2000
DOI: 10.1046/j.1365-2885.2000.00253.x
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The pharmacokinetics and effects of intravenously administered carprofen and salicylate on gastrointestinal mucosa and selected biochemical measurements in healthy cats

Abstract: The pharmacokinetics of carprofen, a propionic acid-derived nonsteroidal anti-inflammatory (NSAID), and its effect on gastrointestinal mucosa, complete blood counts (CBC) and biochemical indicators of liver and renal function were investigated in healthy cats using a randomized crossover design. A single dose of 4 mg/kg of carprofen (Zenecarp(R) Injection), normal saline, or 20 mg/kg of DL-lysine acetyl salicylate (Vetalgine(R)) was given intravenously (i.v.) to each of five cats with a washout period of 2 wee… Show more

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Cited by 50 publications
(48 citation statements)
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“…In a recent study in cats, IV administration of carprofen at a dose of 4 mg kg −1 did not cause endoscopically recognizable gastrointestinal lesions, while 20 mg kg −1 of IV acetyl salicylate produced minor pinpoint erosions in the gastrointestinal tract of one cat 8 hours post‐injection. BUN, ALT, ALP and CBCs were not significantly altered from pretreatment values for both drugs (Parton et al. 2000).…”
Section: Discussionmentioning
confidence: 90%
“…In a recent study in cats, IV administration of carprofen at a dose of 4 mg kg −1 did not cause endoscopically recognizable gastrointestinal lesions, while 20 mg kg −1 of IV acetyl salicylate produced minor pinpoint erosions in the gastrointestinal tract of one cat 8 hours post‐injection. BUN, ALT, ALP and CBCs were not significantly altered from pretreatment values for both drugs (Parton et al. 2000).…”
Section: Discussionmentioning
confidence: 90%
“…However, age did not appear to alter total body clearance. Parton et al . (2000) found huge inter‐cat variability in pharmacokinetics of i.v.…”
Section: Discussionmentioning
confidence: 99%
“…Πρόσφατα η ειδικότητα της αποδόθηκε στο S( + ) ισομερές της (Giraudel et al 2005b). Είναι από τα ελάχιστα ΜΣΑΦ των οποίων τα φαρμακοκινητικά και φαρμακοδυναμικά χαρακτηρι στικά έχουν μελετηθεί στη γάτα (Taylor et al 1996, Parton et al 2000. Στην αναστολή της δράσης της COX-2 πιθανόν να οφείλεται η ασφάλεια της.…”
Section: μη στεροειδή αντιφλεγμονώδη φάρμακαunclassified