Protective effect of extract of Ginkgo biloba on blood-spinal cord barrier after acute spinal cord injury in rat model
Kai Gong
Abstract
Kai Gong
Abstract
[Objective]To observe whether the extract of Ginkgo biloba(EGb761) has protective effect on inflammatory reaction and blood-spinal cord barrier after spinal cord injury in rat model and to study its mechanism.[Method]Totally 120 SD female rats were randomly divided into three groups,group A(sham-operated group),group B(Allen impact SCI group) and group C(EGb761 treated group).Each group had 40 rats for test.Rats in group A underwent laminectomy alone.The modified Allen method was adopted at the T9 level in groups B and C to induce the acute spinal cord injury.For group C,EGb761 was delivered 100 mg/kg/d intraperitoneally half an hour after injury for the first time and per day until killed.At the same time,vehicle-treated animals received physiological saline in the same volumes as in the EGb761-treated group.The rats were sacrificed at 3,6,24 and 72 h post-injury and T9 spinal cord specimen was estracted.The blood-spinal cord barrier(BSCB) of cords was determined by Evans blue content detection,interleukin-1β(IL-1β) expression was detected by ELISA method and intercellular cell adhesion molecule-1(ICAM-1) protein in spinal cord were detected by immunohistochemistry assay.[Result]In group A,there was no obvious leakage of Evans blue around the injuried site and the concentrations of IL-1β and ICAM-1 were maintained at a low level.Compared to group A,the leakage of Evans blue and the concentrations of IL-1β and ICAM-1 were significantly higher.After application of EGb761,the leakage of Evans blue were decreased significantly at all time points except 3 hours post-injury when compared to group B.Additionally,the concentrations of IL-1β and ICAM-1 were decreased significantly at each time point.[Conclusion]In Allen's acute SCI rat model,EGb761 could decrease the local concentration of IL-1β,suppress the abnormal expression of ICAM-1 protein and attenuate disruption of BSCB permeability.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
[Objective]To observe whether the extract of Ginkgo biloba(EGb761) has protective effect on inflammatory reaction and blood-spinal cord barrier after spinal cord injury in rat model and to study its mechanism.[Method]Totally 120 SD female rats were randomly divided into three groups,group A(sham-operated group),group B(Allen impact SCI group) and group C(EGb761 treated group).Each group had 40 rats for test.Rats in group A underwent laminectomy alone.The modified Allen method was adopted at the T9 level in groups B and C to induce the acute spinal cord injury.For group C,EGb761 was delivered 100 mg/kg/d intraperitoneally half an hour after injury for the first time and per day until killed.At the same time,vehicle-treated animals received physiological saline in the same volumes as in the EGb761-treated group.The rats were sacrificed at 3,6,24 and 72 h post-injury and T9 spinal cord specimen was estracted.The blood-spinal cord barrier(BSCB) of cords was determined by Evans blue content detection,interleukin-1β(IL-1β) expression was detected by ELISA method and intercellular cell adhesion molecule-1(ICAM-1) protein in spinal cord were detected by immunohistochemistry assay.[Result]In group A,there was no obvious leakage of Evans blue around the injuried site and the concentrations of IL-1β and ICAM-1 were maintained at a low level.Compared to group A,the leakage of Evans blue and the concentrations of IL-1β and ICAM-1 were significantly higher.After application of EGb761,the leakage of Evans blue were decreased significantly at all time points except 3 hours post-injury when compared to group B.Additionally,the concentrations of IL-1β and ICAM-1 were decreased significantly at each time point.[Conclusion]In Allen's acute SCI rat model,EGb761 could decrease the local concentration of IL-1β,suppress the abnormal expression of ICAM-1 protein and attenuate disruption of BSCB permeability.
Key concepts: Evans Blue, Medicine, Spinal cord, Spinal cord injury, Anesthesia, Laminectomy, Saline, Ginkgo biloba