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The modulating effects of propofol and its lipid carrier on canine neutrophil functions

Propofol (2,6-diisopropylphenol), being used as an intravenous sedative and anesthetic agent, influences not only upon nervous system but also for host inflammatory response through modulating neutrophil functions. This study is designed to evaluate the modulating effects of propofol and its lipid c...

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Autores principales: SATO, Reeko, AOKI, Takuma, KOBAYASHI, Saori, UCHIDA, Naohiro, SIMAMURA, Shunsuke, YAMASAKI, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240761/
https://www.ncbi.nlm.nih.gov/pubmed/27665993
http://dx.doi.org/10.1292/jvms.16-0025
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author SATO, Reeko
AOKI, Takuma
KOBAYASHI, Saori
UCHIDA, Naohiro
SIMAMURA, Shunsuke
YAMASAKI, Masahiro
author_facet SATO, Reeko
AOKI, Takuma
KOBAYASHI, Saori
UCHIDA, Naohiro
SIMAMURA, Shunsuke
YAMASAKI, Masahiro
author_sort SATO, Reeko
collection PubMed
description Propofol (2,6-diisopropylphenol), being used as an intravenous sedative and anesthetic agent, influences not only upon nervous system but also for host inflammatory response through modulating neutrophil functions. This study is designed to evaluate the modulating effects of propofol and its lipid carrier administration at clinically relevant rate on canine neutrophil functions. Clinically healthy beagle dogs were received propofol (8.8 mg/kg) from cephalic vein and maintained with propofol dropping infusion (26.4 mg/kg/hr). Blood samples were collected from the dogs before infusion and 30 min after the start of propofol administration, and neutrophil functions were evaluated. The dogs were also administered lipid carrier, and neutrophil functions were evaluated in the same manner as propofol administration. Peripheral white blood cell and neutrophil counts decreased after the propofol or lipid carrier administration. The administration of propofol or lipid carrier significantly reduced neutrophil adherence ability. The superoxide production of neutrophils was measured by luminol-dependent chemiluminescence response using with opsonized zymosan. Peak height of neutrophil chemiluminescence curve was reduced by propofol and lipid carrier administration, on the contrary, peak time of neutrophil chemiluminescence curve was delayed. Administration of propofol or lipid carrier also reduced neutrophil adherence ability to nylon fibers. In the present study, we showed the modulating effects of propofol and its lipid carrier on canine neutrophil functions. However, there was no significant difference in the modulating effects between propofol group and lipid carrier group. Therefore, the modulating effects observed here were deeply concerned in lipid carrier administration.
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spelling pubmed-52407612017-01-30 The modulating effects of propofol and its lipid carrier on canine neutrophil functions SATO, Reeko AOKI, Takuma KOBAYASHI, Saori UCHIDA, Naohiro SIMAMURA, Shunsuke YAMASAKI, Masahiro J Vet Med Sci Surgery Propofol (2,6-diisopropylphenol), being used as an intravenous sedative and anesthetic agent, influences not only upon nervous system but also for host inflammatory response through modulating neutrophil functions. This study is designed to evaluate the modulating effects of propofol and its lipid carrier administration at clinically relevant rate on canine neutrophil functions. Clinically healthy beagle dogs were received propofol (8.8 mg/kg) from cephalic vein and maintained with propofol dropping infusion (26.4 mg/kg/hr). Blood samples were collected from the dogs before infusion and 30 min after the start of propofol administration, and neutrophil functions were evaluated. The dogs were also administered lipid carrier, and neutrophil functions were evaluated in the same manner as propofol administration. Peripheral white blood cell and neutrophil counts decreased after the propofol or lipid carrier administration. The administration of propofol or lipid carrier significantly reduced neutrophil adherence ability. The superoxide production of neutrophils was measured by luminol-dependent chemiluminescence response using with opsonized zymosan. Peak height of neutrophil chemiluminescence curve was reduced by propofol and lipid carrier administration, on the contrary, peak time of neutrophil chemiluminescence curve was delayed. Administration of propofol or lipid carrier also reduced neutrophil adherence ability to nylon fibers. In the present study, we showed the modulating effects of propofol and its lipid carrier on canine neutrophil functions. However, there was no significant difference in the modulating effects between propofol group and lipid carrier group. Therefore, the modulating effects observed here were deeply concerned in lipid carrier administration. The Japanese Society of Veterinary Science 2016-09-22 2016-12 /pmc/articles/PMC5240761/ /pubmed/27665993 http://dx.doi.org/10.1292/jvms.16-0025 Text en ©2016 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Surgery
SATO, Reeko
AOKI, Takuma
KOBAYASHI, Saori
UCHIDA, Naohiro
SIMAMURA, Shunsuke
YAMASAKI, Masahiro
The modulating effects of propofol and its lipid carrier on canine neutrophil functions
title The modulating effects of propofol and its lipid carrier on canine neutrophil functions
title_full The modulating effects of propofol and its lipid carrier on canine neutrophil functions
title_fullStr The modulating effects of propofol and its lipid carrier on canine neutrophil functions
title_full_unstemmed The modulating effects of propofol and its lipid carrier on canine neutrophil functions
title_short The modulating effects of propofol and its lipid carrier on canine neutrophil functions
title_sort modulating effects of propofol and its lipid carrier on canine neutrophil functions
topic Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240761/
https://www.ncbi.nlm.nih.gov/pubmed/27665993
http://dx.doi.org/10.1292/jvms.16-0025
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