通过粒细胞集落刺激因子(G-CSF)治疗促进创伤性脑损伤(TBI)的恢复需要大麻素受体2型活性。

IF 4.3 Q1 PHARMACOLOGY & PHARMACY
Shijie Song, Bangmei Wang, Xiaoyuan Kong, Niketa Patel, Juan Sanchez-Ramos, Mark S Kindy
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引用次数: 0

摘要

粒细胞集落刺激因子(G-CSF)具有增强脑损伤后脑修复的能力。据报道,啮齿动物TBI后G-CSF治疗可促进脑修复、海马神经发生和行为恢复。德尔塔9-四氢大麻酚治疗还能增强脑外伤后的脑修复,并引发脑中G-CSF的上调,这就提出了G-CSF是否通过脑脊液介导恢复的问题。最近的一份报告显示,CB1和CB2受体的药物阻断并不妨碍CCI的恢复。鉴于受体的药物阻断有局限性,研究在CB2R切除或“敲除”的小鼠(CB2R KO小鼠)中进行。需要验证的假设是,G-CSF增强脑修复不需要CB2受体的活性。CCI后给予G-CSF 3天并没有增强CB2R KO小鼠旋转计测量的平衡和协调性的恢复,这与在正常对照小鼠中观察到的G-CSF治疗的有益作用不同。即使在CCI之前,CB2R小鼠在旋转计上也明显受损,这表明CB2R的活性对调节平衡和协调的神经网络的正常功能很重要。正常小鼠CCI后3天G-CSF处理CB2R表达增加,而CB2R KO小鼠则无升高。有趣的是,通过G-CSF处理,CB2R KO小鼠的CB1R上调,这表明“敲除”或降低CB2R的表达并不影响CB1R的表达。在CB2R KO小鼠中,神经营养因子BDNF和GDNF的表达不随G-CSF处理而改变。内源性大麻素配体2-AG的水平在CB2R KO小鼠中被证明通过G-CSF处理而增加,但2-AG的上调似乎并不促进平衡和协调的恢复。将需要对欧洲经委会的其他组成部分进行进一步研究。结论G-CSF增强脑修复不需要CB2受体活性的假设被本报告的数据所推翻。eCBs,特别是CB2R的活性,对于G-CSF促进CCI损害的平衡和协调恢复至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Promotion of recovery from Traumatic Brain Injury (TBI) by Granulocyte Colony-Stimulating Factor (G-CSF) treatment requires cannabinoid receptor type 2 activity.

Promotion of recovery from Traumatic Brain Injury (TBI) by Granulocyte Colony-Stimulating Factor (G-CSF) treatment requires cannabinoid receptor type 2 activity.

Promotion of recovery from Traumatic Brain Injury (TBI) by Granulocyte Colony-Stimulating Factor (G-CSF) treatment requires cannabinoid receptor type 2 activity.

Promotion of recovery from Traumatic Brain Injury (TBI) by Granulocyte Colony-Stimulating Factor (G-CSF) treatment requires cannabinoid receptor type 2 activity.

Granulocyte colony-stimulating factor (G-CSF) has the capacity to enhance brain repair following various injuries to brain. G-CSF treatment after TBI in rodents has been reported to promote brain repair, hippocampal neurogenesis, and behavioral recovery. Delta9-THC treatment also enhances brain repair after TBI, and triggers upregulation of G-CSF in brain, raising the question as to whether G-CSF mediates recovery via the eCBs. A recent report revealed that pharmacological blockade of CB1 and CB2 receptors did not impede recovery from CCI. Given that pharmacological blockade of receptors has limitations, studies were conducted in mice with ablated or "knocked out" CB2R (CB2R KO mice). The hypothesis to be tested is that G-CSF enhancement of brain repair does not require activity of CB2 receptors.Results and discussion G-CSF administration for 3 days after CCI did not enhance recovery of balance and coordination measured on the rotometer in CB2R KO mice, unlike the beneficial effects of G-CSF treatment observed in normal control mice. Even before CCI, the CB2R mice were markedly impaired on the rotometer, suggesting that activity of CB2R is important for normal function of neural networks that mediate balance and coordination. Expression of CB2R was increased by G-CSF treatment in normal mice 3 days after CCI but not in CB2R KO mice. Interestingly, the CB1R in the CB2R KO mice was upregulated by G-CSF treatment indicating that "knocking-out" or lowering expression of CB2R did not impact expression of CB1R. Expression of the neurotrophic factors BDNF and GDNF did not change with G-CSF treatment in CB2R KO mice. Levels of the endogenous cannabinoid ligand, 2-AG, were shown to be increased by G-CSF treatment in the CB2R KO mice, but upregulation of 2-AG does not appear to promote recovery of balance and coordination. Additional studies will be required of other components of the eCBs.Conclusion The hypothesis that G-CSF enhancement of brain repair does not require activity of CB2 receptors is disproven by data in this report. The eCBs, in particular activity of the CB2R, is critical for G-CSF promotion of recovery of balance and coordination impaired by CCI.

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