Author(s):
Strekalova, Tatyana ; Gorlova, Anna ; Nunes, João ; Litavrin, Aleksandr ; Munter, Johannes P. M. de ; Lyundup, Alexei ; Umriukhin, Aleksei ; Proshin, Andrey ; Kalueff, Allan ; Grünblatt, Edna ; Walitza, Susanna
Date: 2025
Persistent ID: http://hdl.handle.net/10400.5/102614
Origin: Repositório da Universidade de Lisboa
Subject(s): Animal model; Anxiety-like behavior; Benfotiamine; Mice; Neuroinflammation; Oxidative stress; Posttraumatic stress disorder (PTSD); Predator stress; Thiamine (vitamin B1)
Description
Experiences of life-threatening stimuli can induce post-traumatic stress disorder (PTSD), which is associated with long-lasting behavioral and neurochemical abnormalities. Despite its increased global incidence, the current treatment options for PTSD remain limited, highlighting the need for novel therapeutic strategies. As oxidative stress and neuroinflammation contribute to PTSD, the use of powerful antioxidants such as thiamine (B1 vitamin) compounds may counteract disease development. Young C57BL/6 mice received thiamine or benfotiamine in drinking water (each at a dose of 200 mg/kg/day) for 21 days, and for the last five days, they were subjected to rat exposure. Mice were studied for anxiety-like behavior, exploration, locomotion, grooming, social interactions, pain sensitivity, brain changes in protein carbonyl (PC), total glutathione (TG), and gene expression of distress and inflammation markers. Rat exposure induced anxiety-like behavior, excessive grooming, and alteration in locomotion, along with other abnormalities. Stressed, untreated mice had elevated levels of PC and TG in the prefrontal cortex, hippocampus, amygdala, and striatum and increased expression of Il-1β, Tnf, c-Fos, Cox-1, and Cox-2. Treatment with thiamine or benfotiamine significantly ameliorated most of these changes in the stressed groups. Thus, thiamine compounds may have therapeutic potential in patients with PTSD, owing to their antioxidant and anti-inflammatory properties.
