Laboratory of Neurobiology, Centro de Investigación Príncipe Felipe, Valencia, Spain.
CNS Neurosci Ther. 2017 May;23(5):386-394. doi: 10.1111/cns.12688. Epub 2017 Mar 11.
Patients with liver disease may develop hepatic encephalopathy (HE), with cognitive impairment and motor in-coordination. Rats with HE due to portacaval shunts (PCS) show motor in-coordination. We hypothesized that in PCS rats: (i) Motor in-coordination would be due to enhanced GABAergic tone in cerebellum; (ii) increased GABAergic tone would be due to neuroinflammation; (iii) increasing cGMP would reduce neuroinflammation and GABAergic tone and restore motor coordination. To assess these hypotheses, we assessed if (i) treatment with sildenafil reduces neuroinflammation; (ii) reduced neuroinflammation is associated with reduced GABAergic tone and restored motor coordination.
Rats were treated with sildenafil to increase cGMP. Microglia and astrocytes activation were analyzed by immunohistochemistry, extracellular GABA by microdialysis, and motor coordination in the beam walking.
PCS rats show neuroinflammation in cerebellum, with microglia and astrocytes activation, increased IL-1b and TNF-a and reduced YM-1 and IL-4. Membrane expression of the GABA transporter GAT1 is reduced, while GAT3 is increased. Extracellular GABA and motor in-coordination are increased. Sildenafil treatment eliminates neuroinflammation, microglia and astrocytes activation; changes in membrane expression of GABA transporters; and restores motor coordination.
This study supports an interplay between cGMP-neuroinflammation and GABAergic neurotransmission in impairing motor coordination in PCS rats.
患有肝脏疾病的患者可能会发展为肝性脑病(HE),出现认知障碍和运动协调障碍。由于门腔分流术(PCS)导致的 HE 大鼠表现出运动协调障碍。我们假设在 PCS 大鼠中:(i)运动协调障碍是由于小脑 GABA 能神经传递增强所致;(ii)GABA 能神经传递增强是由于神经炎症所致;(iii)增加 cGMP 会减少神经炎症和 GABA 能神经传递,并恢复运动协调。为了评估这些假设,我们评估了(i)西地那非治疗是否会减轻神经炎症;(ii)减轻神经炎症是否与 GABA 能神经传递减少和运动协调恢复有关。
用西地那非增加 cGMP 来治疗大鼠。通过免疫组织化学分析小胶质细胞和星形胶质细胞的激活,通过微透析分析细胞外 GABA,通过在横梁行走中评估运动协调。
PCS 大鼠小脑出现神经炎症,表现为小胶质细胞和星形胶质细胞激活,IL-1b 和 TNF-a 增加,YM-1 和 IL-4 减少。GABA 转运体 GAT1 的膜表达减少,而 GAT3 增加。细胞外 GABA 和运动协调障碍增加。西地那非治疗可消除神经炎症、小胶质细胞和星形胶质细胞激活、GABA 转运体膜表达的改变,并恢复运动协调。
本研究支持 cGMP-神经炎症和 GABA 能神经传递在损害 PCS 大鼠运动协调中的相互作用。