» Articles » PMID: 37606786

Lessons on Brain Edema in HE: from Cellular to Animal Models and Clinical Studies

Overview
Journal Metab Brain Dis
Publisher Springer
Specialties Endocrinology
Neurology
Date 2023 Aug 22
PMID 37606786
Authors
Affiliations
Soon will be listed here.
Abstract

Brain edema is considered as a common feature associated with hepatic encephalopathy (HE). However, its central role as cause or consequence of HE and its implication in the development of the neurological alterations linked to HE are still under debate. It is now well accepted that type A and type C HE are biologically and clinically different, leading to different manifestations of brain edema. As a result, the findings on brain edema/swelling in type C HE are variable and sometimes controversial. In the light of the changing natural history of liver disease, better description of the clinical trajectory of cirrhosis and understanding of molecular mechanisms of HE, and the role of brain edema as a central component in the pathogenesis of HE is revisited in the current review. Furthermore, this review highlights the main techniques to measure brain edema and their advantages/disadvantages together with an in-depth description of the main ex-vivo/in-vivo findings using cell cultures, animal models and humans with HE. These findings are instrumental in elucidating the role of brain edema in HE and also in designing new multimodal studies by performing in-vivo combined with ex-vivo experiments for a better characterization of brain edema longitudinally and of its role in HE, especially in type C HE where water content changes are small.

Citing Articles

Effects of cholestasis and hyperammonemia on dendritic spine density and turnover in rat hippocampal neurons.

Giovannoni L, Pierzchala K, De Roo M, Braissant O, Bruce S, McLin V Sci Rep. 2024; 14(1):29841.

PMID: 39617839 PMC: 11609291. DOI: 10.1038/s41598-024-80871-8.


Ammonia-induced stress response in liver disease progression and hepatic encephalopathy.

Gallego-Duran R, Hadjihambi A, Ampuero J, Rose C, Jalan R, Romero-Gomez M Nat Rev Gastroenterol Hepatol. 2024; 21(11):774-791.

PMID: 39251708 DOI: 10.1038/s41575-024-00970-9.


Response to "Brain Lesions in Liver Cirrhosis May Not Only Be Due to Hepatic Encephalopathy".

Lee H J Korean Soc Radiol. 2024; 85(4):827-828.

PMID: 39130782 PMC: 11310429. DOI: 10.3348/jksr.2024.0073.


Diffusion of brain metabolites highlights altered brain microstructure in type C hepatic encephalopathy: a 9.4 T preliminary study.

Mosso J, Briand G, Pierzchala K, Simicic D, Sierra A, Abdollahzadeh A Front Neurosci. 2024; 18:1344076.

PMID: 38572151 PMC: 10987698. DOI: 10.3389/fnins.2024.1344076.

References
1.
Master S, Gottstein J, Blei A . Cerebral blood flow and the development of ammonia-induced brain edema in rats after portacaval anastomosis. Hepatology. 1999; 30(4):876-80. DOI: 10.1002/hep.510300428. View

2.
Benjamin A, Okamoto K, QUASTEL J . Effects of ammonium ions on spontaneous action potentials and on contents of sodium, potassium, ammonium and chloride ions in brain in vitro. J Neurochem. 1978; 30(1):131-43. DOI: 10.1111/j.1471-4159.1978.tb07044.x. View

3.
Haussinger D, Laubenberger J, Vom Dahl S, Ernst T, Bayer S, Langer M . Proton magnetic resonance spectroscopy studies on human brain myo-inositol in hypo-osmolarity and hepatic encephalopathy. Gastroenterology. 1994; 107(5):1475-80. DOI: 10.1016/0016-5085(94)90552-5. View

4.
Braissant O, Cagnon L, Monnet-Tschudi F, Speer O, Wallimann T, Honegger P . Ammonium alters creatine transport and synthesis in a 3D culture of developing brain cells, resulting in secondary cerebral creatine deficiency. Eur J Neurosci. 2008; 27(7):1673-85. DOI: 10.1111/j.1460-9568.2008.06126.x. View

5.
Sofroniew M, Vinters H . Astrocytes: biology and pathology. Acta Neuropathol. 2009; 119(1):7-35. PMC: 2799634. DOI: 10.1007/s00401-009-0619-8. View