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研究生:楊崇君
研究生(外文):Chung-Chun Yang
論文名稱:評估單獨使用Xylazine或Dexmedetomidine於白鼻心之作用與Atipamezole之翻轉效果
論文名稱(外文):Evaluation of the Effects of Xylazine or Dexmedetomidine and the Reversal Effects of Atipamezole in Formosan Gem-faced Civet (Paguma larvata taivana)
指導教授:董光中董光中引用關係
指導教授(外文):Kwong-Chung Tung
口試委員:吳應寧何素鵬
口試日期:2011-05-25
學位類別:碩士
校院名稱:國立中興大學
系所名稱:獸醫學系暨研究所
學門:獸醫學門
學類:獸醫學類
論文種類:學術論文
論文出版年:2011
畢業學年度:99
語文別:中文
論文頁數:60
中文關鍵詞:白鼻心鎮靜dexmedetomidinexylazineatipamezole
外文關鍵詞:Formosan Gem-faced Civetsedationdexmedetomidinexylazineatipamezole
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白鼻心生性容易緊張,若感受到威脅時,常會表現出攻擊行為。因其四肢粗壯具有利爪且咬合力大,因此常成為臨床診療上之阻礙,若進行需碰觸到白鼻心的檢查,對醫療人員具有一定程度之風險,因此選擇適當的鎮靜劑能使醫療處理的過程更為順利,且同時減少動物緊迫,使得雙方皆能獲得最大的安全。
Xylazine(XYL)和dexmedetomidine(DEX)皆為α2腎上腺素性受體致效劑的一種,這類的鎮靜安神藥物時常用來做為誘導鎮靜,並有止痛作用,皆有拮抗劑可迅速反轉鎮靜之效果可使動物迅速恢復。XYL在過去廣泛地被獸醫應用在各種不同的物種作為鎮靜和止痛之用,相關研究甚多;DEX則為一具有高度選擇性和特異性的α2腎上腺素性受體致效劑,近年來在臨床上常被應用於犬貓。有關白鼻心麻醉的研究很少,本研究探討單獨使用兩種不同的α2腎上腺素性受體致效劑對白鼻心之鎮靜作用和止痛效果,以及使用atipamezole(ATI)反轉DEX之效果。
本研究共使用18隻白鼻心進行實驗,選擇的劑量組分別為每公斤體重2、4和8 mg的XYL,以及0.01、0.02和0.04 mg的DEX,於後肢肌肉注射實驗藥物後分別監控其基礎生理值以及各項反射的強弱並予以紀錄。結果顯示僅有DEX 0.02和DEX 0.04 mg/kg這兩組劑量組能使全數(6/6)白鼻心成功進入鎮靜狀態,而進入鎮靜期的時間於六組之間皆沒有顯著差異;鎮靜持續時間則隨劑量之提高而延長,且各劑量組之心搏和呼吸速率皆會下降,體溫則隨鎮靜時間之延長而逐漸降低。在XYL和DEX的比較上,DEX較能使白鼻心維持穩定的鎮靜狀態。探討拮抗劑效果的實驗先以每公斤體重0.04 mg的DEX鎮靜白鼻心後,於實驗的第30分鐘三組再分別肌肉注射saline 0.04 ml/kg、ATI 0.04 mg/kg及ATI 0.2 mg/kg,三組白鼻心分別於注射後77.5、28.5及7分鐘恢復,顯示不論是注射低劑量或高劑量之ATI,皆能顯著使白鼻心之恢復時間縮短,而較高之劑量則更能縮短恢復時間,有助於於臨床診療結束時使動物快速恢復正常。
綜合上述,我們知道DEX相較於XYL有更穩定的鎮靜效果,而使用DEX 0.02 mg/kg或 0.04 mg/kg時可以成功地使白鼻心進入鎮靜狀態,當臨床上需要對白鼻心進行鎮靜檢查時,可以評估所需鎮靜時間的長短來選擇不同的劑量,而於醫療處理結束後可給予ATI結束鎮靜,使動物迅速恢復正常。


Formosan gem-faced civet (Paguma larvata taivana) has the nature of being tense and is prone to be aggressive under menace. The attack behavior could make a clinical crux for the practitioner if physical examination is intended. To strike for a mutual beneficial resolution on both sides of the animal and staff, administration of appropriate sedatives will ensure an uneventful procedure.
Xylazine (XYL) and dexmedetomidine (DEX) are α2 adrenergic agonists, which are used for induction for their sedative and analgesic and antagonists are available to reverse the effect and speed the recovery. XYL was commonly used for its sedative and analgesic in varieties of species, which related studies are many. DEX is a highly selective and specific α2 adrenergic agonist and its clinical use in dogs and cats is more often in recent years. Yet, studies of anesthetics in Formosan gem-faced civets are rarely documented. This study is intended to observe the sedative and analgesic effects of the sole administration of two different α2 adrenergic agonists, respectively, in formosan gem-faced civets and the effect of atipamezole (ATI) to reverse dexmedetomidine.
The experiment group was formed with 18 formosan gem-faced civets. The treated group of XYL was at doses of 2, 4 and 8 mg/kg and so was the treated group of DEX at doses of 0.01, 0.02 and 0.04 mg/kg via the route of intramuscular injection on the hind limb. The vitals and intensity of the reflex were monitored and recorded. As the results presented the groups of DEX 0.02 and DEX 0.04 mg/kg were the only two dosages that made the whole number of the treated animals (6/6) onset steady sedation and no obvious difference was noted in these six groups. The period of sedation sustained longer at higher doses; the heart rate and respiratory rate were decreased and the body temperature declined gradually over sedation. Comparing XYL and DEX, the later proved to maintain a steady sedation better in formosan gem-faced civets. In the study of antagonist reversal, 0.04 mg/kg of DEX was administered to reach the sedation, and three groups of testing animals were treated with IM injection of 0.04 ml/kg of saline, 0.04 mg/kg of ATI and 0.2 mg/kg of ATI, 30 minutes after the treatment, respectively. The treated animals recovered in 77.5, 28.5 and 7 minutes after the injection, which revealed that ATI dramatically speeded the recovery and the higher dose contributed to the less time, which advantages the clinical practice.
In conclusion, DEX provided more stable sedative effects than XYL and the administration of 0.02 or 0.04 mg/kg of DEX succeeded to achieve such goal uneventfully in formosan gem-faced civets. Previous assessment of the time needed for procedures determined what dose is to be administered when sedation is considered for clinical examination of formosan gem-faced civets. After the procedure, the animals can be restored to their normal presedation demeanour effectively and reliably with administration of ATI.


摘要 i
Abstract ii
目次 iv
表目次 vii
圖目次 viii
第一章 緒言 1
第二章 文獻探討 2
第一節 白鼻心介紹 2
一、 科學分類 2
二、 體型特徵 2
三、 食性 2
四、 棲地類型 2
五、 生態習性 3
第二節 應用於野生動物之鎮靜與麻醉 3
一、 鎮靜前的準備 3
二、 鎮靜前的評估 3
三、 應用於白鼻心之麻醉 4
四、 應用於其他靈貓科動物之麻醉 4
五、 應用於其他食肉目野生動物之麻醉 4
第三節 α2型腎上腺素性受體致效劑 6
一、 簡介 6
二、 Xylazine 8
(一) 簡介 8
(二) 藥理作用 9
(三) 應用 15
三、 Dexmedetomidine 17
(一) 簡介 17
(二) 藥理作用 17
(三) 應用 18
第四節 α2型腎上腺素性受體拮抗劑 19
一、 簡介 19
二、 Atipamezole 20
第三章 材料與方法 21
第一節 實驗設計 21
一、 實驗動物 21
二、 實驗藥物 21
三、 實驗前準備(前準備、前置作業) 22
四、 藥物注射方式 23
五、 鎮靜期的評估 24
(一) 測量方法 24
(二) 基礎生理值之監控 24
(三) 反射項目之測量 25
(四) 評分標準 26
(五) 鎮靜指數和止痛指數 26
(六) 鎮靜分期的定義 26
(七) 統計分析方法 27
第二節 評估單獨使用dexmedetomidine或xylazine於白鼻心之鎮靜效果 27
一、 實驗目的 27
二、 實驗步驟 27
第三節 評估不同劑量atipamezole對白鼻心定量dexmedetomidine之拮抗效果 28
一、 實驗目的 28
二、 實驗步驟 28
第四章 結果 29
第一節 評估單獨使用dexmedetomidine或xylazine於白鼻心之鎮靜效果 29
一、 實驗動物之體重 29
二、 鎮靜分期時間 30
(一) Xylazine之鎮靜分期時間 30
(二) Dexmedetomidine之鎮靜分期時間 31
三、 各項反射反應時間 32
(一) Xylazine之各項反射反應時間 32
(二) dexmedetomidine之各項反射反應時間 33
四、 比較dexmedetomidine與xylazine各劑量組成功鎮靜之頭數 34
五、 心搏速率隨時間之變化 35
(一) Xylazine之心搏速率 35
(二) Dexmedetomidine之心搏速率 36
六、 呼吸速率隨時間之變化 37
(一) Xylazine之呼吸速率 37
(二) Dexmedetomidine之呼吸速率 38
七、 體溫隨時間之變化 39
(一) Xylazine之體溫 39
(二) Dexmedetomidine之體溫 40
八、 鎮靜指數隨時間之變化 41
(一) Xylazine之鎮靜指數 41
(二) Dexmedetomidine之鎮靜指數 42
九、 止痛指數隨時間之變化 43
(一) Xylazine之止痛指數 43
(二) Dexmedetomidine之止痛指數 44
第二節 評估不同劑量atipamezole對白鼻心定量dexmedetomidine之拮抗效果 45
一、 實驗動物之體重 45
二、 比較未進行注射及注射slaine兩組之間恢復時間之差異 45
三、 各注射藥物劑量組之間恢復時間之差異 46
四、 各劑量組之間呼吸速率之變化 46
五、 各注射藥物劑量組之間心搏速率之變化 48
第五章 討論 48
參考文獻 53


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