Rutkowski J A, Ross M W, Cullen K
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square 19348.
Am J Vet Res. 1989 Jul;50(7):1096-101.
Effects of xylazine HCl (0.5 mg/kg of body weight, IV) and/or butorphanol tartrate (0.04 mg/kg, IV) or neostigmine methylsulfate (0.022 mg/kg, IV) on myoelectric activity of the cecum and right ventral colon were studied in 4 conscious female ponies. Eight bipolar Ag/AgCl electrodes were sequentially placed on the seromuscular layer of the cecum (6 electrodes) and right ventral colon (2 electrodes). Recordings began 30 minutes before and continued for 90 minutes after drug administration. Each drug or drug combination was studied on 2 occasions in each pony. Two major patterns of coordinated spike bursts were identified. A series of coordinated spike bursts began at the cecal base and was conducted to the cecal apex (pattern I). A series of coordinated spike bursts began at the cecal apex, traversed the cecum, cecocolic orifice, and right ventral colon and was termed a progressive pattern (pattern II). Xylazine administration caused a significant decrease in patterns I and II for 20 minutes (P less than 0.05). Butorphanol tartrate administration caused a significant decrease in the progressive pattern for 10 minutes (P less than 0.05) without affecting the orally directed pattern. Administration of the combination of xylazine/butorphanol significantly decreased the frequency of pattern I for 40 minutes (P less than 0.05) and pattern II for 30 minutes (P less than 0.05). Neostigmine administration caused a significant increase in the frequency of pattern II for 30 minutes (P less than 0.05) without affecting pattern I (P greater than 0.05). Changes in conduction velocity of pattern I or II or the duration of spiking activity were not significantly different because of any treatment.
在4匹清醒的雌性小马中研究了盐酸赛拉嗪(0.5毫克/千克体重,静脉注射)和/或酒石酸布托啡诺(0.04毫克/千克,静脉注射)或甲基硫酸新斯的明(0.022毫克/千克,静脉注射)对盲肠和右腹结肠肌电活动的影响。将8个双极银/氯化银电极依次置于盲肠(6个电极)和右腹结肠(2个电极)的浆肌层上。记录在给药前30分钟开始,并在给药后持续90分钟。每种药物或药物组合在每匹小马身上研究2次。识别出两种主要的协调性尖峰爆发模式。一系列协调性尖峰爆发始于盲肠底部并传导至盲肠顶端(模式I)。一系列协调性尖峰爆发始于盲肠顶端,穿过盲肠、盲结肠口和右腹结肠,被称为进行性模式(模式II)。给予赛拉嗪使模式I和模式II在20分钟内显著减少(P<0.05)。给予酒石酸布托啡诺使进行性模式在10分钟内显著减少(P<0.05),而不影响向口腔方向的模式。给予赛拉嗪/酒石酸布托啡诺组合使模式I的频率在40分钟内显著降低(P<0.05),模式II的频率在30分钟内显著降低(P<0.05)。给予新斯的明使模式II的频率在30分钟内显著增加(P<0.05),而不影响模式I(P>0.05)。由于任何治疗,模式I或II的传导速度或尖峰活动持续时间的变化没有显著差异。