Department of Acupuncture and Moxibustion, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Department of Neurobiology and Acupuncture Research, The Third Clinical Medical College, Zhejiang Chinese Medical University, Key Laboratory of Acupuncture and Neurology of Zhejiang Province, Hangzhou, China.
Neural Plast. 2020 Feb 26;2020:9076042. doi: 10.1155/2020/9076042. eCollection 2020.
Electroacupuncture (EA) can effectively alleviate anxiety disorders and memory impairments caused by various neurodegenerative diseases; however, the molecular mechanisms underlying its neuroprotective effects are unclear. Previous studies have shown that the renin-angiotensin system (RAS) comprises of two axes with mutual antagonism: the classical angiotensin converting enzyme/angiotensin II/angiotensin II type 1 receptor (ACE/Ang II/AT1R) axis and the protective angiotensin converting enzyme 2/angiotensin-(1-7)/Mas receptor (ACE2/Ang-(1-7)/MasR) axis. In this study, we observed that chronic cerebral hypoperfusion (CCH) mediated anxiety-like behavior and memory impairments in spontaneously hypertensive rats (SHR) via upregulation of the hippocampal classical axis (ACE/Ang II/AT1R) and the partial hippocampal protective axis (ACE2/Ang-(1-7)). However, Ang II levels were much higher than those of Ang-(1-7), indicating that the ACE/Ang II/AT1R axis plays a dominant role in the comorbidity of CCH and hypertension. Moreover, candesartan cilexetil (Canc) and perindopril (Peril) were used as positive control drugs. We found that EA, Canc, and Peril attenuated CCH-induced anxiety-like behavior and memory impairments in SHR, potentially via downregulation of the hippocampal classical axis (ACE/Ang II/AT1R) and upregulation of the whole hippocampal protective axis (ACE2/Ang-(1-7)/MasR). These results suggest that EA therapy for CCH with hypertension may be mediated by two hippocampal RAS axes.
电针(EA)可以有效缓解各种神经退行性疾病引起的焦虑症和记忆障碍;然而,其神经保护作用的分子机制尚不清楚。先前的研究表明,肾素-血管紧张素系统(RAS)包含两个相互拮抗的轴:经典的血管紧张素转换酶/血管紧张素 II/血管紧张素 II 型 1 受体(ACE/Ang II/AT1R)轴和保护性的血管紧张素转换酶 2/血管紧张素-(1-7)/Mas 受体(ACE2/Ang-(1-7)/MasR)轴。在这项研究中,我们观察到慢性大脑低灌注(CCH)通过上调海马体经典轴(ACE/Ang II/AT1R)和部分海马体保护轴(ACE2/Ang-(1-7)),在自发性高血压大鼠(SHR)中引起焦虑样行为和记忆障碍。然而,Ang II 的水平远高于 Ang-(1-7),这表明 ACE/Ang II/AT1R 轴在 CCH 和高血压的合并症中起主导作用。此外,坎地沙坦西酯(Canc)和培哚普利(Peril)被用作阳性对照药物。我们发现,EA、Canc 和 Peril 可减轻 SHR 中由 CCH 引起的焦虑样行为和记忆障碍,可能是通过下调海马体经典轴(ACE/Ang II/AT1R)和上调整个海马体保护轴(ACE2/Ang-(1-7)/MasR)。这些结果表明,EA 治疗 CCH 合并高血压可能通过两个海马体 RAS 轴介导。