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肝性脑病:从代谢到神经退行性变。

Hepatic Encephalopathy: From Metabolic to Neurodegenerative.

机构信息

Hepato-Neuro Laboratory, CRCHUM, Université de Montréal, 900, rue Saint-Denis Pavillon R, R08.422, Montreal, QC, H2X-0A9, Canada.

出版信息

Neurochem Res. 2021 Oct;46(10):2612-2625. doi: 10.1007/s11064-021-03372-4. Epub 2021 Jun 15.

DOI:10.1007/s11064-021-03372-4
PMID:34129161
Abstract

Hepatic encephalopathy (HE) is a neuropsychiatric syndrome of both acute and chronic liver disease. As a metabolic disorder, HE is considered to be reversible and therefore is expected to resolve following the replacement of the diseased liver with a healthy liver. However, persisting neurological complications are observed in up to 47% of transplanted patients. Several retrospective studies have shown that patients with a history of HE, particularly overt-HE, had persistent neurological complications even after liver transplantation (LT). These enduring neurological conditions significantly affect patient's quality of life and continue to add to the economic burden of chronic liver disease on health care systems. This review discusses the journey of the brain through the progression of liver disease, entering the invasive surgical procedure of LT and the conditions associated with the post-transplant period. In particular, it will discuss the vulnerability of the HE brain to peri-operative factors and post-LT conditions which may explain non-resolved neurological impairment following LT. In addition, the review will provide evidence; (i) supporting overt-HE impacts on neurological complications post-LT; (ii) that overt-HE leads to permanent neuronal injury and (iii) the pathophysiological role of ammonia toxicity on astrocyte and neuronal injury/damage. Together, these findings will provide new insights on the underlying mechanisms leading to neurological complications post-LT.

摘要

肝性脑病(HE)是一种急性和慢性肝病的神经精神综合征。作为一种代谢紊乱,HE 被认为是可逆的,因此有望在患病肝脏被健康肝脏替代后得到解决。然而,高达 47%的移植患者仍存在持续的神经并发症。几项回顾性研究表明,有 HE 病史的患者,尤其是显性 HE 患者,即使在肝移植(LT)后也存在持续的神经并发症。这些持久的神经状况显著影响患者的生活质量,并继续给慢性肝病的医疗保健系统带来经济负担。本文综述探讨了大脑在肝病进展过程中的变化,以及 LT 这一侵入性手术和移植后相关情况。特别地,它将讨论 HE 大脑对围手术期因素和 LT 后情况的脆弱性,这可能解释了 LT 后未解决的神经损伤。此外,该综述将提供证据:(i)显性 HE 对 LT 后神经并发症的影响;(ii)显性 HE 导致永久性神经元损伤;(iii)氨毒性对星形胶质细胞和神经元损伤/损害的病理生理作用。这些发现将为 LT 后神经并发症的潜在机制提供新的见解。

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Neurochem Res. 2021 Oct;46(10):2612-2625. doi: 10.1007/s11064-021-03372-4. Epub 2021 Jun 15.
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Multiple ammonia-induced episodes of hepatic encephalopathy provoke neuronal cell loss in bile-duct ligated rats.多次氨诱导的肝性脑病发作导致胆管结扎大鼠的神经元细胞丢失。
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Perioperative neurological complications after liver transplantation are best predicted by pre-transplant hepatic encephalopathy.肝移植术后围手术期神经并发症最好通过移植前肝性脑病来预测。
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Reactive astrocyte nomenclature, definitions, and future directions.反应性星形胶质细胞命名、定义和未来方向。
Nat Neurosci. 2021 Mar;24(3):312-325. doi: 10.1038/s41593-020-00783-4. Epub 2021 Feb 15.
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Targeting neuroplasticity in patients with neurodegenerative diseases using brain stimulation techniques.利用脑刺激技术靶向神经退行性疾病患者的神经可塑性。
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Hepatic encephalopathy: Novel insights into classification, pathophysiology and therapy.肝性脑病:分类、病理生理学和治疗的新见解。
睡眠障碍:发病机制与治疗干预
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Elevated serum neurofilament light chain levels are associated with hepatic encephalopathy in patients with cirrhosis.血清神经丝轻链水平升高与肝硬化患者肝性脑病有关。
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Sialyltransferase ST3GAL6 silencing reduces α2,3-sialylated glycans to regulate autophagy by decreasing HSPB8-BAG3 in the brain with hepatic encephalopathy.沉默唾液酸转移酶 ST3GAL6 可减少 α2,3-唾液酸化聚糖,通过降低肝性脑病大脑中的 HSPB8-BAG3 来调节自噬。
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The Importance of Making an Accurate Diagnosis for Hepatic Encephalopathy.准确诊断肝性脑病的重要性。
Gastroenterol Hepatol (N Y). 2023 Dec;19(12):740-748.
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Multiple ammonia-induced episodes of hepatic encephalopathy provoke neuronal cell loss in bile-duct ligated rats.多次氨诱导的肝性脑病发作导致胆管结扎大鼠的神经元细胞丢失。
JHEP Rep. 2023 Sep 11;5(12):100904. doi: 10.1016/j.jhepr.2023.100904. eCollection 2023 Dec.
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Astrocytes in human central nervous system diseases: a frontier for new therapies.人类中枢神经系统疾病中的星形胶质细胞:新疗法的前沿。
Signal Transduct Target Ther. 2023 Oct 13;8(1):396. doi: 10.1038/s41392-023-01628-9.
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