Combined Restraint Stress and Metal Exposure Paradigms in Rats: Unravelling Behavioural and Neurochemical Perturbations
- PMID: 39443350
- PMCID: PMC12145149
- DOI: 10.1007/s12035-024-04570-1
Combined Restraint Stress and Metal Exposure Paradigms in Rats: Unravelling Behavioural and Neurochemical Perturbations
Abstract
Accumulation of heavy metals (Mn and Ni) and prolonged exposure to stress are associated with adverse health outcomes. Various studies have shown the impacts of stress and metal exposures on brain function. However, no study has examined the effects of co-exposure to stress, Mn, and Ni on the brain. This study addresses this gap by evaluating oxidative and glial responses, apoptotic activity, as well as cognitive processes in a rat model. Adult Wistar rats were exposed to vehicle (control), restraint stress, 25 mg/kg of manganese (Mn) or nickel (Ni), or combined restraint stress plus Mn or Ni. Following treatment, rats were subjected to several behavioural paradigms to assess cognitive function. Enzyme activity, as well as ATPase levels, were evaluated. Thereafter, an immunohistochemical procedure was utilised to evaluate neurochemical markers of glial function, myelination, oxidative stress, and apoptosis in the hippocampus, prefrontal cortex (PFC), and striatum. Results showed that stress and metal exposure increased oxidative stress markers and reduced antioxidant levels. Further, combined stress and metal exposure reduced various forms of learning and memory ability in rats. In addition, there were alterations in Iba1 activity and Nrf2 levels, reduced Olig2 and myelin basic protein (MBP) levels, and increased caspase-3 expression. These neurotoxic outcomes were mostly exacerbated by co-exposure to stress and metals. Overall, our findings establish that stress and metal exposures impaired cognitive performance, induced oxidative stress and apoptosis, and led to demyelination effects which were worsened by combined stress and metal exposure.
Keywords: Brain; Chronic stress; Manganese; Memory; Nickel.
© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Ethics Approval: All experimental protocols were in strict adherence with the NIH Guide for the Care and Use of Laboratory Animals (National Research Council 2011) and approved by the Institutional Research Ethics Committee (FUTA/ETH/23/99). Consent to Participate: Not applicable. Consent for Publication: Not applicable. Competing Interests: The authors declare no competing interests.
References
-
- Abad S, Camarasa J, Pubill D, Camins A, Escubedo E (2016). Adaptive plasticity in the hippocampus of young mice intermittently exposed to MDMA could be the origin of memory deficits. Molecular neurobiology 53:7271–7283. - PubMed
-
- Adedara IA, Subair TI, Ego VC, Oyediran O, Farombi EO (2017). Chemoprotective role of quercetin in manganese-induced toxicity along the brain-pituitary-testicular axis in rats. Chemico-biological interactions 263:88–98. - PubMed
-
- Adhikari A, Das M, Mondal S, Darbar S, Das AK, Bhattacharya SS, Pal D, Pal SK (2019). Manganese neurotoxicity: nano-oxide compensates for ion-damage in mammals. Biomaterials science 7:4491–4502. - PubMed
-
- Akingbade GT, Ijomone OM, Imam A, Aschner M, Ajao MS (2021). D-ribose-l-cysteine improves glutathione levels, neuronal and mitochondrial ultrastructural damage, caspase-3 and GFAP expressions following manganese-induced neurotoxicity. Neurotoxicity Research 39:1846–1858. doi:10.1007/s12640-021-00404-3 - DOI - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous
