Lenzlinger Philipp M, Saatman Kathryn E, Hoover Rachel C, Cheney Jessica A, Bareyre Florence M, Raghupathi Ramesh, Arnold Lee D, McIntosh Tracy K
Head Injury Center, Department of Neurosurgery, University of Pennsylvania, School of Medicine, Philadelphia, PA 19104-6316, USA.
Restor Neurol Neurosci. 2004;22(2):73-9.
In the present study we assessed the ability of BSF476921, an inhibitor of vascular endothelial growth factor receptor (VEGFR) kinase signal transduction, to reduce edema formation and neurologic motor dysfunction following lateral fluid percussion (FP) brain injury in rats.
Anesthetized adult male rats were subjected to either lateral FP brain injury of moderate severity (n = 37) or sham injury (n = 22, surgery without brain injury). Animals were randomized to receive i.p. injections of either BSF476921 (30 mg/kg bw; injured n = 15, sham n = 11) or sterile water (injured n = 14, sham n = 11) at 1, 11 and 22 hours post-injury. After assessment of motor function using a standard 28-point neuroscore, animals were sacrificed 24 hours following trauma and their brains evaluated for regional water content using the wet-weight/dry-weight technique.
Although brain-injured animals showed a significant motor deficit compared to uninjured animals, no differences were detected between BSF476921- and vehicle-treated animals at the acute 24 hour post-injury time point. However, BSF476921 significantly attenuated regional edema formation in brain-injured animals in the ipsilateral hippocampus (p < 0.05) and in the cortex adjacent to the injury (p < 0.05) when compared to vehicle treatment.
To our knowledge, this is the first report of a small molecule VEGFR kinase inhibitor reducing cerebral edema in a widely accepted model of brain injury.
在本研究中,我们评估了血管内皮生长因子受体(VEGFR)激酶信号转导抑制剂BSF476921减轻大鼠侧方液压冲击(FP)脑损伤后水肿形成和神经运动功能障碍的能力。
将成年雄性麻醉大鼠分为中度严重侧方FP脑损伤组(n = 37)或假损伤组(n = 22,仅进行手术但无脑损伤)。动物在损伤后1、11和22小时随机接受腹腔注射BSF476921(30 mg/kg体重;损伤组n = 15,假损伤组n = 11)或无菌水(损伤组n = 14,假损伤组n = 11)。使用标准的28分神经评分评估运动功能后,在创伤后24小时处死动物,并用湿重/干重技术评估其大脑区域含水量。
与未受伤动物相比,脑损伤动物表现出明显的运动缺陷,但在损伤后24小时的急性时间点,BSF476921治疗组和溶剂对照组动物之间未检测到差异。然而,与溶剂对照治疗相比,BSF476921显著减轻了脑损伤动物同侧海马体(p < 0.05)和损伤附近皮质(p < 0.05)的局部水肿形成。
据我们所知,这是小分子VEGFR激酶抑制剂在广泛接受的脑损伤模型中减轻脑水肿的首次报道。