Tokuriki M, Matsunami K, Uzuka Y
Department of Veterinary Physiology, Faculty of Agriculture, Yamaguchi University, Japan.
Am J Vet Res. 1990 Jan;51(1):97-102.
Brain stem auditory-evoked potentials (BAEP) were recorded in 4 dogs to analyze the relationship between acoustic stimulus intensities and peak latencies of each wave, and to investigate the relative effects of xylazine-atropine, xylazine-atropine-ketamine, and xylazine-atropine-pentobarbital combinations and the time-course effects of the latter 2 drug combinations on BAEP. Click stimulations fixed at a stimulus rate of 10/s and a frequency of 4 kHz were delivered at intensities ranging from 10- to 110-dB sound pressure level (SPL) in 10-dB steps for analyzing the relationship between the acoustic stimulus intensities and the peak latencies and at an intensity of 110-dB SPL for investigating the effects of the sedative and anesthetic drug combinations and their time-course effects on BAEP. Waves I to VI were identified with stimulus intensity of greater than or equal to 50-dB SPL. Wave VII was observed in some records, but was excluded from statistical analysis. As stimulus intensity was increased from 50- to 110-dB SPL, the latency decreased for all waves during xylazine-atropine-ketamine anesthesia. There were no statistically significant differences in the peak latencies of each wave in BAEP among xylazine-atropine, xylazine-atropine-ketamine, and xylazine-atropine-pentobarbital combinations 20 minutes after drug administration, except that the latency of wave VI during xylazine-atropine sedation was significantly (P less than 0.01) shorter than that detected during xylazine-atropine-ketamine or xylazine-atropine-pentobarbital anesthesia.(ABSTRACT TRUNCATED AT 250 WORDS)
对4只犬记录脑干听觉诱发电位(BAEP),以分析声音刺激强度与各波峰潜伏期之间的关系,并研究赛拉嗪-阿托品、赛拉嗪-阿托品-氯胺酮以及赛拉嗪-阿托品-戊巴比妥组合的相对效应,以及后两种药物组合对BAEP的时程效应。以10次/秒的刺激率和4千赫的频率进行短声刺激,强度范围为10至110分贝声压级(SPL),以10分贝步长递增,用于分析声音刺激强度与峰潜伏期之间的关系;以110分贝SPL的强度用于研究镇静和麻醉药物组合及其对BAEP的时程效应。当刺激强度大于或等于50分贝SPL时可识别出I至VI波。在一些记录中观察到了VII波,但将其排除在统计分析之外。在赛拉嗪-阿托品-氯胺酮麻醉期间,随着刺激强度从50分贝SPL增加到110分贝SPL,所有波的潜伏期均缩短。给药20分钟后,赛拉嗪-阿托品、赛拉嗪-阿托品-氯胺酮和赛拉嗪-阿托品-戊巴比妥组合之间,BAEP各波的峰潜伏期无统计学显著差异,不过赛拉嗪-阿托品镇静期间VI波的潜伏期显著(P<0.01)短于赛拉嗪-阿托品-氯胺酮或赛拉嗪-阿托品-戊巴比妥麻醉期间检测到的潜伏期。(摘要截短于250字)