Chronic NaHS treatment improves spatial and passive avoidance learning and memory and anxiety-like behavior and decreases oxidative stress in rats fed with a high-fat diet

• Published in: Brain research bulletin 2020-11, Vol.164, p.380-391
• Main Authors: Habibitabar, Elahe, Moridi, Heresh, Shateri, Hossein, Karimi, Seyed Asaad, Salehi, Iraj, Komaki, Alireza, Sarihi, Abdolrahman
• Format: Article
• Language: English
• Subjects: High-Fat Diet; Hydrogen Sulfide; Learning and Memory; Oxidative Stress
• ISSN: 0361-9230; 1873-2747
• DOI: 10.1016/j.brainresbull.2020.09.007

•High-fat diet (HFD) induces a decline in spatial and passive memory.•Exogenous H2S can improve HFD-induced MWM and PAL memory impairment.•HFD increased anxiety-like behavior and exogenous H2S reversed this change.•Exogenous H2S reversed HFD-induced oxidative stress.•H2S act as a neuroprotective factor in HFD induced memory impairment. Cognitive function is impaired by increased consumption of a high-fat diet (HFD). Also, HFD consumption can alter hydrogen sulfide (H2S) metabolism. H2S is an important signaling molecule with antioxidant effects that regulates multiple functions in the brain. In the present study, we investigated the effect of sodium hydrosulfide (NaHS, an H2S donor) on cognitive impairment and oxidative stress changes induced by HFD consumption. Following 11 weeks of HFD regimes in Wistar rats, elevated plus-maze (EPM), Morris water maze (MWM), and passive avoidance learning (PAL) tasks were used to evaluate the anxiety-like behavior and spatial and passive learning and memory, respectively. Daily intraperitoneal injection of NaHS was done during the dietary regimen. Serum and hippocampal oxidative stress biomarkers (malondialdehyde (MDA), total antioxidant capacity (TAC), and total oxidant status (TOS)) were measured. We demonstrated that treatment with NaHS ameliorated the impairment in the retrieval of reference memory and passive avoidance learning. Moreover, HFD increased anxiety-like behavior, which was reversed by the administration of NaHS. Additionally, the increase in MDA and TOS and the decrease in TAC induced by HFD in the serum and hippocampus were significantly reduced following administration of NaHS. These results indicate that NaHS could significantly ameliorate HFD-induced spatial and passive learning and memory impairment and anxiety-like behavior, at least in part, via its antioxidant activities. Therefore, the administration of NaHS can provide a therapeutic approach for HFD-induced memory impairment.