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Protective effect of taurine on cognitive deficit induced by 1-bromopropane
- ZHAO Huiwen, XU Lin, SHAN Shan, ZHAO Xiulan
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Journal of Shandong University (Health Sciences). 2022, 60(2):
14-21.
doi:10.6040/j.issn.1671-7554.0.2021.1290
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Abstract
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Objective To explore the protective effect of taurine on cognitive deficit induced by 1-bromopropane(1-BP). Methods A total of 60 SPF adult male Wistar rats were randomly divided into control group, 1-BP group, low-dose taurine intervention group, high-dose taurine intervention group and taurine control group according to body weight. 1-BP was dissolved in corn oil and orally administrated at the dose of 800 mg/kg.bw. The spatial learning and memory function of rats were detected with Morris water maze(MWM)15-20 days after the administration of 1-BP. On Day 21, the rats were sacrificed and the cerebral cortex and hippocampus were separated immediately. The content of taurine was determined with high-performance liquid chromatography(HPLC). The expressions of oxidative phosphorylation protein complex of mitochondria and apoptosis related proteins in brains were detected with Western blotting. Results Morris water maze showed that compared with the control group, 1-BP group had longer escape latency, and decreased frequencies of crossing platform(P<0.01); compared with 1-BP group, the low-dose and high-dose taurine intervention groups had shorter escape latency and increased frequencies of crossing platform(P<0.01). The HPLC results showed that compared with the control group, the 1-BP group had significantly decreased taurine contents in cerebral cortex and hippocampus(P<0.001, P<0.05); compared with 1-BP group, the low-dose and high-dose taurine intervention groups had significantly increased taurine level(P<0.001, P<0.01). Compared with the control group, the 1-BP group had significantly decreased expression of mitochondrial oxidative phosphorylation protein complex(OXPHOS)and Bcl-2(P<0.01, P<0.05), but significantly increased expressions of BAX and cleaved capase-3(P<0.05, P<0.01). The alteration trends of OXPHOS and apoptosis related proteins in low-dose and high-dose taurine intervention groups were significantly reversed(P<0.01, P<0.05, P<0.001). Conclusion Taurine supplementation could inhibit neuronal apoptosis, maintain the normal function of mitochondria, and improve the learning and memory dysfunction caused by 1-BP.