RESEARCH PAPER: Clinical evaluation of intranasal benzodiazepines, alpha sub(2)-agonists and their antagonists in canaries

Objective: To evaluate the effects of intranasal benzodiazepines (midazolam and diazepam), alpha sub(2)-agonists (xylazine and detomidine) and their antagonists (flumazenil and yohimbine) in canaries. Study design: Prospective randomized study. Animals: Twenty-six healthy adult domesticated canaries...

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Veröffentlicht in:Veterinary anaesthesia and analgesia 2006-05, Vol.33 (3), p.143-148
Hauptverfasser: Vesal, Nasser, Zare, Payman
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description Objective: To evaluate the effects of intranasal benzodiazepines (midazolam and diazepam), alpha sub(2)-agonists (xylazine and detomidine) and their antagonists (flumazenil and yohimbine) in canaries. Study design: Prospective randomized study. Animals: Twenty-six healthy adult domesticated canaries of both sexes, weighing 18.3 plus or minus 1.0 g. Methods: In Study 1 an attempt was made to determine the dose of each drug that allowed treated canaries to be laid in dorsal recumbency for at least 5 minutes, i.e. its effective dose. This involved the evaluation of various doses, during which equal volumes of the tested drug were administered slowly into each nostril. In study 2 the onset of action, duration and quality of sedation induced by each drug at its effective dose were evaluated. The efficacy of flumazenil and yohimbine in antagonizing the effects of the sedative drugs was also studied. Results: In study 1 administration of 25 mu L per nostril diazepam (5 mg mL super(-1) solution) or midazolam (5 mg mL super(-1) solution) to each bird caused adequate sedation within 1-2 minutes; birds did not move when placed in dorsal recumbency. After administration of 12 mu L per nostril of either xylazine (20 mg mL super(-1)) or detomidine (10 mg mL super(-1)), birds seemed heavily sedated and assumed sternal recumbency but could not be placed in dorsal recumbency. Higher doses of xylazine (0.5 mg per nostril) or detomidine (0.25 mg per nostril) prolonged sedation but did not produce dorsal recumbency. In study 2 in all treatment groups, onset of action was rapid. Duration of dorsal recumbency was significantly longer (p < 0.05) with diazepam (38.4 plus or minus 10.5 minutes) than midazolam (17.1 plus or minus 2.2 minutes). Intranasal flumazenil (2.5 mu g per nostril) significantly reduced recumbency time. Duration of sedation was longer with alpha sub(2)-agonists compared with benzodiazepines. Detomidine had the longest duration of effect (257.5 plus or minus 1.5 minutes) and midazolam the shortest (36.9 plus or minus 2.4 minutes). Nasally administered flumazenil significantly reduced the duration of sedation with diazepam and midazolam while yohimbine (120 mu g per nostril) effectively antagonized the effects of xylazine and detomidine. Conclusion: Intranasal benzodiazepines produce rapid and effective sedation in canaries. Intranasal alpha sub(2) agonists produce sedation but not sustained recumbency. Specific antagonists are also effective when used by this
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Study design: Prospective randomized study. Animals: Twenty-six healthy adult domesticated canaries of both sexes, weighing 18.3 plus or minus 1.0 g. Methods: In Study 1 an attempt was made to determine the dose of each drug that allowed treated canaries to be laid in dorsal recumbency for at least 5 minutes, i.e. its effective dose. This involved the evaluation of various doses, during which equal volumes of the tested drug were administered slowly into each nostril. In study 2 the onset of action, duration and quality of sedation induced by each drug at its effective dose were evaluated. The efficacy of flumazenil and yohimbine in antagonizing the effects of the sedative drugs was also studied. Results: In study 1 administration of 25 mu L per nostril diazepam (5 mg mL super(-1) solution) or midazolam (5 mg mL super(-1) solution) to each bird caused adequate sedation within 1-2 minutes; birds did not move when placed in dorsal recumbency. After administration of 12 mu L per nostril of either xylazine (20 mg mL super(-1)) or detomidine (10 mg mL super(-1)), birds seemed heavily sedated and assumed sternal recumbency but could not be placed in dorsal recumbency. Higher doses of xylazine (0.5 mg per nostril) or detomidine (0.25 mg per nostril) prolonged sedation but did not produce dorsal recumbency. In study 2 in all treatment groups, onset of action was rapid. Duration of dorsal recumbency was significantly longer (p &lt; 0.05) with diazepam (38.4 plus or minus 10.5 minutes) than midazolam (17.1 plus or minus 2.2 minutes). Intranasal flumazenil (2.5 mu g per nostril) significantly reduced recumbency time. Duration of sedation was longer with alpha sub(2)-agonists compared with benzodiazepines. Detomidine had the longest duration of effect (257.5 plus or minus 1.5 minutes) and midazolam the shortest (36.9 plus or minus 2.4 minutes). Nasally administered flumazenil significantly reduced the duration of sedation with diazepam and midazolam while yohimbine (120 mu g per nostril) effectively antagonized the effects of xylazine and detomidine. Conclusion: Intranasal benzodiazepines produce rapid and effective sedation in canaries. Intranasal alpha sub(2) agonists produce sedation but not sustained recumbency. Specific antagonists are also effective when used by this route. Clinical relevance: Intranasal sedative drug administration is an acceptable alternative method of drug delivery in canaries.</description><identifier>ISSN: 1467-2987</identifier><identifier>EISSN: 1467-2995</identifier><identifier>DOI: 10.1111/j.1467-2995.2005.00244.x</identifier><language>eng</language><ispartof>Veterinary anaesthesia and analgesia, 2006-05, Vol.33 (3), p.143-148</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Vesal, Nasser</creatorcontrib><creatorcontrib>Zare, Payman</creatorcontrib><title>RESEARCH PAPER: Clinical evaluation of intranasal benzodiazepines, alpha sub(2)-agonists and their antagonists in canaries</title><title>Veterinary anaesthesia and analgesia</title><description>Objective: To evaluate the effects of intranasal benzodiazepines (midazolam and diazepam), alpha sub(2)-agonists (xylazine and detomidine) and their antagonists (flumazenil and yohimbine) in canaries. Study design: Prospective randomized study. Animals: Twenty-six healthy adult domesticated canaries of both sexes, weighing 18.3 plus or minus 1.0 g. Methods: In Study 1 an attempt was made to determine the dose of each drug that allowed treated canaries to be laid in dorsal recumbency for at least 5 minutes, i.e. its effective dose. This involved the evaluation of various doses, during which equal volumes of the tested drug were administered slowly into each nostril. In study 2 the onset of action, duration and quality of sedation induced by each drug at its effective dose were evaluated. The efficacy of flumazenil and yohimbine in antagonizing the effects of the sedative drugs was also studied. Results: In study 1 administration of 25 mu L per nostril diazepam (5 mg mL super(-1) solution) or midazolam (5 mg mL super(-1) solution) to each bird caused adequate sedation within 1-2 minutes; birds did not move when placed in dorsal recumbency. After administration of 12 mu L per nostril of either xylazine (20 mg mL super(-1)) or detomidine (10 mg mL super(-1)), birds seemed heavily sedated and assumed sternal recumbency but could not be placed in dorsal recumbency. Higher doses of xylazine (0.5 mg per nostril) or detomidine (0.25 mg per nostril) prolonged sedation but did not produce dorsal recumbency. In study 2 in all treatment groups, onset of action was rapid. Duration of dorsal recumbency was significantly longer (p &lt; 0.05) with diazepam (38.4 plus or minus 10.5 minutes) than midazolam (17.1 plus or minus 2.2 minutes). Intranasal flumazenil (2.5 mu g per nostril) significantly reduced recumbency time. Duration of sedation was longer with alpha sub(2)-agonists compared with benzodiazepines. Detomidine had the longest duration of effect (257.5 plus or minus 1.5 minutes) and midazolam the shortest (36.9 plus or minus 2.4 minutes). Nasally administered flumazenil significantly reduced the duration of sedation with diazepam and midazolam while yohimbine (120 mu g per nostril) effectively antagonized the effects of xylazine and detomidine. Conclusion: Intranasal benzodiazepines produce rapid and effective sedation in canaries. Intranasal alpha sub(2) agonists produce sedation but not sustained recumbency. Specific antagonists are also effective when used by this route. 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Study design: Prospective randomized study. Animals: Twenty-six healthy adult domesticated canaries of both sexes, weighing 18.3 plus or minus 1.0 g. Methods: In Study 1 an attempt was made to determine the dose of each drug that allowed treated canaries to be laid in dorsal recumbency for at least 5 minutes, i.e. its effective dose. This involved the evaluation of various doses, during which equal volumes of the tested drug were administered slowly into each nostril. In study 2 the onset of action, duration and quality of sedation induced by each drug at its effective dose were evaluated. The efficacy of flumazenil and yohimbine in antagonizing the effects of the sedative drugs was also studied. Results: In study 1 administration of 25 mu L per nostril diazepam (5 mg mL super(-1) solution) or midazolam (5 mg mL super(-1) solution) to each bird caused adequate sedation within 1-2 minutes; birds did not move when placed in dorsal recumbency. After administration of 12 mu L per nostril of either xylazine (20 mg mL super(-1)) or detomidine (10 mg mL super(-1)), birds seemed heavily sedated and assumed sternal recumbency but could not be placed in dorsal recumbency. Higher doses of xylazine (0.5 mg per nostril) or detomidine (0.25 mg per nostril) prolonged sedation but did not produce dorsal recumbency. In study 2 in all treatment groups, onset of action was rapid. Duration of dorsal recumbency was significantly longer (p &lt; 0.05) with diazepam (38.4 plus or minus 10.5 minutes) than midazolam (17.1 plus or minus 2.2 minutes). Intranasal flumazenil (2.5 mu g per nostril) significantly reduced recumbency time. Duration of sedation was longer with alpha sub(2)-agonists compared with benzodiazepines. Detomidine had the longest duration of effect (257.5 plus or minus 1.5 minutes) and midazolam the shortest (36.9 plus or minus 2.4 minutes). Nasally administered flumazenil significantly reduced the duration of sedation with diazepam and midazolam while yohimbine (120 mu g per nostril) effectively antagonized the effects of xylazine and detomidine. Conclusion: Intranasal benzodiazepines produce rapid and effective sedation in canaries. Intranasal alpha sub(2) agonists produce sedation but not sustained recumbency. Specific antagonists are also effective when used by this route. Clinical relevance: Intranasal sedative drug administration is an acceptable alternative method of drug delivery in canaries.</abstract><doi>10.1111/j.1467-2995.2005.00244.x</doi></addata></record>
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title RESEARCH PAPER: Clinical evaluation of intranasal benzodiazepines, alpha sub(2)-agonists and their antagonists in canaries
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