Study on the protective effect of zedoary ketone on the cognitive function and nerve function in mice with cerebral ischemia reperfusion injury

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

  Methods A mouse model of cerebral ischemia-reperfusion injury was established by 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/( kg.d), 60mg/(kg.d), observe Morris water maze test, behavioral score, cerebral infarction rate, brain tissue water content of mice in each group, 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, the 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 and p-CREB were significantly reduced (P<0.01). Compared with the model group, curcumin was given 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 the activation of the cAMP/CREB/BDNF signaling pathway.