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Evidence for oxidative/nitrosative stress in the pathogenesis of hepatic encephalopathy

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Abstract

Hepatic encephalopathy (HE) is a serious complication of liver failure. HE manifests as a series of neuropsychiatric and neuromuscular symptoms including personality changes, sleep abnormalities, asterixis and muscle rigidity progressing through stupor to coma. The pathophysiologic basis of HE remains unclear. There is general agreement that ammonia plays a key role. In recent years, it has been suggested that oxidative/nitrosative stress constitutes part of the pathophysiologic cascade in HE. Direct evidence for oxidative/nitrosative stress in the pathogenesis of HE has been demonstrated in experimental animal models of acute or chronic liver failure. However, evidence from studies in HE patients is limited. This review summarizes this evidence for a role of oxidative/nitrosative stress in relation to ammonia toxicity and to the pathogenesis of HE.

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Abbreviations

HE:

hepatic encephalopathy

ALF:

acute liver failure

eNOS:

endothelial nitric oxide synthase

HO-1:

heme oxygenase-1

TAA:

thioacetamide

SOD:

superoxide dismutase

MPT:

mitochondrial permeability transition

PTP:

permeability transition pore

NAC:

n-acetylcysteine

iNOS:

inducible nitric oxide synthase

nNOS:

neuronal nitric oxide synthase

NMDAr:

n-methyl-d-aspartic acid receptors

GS:

glutamine synthetase

MSO:

methionine sulfoximine

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Bemeur, C., Desjardins, P. & Butterworth, R.F. Evidence for oxidative/nitrosative stress in the pathogenesis of hepatic encephalopathy. Metab Brain Dis 25, 3–9 (2010). https://doi.org/10.1007/s11011-010-9177-y

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