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首页> 外文期刊>Journal of neurosurgery. >Reversal of cerebral vasospasm via intravenous sodium nitrite after subarachnoid hemorrhage in primates.
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Reversal of cerebral vasospasm via intravenous sodium nitrite after subarachnoid hemorrhage in primates.

机译:灵长类动物蛛网膜下腔出血后通过静脉注射亚硝酸钠逆转脑血管痉挛。

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Object Subarachnoid hemorrhage (SAH)-induced vasospasm is a significant underlying cause of aneurysm rupture-related morbidity and death. While long-term intravenous infusion of sodium nitrite (NaNO(2)) can prevent cerebral vasospasm after SAH, it is not known if the intravenous administration of this compound can reverse established SAH-induced vasospasm. To determine if the intravenous infusion of NaNO(2) can reverse established vasospasm, the authors infused primates with the compound after SAH-induced vasospasm was established. Methods Subarachnoid hemorrhage-induced vasospasm was created in 14 cynomolgus macaques via subarachnoid implantation of a 5-ml blood clot. On Day 7 after clot implantation, animals were randomized to either control (saline infusion, 5 monkeys) or treatment groups (intravenous NaNO(2) infusion at 300 mug/kg/hr for 3 hours [7 monkeys] or 8 hours [2 monkeys]). Arteriographic vessel diameter was blindly analyzed to determine the degree of vasospasm before, during, and after treatment. Nitric oxide metabolites (nitrite, nitrate, and S-nitrosothiols) were measured in whole blood and CSF. Results Moderate-to-severe vasospasm was present in all animals before treatment (control, 36.2% +/- 8.8% [mean +/- SD]; treatment, 45.5% +/- 12.5%; p = 0.9). While saline infusion did not reduce vasospasm, NaNO(2) infusion significantly reduced the degree of vasospasm (26.9% +/- 7.6%; p = 0.008). Reversal of the vasospasm lasted more than 2 hours after cessation of the infusion and could be maintained with a prolonged infusion. Nitrite (peak value, 3.7 +/- 2.1 mumol/L), nitrate (18.2 +/- 5.3 mumol/L), and S-nitrosothiols (33.4 +/- 11.4 nmol/L) increased significantly in whole blood, and nitrite increased significantly in CSF. Conclusions These findings indicate that the intravenous infusion of NaNO(2) can reverse SAH-induced vasospasm in primates. Further, these findings indicate that a similar treatment paradigm could be useful in reversing cerebral vasospasm after aneurysmal SAH.
机译:对象蛛网膜下腔出血(SAH)诱发的血管痉挛是与动脉瘤破裂相关的发病率和死亡的重要根本原因。虽然长期静脉内输注亚硝酸钠(NaNO(2))可以预防SAH后的脑血管痉挛,但尚不知道该化合物的静脉内给药是否可以逆转已建立的SAH诱导的血管痉挛。为了确定NaNO(2)的静脉输液是否可以逆转已建立的血管痉挛,作者在SAH诱导的血管痉挛建立后向灵长类动物注入了该化合物。方法通过蛛网膜下腔植入5-ml血凝块在14只食蟹猕猴中产生蛛网膜下腔出血引起的血管痉挛。血块植入后第7天,将动物随机分为对照组(盐水输注,5只猴子)或治疗组(静脉输注NaNO(2),以300杯/ kg / hr的速度输注3小时[7只猴子]或8小时[2只猴子] ])。对动脉造影血管直径进行盲法分析,以确定治疗前,治疗中和治疗后的血管痉挛程度。在全血和脑脊液中测量一氧化氮代谢产物(亚硝酸盐,硝酸盐和S-亚硝基硫醇)。结果治疗前所有动物均存在中度至重度血管痉挛(对照组,36.2%+/- 8.8%[平均值+/- SD];治疗,45.5%+/- 12.5%; p = 0.9)。输注生理盐水并不能减少血管痉挛,而NaNO(2)输注可以显着降低血管痉挛的程度(26.9%+/- 7.6%; p = 0.008)。停止输注后,血管痉挛的逆转持续了超过2小时,可以通过长时间输注来维持。全血中亚硝酸盐(峰值,3.7 +/- 2.1μmol/ L),硝酸盐(18.2 +/- 5.3μmol/ L)和S-亚硝基硫醇(33.4 +/- 11.4 nmol / L)在全血中​​显着增加,亚硝酸盐增加在脑脊液中显着。结论这些发现表明,静脉内输注NaNO(2)可以逆转SAH诱导的灵长类动物的血管痉挛。此外,这些发现表明,在动脉瘤性SAH后逆转脑血管痉挛可能使用类似的治疗范例。

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