Department of Neurology , University of Iowa Hospitals and Clinics, Iowa City, IA 52242, United States.
Department of Neurology, Medical College of Wisconsin, Wauwatosa, WI 53226, United States.
Curr Neurovasc Res. 2020;17(4):510-517. doi: 10.2174/1567202617999200831152233.
Hypoxic-ischemic encephalopathy (HIE) is a major cause of pediatric and adult mortality and morbidity. Unfortunately, to date, no effective treatment has been identified. In the striatum, neuronal injury is analogous to the cellular mechanism of necrosis observed during NMethyl- D-Aspartate (NMDA) excitotoxicity. Adenosine acts as a neuromodulator in the central nervous system, the role of which relies mostly on controlling excitatory glutamatergic synapses.
To examine the effect of pretreatment of SCH58261, an adenosine 2A (A2A) receptor antagonist and modulator of NMDA receptor function, following hypoxic-ischemia (HI) on sodium- potassium ATPase (Na+, K+-ATPase) activity and oxidative stress.
Piglets (4-7 days old) were subjected to 30 min hypoxia and 7 min of airway occlusion producing asphyxic cardiac arrest. Groups were divided into four categories: HI samples were divided into HI-vehicle group (n = 5) and HI-A2A group (n = 5). Sham controls were divided into Sham vehicle (n = 5) and Sham A2A (n = 5) groups. Vehicle groups were pretreated with 0.9% saline, whereas A2A animals were pretreated with SCH58261 10 min prior to intervention. Striatum samples were collected 3 h post-arrest. Sodium-potassium ATPase (Na+, K+-ATPase) activity, malondialdehyde (MDA) + 4-hydroxyalkenals (4-HDA) and glutathione (GSH) levels were compared.
Pretreatment with SCH58261 significantly attenuated the decrease in Na+, K+-ATPase, decreased MDA+4-HDA levels and increased GSH in the HI-A2A group when compared to HIvehicle.
A2A receptor activation may contribute to neuronal injury in newborn striatum after HI in association with decreased Na+, K+-ATPase activity and increased oxidative stress.
缺氧缺血性脑病(HIE)是小儿和成人死亡和发病的主要原因。不幸的是,迄今为止,尚未发现有效的治疗方法。在纹状体中,神经元损伤类似于 NMDA 兴奋性毒性观察到的细胞坏死机制。腺苷作为中枢神经系统中的神经调节剂,其作用主要依赖于控制兴奋性谷氨酸能突触。
研究缺氧缺血(HI)后,预先给予腺苷 2A(A2A)受体拮抗剂和 NMDA 受体功能调节剂 SCH58261 对钠离子-钾离子 ATP 酶(Na + ,K + -ATPase)活性和氧化应激的影响。
将仔猪(4-7 天大)置于 30 分钟缺氧和 7 分钟气道阻塞导致窒息性心脏骤停。将各组分为 4 类:HI 组分为 HI-vehicle 组(n = 5)和 HI-A2A 组(n = 5)。假手术对照组分为 Sham-vehicle 组(n = 5)和 Sham-A2A 组(n = 5)。载体组用 0.9%生理盐水预处理,而 A2A 动物在干预前用 SCH58261 预处理 10 分钟。在心跳骤停后 3 小时收集纹状体样本。比较钠离子-钾离子 ATP 酶(Na + ,K + -ATPase)活性、丙二醛(MDA)+4-羟基烯醛(4-HDA)和谷胱甘肽(GSH)水平。
与 HI-vehicle 组相比,SCH58261 预处理可显著减轻 HI-A2A 组 Na + ,K + -ATPase 活性降低、MDA+4-HDA 水平降低和 GSH 水平升高。
A2A 受体激活可能与 Na + ,K + -ATPase 活性降低和氧化应激增加有关,导致 HI 后新生纹状体神经元损伤。