Department of Physiology, School of Medicine, Tehran University of Medical Sciences, PourSina St., 1417613151, Tehran, Iran.
Metab Brain Dis. 2022 Jun;37(5):1503-1516. doi: 10.1007/s11011-022-00985-8. Epub 2022 May 2.
Multiple neuronal injury pathways are activated during cerebral ischemia and reperfusion (I/R). This study was designed to decrease potential neuronal injuries by using both transcranial direct current stimulation (tDCS) polarities in cerebral ischemia and its following reperfusion period. Ninety rats were randomly divided into six groups. In the sham group, rats were intact. In the I/R group, global cerebral I/R was only induced. In the I/R + c-tDCS and I/R + a-tDCS groups, cathodal and anodal currents were applied, respectively. In the I/R + c/a-tDCS, cathodal current was used in the cerebral ischemia and anodal in the reperfusion. In the I/R + a/c-tDCS group, cathodal and anodal currents were applied in the I/R, respectively. Hippocampal tissue was used to determine the levels of IL-1β, TNF-α, NOS, SOD, MDA, and NMDAR. Hot plate and open field tests evaluated sensory and locomotor performances. The cerebral edema was also measured. Histological assessment was assessed by H/E and Nissl staining of the hippocampal CA1 region. All tDCS modes significantly decreased IL-1β and TNF-α levels, especially in the c/a-tDCS. All tDCS caused a significant decrease in MDA and NOS levels while increasing SOD activity compared to the I/R group, especially in the c/a-tDCS mode. In the c-tDCS and a/c-tDCS groups, the NMDAR level was significantly decreased. The c/a-tDCS group improved sensory and locomotor performances more than other groups receiving tDCS. Furthermore, the least neuronal death was observed in the c/a-tDCS mode. Using two different polarities of tDCS could induce more neuroprotective versus pathophysiological pathways in cerebral I/R, especially in c/a-tDCS mode. HIGHLIGHTS: Multiple pathways of neuronal injury are activated in cerebral ischemia and reperfusion (I/R). Using tDCS could modulate neuroinflammation and oxidative stress pathways in global cerebral I/R. Using c/a-tDCS mode during cerebral I/R causes more neuroprotective effects against neuronal injuries of cerebral I/R.
在脑缺血再灌注(I/R)期间,多个神经元损伤途径被激活。本研究旨在通过在脑缺血及其随后的再灌注期间使用两种经颅直流电刺激(tDCS)极性来减少潜在的神经元损伤。90 只大鼠被随机分为六组。在假手术组中,大鼠完整无损。在 I/R 组中,仅诱导全脑 I/R。在 I/R+c-tDCS 和 I/R+a-tDCS 组中,分别施加阴极和阳极电流。在 I/R+c/a-tDCS 中,在脑缺血期间使用阴极电流,在再灌注期间使用阳极电流。在 I/R+a/c-tDCS 组中,在 I/R 期间施加阴极和阳极电流。使用海马组织来确定 IL-1β、TNF-α、NOS、SOD、MDA 和 NMDAR 的水平。热板和旷场试验评估感觉和运动表现。还测量了脑水肿。通过海马 CA1 区的 H/E 和尼氏染色评估组织学评估。所有 tDCS 模式均显著降低了 IL-1β 和 TNF-α 水平,尤其是在 c/a-tDCS 中。与 I/R 组相比,所有 tDCS 均显著降低 MDA 和 NOS 水平,同时增加 SOD 活性,尤其是在 c/a-tDCS 模式下。在 c-tDCS 和 a/c-tDCS 组中,NMDAR 水平显著降低。c/a-tDCS 组比接受 tDCS 的其他组更能改善感觉和运动表现。此外,在 c/a-tDCS 模式下观察到的神经元死亡最少。在脑 I/R 中使用两种不同极性的 tDCS 可以诱导更多的神经保护与病理生理途径,尤其是在 c/a-tDCS 模式下。重点:在脑缺血再灌注(I/R)期间,多个神经元损伤途径被激活。使用 tDCS 可以调节全脑 I/R 中的神经炎症和氧化应激途径。在脑 I/R 期间使用 c/a-tDCS 模式会对脑 I/R 的神经元损伤产生更多的神经保护作用。