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Zingiber officinale (Ginger) hydroalcoholic extract improved avoidance memory in rat model of streptozotocin-induced diabetes by regulating brain oxidative stress

  • Narges Marefati , Tara Abdi , Farimah Beheshti , Farzaneh Vafaee , Maryam Mahmoudabady ORCID logo and Mahmoud Hosseini EMAIL logo
Published/Copyright: October 22, 2021

Abstract

Objectives

Diabetes mellitus associated cognitive impairment is suggested to be due to oxidative stress. Considering the anti-diabetic, antioxidant, antihyperlipidemic, and anti-inflammatory effects of Zingiber officinale, the present study aimed to investigate its effect on memory and oxidative stress factors in streptozotocin (STZ)-induced diabetic rats.

Methods

The rats were allocated into five groups: Control, Diabetic, Diabetic + Ginger 100, Diabetic + Ginger 200, and Diabetic + Ginger 400. Following diabetes induction by STZ (60 mg/kg), 100, 200, or 400 mg/kg Ginger was given for eight weeks. Passive avoidance test (PA) was done and thiol, malondialdehyde (MDA), superoxide dismutase (SOD), and catalase (CAT) measurements were carried out in the brain.

Results

The latency into the dark compartment decreased (p<0.001) and the number of entries and time spent in the dark chamber increased in the Diabetic group compared to the Control (p<0.001 for all). All three doses of extract improved performance of the rats in the PA test (p<0.001 for all). The hippocampal and cortical MDA level was higher (p<0.001) while CAT, SOD, and total thiol were lower (p<0.01–p<0.001) in the Diabetic group than the Control. Treatment with 200 and 400 mg/kg Z. officinale extract reduced hippocampal and cortical MDA (p<0.001) and improved CAT (p<0.001) while, just the dose of 400 mg/kg of the extract increased SOD and total thiol in hippocampal and cortical tissues (p<0.001) compared with Diabetic group.

Conclusions

Z. officinale extract could improve memory by reducing the oxidative stress in STZ-induced diabetes model.


Corresponding author: Mahmoud Hosseini, PhD, Division of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran; and Department of Physiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran, Phone: +98 51 38828565, Fax: +98 51 38828564, E-mail:

Funding source: Mashhad University of Medical Sciences

Award Identifier / Grant number: 980070

  1. Research funding: This study was financially supported by the Vice Presidency of Research, Mashhad University of Medical Sciences (NO: 980070).

  2. Competing interests: We declare that we have no conflict of interest.

  3. Ethical approval: Animal procedures were carried out considering the Guide for the Care and Use of Laboratory Animals and were approved by the Committee on Animal Research of Mashhad University of Medical Sciences. The document number was IR.MUMS.MEDICAL.REC.1398.517.

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Received: 2021-04-07
Accepted: 2021-10-06
Published Online: 2021-10-22

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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