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葡萄籽原花青素对异氟醚诱导的小鼠认知功能障碍的保护作用。

Protective effects of grape seed procyanidin on isoflurane-induced cognitive impairment in mice.

机构信息

Department of Anesthesiology, Nanjing University Medical School Affiliated Nanjing Drum Tower Hospital, Nanjing, China.

Jiangsu Key Laboratory of Molecular Medicine, Nanjing University Medical School, Nanjing, China.

出版信息

Pharm Biol. 2020 Dec;58(1):200-207. doi: 10.1080/13880209.2020.1730913.

Abstract

Oxidative imbalance-induced cognitive impairment is among the most urgent clinical concerns. Isoflurane has been demonstrated to impair cognitive function via an increase in oxidative stress. GSP has strong antioxidant capacities, suggesting potential cognitive benefits. This study investigates whether GSP pre-treatment can alleviate isoflurane-induced cognitive dysfunction in mice. C57BL/6J mice were pre-treated with either GSP 25-100 mg/kg/d for seven days or GSP 100-400 mg/kg as a single dose before the 6 h isoflurane anaesthesia. Cognitive functioning was examined using the fear conditioning tests. The levels of SOD, p-NR2B and p-CREB in the hippocampus were also analysed. Pre-treatment with either a dose of GSP 50 mg/kg/d for seven days or a single dose of GSP 200 mg/kg significantly increased the % freezing time in contextual tests on the 1st (72.18 ± 12.39% vs. 37.60 ± 8.93%; 78.27 ± 8.46% vs. 52.72 ± 2.64%), 3rd (93.80 ± 7.62% vs. 52.94 ± 14.10%; 87.65 ± 10.86% vs. 52.89 ± 1.73%) and 7th (91.36 ± 5.31% vs. 64.09 ± 14.46%; 93.78 ± 3.92% vs. 79.17 ± 1.79%) day after anaesthesia. In the hippocampus of mice exposed to isoflurane, GSP 200 mg/kg increased the total SOD activity on the 1st and 3rd day and reversed the decreased activity of the NR2B/CREB pathway. These findings suggest that GSP improves isoflurane-induced cognitive dysfunction by protecting against perturbing antioxidant enzyme activities and NR2B/CREB pathway. Therefore, GSP may possess a potential prophylactic role in isoflurane-induced and other oxidative stress-related cognitive decline.

摘要

氧化失衡诱导的认知障碍是最紧迫的临床关注点之一。异氟醚已被证明通过增加氧化应激来损害认知功能。GSP 具有很强的抗氧化能力,提示可能具有认知益处。本研究旨在探讨 GSP 预处理是否可以减轻异氟醚麻醉诱导的小鼠认知功能障碍。C57BL/6J 小鼠连续 7 天给予 GSP25-100mg/kg/d 或单次给予 GSP100-400mg/kg 预处理,然后进行 6 小时异氟醚麻醉。使用恐惧条件测试检查认知功能。还分析了海马中 SOD、p-NR2B 和 p-CREB 的水平。连续 7 天给予 GSP50mg/kg/d 或单次给予 GSP200mg/kg 预处理可显著增加第 1 天(72.18±12.39%vs.37.60±8.93%;78.27±8.46%vs.52.72±2.64%)、第 3 天(93.80±7.62%vs.52.94±14.10%;87.65±10.86%vs.52.89±1.73%)和第 7 天(91.36±5.31%vs.64.09±14.46%;93.78±3.92%vs.79.17±1.79%)后麻醉后的冷冻时间百分比。在异氟醚暴露的小鼠海马中,GSP200mg/kg 增加了第 1 天和第 3 天的总 SOD 活性,并逆转了 NR2B/CREB 途径活性的降低。这些发现表明,GSP 通过保护抗氧化酶活性和 NR2B/CREB 途径免受干扰来改善异氟醚诱导的认知功能障碍。因此,GSP 可能在异氟醚诱导和其他氧化应激相关认知衰退中具有潜在的预防作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/7067175/0f265ad37fba/IPHB_A_1730913_F0001_B.jpg

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