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成像研究 β-羟丁酸对梗死周边神经血管功能和代谢的影响。

Imaging the Effects of β-Hydroxybutyrate on Peri-Infarct Neurovascular Function and Metabolism.

机构信息

From the Physical Sciences Platform (P.B., E.M.L., T.L.B., M.M.K., I.W., J.M., R.J., A.D., G.J.S., B.S.).

Sunnybrook Research Institute, Toronto, Canada; Fundamental Neurobiology, Krembil Research Institute, Toronto, Canada (P.B., I.W., P.L.C.).

出版信息

Stroke. 2018 Sep;49(9):2173-2181. doi: 10.1161/STROKEAHA.118.020586.

Abstract

Background and Purpose- Recent evidence suggests great potential of metabolically targeted interventions for treating neurological disorders. We investigated the use of the endogenous ketone body β-hydroxybutyrate (BHB) as an alternate metabolic substrate for the brain in the acute phase of ischemia because postischemic hyperglycemia and brain glucose metabolism elevation compromise functional recovery. Methods- We delivered BHB (or vehicle) 1 hour after ischemic insult induced by cortical microinjection of endothelin-1 in sensorimotor cortex of rats. Two days after ischemic insult, the rats underwent multimodal characterization of the BHB effects. We examined glucose uptake on 2-Deoxy-d-glucose chemical exchange saturation transfer magnetic resonance imaging, cerebral hemodynamics on continuous arterial spin labeling magnetic resonance imaging, resting-state field potentials by intracerebral multielectrode arrays, Neurological Deficit Score, reactive oxygen species production, and astrogliosis and neuronal death. Results- When compared with vehicle-administered animals, BHB-treated cohort showed decreased peri-infarct neuronal glucose uptake which was associated with reduced oxidative stress, diminished astrogliosis and neuronal death. Functional examination revealed ameliorated neuronal functioning, normalized perilesional resting perfusion, and ameliorated cerebrovascular reactivity to hypercapnia, suggesting improved functioning. Cellular and functional recovery of the neurogliovascular unit in the BHB-treated animals was associated with improved performance on the withdrawal test. Conclusions- We characterize the effects of the ketone body BHB administration at cellular and system levels after focal cortical stroke. The results demonstrate that BHB curbs the peri-infarct glucose-metabolism driven production of reactive oxygen species and astrogliosis, culminating in improved neurogliovascular and functional recovery.

摘要

背景与目的- 最近的证据表明,代谢靶向干预在治疗神经疾病方面具有巨大潜力。我们研究了内源性酮体β-羟丁酸(BHB)在缺血急性期作为大脑替代代谢底物的用途,因为缺血后高血糖和脑葡萄糖代谢升高会损害功能恢复。方法- 我们在大脑感觉运动皮层内皮素-1 微注射诱导缺血后 1 小时给予 BHB(或载体)。在缺血后 2 天,对大鼠进行 BHB 影响的多模态特征分析。我们通过 2-脱氧-d-葡萄糖化学交换饱和转移磁共振成像检查葡萄糖摄取,通过连续动脉自旋标记磁共振成像检查脑血流动力学,通过颅内多电极阵列检查静息状态场电位,通过神经功能缺损评分、活性氧物质产生、星形胶质细胞增生和神经元死亡检查。结果- 与给予载体的动物相比,BHB 治疗组显示出梗死周边区神经元葡萄糖摄取减少,这与氧化应激减少、星形胶质细胞增生和神经元死亡减少有关。功能检查显示神经元功能改善,病变周围的静息灌注正常化,以及对高碳酸血症的脑血管反应性改善,表明功能改善。BHB 治疗动物的神经胶质血管单元的细胞和功能恢复与撤回测试中的表现改善相关。结论- 我们在局灶性皮质卒中后从细胞和系统水平描述了酮体 BHB 给药的效果。结果表明,BHB 抑制了梗死周边区葡萄糖代谢驱动的活性氧物质和星形胶质细胞增生的产生,最终导致神经胶质血管和功能恢复改善。

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