderi - Department of Pharmacology and Toxicology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Keyvan Yaghoobi - Neuroscience Research center, Shahid Beheshti Univ ersity of Medical Sciences, Tehran, Iran
Behzad Parsi - Department of Physiology and Pharmacology, Psychia try and Behavioral Sciences Research Center, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Sahar Berijani - Neuroscience Research center, Shahid Beheshti Univ ersity of Medical Sciences, Tehran, Iran

Background: The memory impairment, obtained from intracerebroventricular (i.c.v.) infusion of streptozotocin (STZ) in rats through activation of oxidative stress, is accepted as sporadic Alzheimer’s disease (AD) model in most experimental studies. Dimethyl sulfoxide (DMSO) as a solvent is widely used in animal studies to have antioxidant effects as well. However, no report is available about DMSO effect on oxidative stress-induced cognition deficit i.e. AD. The present work was designed to assess the effect of chronic treatment of DMSO on STZ-treated rats. Materials and Methods: STZ (۳ mg/ kg i.c.v. bilateral with ۱۰ µl volume in either side days ۱ and ۳) using a single-day version of Morris water maze (MWM). The DMSO (۲.۵, ۵ and ۱۰ %v/v in saline), started from the first day, was infused for ۱۴ days. Results: The chronic administration of DMSO ۱۰% (but not ۲.۵ and ۵%) improved the distance to hidden platform (P<۰.۰۱) in training sessions and time spent in the target quadrant (P<۰.۰۱) in probe tests. Neither STZ nor DMSO had any intervention on velocity and visuo-motor coordination in the visible version of MWM. Conclusion: Taken together, the results suggest that DMSO may be appropriate as adjuvant therapies for the prevention of memory impairment in the experimental models of AD. Therefore, use of DMSO as a solvent in AD animal studies should be considered having beneficial effects on cognitive function.

Alzheimer’s disease, dimethyl sulfoxide, Morris water maze, streptozotocin