Liu Luyu, Gong Maowei, Liao Guosong, Zhao Weixing, Fu Qiang
Department of Anesthesiology, First Medical Center.
Graduate School, Chinese PLA General Hospital, Beijing 100853, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2025 Apr 20;45(4):725-735. doi: 10.12122/j.issn.1673-4254.2025.04.07.
To explore the correlation of hypertension with postoperative cognitive dysfunction and its possible mechanism.
Twelve-week-old spontaneously hypertensive rats (SHRs) and Wistar-Kyoto (WKY) rats were both randomized into control group and surgical group (8). In the latter group, the rats received carotid artery exposure surgery under sevoflurane anesthesia to establish models of postoperative learning and memory impairment. Postoperative cognitive function changes of the rats were evaluated using behavioral tests. The hippocampus of the rats were collected for determining ATP level and mitochondrial membrane potential (MMP) and for detecting expressions of UCP2 and astrocyte markers (GFAP and NOX4) using Western blotting and immunofluorescence staining. Serum levels of ROS, IL-6, IL-1β and TNF‑α were detected using ELISA. Nissl staining was used to examine hippocampal neuronal loss in the CA1 region.
The SHRs exhibited exacerbated learning and memory deficits following the surgery as shown by significantly reduced performance in novel object recognition tests and context-related and tone-related fear conditioning experiments. Compared with WKY rats, the SHRs had significantly decreased mitochondrial UCP2 expression and MMP in the hippocampus, increased hippocampal ATP level, and markedly increased serum levels of ROS and inflammatory factors, showing also increased activation of hippocampal astrocytes and microglia and reduced number of neurons positive for Nissl staining.
Hypertension can exacerbate major postoperative learning and memory impairment in rats possibly as a result of UCP2-mediated mitochondrial dysfunction and oxidative stress damage, which further leads to astrocyte overactivation and neuronal damage.
探讨高血压与术后认知功能障碍的相关性及其可能机制。
将12周龄的自发性高血压大鼠(SHRs)和Wistar-Kyoto(WKY)大鼠均随机分为对照组和手术组(每组8只)。手术组大鼠在七氟醚麻醉下接受颈动脉暴露手术,以建立术后学习和记忆障碍模型。采用行为学测试评估大鼠术后认知功能变化。采集大鼠海马组织,测定ATP水平和线粒体膜电位(MMP),并通过蛋白质免疫印迹法和免疫荧光染色检测UCP2及星形胶质细胞标志物(GFAP和NOX4)的表达。采用酶联免疫吸附测定法(ELISA)检测血清中活性氧(ROS)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)水平。采用尼氏染色法检测海马CA1区神经元丢失情况。
与WKY大鼠相比,SHRs术后学习和记忆缺陷加剧,表现为新物体识别试验以及与情境相关和与音调相关的恐惧条件反射实验中的表现显著降低。SHRs海马组织中线粒体UCP2表达和MMP显著降低,海马ATP水平升高,血清ROS和炎性因子水平显著升高,海马星形胶质细胞和小胶质细胞激活增加,尼氏染色阳性神经元数量减少。
高血压可能通过UCP2介导的线粒体功能障碍和氧化应激损伤,加剧大鼠术后主要的学习和记忆障碍,进而导致星形胶质细胞过度激活和神经元损伤。