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错配后怀孕母犬中前列腺素诱导流产

Prostaglandin induction of abortion in pregnant bitches after misalliance.

作者信息

Feldman E C, Davidson A P, Nelson R W, Nyland T G, Munro C

机构信息

Department of Reproduction, University of California, Davis 95616.

出版信息

J Am Vet Med Assoc. 1993 Jun 1;202(11):1855-8.

PMID:8320154
Abstract

Of 48 privately-owned bitches evaluated 30 to 35 days after a single, unplanned breeding, 30 (62%) dogs were determined not to be pregnant by abdominal ultrasonography and 18 dogs were confirmed to be pregnant. Each pregnant dog was hospitalized, allotted to a treatment group, and given prostaglandin F2 alpha, SC, at 1 of 3 dosages: group 1, 0.1 mg/kg of body weight, every 8 hours; group 2, 0.25 mg/kg, every 12 hours; and group 3, 0.1 mg/kg, every 8 hours for 2 days and then 0.2 mg/kg every 8 hours thereafter. Plasma from each dog was assayed for progesterone concentration before treatment and daily until abortion was completed. Physical examinations and abdominal ultrasonography were performed every 12 and 48 hours, respectively. Treatment was continued until abortion was complete as determined by results of abdominal ultrasonography. Ultrasonography was performed earlier than the scheduled 48 hours if abdominal contractions, fetuses, or bloody or dark colored vaginal discharge was observed. Dogs of 14 breeds were treated; body weight ranged from 5.4 to 37.7 kg. All dogs aborted all fetuses within 9 days of beginning treatment. Abdominal palpation was not satisfactory in confirming whether the abortion process had been completed; however, results of ultrasonography were a reliable indicator. Plasma progesterone concentrations prior to treatment were typical of the middle phase of gestation, with all concentrations > 6.0 ng/ml. The plasma progesterone concentration decreased significantly in each dog after the first 48 hours of therapy. None of the bitches aborted any fetal material until at least 24 hours after the plasma progesterone concentration was < 2.0 ng/ml.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在48只未经计划的单次配种后30至35天接受评估的私有母犬中,通过腹部超声检查确定30只(62%)犬未怀孕,18只犬被确认怀孕。每只怀孕犬住院,分配到一个治疗组,并皮下注射前列腺素F2α,剂量为以下三种之一:第1组,0.1mg/kg体重,每8小时一次;第2组,0.25mg/kg,每12小时一次;第3组,0.1mg/kg,每8小时一次,持续2天,之后每8小时0.2mg/kg。在治疗前及每天直至流产完成时,检测每只犬的血浆孕酮浓度。分别每12小时和48小时进行体格检查和腹部超声检查。根据腹部超声检查结果,持续治疗直至流产完成。如果观察到腹部收缩、胎儿或血性或深色阴道分泌物,则超声检查比预定的48小时提前进行。治疗了14个品种的犬;体重范围为5.4至37.7kg。所有犬在开始治疗后9天内流产了所有胎儿。腹部触诊在确认流产过程是否完成方面并不令人满意;然而,超声检查结果是一个可靠的指标。治疗前血浆孕酮浓度处于妊娠中期的典型水平,所有浓度均>6.0ng/ml。治疗开始后的前48小时后,每只犬的血浆孕酮浓度均显著下降。直到血浆孕酮浓度<2.0ng/ml至少24小时后,才会有母犬流产任何胎儿物质。(摘要截断于250字)

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1
Prostaglandin induction of abortion in pregnant bitches after misalliance.错配后怀孕母犬中前列腺素诱导流产
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2
Clinical use of prostaglandin F2 alpha to induce early abortion in bitches: serum progesterone, treatment outcome and interval to subsequent oestrus.前列腺素F2α在母犬中诱导早期流产的临床应用:血清孕酮、治疗结果及至随后发情的间隔时间
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Hormonal variation in bitches after early or mid-pregnancy termination with aglepristone (RU534).使用阿格列司酮(RU534)在妊娠早期或中期终止妊娠后母犬的激素变化。
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Plasma concentrations of 13,14-dihydro-15-keto prostaglandin F2-alpha (PGFM), progesterone and estradiol in pregnant and nonpregnant diestrus cross-bred bitches.怀孕和非怀孕发情后期杂交母犬的血浆中13,14-二氢-15-酮前列腺素F2-α(PGFM)、孕酮和雌二醇的浓度。
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Intra-vesicle administration of D-cloprostenol for induction of abortion in mid-gestation bitches.在妊娠中期母犬中,通过囊内给药法使用D-氯前列醇诱导流产。
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[Plasma concentrations of folic acid, vitamin B12 and progesterone of cyclic bitches, bitches during pregnancy and induced abortion and bitches with pyometra].[发情周期母犬、妊娠及人工流产母犬和子宫蓄脓母犬的血浆叶酸、维生素B12和孕酮浓度]
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[Use of a low dose prostaglandin F2 alpha in bitches].
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Evaluation of progesterone deficiency as a cause of fetal death in mares with experimentally induced endotoxemia.评估孕酮缺乏作为实验性诱导内毒素血症母马胎儿死亡原因的研究。
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The use of ultrasonography for pregnancy diagnosis in the bitch.超声检查在母犬妊娠诊断中的应用。
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引用本文的文献

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Ultrasound-guided induced fetal death, an alternative method for induction of abortion in the bitch.超声引导下诱导胎儿死亡,一种母犬引产的替代方法。
Vet Res Forum. 2020 Spring;11(2):165-170. doi: 10.30466/vrf.2018.68229.1964. Epub 2020 Jun 15.
2
Pharmacologic advances in canine and feline reproduction.犬猫繁殖领域的药理学进展。
Top Companion Anim Med. 2009 May;24(2):71-99. doi: 10.1053/j.tcam.2008.12.004.