1995
DOI: 10.4327/jsnfs.48.181
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Effects of Oligosaccharides on Galactosamine Hepatitis in Rats.

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Cited by 10 publications
(3 citation statements)
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“…8,9,[23][24][25] Some investigators have also observed that liver weight decreases 24 h after GalN injection as a result of atrophy followed by necrosis. 26,27) In this study, serum ALT, AST, and LDH activities that were increased by GalN treatment were significantly decreased by pretreated PPE. Furthermore, although there was no significant difference in liver weight between the two GalN-treated groups, the PPE + GalN group tended to increase in liver weight more than the control + GalN group.…”
Section: Discussionmentioning
confidence: 81%
“…8,9,[23][24][25] Some investigators have also observed that liver weight decreases 24 h after GalN injection as a result of atrophy followed by necrosis. 26,27) In this study, serum ALT, AST, and LDH activities that were increased by GalN treatment were significantly decreased by pretreated PPE. Furthermore, although there was no significant difference in liver weight between the two GalN-treated groups, the PPE + GalN group tended to increase in liver weight more than the control + GalN group.…”
Section: Discussionmentioning
confidence: 81%
“…On the other hand, it has been reported that GalN causes a decrease in liver weight as a result of atrophy followed by necrosis in rats. 20,21) This phenomenon might originate in hepatocellular injury secondary to loss of proteins, because GalN reduces the intracellular pool of uracil nucleotide in hepatocytes, thus inhibiting RNA and protein synthesis. 22) As Table 1 shows, liver weight in the GalN-treated groups was significantly (p < 0:05) lower than in the control group.…”
Section: )mentioning
confidence: 99%
“…25 Protective effects on galactosamine-induced liver damage have been reported for green tea and dietetic fibers, although the mechanism of such protection has not been explained. 41,42 D-003 has been found to be effective for preventing liver damage induced with agents like CCl 4 and paracetamol, 39,40 whose hepatotoxicity has been linked to contributions by augmented LP and free radicals. [16][17][18][19][20][21][22][23][24] In fact, the hypothesis underlying the rationale for investigating the putative protection of D-003 on the liver damage induced with both paracetamol and CCl 4 was based in the effective antioxidant profile of D-003 to prevent LP induced with several agents in rats 34 and humans.…”
Section: Discussionmentioning
confidence: 98%