Department of Neurosurgery, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark; Clinical Experimental Research Unit, Translational Research Centre, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark.
Clinical Experimental Research Unit, Translational Research Centre, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark; Center for RNA Medicine, Aalborg University, Copenhagen, Denmark.
J Stroke Cerebrovasc Dis. 2024 Jul;33(7):107728. doi: 10.1016/j.jstrokecerebrovasdis.2024.107728. Epub 2024 Apr 19.
Subarachnoid haemorrhage (SAH) carries a high burden of morbidity and mortality. One in three patients develop vasospasm, which is associated with Delayed Cerebral Ischemia. The pathophysiology includes vasoconstrictor receptor upregulation in cerebral arteries. The protein kinase C - inhibitor RO-31-7549 reduces the expression of several vasoconstrictor receptors and normalizes cerebral blood flow in experimental SAH but functional and behavioural effects are unknown. This study was undertaken to analyse functional outcomes up to 14 days after experimental SAH.
54 male rats were randomised to experimental SAH or sham, using the pre-chiasmatic, single injection model, and subsequent treatment or vehicle. 42 remained for final analysis. The animals were euthanized on day 14 or when reaching a humane endpoint. The primary endpoint was overall survival, defined as either spontaneous mortality or when reaching a predefined humane endpoint. The secondary outcomes were differences in the rotating pole test, weight, open field test, novel object recognition and qPCR of selected inflammatory markers.
In the vehicle group 6/15 rats reached the humane endpoint of >20 % weight loss compared to 1/14 in the treatment group. This resulted in a significant reduced risk of early euthanasia due to >20 % weight loss of HR 0.15 (0.03-0.66, p = 0.04). Furthermore, the treatment group did significantly better on the rotating pole test, RR 0.64 (0.47-0.91, p = 0.02).
RO-31-7549 improved outcomes in terms >20 % weight loss and rotating pole performance after experimental SAH and could be investigated.
蛛网膜下腔出血(SAH)发病率和死亡率高。三分之一的患者发生血管痉挛,与迟发性脑缺血有关。病理生理学包括脑血管中血管收缩剂受体的上调。蛋白激酶 C 抑制剂 RO-31-7549 可降低几种血管收缩剂受体的表达,并使实验性 SAH 中的脑血流正常化,但功能和行为影响尚不清楚。本研究旨在分析实验性 SAH 后 14 天内的功能结果。
54 只雄性大鼠随机分为实验性 SAH 或假手术组,采用视交叉前、单次注射模型,随后进行治疗或载体治疗。42 只大鼠用于最终分析。动物在第 14 天或达到人道终点时安乐死。主要终点是总生存率,定义为自发性死亡率或达到预定的人道终点。次要终点是旋转杆试验、体重、旷场试验、新物体识别和选定炎症标志物的 qPCR 的差异。
在载体组中,有 6/15 只大鼠达到了>20%体重减轻的人道终点,而在治疗组中只有 1/14 只大鼠达到了这一终点。这导致由于>20%体重减轻而早期安乐死的风险显著降低,HR 为 0.15(0.03-0.66,p=0.04)。此外,治疗组在旋转杆试验中表现明显更好,RR 为 0.64(0.47-0.91,p=0.02)。
RO-31-7549 改善了实验性 SAH 后>20%体重减轻和旋转杆性能的预后,可以进一步研究。