Why the study?
This study was designed to evaluate whether neuregulin-1β plays a protective role in spinal cord ischemia and reperfusion injury.
Does neuregulin-1β reduce spinal cord ischemia reperfusion injury in a rat model?
Does neuregulin-1β reduce spinal cord ischemia reperfusion injury in a rat model?
Neuregulin-1β reduces spinal cord ischemia-reperfusion injury in a rat model, potentially by downregulating MMP-9 and upregulating TIMP-1 expression.
NRG-1β reduces rat SCII damage; leaves open whether it protects human spinal cord during ischemia-reperfusion.
Objective: This study was designed to see if neuregulin-1β (NRG-1β) plays a protective role in spinal cord ischemia and reperfusion injury (SCII).Design: Animal research.Setting: China.Participants: NA.Interventions: Forty-eight SD rats were randomly divided into control group (n = 16), SCII model group (n = 16) and NRG-1β-treated group (n = 16). In control group, the abdominal aorta was isolated but not clipped. The rats in NRG-1β-treated group were treated with 10μg/kg NRG-1β during developing SCII model.Outcome Measures: Neurological scores were evaluated. At 3, 6, 12 and 24 h after the reperfusion, rats were killed. Pathological changes of spinal cord were assessed with HE staining, and immunohistochemical staining of matrix metalloproteinases-9 (MMP-9) and tissue inhibitor of metalloproteinase-1 (TIMP-1). MMP-9 and TIMP-1 mRNA levels were assessed using real-time PCR.Results: NRG-1β reduced the damage of SCII in the rats. The expression of MMP-9 protein and mRNA in NRG-1β treatment group was significantly lower than the model group (P < 0.05) at 6 h, 12 h and 24 h after the perfusion. The expression of TIMP-1 protein and mRNA in the treatment group was significantly higher than the model group at 12 h and 24 h after the perfusion.Conclusion: NRG-1β reduced the reperfusion damage in rat model of SCII, in which process MMP-9 and TIMP-1 were probably involved.
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Jing et al. (2019) studied this question.
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