The neuroprotection of Rattin against amyloid β peptide in spatial memory and synaptic plasticity of rats.
Wang. Zhao-Jun ZJ; Han. Wei-Na WN; Yang. Guang-Zhao GZ; Yuan. Li L; Liu. Xiao-Jie XJ; Li. Qing-Shan QS; Qi. Jin-Shun JS
Key Findings
- Rattin prevents amyloid‑beta‑induced spatial memory deficits in rats
- Rattin preserves hippocampal long‑term potentiation despite amyloid‑beta exposure
- The protective effect involves inhibition of caspase‑3 activation and maintenance of STAT3 signaling
Practical Outcomes
- The findings show a potential brain‑protective role for humanin‑derived peptides, but the required intracerebral injection isn’t practical for humans. It points to the idea of developing drugs that mimic Rattin or target its STAT3/caspase pathways, though no dosage or supplement protocol can be recommended yet.
Summary
A rat study found that injecting Rattin, a humanin‑like peptide, directly into the brain blocks memory loss and synaptic problems caused by amyloid‑beta, likely by keeping STAT3 active and stopping caspase‑3 from killing cells.
Abstract
Rattin, a specific derivative of humanin in rats, shares the ability with HN to protect neurons against amyloid β (Aβ) peptide-induced cellular toxicity. However, it is still unclear whether Rattin can protect against Aβ-induced deficits in cognition and synaptic plasticity in rats. In the present study, we observed the effects of Rattin and Aβ31-35 on the spatial reference memory and in vivo hippocampal Long-term potentiation of rats by using Morris water maze test and hippocampal field potential recording. Furthermore, the probable molecular mechanism underlying the neuroprotective roles of Rattin was investigated. We showed that intra-hippocampal injection of Rattin effectively prevented the Aβ31-35-induced spatial memory deficits and hippocampal LTP suppression in rats; the Aβ31-35-induced activation of Caspase-3 and inhibition of STAT3 in the hippocampus were also prevented by Rattin treatment. These findings indicate that Rattin treatment can protect spatial memory and synaptic plasticity of rats against Aβ31-35-induced impairments, and the underlying protective mechanism of Rattin may be involved in STAT3 and Caspases-3 pathways. Therefore, application of Rattin or activation of its signaling pathways in the brain might be beneficial to the prevention of Aβ-related cognitive deficits.
Study Information
pubmed
2013
2013-09-30T00:00:00.000Z
10.1002/hipo.22202
17
75