Burger D M, Wiestner T, Hubler M, Binder H, Keiser M, Arnold S
Department of Reproduction, Vetsuisse-Faculty, University of Zurich, CH-8057 Zurich, Switzerland.
J Vet Med A Physiol Pathol Clin Med. 2006 Mar;53(2):97-107. doi: 10.1111/j.1439-0442.2006.00787.x.
The effect of atropine, glycopyrrolate, metoclopramide and cisapride on the antral motility was investigated in eight dogs (four Beagles and four Labradors) using passive telemetry. Both anticholinergics induced a pronounced and lasting reduction of the intensity and frequency of the contractions. A definite dose-related inhibition of the antral motility was seen in Beagles, similar for both active substances. Low doses of atropine (0.02 mg/kg BW i.m.) and glycopyrrolate (0.005 mg/kg BW i.m.) completely inhibited the gastric motility for at least 30 min, whereas higher doses (0.04 or 0.01 mg/kg BW) caused a cessation of activity for more than 3 h. In Labradors, the effects of both active substances were not so dose related and the effect of glycopyrrolate lasted at least 6 h, whereas the effect of atropine gradually decreased after 3 h. A distinct breed difference regarding the effect of the two prokinetics on the antral motility was also observed. In Beagles, the prokinetics, at a low dose (metoclopramide 0.3 mg/kg BW, cisapride 0.2 mg/kg BW), resulted in a significant increase in the amplitude integral. Higher doses (metoclopramide 0.6 mg/kg BW, cisapride 0.5 mg/kg BW) also increased the integrals of the pressure profiles, but significantly less than with the lower doses. In Labradors, both medications, mainly at higher doses, resulted in an increase of the contraction amplitudes. The low dose had no (cisapride) or only a transient effect (metoclopramide). The frequency of the antral contractions was not at all influenced by cisapride, and only in Beagles metoclopramide resulted in a dose-related increase. It is not clear if the different results in Labradors and Beagles are because of breed or body weight.
使用被动遥测技术,在8只犬(4只比格犬和4只拉布拉多犬)中研究了阿托品、格隆溴铵、甲氧氯普胺和西沙必利对胃窦运动的影响。两种抗胆碱能药物均引起收缩强度和频率显著且持久的降低。在比格犬中观察到胃窦运动有明确的剂量相关抑制,两种活性物质情况相似。低剂量的阿托品(0.02mg/kg体重,肌肉注射)和格隆溴铵(0.005mg/kg体重,肌肉注射)至少30分钟完全抑制胃动力,而较高剂量(0.04或0.01mg/kg体重)导致活动停止超过3小时。在拉布拉多犬中,两种活性物质的作用与剂量关系不那么明显,格隆溴铵的作用持续至少6小时,而阿托品的作用在3小时后逐渐减弱。还观察到两种促动力药对胃窦运动的影响存在明显的品种差异。在比格犬中,低剂量的促动力药(甲氧氯普胺0.3mg/kg体重,西沙必利0.2mg/kg体重)导致振幅积分显著增加。较高剂量(甲氧氯普胺0.6mg/kg体重,西沙必利0.5mg/kg体重)也增加了压力曲线的积分,但显著低于较低剂量时。在拉布拉多犬中,两种药物主要在较高剂量时导致收缩幅度增加。低剂量时西沙必利无作用或仅有短暂作用(甲氧氯普胺)。胃窦收缩频率完全不受西沙必利影响,仅在比格犬中,甲氧氯普胺导致剂量相关增加。尚不清楚拉布拉多犬和比格犬的不同结果是由于品种还是体重。