<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1019-9128</journal-id>
<journal-title><![CDATA[Journal of the South African Veterinary Association ]]></journal-title>
<abbrev-journal-title><![CDATA[J. S. Afr. Vet. Assoc.]]></abbrev-journal-title>
<issn>1019-9128</issn>
<publisher>
<publisher-name><![CDATA[South African Veterinary Association of South Africa ]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1019-91282012000100006</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Clinical evaluation of general anaesthesia in pigeons using a combination of ketamine and diazepam]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Azizpour]]></surname>
<given-names><![CDATA[Aidin]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hassani]]></surname>
<given-names><![CDATA[Yashar]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Islamic Azad University Young Researchers Club ]]></institution>
<addr-line><![CDATA[Ardabil ]]></addr-line>
<country>Iran</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Islamic Azad University Department of Animal Science ]]></institution>
<addr-line><![CDATA[Ardabil ]]></addr-line>
<country>Iran</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2012</year>
</pub-date>
<volume>83</volume>
<numero>1</numero>
<fpage>01</fpage>
<lpage>04</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.za/scielo.php?script=sci_arttext&amp;pid=S1019-91282012000100006&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.org.za/scielo.php?script=sci_abstract&amp;pid=S1019-91282012000100006&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.org.za/scielo.php?script=sci_pdf&amp;pid=S1019-91282012000100006&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[This study was undertaken to investigate the clinical effects of ketamine, diazepam and a ketamine and diazepam combination in the general anaesthesia of pigeons. Thirty-two pigeons of both sexes with body weights ranging from 280 g to 300 g were allocated randomly to four groups comprising eight birds each. Group D received a 0.5 mL mixture of diazepam (0.2 mg/kg) and normal saline, group K a 0.5 mL mixture of ketamine 5% (30 mg/kg) and normal saline, group D, group KD a 0.5 mL mixture of ketamine 5% (10 mg/kg), diazepam (0.2 mg/kg) and normal saline, whilst group C (control) received 0.5 mL of normal saline only. Each mixture was administered intramuscularly. Under standard operating room conditions, general anaesthesia was not observed in group C (normal saline alone). In group D, sedation and muscle relaxation without complete loss of consciousness was observed. Induction time of anaesthesia in group KD was significantly quicker than group K (p < 0.05). Duration of anaesthesia in group KD was significantly longer than group K (p < 0.05). Recovery took longer in group KD in comparison with group K, but the difference was not statistically significant (p &gt; 0.05). The birds in group KD were calm and sedated, with good muscle relaxation, whilst in group K the birds were excited and showed a drop in body temperature. According to the results of this study, the combination of low dose ketamine hydrochloride (HCL) and diazepam overcame the adverse effects of ketamine alone. This combination produced a more rapid induction of anaesthesia, as well as an increase in anaesthesia duration, with good muscle relaxation and a smooth and slow recovery. Use of a combination of ketamine HCL given at 10 mg/kg and diazepam given at 0.2 mg/kg for anaesthesia in pigeons is therefore recommended.]]></p></abstract>
</article-meta>
</front><body><![CDATA[ <p align="right"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>ORIGINAL    RESEARCH</b></font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="4"><b><a name="top"></a>Clinical    evaluation of general anaesthesia in pigeons using a combination of ketamine    and diazepam</b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Aidin Azizpour<sup>I</sup>;    Yashar Hassani<sup>II</sup></b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><sup>I</sup>Young    Researchers Club; Ardabil Branch, Islamic Azad University, Ardabil, Iran    <br>   <sup>II</sup>Department of Animal Science, Ardabil Branch, Islamic Azad University,    Ardabil, Iran</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><a href="#back">Correspondence    to</a></font></p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p> <hr size="1" noshade>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>ABSTRACT</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">This study was    undertaken to investigate the clinical effects of ketamine, diazepam and a ketamine    and diazepam combination in the general anaesthesia of pigeons. Thirty-two pigeons    of both sexes with body weights ranging from 280 g to 300 g were allocated randomly    to four groups comprising eight birds each. Group D received a 0.5 mL mixture    of diazepam (0.2 mg/kg) and normal saline, group K a 0.5 mL mixture of ketamine    5% (30 mg/kg) and normal saline, group D, group KD a 0.5 mL mixture of ketamine    5% (10 mg/kg), diazepam (0.2 mg/kg) and normal saline, whilst group C (control)    received 0.5 mL of normal saline only. Each mixture was administered intramuscularly.    <br>   Under standard operating room conditions, general anaesthesia was not observed    in group C (normal saline alone). In group D, sedation and muscle relaxation    without complete loss of consciousness was observed. Induction time of anaesthesia    in group KD was significantly quicker than group K <i>(p</i> &lt; 0.05). Duration    of anaesthesia in group KD was significantly longer than group K <i>(p</i> &lt;    0.05). Recovery took longer in group KD in comparison with group K, but the    difference was not statistically significant (p &gt; 0.05). The birds in group    KD were calm and sedated, with good muscle relaxation, whilst in group K the    birds were excited and showed a drop in body temperature.    <br>   According to the results of this study, the combination of low dose ketamine    hydrochloride (HCL) and diazepam overcame the adverse effects of ketamine alone.    This combination produced a more rapid induction of anaesthesia, as well as    an increase in anaesthesia duration, with good muscle relaxation and a smooth    and slow recovery. Use of a combination of ketamine HCL given at 10 mg/kg and    diazepam given at 0.2 mg/kg for anaesthesia in pigeons is therefore recommended.</font></p> <hr size="1" noshade>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Introduction</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Avian anaesthetic    and surgical techniques have progressed greatly in the last decade. The choice    of anaesthesia and route of administration is often as important as the surgical    procedure itself.<sup>1 </sup>General anaesthesia in various avian species may    be produced by administration of either inhalation or injectable agents.<sup>2,3</sup>    Injectable anaesthetics and sedatives can be administered intramuscularly, intravenously    or intraosseously.<sup>4</sup> Inhalation of anaesthesia is preferred for birds    but requires expensive equipment. The use of an injectable agent in comparison    with an inhalation agent has the advantage of increased speed of anaesthesia    induction, the need for minimal equipment and a low cost.<sup>2,3,5</sup></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Several injectable    drugs are used in birds. These include barbiturates, chloral hydrate, phenothiazine    derivatives, alpha-2 adrenergic agonists, ketamine and propofol.<sup>6,7,8</sup>    Pigeons are very sensitive birds and any mismanagement in a crisis can lead    to immediate shock and death. Pigeons are often referred to a hospital in a    critical condition and these birds require safe anaesthesia and painless surgery.    In these situations, careful selection of the safest possible anaesthetic agent    is very important.<sup>9,10</sup></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Ketamine is a dissociative    anaesthetic agent which can be used for the induction of general anaesthesia    in many species by either the intravenous, intramuscular or intraosseous route.<sup>1,5,6    </sup>However, ketamine is rarely used as the sole sedative agent in birds.    According to Athar et al.<sup>2</sup>, ketamine has a wide safety margin in    birds and as much as 10 times the therapeutic dose is normally required before    symptoms of toxicity appear. For respiratory depression that may result from    ketamine, supportive ventilation and administration of doxapram can be applied.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">When ketamine is    used as the sole anaesthetic agent, it produces poor muscle relaxation, muscle    tremors, myotonic contractions, opisthotonos, persistent pain reflexes and stormy    recoveries.<sup>11,12,13</sup> Therefore, it is most often combined with other    agents (alpha-2 adrenergic agonists, diazepam or azaperone), depending on the    species involved.<sup>10,14,15</sup> A combination of</font> <font face="Verdana, Arial, Helvetica, sans-serif" size="2">ketamine    and benzodiazepines (diazepam and midazolam) or ketamine and alpha-2 adrenergic    agonists are commonly used for general anaesthesia in pigeons.<sup>9</sup>'<sup>10</sup>'<sup>15</sup>-<sup>16</sup>    Diazepam has potent muscle relaxant and anticonvulsant properties and has been    used in a wide range of wild and domestic animals and birds.<sup>15-16-17</sup>    When used together, diazepam and ketamine have a synergistic effect, resulting    in a smooth recovery and better muscle relaxation.<sup>11-18</sup> Their efficacy    is enhanced whilst minimising their unwanted adverse effects.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The purpose of    this study was to compare the effects (time to onset of anaesthesia, duration    of anaesthesia, duration of recovery, response to external stimuli, muscular    relaxation, palpebral and pedal reflexes, and cloacal temperature) of diazepam    and ketamine in pigeons when administered intramuscularly alone or combined.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Materials and    methods</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Birds</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Thirty-two healthy    adult pigeons of both sexes (9 males and 23 females) with body weights ranging    from 280 g to 300 g were used in the study. All the pigeons were from the same    flock and their ages were between 1 and 2 years. All the birds were acclimatised    in a quiet room for 2 weeks. They were fed a wheat-based diet similar to their    previous diet and had free access to water and food, except for a period of    1 h prior to drug administration. This minimised the chances of vomiting. Before    the commencement of the study, the birds were found to be in good health, based    on physical examinations.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Trial procedure</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The pigeons were    allocated randomly to four equal groups of eight birds each. The groups were    differentiated as follows: in group D, diazepam was administered at a dose of    0.2 mg/kg, in group K, ketamine 5% was administered at a dose of 30 mg/kg, in    group KD, a ketamine (5%) and diazepam combination was administered at a dose    of 10 mg/kg and 0.2 mg/kg, respectively, whilst in group C (control), a 0.5    mL dose of normal saline was given per bird.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">All medications    were administered intramuscularly into the deep pectoral muscle using an insulin    syringe. The medications in groups D, K and KD were diluted with normal saline    to make a final volume of 0.5 mL.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Post-treatment    monitoring</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">After drug administration,    each bird was placed in sternal recumbency in separate cages, so that each bird    could be observed individually and external stimulation was kept to a minimum.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The clinical parameters    for each pigeon were as follows:</font></p> <ul>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">he severity      of opisthotonos was scored on a scale of 0-4: lack of opisthotonos was scored      as 0 and those with severest opisthotonos were scored as 4.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Onset of anaesthesia:      Time interval (in minutes) from administration through the stages of anaesthesia      to loss of consciousness.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Duration of      anaesthesia: Time interval (in minutes) from loss of consciousness to reappearance      of sensation.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Eyelids: scored      as - for closed, + for half-opened and ++ for opened.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Duration of      recovery: Time interval (in minutes) from the return of reflexes to complete      consciousness.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The severity      of excitability, such as wing flapping and ataxia was scored from 0 to 1.      No excitability was scored as 0 and the birds showing most excitability were      scored as 1.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Muscle relaxation      was tested in the muscles of the neck, wings and legs. The ease with which      the wings of the birds could be pulled, their hind limbs could be flexed and      the neck could be extended was recorded as the degree of muscle relaxation.      It was graded on a scale of 0.0-3.0, where 0.0 represented weak relaxation.      Birds given this score showed closed wings and stiff limbs. A score of 1.5      represented moderate relaxation where there was mild resistance to extension      of the neck, opening of the wings and flexing of the limbs, whilst a score      of 3.0 represented excellent relaxation where the birds showed a flaccid neck,      no resistance to opening of the wings and flexing of limbs.</font></li>       ]]></body>
<body><![CDATA[<li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Pedal reflex      was evaluated by using a towel clamp forceps. The presence and strength of      the reflex was scored based on a scale of 0-4, with 0 being a weak reflex      and 4 being a strong reflex.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Palpebral reflexes      were tested by touching the eyelids with a sterile cotton tip swab. Lack or      presence of the reflexes were scored as - or +, respectively.</font></li>       <li><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Cloacal temperature      was measured before anaesthesia and again 10 min after induction of anaesthesia.      A digital thermometer was used.</font></li>     </ul>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Statistical    analysis</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Opisthotonos, onset    of anaesthesia, duration of anaesthesia and duration of recovery were compared    using an independent f-test. The Kruskal-Wallis test was used to compare the    mean scores amongst the different groups. Cloacal temperature was analysed by    one-way ANOVA and Duncan's multiple-range test. All statements of significance    were based on the 0.05 level of probability.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Ethical considerations</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The Institutional    Animal Care and Use Committee approved the protocol for this project, under    the following project number 671.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Results</b></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">No anaesthesia    or opisthotonos was observed in groups C and D. Diazepam alone produced better    muscle relaxation than ketamine alone, but the muscle relaxation was not as    good as with the ketamine and diazepam combination. Opisthotonos in the ketamine    and diazepam combination was more severe than with ketamine alone, but the difference    was not statistically significant <i>(p</i> &gt; 0.05) (<a href="/img/revistas/jsava/v83n1/06t01.jpg">Table    1</a>). The onset of anaesthesia after injection was significantly quicker with    the ketamine and diazepam combination (1.50 min &plusmn; 0.23 min) than with    ketamine alone (4.50 min &plusmn; 0.41 min) <i>(p</i> &lt; 0.05) (<a href="/img/revistas/jsava/v83n1/06t01.jpg">Table    1</a>). The duration of anaesthesia in the KD group (14.10 min &plusmn; 1.48    min) was significantly higher than group K, where ketamine was used alone (8.13    min &plusmn; 1.41 min) <i>(p</i> &lt; 0.05) (<a href="/img/revistas/jsava/v83n1/06t01.jpg">Table    1</a>). Recovery from anaesthesia took longer with the ketamine and diazepam    combination (23.12 min &plusmn; 2.85 min) compared with ketamine alone (19.25    min &plusmn; 2.69 min), but the difference was not statistically significant    <i>(p</i> &gt; 0.05) (<a href="/img/revistas/jsava/v83n1/06t01.jpg">Table 1</a>).    The excitability during the recovery was significantly less in group KD as compared    with group K <i>(p</i> &lt; 0.05). The pigeons that were treated with diazepam    alone were calm and sedated during recovery (<a href="/img/revistas/jsava/v83n1/06t01.jpg">Table    1</a>).</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Muscle relaxation    following the administration of the ketamine and diazepam combination was twice    as pronounced than with diazepam alone <i>(p</i> &lt; 0.05). Muscle relaxation    was not observed in groups K and C (<a href="#f1">Figure 1</a>). The pigeons'    pedal reflexes were significantly weaker in groups K and KD when compared with    groups C and D (p &lt; 0.05). This reflex was markedly weaker with the ketamine    and diazepam combination than with ketamine alone (<a href="#f2">Figure 2</a>).</font></p>     <p><a name="f1"></a></p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/jsava/v83n1/06f01.jpg"></p>     <p>&nbsp;</p>     <p><a name="f2"></a></p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/jsava/v83n1/06f02.jpg"></p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">There were significant    differences in eyelid status between group KD and groups C, D and K <i>(p</i>    &lt; 0.05). The eyelids of pigeons treated with the ketamine and diazepam combination    were completely closed. With ketamine alone, the pigeons' eyes were completely    open during anaesthesia (<a href="#t2">Table 2</a>). There were no significant    differences in the palpebral reflexes in the different groups and these were    present in all the groups (<a href="#t2">Table 2</a>). The cloacal temperature    was 41.30 &deg;C &plusmn; 0.72 &deg;C before medication. When measured 10 min    after drug administration in groups K and D, the cloacal temperature was recorded    to have decreased significantly <i>(p</i> &lt; 0.05). However, in pigeons from    group KD, the cloacal temperature remained within the initial range, measuring    at 40.93 &deg;C &plusmn; 0.86 &deg;C (<a href="#t2">Table 2</a>).</font></p>     <p><a name="t2"></a></p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/jsava/v83n1/06t02.jpg"></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Discussion</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The dose and anaesthetic    response of ketamine varies across different bird species.<sup>13</sup> The    recommended dosage of ketamine is approximately 10 mg/kg - 60 mg/kg, given intramuscularly    or intravenously. Larger birds (greater than 1000 g) require a lower dose per    kilogram (10 mg/kg). The recommended intramuscular and/or intravenous dosage    of diazepam in birds is 0.2 mg/kg - 1 mg/kg.<sup>11</sup> In this study,the    dosage of ketamine was about half the normal dose used in pigeons.<sup>9,10,15</sup>    There are very few articles in the current literature on the ideal intramuscular    dosage of the diazepam and ketamine combination in pigeons. For this reason    a low dosage of ketamine and diazepam was used.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">A ketamine and    diazepam combination produced a fast and smooth induction of anaesthesia, whilst    a dosage of ketamine alone produced a slow and smooth anaesthesia. The duration    of anaesthesia with a ketamine and diazepam combination (14.10 min &plusmn;    1.48 min) obtained in this study was longer than the 8.13 min &plusmn; 1.41    min obtained with ketamine alone. Diazepam is distributed widely throughout    the body after administration and, being fat soluble, it can be deposited into    muscle and fat tissue.<sup>19</sup> The diazepam that was absorbed by the fat    and muscle tissue is then released slowly into the system, resulting in a longer    duration of anaesthesia than with ketamine alone. Paul-Murphy et al.<sup>20</sup>    reported that the average surgical time needed for most perching bird species    was 15 min. Therefore, the increase in anaesthesia duration through this combination    provides enough time for most surgical procedures.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">In the present    study, the recovery was smooth but slow in the pigeons anaesthetised with the    ketamine and diazepam combination. This observation is similar to those reported    by Lumeij and Deenik<sup>15</sup> and Varner et al.<sup>18</sup> In the ketaminetreated    pigeons, recovery was stormy. These birds showed severe convulsions and wing    flapping. This was also found by Atalan et al.<sup>14</sup>, who reported that    the stormy recovery is caused by the dissociative characteristics of ketamine    anaesthesia. With the ketamine and diazepam combination, the reduction of side    effects during the recovery could be the result of the low dose of ketamine    used in this group, as compared with ketamine alone (used at a higher dosage),    as well as the simultaneous administration of sedatives such as diazepam.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">In this study,    muscle relaxation was significantly more pronounced in the ketamine and diazepam    combination than with diazepam alone <i>(p</i> &lt; 0.05). Improvement of muscular    relaxation in this combination was associated with the muscle relaxant properties    of diazepam.<sup>15,18,19</sup> Poor muscle relaxation was found when ketamine    was used alone.<sup>13,14</sup> The presence of palpebral reflex in the ketamine-treated    pigeons was reported previously by many studies<sup>9,10</sup> and was also    observed in our study. In the present study, the cloacal temperature 10 min    after anaesthetic administration dropped to 39.17 &deg;C &plusmn; 0.59 &deg;C    in the ketamine group. Yet, it remained at 40.93 &deg;C &plusmn; 0.86 &deg;C    in pigeons treated with the ketamine and diazepam combination.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The present study    showed that intramuscular injection of the diazepam and normal saline mixture    could not induce anaesthesia, but sedation and muscle relaxation were observed.    Normal saline alone produced no sedation, muscle relaxation or anaesthesia.    Solution volume alone therefore plays no role. This finding correlates with    previous investigations.<sup>15,18</sup></font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Conclusion</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The combination    of ketamine HCL given at 10 mg/kg and diazepam given at 0.2 mg/kg provides more    ideal conditions for the veterinary surgeon. This is, to a large extent, thanks    to the sedation and the prolongation of the anaesthetic effect produced by diazepam.    The ketamine and diazepam combination produced more a rapid induction of anaesthesia,    an increase in the duration of anaesthesia, as well as smooth recovery and more    muscle relaxation without any adverse effects. It can therefore be considered    an important tool for the light anaesthesia of pigeons.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Acknowledgements</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The authors are    thankful to Dr G. Sadeghi-Hashjin from the Department of Pharmacology in the    Faculty of Veterinary Medicine at Tehran University, Iran for his technical    help.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Competing interests</b></font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The authors declare    that they have no financial or personal relationship(s) which may have inappropriately    influenced them in writing this paper.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Authors' contributions</b></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The authors made    equal contributions to the experimental project design and acquisition of data.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>References</b></font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">1.&nbsp;Forbes    NA. Avian anesthesia. Vet Q. 1998;20:265-266.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216052&pid=S1019-9128201200010000600001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">2.&nbsp;Athar M,    Shakoor A, Muhammad G, Sarwar MN, Chaudhry NI. Clinical perspectives of intravenous    ketamine anesthesia in peafowl <i>(Pavo cristatus).</i> Acta Vet Hung. 1996;44:357-361.    PMid:9055460</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216054&pid=S1019-9128201200010000600002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">3.&nbsp;Christense    J, Fosse RT, Halvorsen OJ, Moril I. Comparison of various anesthetic regimens    in the domestic fowl. Am J Vet Res. 1987;48:1649-1657.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216055&pid=S1019-9128201200010000600003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">4.&nbsp;Harrison,    GJ. Anesthesiology. In: Harrison J, Harrison LR, editors. Clinical avian medicine    and surgery. 7th edn. Philadelphia: WB Saunders, 1986; p. 520-545.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216057&pid=S1019-9128201200010000600004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     ]]></body>
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<body><![CDATA[<!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">17.&nbsp;Lees P.    Sedatives. In: Lees P, editor. Veterinary applied pharmacology and therapeutics.    5th edn. Oxford: Baillière Tindall, 1991; p. 337-339.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216079&pid=S1019-9128201200010000600017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">18.&nbsp;Varner    J, Clifton KR, Poulos S, Broderson JR, Wyatt RD. Lack of efficacy of injectable    ketamine with xylazine or diazepam for anesthesia in chickens. Lab Anim. 2004;33:36-39.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216081&pid=S1019-9128201200010000600018&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">19.&nbsp;Bateson    AN. Basic pharmacologic mechanisms involved in benzodiazepine tolerance and    withdrawal. Curr Pharm Des. 2002;8:5-21. PMid:11812247</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216083&pid=S1019-9128201200010000600019&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">20.&nbsp;Paul-Murphy    JR, Brunson DB, Miletic VA. Technique for evaluating analgesia in conscious    perching birds. Am J Vet Res. 1999;60:1213-1217. PMid:10791932</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=216084&pid=S1019-9128201200010000600020&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>&nbsp;</p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><a name="back"></a><a href="#top"><img src="/img/revistas/jsava/v83n1/seta.jpg" border="0"></a>    Correspondence to:    <br>   </b> Yashar Hassani    ]]></body>
<body><![CDATA[<br>   Email:<a href="mailto:yhassani86@yahoo.com">yhassani86@yahoo.com</a>    <br>   PO Box 56157-83137,    <br>   Department of Animal Science,    <br>   Ardabil Branch, Islamic Azad University,    <br>   Ardabil, Iran</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Received: 08 Sept.    2011    <br>   Accepted: 09 Mar. 2012    <br>   Published: 06 June 2012</font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">&copy; 2012. The    Authors. Licensee: AOSIS OpenJournals. This work is licensed under the Creative    Commons Attribution License.</font></p>      ]]></body>
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