[Animal experiment]-Study on the protective effect of zedoary dione on the cognitive function and nerve function of mice with cerebral ischemia reperfusion injury

  Objective   To investigate the effects of curcuma dione on cognitive function, neurological function and mechanism of cerebral ischemia-reperfusion injury in mice.

  Methods A mouse model of cerebral ischemia-reperfusion injury was established by the suture method. The low-molecular-weight heparin sodium group, the low- and high-dose turmeric dione group and the model were given 1 mg/(kg.d) and 20 mg/( respectively). kg.d), 60mg/(kg.d), observe the Morris water maze test, behavioral score, cerebral infarction rate, brain tissue water content in each group of mice, and determine serum 6-keto-PGF1α and 6-keto-PGF1α/ The ratio of TXB2, the expression level of cAMP and p-CREB in brain homogenate.

  Results Compared with the sham operation group, mice in the model group had significantly longer escape latency, significantly reduced the number of platform crossings (P<0.01), behavioral score, cerebral infarction rate, brain tissue water content, and serum TXB2 content significantly increased (P <0.01), serum 6-keto-PGF1α, 6-keto-PGF1α/TXB2 ratio, brain homogenate cAMP, p-CREB were significantly reduced (P<0.01), compared with the model group, curcuma In the drug group, the escape latency was significantly shortened (P<0.05), the number of platform crossings was significantly increased (P<0.05), the behavioral score, cerebral infarction rate and brain tissue water content were significantly reduced (P<0.05), serum TXB2 content was significantly reduced (P<0.01), serum 6-keto-PGF1α, 6-keto-PGF1α/TXB2 ratio, brain homogenate cAMP and p-CREB were significantly increased (P<0.05), and showed Dose dependent.

  Conclusion  Curcuma dione has a good protective effect on the cognitive and neurological functions of mice with cerebral ischemia-reperfusion injury, and its mechanism may be related to the improvement of microcirculation disorders and activation of the cAMP/CREB/BDNF signaling pathway.