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将胰岛素样生长因子衍生物与咖啡诺醇联合使用可在大鼠中风后产生强大的神经保护作用。

Combining insulin-like growth factor derivatives plus caffeinol produces robust neuroprotection after stroke in rats.

作者信息

Zhao Xiurong, Liu Shi-Jie, Zhang Jie, Strong Roger, Aronowski Jarek, Grotta James C

机构信息

Vascular Neurology Program, Department of Neurology, University of Texas-Houston Medical School, Houston, Tex 77030, USA.

出版信息

Stroke. 2005 Jan;36(1):129-34. doi: 10.1161/01.STR.0000149624.87661.18. Epub 2004 Nov 29.

Abstract

BACKGROUND AND PURPOSE

Insulin-like growth factor-1 (IGF-1) and caffeinol are both neuroprotective and probably have different mechanisms of action; therefore, they may be more effective in combination.

METHODS

We tested the N-terminal tripeptide of IGF-1, Gly-Pro-Glu (GPE), and its analogue, G2MePE, alone and with caffeinol in a rat middle cerebral artery (MCA) suture occlusion model. We randomly assigned rats to 6 groups of 8 to 12 animals: (1) control; (2) GPE, 3 mg/kg per hour; (3) G2MePE, 0.3 mg/kg per hour; (4) caffeinol, a mixture of caffeine (10 mg/kg) with ethanol (0.32 g/kg); (5) GPE with caffeinol (combination of group 2 with 4); and (6) G2MePE with caffeinol (combination of group 3 with 4). Drugs were started 75 minutes after suture occlusion, at the start of reperfusion. Three days after MCA occlusion, neurological deficit (Neurological Deficit Score [NDS]) and lesion volume were measured.

RESULTS

GPE and caffeinol improved NDS by 34% and 36%, respectively (P<0.01), and also decreased cortical but not striatal lesion volume compared with control (GPE cortex, 121 mm3; caffeinol cortex, 134 mm3; and control, 221 mm3; P<0.01). GPE plus caffeinol did not have more efficacy than either GPE or caffeinol alone. G2MePE slightly improved NDS (19.7%, P=0.05) but not lesion volume. However, G2MePE plus caffeinol very significantly improved NDS (64%) and lesion volume in both cortex (combination 95 mm3 versus control 221 mm3) and striatum (combination 74 mm3 versus control 110 mm3) (P<0.001), and was significantly more effective than either caffeinol or G2MePE alone.

CONCLUSIONS

Both GPE and caffeinol significantly protect cortex after MCA occlusion. At the doses used in this study, the GPE analogue G2MePE by itself had minimal protective effects, but when combined with caffeinol, it demonstrated robust beneficial effects on cortical and subcortical lesion size and behavioral deficit. Further study of this combination appears justified.

摘要

背景与目的

胰岛素样生长因子-1(IGF-1)和咖啡诺尔都具有神经保护作用,且可能具有不同的作用机制;因此,它们联合使用可能更有效。

方法

我们在大鼠大脑中动脉(MCA)缝合闭塞模型中,单独及联合咖啡诺尔测试了IGF-1的N端三肽甘氨酸-脯氨酸-谷氨酸(GPE)及其类似物G2MePE。我们将大鼠随机分为6组,每组8至12只动物:(1)对照组;(2)GPE,每小时3mg/kg;(3)G2MePE,每小时0.3mg/kg;(4)咖啡诺尔,咖啡因(10mg/kg)与乙醇(0.32g/kg)的混合物;(5)GPE与咖啡诺尔联合(第2组与第4组联合);(6)G2MePE与咖啡诺尔联合(第3组与第4组联合)。在缝合闭塞75分钟后、再灌注开始时给予药物。MCA闭塞3天后,测量神经功能缺损(神经功能缺损评分[NDS])和梗死体积。

结果

GPE和咖啡诺尔分别使NDS改善了34%和36%(P<0.01),与对照组相比,还减少了皮质梗死体积,但未减少纹状体梗死体积(GPE皮质梗死体积为121mm³;咖啡诺尔皮质梗死体积为134mm³;对照组为221mm³;P<0.01)。GPE加咖啡诺尔的疗效并不比单独使用GPE或咖啡诺尔更显著。G2MePE使NDS略有改善(19.7%,P=0.05),但未减少梗死体积。然而,G2MePE加咖啡诺尔非常显著地改善了NDS(64%)以及皮质(联合用药组95mm³,对照组221mm³)和纹状体(联合用药组74mm³,对照组110mm³)的梗死体积(P<0.001),且比单独使用咖啡诺尔或G2MePE更有效。

结论

GPE和咖啡诺尔在MCA闭塞后均能显著保护皮质。在本研究使用的剂量下,GPE类似物G2MePE本身的保护作用极小,但与咖啡诺尔联合使用时,对皮质和皮质下梗死大小及行为缺损显示出强大的有益作用。对这种联合用药进行进一步研究似乎是合理的。

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