RESUMEN
The aim of this study was to evaluate the effectiveness of the original sperm chromatin dispersion (SCD) assay and the toluidine blue (TB) stain to assess DNA fragmentation and chromatin condensation, respectively, in cat sperm obtained by urethral catheterization (CT) and epididymis slicing (EP). CT and EP samples were collected from the same cat, and sperm motility, concentration, morphology, DNA integrity and chromatin condensation were evaluated. As controls, aliquots of the samples were incubated with 0.3 M NaOH and with 1% of dithiothreitol (DTT) to promote DNA fragmentation and chromatin decondensation, respectively. With SCD, four DNA dispersion halo patterns were observed: large, medium, small and no halo. TB staining patterns were as follows: light blue (condensed chromatin), light violet (moderate chromatin decondensation) and dark blue-violet (high chromatin decondensation). Sperm incubations with NaOH and with DTT were effective in inducing DNA fragmentation and chromatin decondensation, respectively. No significant differences were observed in the percentages of the SCD and TB patterns between samples (CT and EP) and no correlation was observed between sperm head abnormalities and the different SCD and TB patterns. The original SCD technique and the TB stain were adapted to evaluate DNA integrity and chromatin condensation in cat sperm obtained by CT and EP.
Asunto(s)
Cromatina , Cateterismo Urinario , Masculino , Animales , Cateterismo Urinario/veterinaria , Epidídimo , Hidróxido de Sodio , Semen , Motilidad Espermática , Espermatozoides , ADN , Colorantes , Cloruro de Tolonio , Fragmentación del ADNRESUMEN
A combination of tiletamine-zolazepam, medetomidine, and azaperone was used to immobilize captive Chacoan peccaries (Catagonus wagneri) for health assessments and biological sample collection at the Centro Chaqueño para la Conservación e Investigación (CCCI) in the Paraguayan Chaco during July in 2017 and 2018. In total, 83 peccaries kept in 0.25-1.50 hectare enclosures were immobilized via dart-administered anesthetic. Mean animal weight was 33.89±3.74 kg (standard deviation; n=77). The mean intramuscular (IM) anesthetic drug and dosages were 0.03±0.00 mg/kg of medetomidine, 0.91±0.10 mg/kg of Zoletil 50 (tiletamine-zolazepam), and 0.30±0.03 mg/kg azaperone. The mean time to recumbency after darting was 6.07±2.65 min. The mean time to reach the anesthetic plane postdarting was 10.00±2.00 min. Muscle relaxation was adequate to allow minor veterinary procedures. A mean dosage of 0.15±0.02 mg/kg of atipamezole was given IM to reverse the medetomidine. Recoveries were smooth and animals were standing by 59.17±30.18 min postreversal. Full recovery and release back to enclosures occurred 90±30 min postreversal. A single dose of this drug combination provided adequate anesthesia for 88% of adult Chacoan peccaries; 12% needed a supplemental dose of tiletamine-zolazepam because of failure to receive the full dose from the anesthetic dart. Sex and age did not impact the dosage required to achieve immobilization. Confinement during recovery from anesthesia is required with this protocol. Aside from mild hypoxemia, no adverse effects from anesthesia were observed. However, oxygen supplementation as a part of this protocol is recommended to support circulatory and respiratory capacity.
Asunto(s)
Anestésicos , Artiodáctilos , Animales , Medetomidina/farmacología , Tiletamina , Zolazepam , Azaperona/farmacología , Oxígeno , Paraguay , Combinación de Medicamentos , Artiodáctilos/fisiología , Terapia por Inhalación de Oxígeno/veterinaria , Inmovilización/veterinaria , Inmovilización/métodos , Hipnóticos y Sedantes , Anestésicos DisociativosRESUMEN
A combination of intramuscular medetomidine and ketamine was used to immobilize 46 free-ranging huemul deer (Hippocamelus bisulcus) with a remote drug delivery system in Chilean Patagonia for tagging and biological sampling. Captures occurred in May-October of 2005-09 between fall and early spring in the southern hemisphere. An initial dose of 6.6 mg medetomidine and 185 mg ketamine was adjusted after 17 captures to 3 mg and 200 mg, respectively, in the 29 remaining deer. Mean±SD adjusted dose was 0.042±0.012 mg/kg of medetomidine and 2.929±0.427 mg/kg of ketamine. Inductions were calm and the mean±SD time to sternal recumbency was 10.3±10.1 min. Palpebral reflex and jaw tone were present during immobilization. Atipamezole at 5 mg/mg of medetomidine was administered intramuscularly for reversal after 55.3±18.8 min procedure time. Recoveries were smooth and mean±SD time to standing was 10.2±3.3. All immobilized animals were hypoxemic by pulse oximetry (blood oxygen saturation approximately 81%). Three animals that developed apnea were resuscitated through chest compression and atipamezole administration, another regurgitated during capture, and all developed tachypnea. The combination of medetomidine-ketamine and atipamezole can be used for partially reversible immobilization of huemul, but supplemental oxygen should be administered, blood oxygenation should be monitored, and equipment for intubation and manual ventilation should be available.
Asunto(s)
Ciervos , Ketamina , Anestésicos Disociativos/farmacología , Animales , Frecuencia Cardíaca , Hipnóticos y Sedantes/farmacología , Imidazoles , Inmovilización/métodos , Inmovilización/veterinaria , Ketamina/farmacología , Medetomidina/farmacologíaRESUMEN
OBJECTIVES: We compared the effects of two alpha (α)2-adrenergic agonists on semen traits. METHODS: In this study, 13 adult domestic cats were divided into two experimental groups, according to the chemical ejaculation protocol used: the first group received medetomidine hydrochloride (100 µg/kg) and ketamine (5000 µg/kg); the second group received dexmedetomidine hydrochloride (25 µg/kg) and ketamine (5000 µg/kg), both by the intramuscular route. RESULTS: The animals responded positively (P >0.05) to chemical collection. Seminal parameters evaluated included volume, sperm vigor, total motility, progressive motility, sperm concentration, and the structural and functional integrity of the plasma membrane; sperm morphology values did not differ between groups (P >0.05). CONCLUSIONS AND RELEVANCE: The results indicated that dexmedetomidine is a more viable and economical alternative to medetomidine in domestic cats submitted to semen collection by urethral catheterization. Semen collection by urethral catheterization after using α2-adrenergic agonists is a recently developed technique in feline species that is considered to be quick and highly applicable to assisted reproduction programs in felids.
Asunto(s)
Felidae , Semen , Agonistas Adrenérgicos , Animales , Gatos , Masculino , Análisis de Semen/veterinaria , Cateterismo Urinario/efectos adversos , Cateterismo Urinario/veterinariaRESUMEN
Objetivou-se, por meio do presente estudo, avaliar o método de colheita farmacológica de sêmen com sondagem uretral, em machos de onças-pardas (Puma concolor) mantidos em cativeiro. A técnica proposta (Cat; N=3) foi comparada com a eletroejaculação (EE; N=4). Para a colheita farmacológica, utilizou-se medetomidina para induzir a liberação de sêmen na uretra e sonda uretral para gatos, sem janela lateral, para colheita do sêmen por capilaridade. O método foi eficaz em todos os animais usados. Por meio dessa técnica, colheram-se amostras com menor volume (106,7±30,5aµL) e maior concentração (524,1±54,3b x 106 espermatozoides/mL) em relação à EE (450,0±0,1bµL e 205,0±141,8a x 106 espermatozoides/mL). As avaliações de vigor, motilidade e patologia espermática demonstraram que a técnica não afeta a qualidade do sêmen em relação à EE (P>0,05). Dessa forma, o método proposto consiste em uma técnica mais prática e eficiente para a colheita de sêmen com boa qualidade, dispensando o eletroejaculador.(AU)
The aim of this study was to evaluate the pharmacological semen collection method with urethral catheterization (CT) in captive cougar (Puma concolor) males. The pharmacological method (CT; N= 3) was compared to the electroejaculation technique (EE; N= 4). For CT collection, medetomidine was administrated to induce semen release using a tomcat catheter inserted into the urethra to collect by capillarity. The proposed method was efficacious on all animals used. Through the CT method, semen collected yielded smaller volume (106,7±30,5aµL) and higher concentration (524,1±54,3b x 106sperm/mL) compared to EE (450,0±0,1bµL and 205,0±141,8a x 106 sperm /mL). Evaluations of vigor, motility and sperm pathology demonstrated that CT does not affect semen quality when compared to EE (P> 0.05). Thus, the proposed method consists of a more practical and efficient technique for semen collection with good quality, eliminating the need for eletroejaculation.(AU)
Asunto(s)
Animales , Masculino , Manejo de Especímenes/veterinaria , Puma/anatomía & histología , Análisis de Semen/veterinaria , Motilidad Espermática , Espermatozoides , Medetomidina/administración & dosificaciónRESUMEN
Objetivou-se, por meio do presente estudo, avaliar o método de colheita farmacológica de sêmen com sondagem uretral, em machos de onças-pardas (Puma concolor) mantidos em cativeiro. A técnica proposta (Cat; N=3) foi comparada com a eletroejaculação (EE; N=4). Para a colheita farmacológica, utilizou-se medetomidina para induzir a liberação de sêmen na uretra e sonda uretral para gatos, sem janela lateral, para colheita do sêmen por capilaridade. O método foi eficaz em todos os animais usados. Por meio dessa técnica, colheram-se amostras com menor volume (106,7±30,5aµL) e maior concentração (524,1±54,3b x 106 espermatozoides/mL) em relação à EE (450,0±0,1bµL e 205,0±141,8a x 106 espermatozoides/mL). As avaliações de vigor, motilidade e patologia espermática demonstraram que a técnica não afeta a qualidade do sêmen em relação à EE (P>0,05). Dessa forma, o método proposto consiste em uma técnica mais prática e eficiente para a colheita de sêmen com boa qualidade, dispensando o eletroejaculador.(AU)
The aim of this study was to evaluate the pharmacological semen collection method with urethral catheterization (CT) in captive cougar (Puma concolor) males. The pharmacological method (CT; N= 3) was compared to the electroejaculation technique (EE; N= 4). For CT collection, medetomidine was administrated to induce semen release using a tomcat catheter inserted into the urethra to collect by capillarity. The proposed method was efficacious on all animals used. Through the CT method, semen collected yielded smaller volume (106,7±30,5aµL) and higher concentration (524,1±54,3b x 106sperm/mL) compared to EE (450,0±0,1bµL and 205,0±141,8a x 106 sperm /mL). Evaluations of vigor, motility and sperm pathology demonstrated that CT does not affect semen quality when compared to EE (P> 0.05). Thus, the proposed method consists of a more practical and efficient technique for semen collection with good quality, eliminating the need for eletroejaculation.(AU)
Asunto(s)
Animales , Masculino , Manejo de Especímenes/veterinaria , Puma/anatomía & histología , Análisis de Semen/veterinaria , Motilidad Espermática , Espermatozoides , Medetomidina/administración & dosificaciónRESUMEN
Cryptorchidism is a genital alteration wherein one or both testicles fail to descend into the scrotum and has multifactorial causes. A free-range adult male was captured twice in the Pantanal of Nhecolândia to put a GPS collar and semen collection. Pharmacological semen collection, andrological examination and semen analysis were performed. At the first capture and during the andrological examination only the left testis was found, and the male qualified as cryptorchid. The penis had no penile spines at either procedure. The semen volume obtained at first and second capture was 435 and 160 µL, respectively, with a concentration of 618 and 100 x 106 sperm/mL, progressive motility of ~ 5% and ~ 1% and total morphological sperm abnormalities of 74% and 86%. The male was monitored by a GPS collar, but the signal was lost, making it difficult to re-captures and perform new seminal and ultrasound evaluations to discard monorchidism - exceedingly rare in felids. Genetic studies to assess the individual's homozygosity are necessary to verify whether cryptorchidism in this individual has a genetic factor.
RESUMEN
Cryptorchidism is a genital alteration wherein one or both testicles fail to descend into the scrotum and has multifactorial causes. A free-range adult male was captured twice in the Pantanal of Nhecolândia to put a GPS collar and semen collection. Pharmacological semen collection, andrological examination and semen analysis were performed. At the first capture and during the andrological examination only the left testis was found, and the male qualified as cryptorchid. The penis had no penile spines at either procedure. The semen volume obtained at first and second capture was 435 and 160 L, respectively, with a concentration of 618 and 100 x 106 sperm/mL, progressive motility of ~ 5% and ~ 1% and total morphological sperm abnormalities of 74% and 86%. The male was monitored by a GPS collar, but the signal was lost, making it difficult to re-captures and perform new seminal and ultrasound evaluations to discard monorchidism exceedingly rare in felids. Genetic studies to assess the individual's homozygosity are necessary to verify whether cryptorchidism in this individual has a genetic factor.
Asunto(s)
Masculino , Animales , Criptorquidismo/clasificación , Criptorquidismo/diagnóstico , Medetomidina/análisis , Panthera/anomalíasRESUMEN
Cryptorchidism is a genital alteration wherein one or both testicles fail to descend into the scrotum and has multifactorial causes. A free-range adult male was captured twice in the Pantanal of Nhecolândia to put a GPS collar and semen collection. Pharmacological semen collection, andrological examination and semen analysis were performed. At the first capture and during the andrological examination only the left testis was found, and the male qualified as cryptorchid. The penis had no penile spines at either procedure. The semen volume obtained at first and second capture was 435 and 160 L, respectively, with a concentration of 618 and 100 x 106 sperm/mL, progressive motility of ~ 5% and ~ 1% and total morphological sperm abnormalities of 74% and 86%. The male was monitored by a GPS collar, but the signal was lost, making it difficult to re-captures and perform new seminal and ultrasound evaluations to discard monorchidism exceedingly rare in felids. Genetic studies to assess the individual's homozygosity are necessary to verify whether cryptorchidism in this individual has a genetic factor.(AU)
Asunto(s)
Animales , Masculino , Panthera/anomalías , Criptorquidismo/clasificación , Criptorquidismo/diagnóstico , Medetomidina/análisisRESUMEN
To define a protocol of anesthesia for long-duration invasive surgery in a lizard, eight young adult Argentine tegus ( Salvator merianae) of mean body weight 3.0 kg (interquartile range [IQR] 3.40-2.65) were anesthetized with a mixture of ketamine (K) and medetomidine (M) at 19°C, injected intramuscularly and equally distributed in the four limbs. As the experimental surgery procedure required a prolonged deep anesthesia with a good myorelaxation (between 16 and 21 hr), reinjections were required and reflexes were checked during surgery. Times for anesthetic induction, anesthetic reinjection, and recovery periods were recorded for five different combinations of ketamine-medetomidine: 1) 66 mg/kg K + 100 µg/kg M; 2) 80 mg/kg K + 100 µg/kg M; 3) 100 mg/kg K + 130 µg/kg M; 4) 125 mg/kg K + 200 µg/kg M; and 5) 150 mg/kg K + 200 µg/kg M. The effect on the recovery speed of the postoperative atipamezole injection was also evaluated. The median induction time was 30 (IQR 35-27.5) min with no statistical difference between all the concentrations tested. The first reinjection of half a dose was administered after a mean of 5 hr (5.64 hr, IQR 5.95-4.84) as were the subsequent reinjections of a quarter dose (3.99 hr, IQR 5.98-3.23). Intramuscular administration of the ketamine-medetomidine combination is a simple, rapid, and efficient anesthesia for long-term surgery (>12 hr). A mix of 100 mg/kg ketamine and 200 µg/kg medetomidine, with reinjections every 4 hr of half a dose of the previous injection can maintain a good quality of anesthesia for at least 16 hr. The injection of atipamezole after the surgery reverses the effects of medetomidine and permits a reduction of the recovery period.
Asunto(s)
Anestesia/veterinaria , Anestésicos Disociativos/farmacología , Hipnóticos y Sedantes/farmacología , Ketamina/farmacología , Lagartos/fisiología , Medetomidina/farmacología , Anestésicos Disociativos/administración & dosificación , Animales , Relación Dosis-Respuesta a Droga , Combinación de Medicamentos , Femenino , Hipnóticos y Sedantes/administración & dosificación , Inyecciones Intramusculares/veterinaria , Ketamina/administración & dosificación , Masculino , Medetomidina/administración & dosificaciónRESUMEN
Purpose: To investigate the effects of dexmedetomidine (DEX) on amino acid contents and the cerebral ultrastructure of rats with cerebral ischemia-reperfusion injury (I/R). Methods: Thirty-six, male, Wistar rats were randomly divided into three groups: the sham operation group (group C), the ischemia-reperfusion group (group I/R), and the DEX group (group D). The middle cerebral artery occlusion model was prepared by the modified Longa method. The time of ischemia was 180 min, and 120 min after reperfusion, the amount of glutamate (Glu), and -aminobutyric acid (GABA) in the brain were measured, and the ultrastructure-level changes in the cerebral cortex were examined using electron microscopy. Results: Compared to group C, Glu contents in group D, and I/R significantly increased. Compared to group I/R, Glu contents in group D significantly decreased. Compared to group C, GABA contents in group D, and I/R significantly increased, and those in group D significantly increased, as compared to group I/R. The cerebral ultrastructure was normal in group C. Vacuolar degeneration in the plastiosome and nervous processes, was more critical than in group D. Vascular endothelial cells (VEC) were damaged. On the contrary, these changes in group D significantly improved. Conclusion: Dexmedetomidine is capable of decreasing glutamergic content, and increasing GABAergic content, in order to decrease the injury of the cerebral ultrastructure, following cerebral ischemia-reperfusion injury.(AU)
Asunto(s)
Animales , Ratas , Ratas/metabolismo , Isquemia Encefálica/tratamiento farmacológico , Isquemia Encefálica/veterinaria , Dexmedetomidina/análisis , Dexmedetomidina/farmacocinéticaRESUMEN
Abstract Purpose: To investigate the effects of dexmedetomidine (DEX) on amino acid contents and the cerebral ultrastructure of rats with cerebral ischemia-reperfusion injury (I/R). Methods: Thirty-six, male, Wistar rats were randomly divided into three groups: the sham operation group (group C), the ischemia-reperfusion group (group I/R), and the DEX group (group D). The middle cerebral artery occlusion model was prepared by the modified Longa method. The time of ischemia was 180 min, and 120 min after reperfusion, the amount of glutamate (Glu), and γ-aminobutyric acid (GABA) in the brain were measured, and the ultrastructure-level changes in the cerebral cortex were examined using electron microscopy. Results: Compared to group C, Glu contents in group D, and I/R significantly increased. Compared to group I/R, Glu contents in group D significantly decreased. Compared to group C, GABA contents in group D, and I/R significantly increased, and those in group D significantly increased, as compared to group I/R. The cerebral ultrastructure was normal in group C. Vacuolar degeneration in the plastiosome and nervous processes, was more critical than in group D. Vascular endothelial cells (VEC) were damaged. On the contrary, these changes in group D significantly improved. Conclusion: Dexmedetomidine is capable of decreasing glutamergic content, and increasing GABAergic content, in order to decrease the injury of the cerebral ultrastructure, following cerebral ischemia-reperfusion injury.
Asunto(s)
Animales , Masculino , Ratas , Daño por Reperfusión/metabolismo , Corteza Cerebral/química , Isquemia Encefálica/tratamiento farmacológico , Fármacos Neuroprotectores/farmacología , Dexmedetomidina/farmacología , Glutamina/metabolismo , Corteza Cerebral/ultraestructura , Isquemia Encefálica/metabolismo , Ratas Wistar , Ácido gamma-Aminobutírico/efectos de los fármacos , Ácido gamma-Aminobutírico/metabolismo , Aminoácidos/efectos de los fármacos , Aminoácidos/metabolismoRESUMEN
Procedimentos cirúrgicos em equinos requerem uma anestesia potencialmente prolongada, segura, e com recuperação suave. As necessidades clínicas e cirúrgicas têm sido atendidas com anestésicos inalatórios ou ainda técnicas anestésicas injetáveis. A anestesia intravenosa total demonstrou manter melhor os parâmetros cardiovasculares durante procedimentos de curta duração, sempre associado a relaxantes musculares, como por exemplo a a2-adrenoceptores. O propofol é ideal a ser utilizado por sua ação rápida e de curta duração. Pode ser utilizado na indução ou manutenção. Contudo, possui uma principal desvantagem, que é a possibilidade de provocar uma depressão respiratória substancial. Apesar de muitos estudos ainda existem lacunas, e a busca do "uso perfeito"de fármacos injetáveis para cavalos é constante.
Surgical procedures in horses require a potentially prolonged anesthesia, safe, and smooth recovery. The clinical and surgical needs have been met with inhaled anesthetics or injected anesthetic techniques. Total intravenous anesthesia demonstrated better to keep the cardiovascular parameters durantes short procedures, always associated with muscle relaxants or the a2-adrenoceptor. Propofol is ideal for use by its quick action and short-lived. Itcan be used for the induction or maintenance. However, it has a major disadvantage, which is the possibility of causinga substantial respiratory depression. Although many studies there are still gaps, and the pursuit of "perfect use" ofinjectable drugs for horses is constant.
Los procedimientos quirúrgicos en los caballos requiere una anestesia potencialmente prolongada, seguray recuperación sin problemas. Las necesidades clínicas y quirúrgicas se han cumplido con los anestésicos inhaladoso técnicas anestésicas inyectados. EI total de Ia anestesia por vía intravenosa mostraron mejor mantener los parámetros cardiovasculares durante procedimientos cortos, siempre asociados aios relajantes musculares, como a2-adrenérgicos.EI propofol es ideal para su uso por su acción rápida y de corta duración. Se puede utilizar para Ia inducción o mantenimiento. Sin embargo, tiene una desventaja importante, que es Ia posibilidad de causar una depresión respiratoria importante. Aunque muchos estudios todavía hay lagunas, y Ia búsqueda de "uso perfecto" de los medicamentos inyectables para los caballos es constante.
Asunto(s)
Animales , Anestesia Intravenosa/veterinaria , Caballos/fisiología , Procedimientos Quirúrgicos Operativos/veterinaria , Propofol/administración & dosificación , Propofol/uso terapéutico , Ketamina/uso terapéutico , Medetomidina/uso terapéuticoRESUMEN
Procedimentos cirúrgicos em equinos requerem uma anestesia potencialmente prolongada, segura, e com recuperação suave. As necessidades clínicas e cirúrgicas têm sido atendidas com anestésicos inalatórios ou ainda técnicas anestésicas injetáveis. A anestesia intravenosa total demonstrou manter melhor os parâmetros cardiovasculares durante procedimentos de curta duração, sempre associado a relaxantes musculares, como por exemplo a a2-adrenoceptores. O propofol é ideal a ser utilizado por sua ação rápida e de curta duração. Pode ser utilizado na indução ou manutenção. Contudo, possui uma principal desvantagem, que é a possibilidade de provocar uma depressão respiratória substancial. Apesar de muitos estudos ainda existem lacunas, e a busca do "uso perfeito"de fármacos injetáveis para cavalos é constante.(AU)
Surgical procedures in horses require a potentially prolonged anesthesia, safe, and smooth recovery. The clinical and surgical needs have been met with inhaled anesthetics or injected anesthetic techniques. Total intravenous anesthesia demonstrated better to keep the cardiovascular parameters durantes short procedures, always associated with muscle relaxants or the a2-adrenoceptor. Propofol is ideal for use by its quick action and short-lived. Itcan be used for the induction or maintenance. However, it has a major disadvantage, which is the possibility of causinga substantial respiratory depression. Although many studies there are still gaps, and the pursuit of "perfect use" ofinjectable drugs for horses is constant.(AU)
Los procedimientos quirúrgicos en los caballos requiere una anestesia potencialmente prolongada, seguray recuperación sin problemas. Las necesidades clínicas y quirúrgicas se han cumplido con los anestésicos inhaladoso técnicas anestésicas inyectados. EI total de Ia anestesia por vía intravenosa mostraron mejor mantener los parámetros cardiovasculares durante procedimientos cortos, siempre asociados aios relajantes musculares, como a2-adrenérgicos.EI propofol es ideal para su uso por su acción rápida y de corta duración. Se puede utilizar para Ia inducción o mantenimiento. Sin embargo, tiene una desventaja importante, que es Ia posibilidad de causar una depresión respiratoria importante. Aunque muchos estudios todavía hay lagunas, y Ia búsqueda de "uso perfecto" de los medicamentos inyectables para los caballos es constante.(AU)
Asunto(s)
Animales , Propofol/administración & dosificación , Propofol/uso terapéutico , Procedimientos Quirúrgicos Operativos/veterinaria , Anestesia Intravenosa/veterinaria , Caballos/fisiología , Ketamina/uso terapéutico , Medetomidina/uso terapéuticoRESUMEN
Background: Bispectral index (BIS) monitor was developed to utilize the depth of anesthesia by estimating electroencephalogram (EEG) signals. BIS, which is the numerical value of EEG derivative, is used for evaluation of depression of central nervous system (CNS) in human medicine. The depressive effect of sedative and anaesthetic agents on CNS in human is correlated to BIS. Dexmedetomidine (DEX) is administered as continuous infusion during anesthesia and surgery in humans. DEX is a hypnotic with high selectivity for 2-adrenergic receptors.Materials, Methods & Results: Adult female New Zealand rabbits (mean ± SD body weight 3.8 ± 0.5 kg) were procured from a certified commercial source to use in medical researches. The animal number in each of the two study groups was four, for a total of eight. The rabbits were randomly divided into two equal groups (n = 4). The rabbits DEX group were administered 20 mcg/kg of iv. DEX HCI for premedication. Medetomidine (MED) group was administered 20 mcg/ kg of iv MED for premedication. Induction was provided by 5% of sevoflurane + 4 L/min oxygen via glove mask in the both groups. General anesthesia was maintained with 3% of sevoflurane + oxygen on spontaneous respiration for 30 min. The animals temporomandibular region was shaved; its fat was eliminated with ether before the study. Human sensors were used as BIS sensor consisted of...
Asunto(s)
Dexmedetomidina/administración & dosificación , Dexmedetomidina/análisis , Medetomidina/administración & dosificación , Medetomidina/análisis , Sevoflurano/administración & dosificación , Sevoflurano/análisis , Análisis Espectral/veterinariaRESUMEN
Background: Bispectral index (BIS) monitor was developed to utilize the depth of anesthesia by estimating electroencephalogram (EEG) signals. BIS, which is the numerical value of EEG derivative, is used for evaluation of depression of central nervous system (CNS) in human medicine. The depressive effect of sedative and anaesthetic agents on CNS in human is correlated to BIS. Dexmedetomidine (DEX) is administered as continuous infusion during anesthesia and surgery in humans. DEX is a hypnotic with high selectivity for 2-adrenergic receptors.Materials, Methods & Results: Adult female New Zealand rabbits (mean ± SD body weight 3.8 ± 0.5 kg) were procured from a certified commercial source to use in medical researches. The animal number in each of the two study groups was four, for a total of eight. The rabbits were randomly divided into two equal groups (n = 4). The rabbits DEX group were administered 20 mcg/kg of iv. DEX HCI for premedication. Medetomidine (MED) group was administered 20 mcg/ kg of iv MED for premedication. Induction was provided by 5% of sevoflurane + 4 L/min oxygen via glove mask in the both groups. General anesthesia was maintained with 3% of sevoflurane + oxygen on spontaneous respiration for 30 min. The animals temporomandibular region was shaved; its fat was eliminated with ether before the study. Human sensors were used as BIS sensor consisted of...(AU)
Asunto(s)
Dexmedetomidina/administración & dosificación , Dexmedetomidina/análisis , Sevoflurano/administración & dosificación , Sevoflurano/análisis , Medetomidina/administración & dosificación , Medetomidina/análisis , Análisis Espectral/veterinariaRESUMEN
OBJECTIVE: To evaluate the effects of intravenous (IV) or intramuscular (IM) hyoscine premedication on physiologic variables following IV administration of medetomidine in horses. STUDY DESIGN: Randomized, crossover experimental study. ANIMALS: Eight healthy crossbred horses weighing 330 ± 39 kg and aged 7 ± 4 years. METHODS: Baseline measurements of heart rate (HR), cardiac index (CI), respiratory rate, systemic vascular resistance (SVR), percentage of patients with second degree atrioventricular (2(o) AV) block, mean arterial pressure (MAP), pH, and arterial partial pressures of carbon dioxide (PaCO2 ) and oxygen (PaO2 ) were obtained 5 minutes before administration of IV hyoscine (0.14 mg kg(-1) ; group HIV), IM hyoscine (0.3 mg kg(-1) ; group HIM), or an equal volume of physiologic saline IV (group C). Five minutes later, medetomidine (7.5 µg kg(-1) ) was administered IV and measurements were recorded at various time points for 130 minutes. RESULTS: Medetomidine induced bradycardia, 2(o) AV blocks and increased SVR immediately after administration, without significant changes in CI or MAP in C. Hyoscine administration induced tachycardia and hypertension, and decreased the percentage of 2(o) AV blocks induced by medetomidine. Peak HR and MAP were higher in HIV than HIM at 88 ± 18 beats minute(-1) and 241 ± 37 mmHg versus 65 ± 16 beats minute(-1) and 192 ± 38 mmHg, respectively. CI was increased significantly in HIV (p ≤ 0.05). Respiratory rate decreased significantly in all groups during the recording period. pH, PaCO2 and PaO2 were not significantly changed by administration of medetomidine with or without hyoscine. CONCLUSION AND CLINICAL RELEVANCE: Hyoscine administered IV or IM before medetomidine in horses resulted in tachycardia and hypertension under the conditions of this study. The significance of these changes, and responses to other dose rates, requires further investigation.
Asunto(s)
Bromuro de Butilescopolamonio/farmacología , Caballos , Hipnóticos y Sedantes/farmacología , Medetomidina/farmacología , Antagonistas Muscarínicos/farmacología , Animales , Bloqueo Atrioventricular , Presión Sanguínea/efectos de los fármacos , Gasto Cardíaco/efectos de los fármacos , Estudios Cruzados , Femenino , Frecuencia Cardíaca/efectos de los fármacos , Hipnóticos y Sedantes/administración & dosificación , Inyecciones Intramusculares , Inyecciones Intravenosas , Masculino , PremedicaciónRESUMEN
Objetivou-se verificar a existência de potenciais associações entre medetomidina e atipemazole na eletroejaculação de catetos anestesiados com propofol. Os doze catetos receberam os tratamentos: controle, sem pré medicação; medetomidina 40 μg.Kg -1IV ou atipemazole 200 μg.Kg -1 IV. Todos os animais receberam propofol 5 mg.Kg -1 IV na indução e manutenção da anestesia. Foram avaliados: frequência cardíaca, respiratória, pressão arterial sistólica, diastólica, e média, temperatura, hemogasometria e cortisol. Em relação aos parâmetros reprodutivos, avaliou-se o tempo de latência da ejaculação, ereção, e variáveis seminais. Analisamos os dados por one way ANOVA para medidas repetidas seguidas por Tukey. P < 0,05 foram considerados significativos. Para o sêmen, obtive-se diferença significativa na concentração espermática entre atipemazole (100,00 25,96 x 106) e medetomidina (220,20 49,74 x 106), contudo ambos não diferiram estatisticamente do controle (180,00 50,71 x 106). Medetomidina promoveu alterações cardiovasculares mais significativas. Não foram observadas diferenças significativas nos valores de cortisol entre os tratamentos comparados. Recuperação com propofol foi significativamente mais rápida. Os fármacos medetomidina e atipemazole não incrementam a função erétil de catetos. Entretanto, influenciam na concentração espermática e na função ejaculatória destes. O propofol isolado proporcionou uma anestesia mais eficiente na coleta de sêmen catetos submetidos à eletroejaculação.
The objective was to verify the existence of potential associations between medetomidine and atipemazole in electroejaculation of peccaries anesthetized with propofol. The twelve peccary received the following treatments: control, none pre medication; medetomidine 40 microg.Kg-1 IV or atipemazole 200 microg.Kg-1 IV. All animals received 5 mg.Kg-1 IV propofol induction and maintenance of anesthesia. Were evaluated: heart rate, respiratory rate, systolic, diastolic, and mean blood pressure, temperature, blood gas and cortisol. For the semen evaluated the onset time of ejaculation, erection, and seminal variables. We analyzed the data by one way ANOVA for repeated measures followed by Tukey. P < 0.05 were considered significant. For semen, we obtained only a significant difference in sperm concentration between atipemazole (100.00 25.96 x 106) and medetomidine (220.20 49.74 x 106), yet both did not differ from controls (180.00 50.71 x 106). Medetomidine promoted cardiovascular changes more significant. There was no significant difference in cortisol levels between the treatments compared. Atipamezole and medetomidine do not increase the peccarys erectile function. However, they influence the concentration of sperm and ejaculatory function in the peccary undergoing electroejaculation. Propofol alone, resulted in a more efficient anesthesia for peccary collection semen.
Asunto(s)
Animales , /administración & dosificación , Artiodáctilos/metabolismo , Medetomidina/administración & dosificación , Propofol/administración & dosificación , Sinergismo Farmacológico , Eyaculación , Erección PenianaRESUMEN
The objectives of this study were to compare the clinical effects and glycemia induced by medetomidine and xylazine in healthy cats and to demonstrate the reversal of the effects by atipamezole. A prospective blinded randomized experimental trial was used with twenty-four healthy adult cats. The animals were allocated into 4 groups of 6 animals each to receive by intramuscular route (IM): Group M (medetomidine - 50 g/ kg); Group X (xylazine - 1.1 mg/kg); Group MA (medetomidine - 50 g/kg and 60 minutes later atipamezole - 0.2 mg/kg); Group XA (xylazine - 1.1 mg/kg and 60 minutes later atipamezole - 0.2 mg/kg). Rectal temperature, respiratory rate, heart rate, systolic arterial pressure, electrocardiogram, intraocular pressure, degree of sedation were measured at 0, 30, 60, 120 and 180 minutes, and the serum glucose concentration was measured at 0, 60, 120 and 180 minutes. The xylazine at a dose of 1.1 mg/kg and medetomidine at a dose of 50 g/kg (both intramuscular) induced hypothermia, decreased heart rate, respiration and blood pressure and also 1st-degree A-V block in some cats, but it did not interfere significantly with intraocular pressure. The medetomidine induced a more pronounced hypothermia, sedation and hyperglycemia than xylazine in cats. The atipamezole was an excellent antagonist of the effects induced by medetomidine and xylazine in cats. Also, it did not interf
RESUMEN
The objectives of this study were to compare the clinical effects and glycemia induced by medetomidine and xylazine in healthy cats and to demonstrate the reversal of the effects by atipamezole. A prospective blinded randomized experimental trial was used with twenty-four healthy adult cats. The animals were allocated into 4 groups of 6 animals each to receive by intramuscular route (IM): Group M (medetomidine - 50 g/ kg); Group X (xylazine - 1.1 mg/kg); Group MA (medetomidine - 50 g/kg and 60 minutes later atipamezole - 0.2 mg/kg); Group XA (xylazine - 1.1 mg/kg and 60 minutes later atipamezole - 0.2 mg/kg). Rectal temperature, respiratory rate, heart rate, systolic arterial pressure, electrocardiogram, intraocular pressure, degree of sedation were measured at 0, 30, 60, 120 and 180 minutes, and the serum glucose concentration was measured at 0, 60, 120 and 180 minutes. The xylazine at a dose of 1.1 mg/kg and medetomidine at a dose of 50 g/kg (both intramuscular) induced hypothermia, decreased heart rate, respiration and blood pressure and also 1st-degree A-V block in some cats, but it did not interfere significantly with intraocular pressure. The medetomidine induced a more pronounced hypothermia, sedation and hyperglycemia than xylazine in cats. The atipamezole was an excellent antagonist of the effects induced by medetomidine and xylazine in cats. Also, it did not interf