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Chinese Journal of Neurotraumatic Surgery(Electronic Edition) ›› 2021, Vol. 07 ›› Issue (04): 199-202. doi: 10.3877/cma.j.issn.2095-9141.2021.04.002

• Traumatic Brain and Spinal Cord Injury • Previous Articles     Next Articles

Effects of isoliquiritigenin on the expression of MMP-9 and TIMP-1 protease after brain injury in rats

Changdong Li1, Jie Zhou1,(), Zhibiao Cai1, Kai Wang1   

  1. 1. Department of Neurosurgery, The 940 Hospital of Joint Logistics Support Force of Chinese People’s Liberation Army, Lanzhou 730050, China
  • Received:2021-01-19 Online:2021-08-11 Published:2021-08-31
  • Contact: Jie Zhou

Abstract:

Objective

To observe the effect of isoliquiritigenin (ISL) on the expression of matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of metalloproteinase-1 (TIMP-1) in brain tissue of rats with traumatic brain injury (TBI).

Methods

Thirty clean grade Wistar rats, weighing 200-250 g, were randomly divided into normal control group (n=10), TBI model group (n=10) and ISL group (n=10). The normal control group was given normal feeding; TBI model group and ISL group were established by modified Feeney method, and closed TBI was induced by free fall impact; The ISL group was given ISL intervention 2-4 h after successful modeling, and the dosage was 30 mg/(kg·d) by gavage for 2 weeks. The expressions of MMP-9 and TIMP-1 were detected by ELISA.

Results

The expression of MMP-9 was strong in normal control group and decreased in TBI model group, and the expression of MMP-9 in ISL group was weaker than in the TBI model group (P<0.05). The expression of TIMP-1 in the normal control group was evident and decreased in TBI model group, and the expression of TIMP-1 in ISL group was significantly higher than that in the TBI model group (P<0.05).

Conclusion

ISL can reduce the permeability of microvascular basement and reduce the degree of brain edema in rats with TBI, and its mechanism may be related to increasing the expression of TIMP-1 to regulate the balance of MMP-9.

Key words: Craniocerebral injury, Isoliquiritigenin, Matrix metalloproteinase-9, Tissue inhibitor of metalloproteinase-1

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