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静脉输注 DL-3-β-羟基丁酸钠可降低实验性心脏骤停复苏后脑损伤生物标志物水平。

Infusion of sodium DL-3-ß-hydroxybutyrate decreases cerebral injury biomarkers after resuscitation in experimental cardiac arrest.

机构信息

Department of Intensive Care, Erasme Hospital, Université Libre de Bruxelles, Lennik Road 808, 1070, Brussels, Belgium.

Experimental Laboratory of Intensive Care, Free University of Brussels, Brussels, Belgium.

出版信息

Crit Care. 2024 Sep 20;28(1):314. doi: 10.1186/s13054-024-05106-8.

Abstract

AIMS

Cerebral complications after cardiac arrest (CA) remain a major problem worldwide. The aim was to test the effects of sodium-ß-hydroxybutyrate (SBHB) infusion on brain injury in a clinically relevant swine model of CA.

RESULTS

CA was electrically induced in 20 adult swine. After 10 min, cardiopulmonary resuscitation was performed for 5 min. After return of spontaneous circulation (ROSC), the animals were randomly assigned to receive an infusion of balanced crystalloid (controls, n = 11) or SBHB (theoretical osmolarity 1189 mOsm/l, n = 8) for 12 h. Multimodal neurological and cardiovascular monitoring were implemented in all animals. Nineteen of the 20 animals achieved ROSC. Blood sodium concentrations, osmolarity and circulating KBs were higher in the treated animals than in the controls. SBHB infusion was associated with significantly lower plasma biomarkers of brain injury at 6 (glial fibrillary acid protein, GFAP and neuron specific enolase, NSE) and 12 h (neurofilament light chain, NFL, GFAP and NSE) compared to controls. The amplitude of the stereoelectroencephalograph (sEEG) increased in treated animals after ROSC compared to controls. Cerebral glucose uptake was lower in treated animals.

CONCLUSIONS

In this experimental model, SBHB infusion after resuscitated CA was associated with reduced circulating markers of cerebral injury and increased sEEG amplitude.

摘要

目的

心脏骤停(CA)后的脑部并发症仍然是全球的一个主要问题。本研究旨在检测 SBHB 输注对复律后猪 CA 模型脑损伤的影响。

结果

20 头成年猪诱导发生 CA。CA 发生 10 min 后,进行心肺复苏 5 min。自主循环恢复(ROSC)后,动物随机分为接受平衡晶体液输注(对照组,n=11)或 SBHB 输注(理论渗透压 1189 mOsm/L,n=8)12 h。所有动物均进行多模式神经和心血管监测。20 只动物中有 19 只达到 ROSC。与对照组相比,治疗组的血钠浓度、渗透压和循环 KBs 更高。与对照组相比,SBHB 输注在 6 小时(胶质纤维酸性蛋白,GFAP 和神经元特异性烯醇化酶,NSE)和 12 小时(神经丝轻链,NFL、GFAP 和 NSE)时,血浆脑损伤生物标志物明显降低。与对照组相比,ROSC 后治疗组立体脑电图(sEEG)的振幅增加。治疗组的脑葡萄糖摄取量较低。

结论

在这个实验模型中,CA 复律后 SBHB 输注与循环脑损伤标志物减少和 sEEG 振幅增加有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dba5/11414246/a83cca9302e6/13054_2024_5106_Fig1_HTML.jpg

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