2017
DOI: 10.1016/j.vaa.2016.09.003
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Hyaluronidase administered with xylazine–tiletamine–zolazepam into adipose tissue shortens recovery from anesthesia in pigs

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Cited by 4 publications
(2 citation statements)
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“…Tiletamine is a competitive N-methyl-D-aspartic acid (NMDA) receptor antagonist that exerts analgesia and immobilization, while zolazepam is a benzodiazepine drug for muscle relaxation and sedation [11][12][13]. Xylazine is an α2 receptor agonist for sedation, analgesia, and muscle relaxation [14].…”
Section: Introductionmentioning
confidence: 99%
“…Tiletamine is a competitive N-methyl-D-aspartic acid (NMDA) receptor antagonist that exerts analgesia and immobilization, while zolazepam is a benzodiazepine drug for muscle relaxation and sedation [11][12][13]. Xylazine is an α2 receptor agonist for sedation, analgesia, and muscle relaxation [14].…”
Section: Introductionmentioning
confidence: 99%
“…A xilazina e a detomidina são utilizadas principalmente para contenção química e como medicação pré-anestésica objetivando reduzir a dose de anestésicos gerais. A associação desses fármacos é feita com agentes dissociativos, tais como opioides, fenotiazinas, benzodiazepínicos, agentes inalatórios, butirofenonas e agentes anestésicos como o propofol (ALBUQUERQUE et al, 2016;SCHMITZ et al, 2016;BISETTO et al, 2017;RAJPUT et al, 2017). Uma vantagem no emprego desses α-2 adrenérgicos é a possibilidade da reversão de seus efeitos por antagonistas, como a ioimbina e o atipamezole (FAHLMAN et al, 2005;ALLAN, 2015;ESTERUELAS et al, 2017;JANSSEN et al, 2017…”
Section: 4-agonistas De Receptores Alfa-2 Adrenérgicosunclassified