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使用新型多巴胺激动剂卡麦角林和合成的前列腺素F2α氯前列醇联合终止猫的妊娠。

Termination of pregnancy in cats using a combination of cabergoline, a new dopamine agonist, and a synthetic PGF2 alpha, cloprostenol.

作者信息

Onclin K, Verstegen J

机构信息

Department of Small Animal Reproduction, Veterinary College, University of Liège, Belgium.

出版信息

J Reprod Fertil Suppl. 1997;51:259-63.

PMID:9404294
Abstract

The objective of this study was to increase efficacy of treatment with the dopamine agonist, cabergoline, for inducing abortion in cats by combining it with a synthetic PGF2 alpha analogue, cloprostenol. Side effects of cloprostenol were avoided by using low doses. An oral formulation of cabergoline was chosen to facilitate administration. Cabergoline was given daily (5 micrograms kg-1 day-1) while s.c. injections of cloprostenol were administered every 2 days (5 micrograms kg-1) (2 days)-1). Plasma concentrations of progesterone, side effects and pregnancy outcome were compared with those of five untreated pregnant queens. The treatment was administered from day 30 after first mating in five queens confirmed as pregnant and lasted a mean of 11 +/- 1 days. All treated animals aborted in 9 +/- 1 days without any side effect, except a mild haemorrhagic vulvar discharge. Subsequent fertility of the queens was not compromised. Abortion was mediated by an abrupt and constant decrease in plasma concentrations of progesterone. Progesterone concentrations were lower than 1 ng ml-1 from day 38 onwards in all treated animals and remained at this value thereafter, except for one queen which showed a further increase in plasma progesterone concentration from day 44 without any clinical consequence. In conclusion, a combination of daily oral administration of cabergoline and cloprostenol injections every 2 days appears to be a reliable, safe and practical method for terminating pregnancy in cats at day 30 of pregnancy, when a diagnosis of pregnancy by palpation or ultrasonography can easily be made.

摘要

本研究的目的是通过将多巴胺激动剂卡麦角林与合成的前列腺素F2α类似物氯前列醇联合使用,提高其诱导猫流产的治疗效果。通过使用低剂量避免了氯前列醇的副作用。选择卡麦角林的口服制剂以方便给药。卡麦角林每日给药(5微克/千克/天),而氯前列醇皮下注射每2天给药一次(5微克/千克)(每2天一次)。将孕酮的血浆浓度、副作用和妊娠结局与五只未治疗的怀孕母猫进行比较。在五只确认怀孕的母猫中,从首次交配后第30天开始进行治疗,平均持续11±1天。所有接受治疗的动物在9±1天内流产,除了轻度的外阴出血性分泌物外,没有任何副作用。母猫随后的生育能力未受影响。流产是由孕酮血浆浓度的突然持续下降介导的。在所有接受治疗的动物中,从第38天起孕酮浓度低于1纳克/毫升,此后一直保持在该水平,只有一只母猫在第44天后血浆孕酮浓度进一步升高,但没有任何临床后果。总之,每天口服卡麦角林和每2天注射氯前列醇的联合使用似乎是一种可靠、安全且实用的方法,可在妊娠第30天终止猫的妊娠,此时通过触诊或超声检查很容易做出妊娠诊断。

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1
Termination of pregnancy in cats using a combination of cabergoline, a new dopamine agonist, and a synthetic PGF2 alpha, cloprostenol.使用新型多巴胺激动剂卡麦角林和合成的前列腺素F2α氯前列醇联合终止猫的妊娠。
J Reprod Fertil Suppl. 1997;51:259-63.
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