Amelioration of Hepatic Encephalopathy Using Dunaliella salina Microalgae in Rats: Modulation of Hyperammonemia/TLR4

Biomed Res Int. 2021 Mar 28:2021:8843218. doi: 10.1155/2021/8843218. eCollection 2021.

Abstract

Hepatic encephalopathy (HE) is a neuropsychiatric disease that is developed as a complication of both acute and chronic liver failure affecting psychomotor dysfunction, memory, and concentration. This study is aimed at evaluating the therapeutic effects of Dunaliella salina (D. salina) microalgae in thioacetamide- (TAA-) induced HE in rats. HE was induced by TAA (200 mg/kg; i.p.) for three successive days. Forty male Wister albino rats were divided into 4 groups; the first group was served as a normal, and the second group was injected with TAA and served as TAA control. The third and fourth groups were administered D. salina (100 and 200 mg/kg; p.o.), respectively, after TAA injection for 7 days. The behavioral and biochemical markers as well as histological aspects of HE were estimated. This study revealed that TAA caused behavioral changes, oxidative stress, neuroinflammation, nuclear pyknosis, and neurons degeneration. D. salina improved liver function and decreased oxidative stress and inflammatory mediator as TLR4 protein expression. Also, D. salina elevated HSP-25 and IGF-1 as well as improved brain histopathological alterations. In conclusion, D. salina exerted a therapeutic potential against HE via its antioxidant, antiinflammatory and cytoprotective effects.

MeSH terms

  • Ammonia / blood
  • Animals
  • Behavior, Animal
  • Biomarkers / blood
  • Brain / metabolism
  • Brain / pathology
  • HSP27 Heat-Shock Proteins / metabolism
  • Hepatic Encephalopathy / blood
  • Hepatic Encephalopathy / complications*
  • Hepatic Encephalopathy / metabolism*
  • Hyperammonemia / blood
  • Hyperammonemia / complications*
  • Hyperammonemia / metabolism*
  • Insulin-Like Growth Factor I / metabolism
  • Liver / enzymology
  • Male
  • Microalgae / chemistry*
  • Models, Biological
  • Oxidative Stress
  • Powders
  • Rats
  • Rats, Wistar
  • Toll-Like Receptor 4 / metabolism*

Substances

  • Biomarkers
  • HSP27 Heat-Shock Proteins
  • Hspb1 protein, rat
  • Powders
  • Toll-Like Receptor 4
  • Insulin-Like Growth Factor I
  • Ammonia