Eslami Maesumeh, Oryan S Hahrbanoo, Rahnema Mehdi, Bigdeli Mohammad Reza
Department of Animal Physiology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran. Email:
Department of Animal Physiology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
Cell J. 2021 Aug;23(3):303-312. doi: 10.22074/cellj.2021.7204. Epub 2021 Jul 17.
Choroid plexus epithelial cells (CPECs) have the epithelial characteristic, produce cerebrospinal fluid, contribute to the detoxification process in the central nervous system (CNS), and are responsible for the synthesis and release of many nerve growth factors. On the other hand, studies suggest that normobaric hyperoxia (HO) by induction of ischemic tolerance (IT) can protect against brain damage and neurological diseases. We examined the effect of combination therapy of encapsulated CPECs and HO to protect against ischemic brain injury.
In this experimental study, six groups of adult male Wistar rats were randomly organized: sham, room air (RA)+middle cerebral artery occlusion (MCAO), HO+MCAO, RA+MCAO+encapsulated CPECs, HO+MCAO+encapsulated CPECs, RA+MCAO+empty capsules. RA/HO were pretreatment. The CPECs were isolated from the brain of neonatal Wistar rats, cultured, and encapsulated. Then microencapsulated CPECs were transplanted in the neck of the animal immediately after the onset of reperfusion in adult rats that had been exposed to 60 minutes MCAO. After 23 hours of reperfusion, the neurologic deficit score (NDS) was assessed. Next, rats were killed, and brains were isolated for measuring brain infarction volume, blood-brain barrier (BBB) permeability, edema, the activity of superoxide dismutase (SOD), and catalase (CAT) and also, the level of malondialdehyde (MDA).
Our results showed that NDS decreased equally in HO+MCAO, RA+MCAO+encapsulated CPECs, and HO+MCAO+encapsulated CPECs groups. Brain infarction volume decreased up 79%, BBB stability increased, edema decreased, SOD and CAT activities increased, and MDA decreased in the combination group of HO and transplantation of encapsulated CPECs in the ischemic brain as compared with when HO or transplantation of encapsulated CPECs was applied alone.
The combination of HO and transplantation of encapsulated CPECs for stroke in rats was more effective than the other treatments, and it can be taken into account as a promising treatment for ischemic stroke.
脉络丛上皮细胞(CPECs)具有上皮细胞特征,可产生脑脊液,有助于中枢神经系统(CNS)的解毒过程,并负责多种神经生长因子的合成与释放。另一方面,研究表明,通过诱导缺血耐受(IT)的常压高氧(HO)可预防脑损伤和神经疾病。我们研究了封装的CPECs与HO联合治疗对缺血性脑损伤的保护作用。
在本实验研究中,将成年雄性Wistar大鼠随机分为六组:假手术组、常氧(RA)+大脑中动脉闭塞(MCAO)组、HO+MCAO组、RA+MCAO+封装的CPECs组、HO+MCAO+封装的CPECs组、RA+MCAO+空胶囊组。RA/HO为预处理。从新生Wistar大鼠脑中分离CPECs,进行培养并封装。然后,在成年大鼠MCAO 60分钟后再灌注开始时,将微封装的CPECs立即移植到动物颈部。再灌注23小时后,评估神经功能缺损评分(NDS)。接下来,处死大鼠,分离大脑以测量脑梗死体积、血脑屏障(BBB)通透性、水肿、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性,以及丙二醛(MDA)水平。
我们的结果显示,HO+MCAO组、RA+MCAO+封装的CPECs组和HO+MCAO+封装的CPECs组的NDS均同等程度降低。与单独应用HO或封装的CPECs移植相比,HO与封装的CPECs移植联合应用于缺血性脑时,脑梗死体积减少了79%,BBB稳定性增加,水肿减轻,SOD和CAT活性增加,MDA降低。
HO与封装的CPECs移植联合治疗大鼠中风比其他治疗更有效,可被视为缺血性中风的一种有前景的治疗方法。