• 제목/요약/키워드: liletamine/zolazepam

검색결과 2건 처리시간 0.014초

그린 이구아나에서 medetomidine-tiletamine/zolazepam의 병용 마취시 atipamezole의 길항작용 (The Reverse Effects of Atipamezole on Medetomidine-tiletamine/zolazepam Combination Anesthesia in the Green Iguana (Iguana iguana))

  • 정소영;김민수;이나영;김순영;서강문;남치주
    • 한국임상수의학회지
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    • 제23권1호
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    • pp.18-21
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    • 2006
  • 그린 이구아나에서 medetomidine과 tiletamine/zolazepam의 병용마취시 atipamezole에 의한 길항효과를 알아 보기 위하여 본 실험을 실시하였다. 심박동수, 호흡수 그리고 체온을 측정하였으며 righting reflex에 의하여 마취의 심도 및 회복을 평가하였다. 두군 모두에서 심박동수와 호흡수는 마취주사 5분 후에 유의성 있는 감소를 보였으며 (p<0.05) atipamezole 주사 후에는 지속적으로 증가하는 양상을 보였다. 본 연구결과 atipamezole $500{\mu}g/kg$은 medetomidine $500{\mu}g/kg$과 liletamine/zolazepam 10mg/kg의 병용마취를 실시한 그린 이구아나에서 효과적인 길항 용량이라고 생각된다.

개에서 Tiletamine-Zolazepam 마취에 대한 Doxapram과 Yohimbine의 길항효과 (Antagonistic Effects of Doxapram and Yohimbine on Tiletamine-Zolazepam Anesthesia in Dogs)

  • 박명호;김명철
    • 한국임상수의학회지
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    • 제12권1호
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    • pp.799-818
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    • 1995
  • This study was performed to examine the general anesthetic efficacy of tiletamine-zolazepam, a mixture of phencyclidine-derived tiletamine and benzodiazepine-related zolazepam. The antagonistic activities of doxapram and yohimbine to the anesthetic effects of tiletamine-zolazepam were also studied. Thirty healthy mongrel dogs were divided into three groups (each of 10) twenty minutes after being anesthetized with tiletamine-zolazepam : T-Z-S group(tiletamine-zolazepam-saline), T-Z-D group (tiletamine -zolazepam-doxapram), T-Z-Y group (tiletamine-zolaz.pam-yohim bine). Various parameters wert evaluated in terms of the onset and recovery time of analgesia, respiration rates, hear rates, body temperature, electrocardiogram, blood chemistry, and lymphocyte blastogenesis. The results obtained through these experiment could be summarized as follows: 1. he anesthetic efficacy of tiletamine-zolazepam was considered desirable, with the onset time of anesthesia being as short as 0.23-0.24 minutes. 2. Both of the antagonistic effects of yohimbine and doxapram on the anesthesia induced by liletamine-zolazepan were evaluated statistically significant(p<0.05) as the recovery time was shortened from 39.3$\pm$4.9 min(T-Z-S group) to 25.3$\pm$2.9 nin(T-Z-Y group) and 29.9$\pm$8.8min(T-Z-D group), respectively. 3. Respiration rates were not changed by the treatments of both doxapram and yohimbine, with the only transient increase in the T-Z-D group. The changes in the respiration rate were not observed during the whole time course of the experiment. 4. Yohimbine(T-Z-Y group) increased the heart rate significantly from 30 minutes after the adminstration compared to the T-Z-S group and T-Z-D group (p<0.05). 5. The decreases in th, body temporature were observed from 30 minutes in the T-Z-S group(p<0.05) and 40 minutes in th, T-Z-D group(p<0.05), after the adminstration. On the other hand, there was no hypothermia in the T-Z-Y group. 6. In the all experimental groups of the T-Z-S, T-Z-D and T-Z-Y, there were no specific findings on the electrocardiograph incept slight shift to the tachycardia in all cases. 1. We could not find any differences in the blood chemistry between all experimental groups (T-Z-S, T-Z-D and T-Z-Y). 8. the inhibition of the lymphocyte blastogenesis shown in the T-Z-S with 3 hours decreasing and thereafter restoring to the normal values up to the point 5 hours were not occurred in the T-Z-D and T-Z-Y groups. With the above results, we could conclude that both doxapram and yohimbine can be clinically used as recovery agents towards anesthesia by tiletamine- zolazepam fi:on the efficacy point of view, but yohimbine is more recommendable in this case if considering the recovery time and lymphocyte blastogenesis.

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