Abstract | PURPOSE: METHODS: Wistar rats were used (8 in each group). Three groups had IRI induced by lobar vascular occlusion (60 minutes) and reperfusion (24 hours) and received HES (13 mL/kg iv), 7.5% saline (HS) (13 mL/kg iv) or no fluid. Three other groups were sham-operated and received the same fluid as the test groups. After 24 hours of reperfusion, blood was drawn for alanine aminotransferase (ALT) quantification and ischemic liver samples were taken for histological study ( hematoxylin and eosin and chloroacetate staining of neutrophils). RESULTS: HES treatment attenuated the elevation in serum ALT (P=0.001) and reduced the extent of hepatocellular necrosis (P<0.01) compared with the IRI controls. HES-mediated cytoprotection was associated with a decrease of infiltration of neutrophils in the necrotic areas (P<0.05) compared with the untreated IRI rats, but not with the volume control IRI rats (P>0.05). CONCLUSION:
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Authors | Dora Catré, Maria Francelina Lopes, Celeste Bento, António Silvério Cabrita |
Journal | Acta cirurgica brasileira
(Acta Cir Bras)
Vol. 26
Issue 6
Pg. 456-62
(Dec 2011)
ISSN: 1678-2674 [Electronic] Brazil |
PMID | 22042108
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- HES 130-0.4
- Hydroxyethyl Starch Derivatives
- Plasma Substitutes
- Alanine Transaminase
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Topics |
- Alanine Transaminase
(blood)
- Animals
- Blood Volume
- Disease Models, Animal
- Hydroxyethyl Starch Derivatives
(therapeutic use)
- Liver
(blood supply, pathology)
- Male
- Neutrophil Infiltration
(drug effects)
- Plasma Substitutes
(therapeutic use)
- Rats
- Rats, Wistar
- Reperfusion Injury
(pathology, prevention & control)
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