Electrophysiology of cerebral ischemia and reperfusion: First evidence for the role of synapse in ischemic tolerance
Autor: | Ali Rafati, Somaye Keshavarz, Masoud Haghani, Maryam Nazari |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
medicine.medical_specialty business.industry Ischemia Long-term potentiation Stimulation Neurotransmission medicine.disease Lesion Brain ischemia 03 medical and health sciences Cellular and Molecular Neuroscience chemistry.chemical_compound Electrophysiology 030104 developmental biology 0302 clinical medicine chemistry Internal medicine Anesthesia Cardiology Medicine medicine.symptom business Neurotransmitter 030217 neurology & neurosurgery |
Zdroj: | Synapse. 70:351-360 |
ISSN: | 0887-4476 |
DOI: | 10.1002/syn.21910 |
Popis: | Objective The subthreshold brain-damaging stimulus may protect the brain from subsequent ischemia; this phenomenon has been named "ischemic tolerance" (IT). We focused on the synaptic properties of the neurons after mild and severe ischemia to determine the association between IT and synaptic efficacy. Experimental design Adult male rats were randomly divided into four experimental groups including control, sham, permanent ischemia (pI/R), and mild ischemia (mI/R). Middle cerebral artery occlusion (MCAO) method was applied to induce brain ischemia. Seven days after the insult, long-term potentiation (LTP) induced by high-frequency stimulation (HFS) and paired-pulse ratio (PPR) were monitored before and after the HFS delivery. Results The field potential recording demonstrated that mild ischemia significantly increased the basal synaptic transmission. Additionally, the HFS produced a significant potentiation compared to its baseline level in the mI/R group. Moreover, mild ischemia prevented depression of PPR by HFS. This effect was accompanied by a significant increase in the normalized PPR (PPR after HFS/PPR before HFS) in this group. Conclusions Our data indicated that a mild reduction in brain perfusion without permanent lesion can dramatically increase the basal synaptic transmission. This effect may be associated with an increase in the neurotransmitter content of the pre-synaptic neurons. This hypothesis could provide a new insight into the relationship between IT and synaptic efficacy. Synapse 70:351-360, 2016. © 2016 Wiley Periodicals, Inc. |
Databáze: | OpenAIRE |
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