2016Zhonghua wuli yixue zazhiRequires access

An enriched environment enhances synaptic plasticity and cognition post-stroke

Xin Wang, Caihua Sun, Zhen Qian, Wei Shi, ZhiYong Sun, Min Yang

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Abstract

Objective To observe the effects of an enriched environment (EE) on cognitive functioning and the synaptic plasticity of mice modeling post-stroke cognitive impairment (PSCI) and explore the possible mechanisms involved. Methods Mice modeling PSCI and sham-operated mice were randomly divided into 3 groups: sham-operated mice in a standard environment (the Sham+ SE group), PSCI mice in a standard environment (the PSCI+ SE group) and PSCI mice in an enriched environment (the PSCI+ EE group). The cognitive functioning of all of the mice was quantified using a Morris water maze and their hippocampal long-term potentiation (LTP) was recorded using an electrophysiological method. The level of synaptophysin was detected using Western blotting. Synaptic ultrastructure in the hippocampus was imaged using electron microscopy. Results Compared with the Sham+ SE group, the PSCI+ SE group showed significantly poorer water maze performance and failed induction of contralateral LTP. Their average level of synaptophysin was significantly lower, and significant adverse changes in the synaptic ultrastructure of the hippocampus were observed, including a decreased number of synapses. The average width of the synaptic cleft, postsynaptic density and the interface curvature of the synapses were all less desirable. All of the measurements of the PSCI+ EE group improved significantly compared to those of the PSCI+ SE group, but were still significantly poorer than those of the Sham+ SE group. Conclusions An enhanced environment can improve the cognitive functioning of mice modelling PSCI. It may be that an EE can improve synaptic plasticity in the hippocampus contralateral to the stroke. Key words: Stroke; Cognitive impairment; Enriched environments; Synaptic plasticity

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Objective To observe the effects of an enriched environment (EE) on cognitive functioning and the synaptic plasticity of mice modeling post-stroke cognitive impairment (PSCI) and explore the possible mechanisms involved. Methods Mice modeling PSCI and sham-operated mice were randomly divided into 3 groups: sham-operated mice in a standard environment (the Sham+ SE group), PSCI mice in a standard environment (the PSCI+ SE group) and PSCI mice in an enriched environment (the PSCI+ EE group). The cognitive functioning of all of the mice was quantified using a Morris water maze and their hippocampal long-term potentiation (LTP) was recorded using an electrophysiological method. The level of synaptophysin was detected using Western blotting. Synaptic ultrastructure in the hippocampus was imaged using electron microscopy. Results Compared with the Sham+ SE group, the PSCI+ SE group showed significantly poorer water maze performance and failed induction of contralateral LTP. Their average level of synaptophysin was significantly lower, and significant adverse changes in the synaptic ultrastructure of the hippocampus were observed, including a decreased number of synapses. The average width of the synaptic cleft, postsynaptic density and the interface curvature of the synapses were all less desirable. All of the measurements of the PSCI+ EE group improved significantly compared to those of the PSCI+ SE group, but were still significantly poorer than those of the Sham+ SE group. Conclusions An enhanced environment can improve the cognitive functioning of mice modelling PSCI. It may be that an EE can improve synaptic plasticity in the hippocampus contralateral to the stroke. Key words: Stroke; Cognitive impairment; Enriched environments; Synaptic plasticity

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Available abstract

Objective To observe the effects of an enriched environment (EE) on cognitive functioning and the synaptic plasticity of mice modeling post-stroke cognitive impairment (PSCI) and explore the possible mechanisms involved. Methods Mice modeling PSCI and sham-operated mice were randomly divided into 3 groups: sham-operated mice in a standard environment (the Sham+ SE group), PSCI mice in a standard environment (the PSCI+ SE group) and PSCI mice in an enriched environment (the PSCI+ EE group). The cognitive functioning of all of the mice was quantified using a Morris water maze and their hippocampal long-term potentiation (LTP) was recorded using an electrophysiological method. The level of synaptophysin was detected using Western blotting. Synaptic ultrastructure in the hippocampus was imaged using electron microscopy. Results Compared with the Sham+ SE group, the PSCI+ SE group showed significantly poorer water maze performance and failed induction of contralateral LTP. Their average level of synaptophysin was significantly lower, and significant adverse changes in the synaptic ultrastructure of the hippocampus were observed, including a decreased number of synapses. The average width of the synaptic cleft, postsynaptic density and the interface curvature of the synapses were all less desirable. All of the measurements of the PSCI+ EE group improved significantly compared to those of the PSCI+ SE group, but were still significantly poorer than those of the Sham+ SE group. Conclusions An enhanced environment can improve the cognitive functioning of mice modelling PSCI. It may be that an EE can improve synaptic plasticity in the hippocampus contralateral to the stroke. Key words: Stroke; Cognitive impairment; Enriched environments; Synaptic plasticity

Key concepts: Synaptophysin, Synaptic plasticity, Morris water navigation task, Postsynaptic density, Hippocampus, Hippocampal formation, Long-term potentiation, Environmental enrichment

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