Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Acta cir. bras ; 32(5): 396-406, May 2017. tab, graf
Article in English | LILACS | ID: biblio-837708

ABSTRACT

Abstract Purpose: To determine the effects of propofol and ketamine anesthesia on liver regeneration in rats after partial hepatectomy (PHT). Methods: Male Wistar albino rats were assigned randomly to four groups of 10. Anesthesia was induced and maintained with propofol in groups 1 and 2, and with ketamine in groups 3 and 4. PHT was undertaken in groups 1 and 3. Rats in groups 2 and 4 (control groups) underwent an identical surgical procedure, but without PHT. At postoperative day-5, rats were killed. Regenerated liver was removed, weighed, and evaluated (by immunohistochemical means) for expression of inducible nitric oxide synthase (iNOS), endothelial NOS (eNOS), apoptosis protease-activating factor (APAF)-1, and proliferating cell nuclear antigen (PCNA). Also, blood samples were collected for measurement of levels of tumor necrosis factor (TNF)-α and interleukin (IL)-6. Results: Between groups 2 and 4, there were no differences in tissue levels of iNOS, eNOS, and APAF-1 or plasma levels of TNF-α and IL-6. eNOS expression was similar in group 1 and group 3. Expression of iNOS and APAF-1 was mild-to-moderate in group 1, but significantly higher in group 3. Groups 1 and 3 showed an increase in PCNA expression, but expression in both groups was comparable. Plasma levels of TNF-α and IL-6 increased to a lesser degree in group 1 than in group 3. Conclusion: Propofol, as an anesthetic agent, may attenuate cytokine-mediated upregulation of iNOS expression and apoptosis in an animal model of liver regeneration after partial hepatectomy.


Subject(s)
Animals , Male , Propofol/pharmacology , Apoptosis , Anesthetics, Intravenous/pharmacology , Nitric Oxide Synthase Type II/metabolism , Ketamine/pharmacology , Liver Regeneration/drug effects , Random Allocation , Propofol/metabolism , Up-Regulation , Interleukin-6/metabolism , Interleukin-6/blood , Rats, Wistar , Proliferating Cell Nuclear Antigen/metabolism , Anesthetics, Intravenous/metabolism , Models, Animal , Nitric Oxide Synthase Type III/metabolism , Apoptotic Protease-Activating Factor 1/metabolism , Hepatectomy , Ketamine/metabolism
2.
Acta cir. bras ; 31(5): 314-319, May 2016. tab, graf
Article in English | LILACS | ID: lil-783800

ABSTRACT

ABSTRACT PURPOSE : To evaluate the effects of platelet rich plasma (PRP) on the healing of fascia wherein peritonitis has been created. METHODS: Twenty eight Wistar Albino rats were divided into four groups. Only a primary fascial repair following laparotomy was performed on Group 1, a primary fascial repair performed and PRP treatment applied following laparotomy on Group 2, and a fecal peritonitis created following laparotomy and a primary fascial repair carried out on Group 3. A fecal peritonitis was created following laparotomy and primary fascial repair and PRP treatment on the fascia was carried out on Group 4. RESULTS: TNF-α was found to be significantly lower in the control group (Group 1). It was detected at the highest level in the group in which fecal peritonitis was created and PRP applied (Group 4). TGF-β was determined as being significantly higher only in Group 4. Histopathologically, the differences between the groups in terms of cell infiltration and collagen deposition were not found to be significant. CONCLUSION: When platelet rich plasma was given histologically and biochemicaly as wound healing parameters cellular infiltration, collagen accumulation, and tissue hydroxyiproline levels were not increased but neovascularization, fibroblast activation and TNF Alfa levels were increased and PRP accelerated wound healing.


Subject(s)
Animals , Peritonitis/complications , Wound Healing , Platelet-Rich Plasma , Fascia/physiology , Peritonitis/metabolism , Serine Endopeptidases/metabolism , Random Allocation , Transforming Growth Factor beta/analysis , Transforming Growth Factor beta/metabolism , Collagen/drug effects , Collagen/metabolism , Tumor Necrosis Factor-alpha/analysis , Tumor Necrosis Factor-alpha/metabolism , Rats, Wistar , Gelatinases/metabolism , Neovascularization, Physiologic , Models, Animal , Fascia/blood supply , Hydroxyproline/analysis , Hydroxyproline/metabolism , Membrane Proteins/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL