Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, Illinois, USA.
Department of Comparative Biosciences, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, Illinois, USA.
Equine Vet J. 2019 Jul;51(4):544-551. doi: 10.1111/evj.13044. Epub 2019 Jan 2.
In selective cases, enrofloxacin may be an alternative antibacterial agent to treat unresponsive infections in pregnant mares. Supratherapeutic doses of enrofloxacin are toxic to adult horses and also to newborn foals, however, it is unknown if enrofloxacin crosses the equine placenta or if it is toxic to the fetus.
To assess the diffusion of enrofloxacin and its metabolite to fetal fluids and its effects on fetal cartilage when administered to pregnant mares.
In vivo and terminal controlled experiment.
Healthy mares at 260 days of gestation were allocated into three groups: untreated (n = 3), therapeutic treatment (5 mg/kg enrofloxacin, i.v., n = 7) or supratherapeutic treatment (10 mg/kg, i.v., n = 6) for 11 days. Fetal fluids were collected on days 1, 5 and 11 of treatment. Premature delivery was induced on day 11 with oxytocin and fetal fluids and plasma were collected during delivery. Plasma and fetal fluid enrofloxacin and ciprofloxacin concentrations were measured by liquid chromatography-mass spectrometry. Fetal articular cartilage was examined macroscopically and histologically for lesions.
Enrofloxacin and ciprofloxacin reached the minimum inhibitory concentrations for common pathogens in all fluids. Ciprofloxacin did not increase with the double enrofloxacin dose in maternal plasma, but allantoic fluid showed a 10-fold increase relative to fetal trough plasma concentrations. Administration of enrofloxacin at recommended doses did not result in cartilaginous lesions in fetuses.
Only one time point in gestation was evaluated and mares treated in the study were healthy at the time of treatment. It remains to be determined if enrofloxacin shows toxicity at other stages of pregnancy, after a longer duration of treatment, or once the foals are delivered and articular surfaces are weightbearing.
Short-term administration of enrofloxacin to late gestation mares resulted in detectable enrofloxacin and ciprofloxacin concentrations in fetal fluids and did not result in macroscopic or microscopic lesions in the fetus. While further research is needed to address long-term foal outcomes, enrofloxacin may be useful for select bacterial infections in pregnant mares.
在某些选择性病例中,恩诺沙星可能是一种替代抗菌药物,用于治疗怀孕母马中无反应性感染。超治疗剂量的恩诺沙星对成年马和新生驹都是有毒的,然而,目前尚不清楚恩诺沙星是否穿过马胎盘,或者对胎儿是否有毒。
评估恩诺沙星及其代谢物在给予怀孕母马时向胎儿液的扩散及其对胎儿软骨的影响。
体内和终末对照实验。
260 天妊娠的健康母马分为三组:未治疗组(n = 3)、治疗组(5mg/kg 恩诺沙星,静脉注射,n = 7)或超治疗组(10mg/kg,静脉注射,n = 6),治疗 11 天。在治疗的第 1、5 和 11 天采集胎儿液。第 11 天用催产素诱导早产,并在分娩期间采集胎儿液和血浆。通过液相色谱-质谱法测量血浆和胎儿液中的恩诺沙星和环丙沙星浓度。对胎儿关节软骨进行大体和组织学检查以评估病变。
恩诺沙星和环丙沙星在所有液体中均达到常见病原体的最低抑菌浓度。母血浆中环丙沙星没有随恩诺沙星剂量加倍而增加,但羊膜腔液中与胎儿谷血浆浓度相比增加了 10 倍。以推荐剂量给予恩诺沙星不会导致胎儿软骨病变。
仅在妊娠的一个时间点进行评估,并且在治疗时治疗的母马是健康的。恩诺沙星在妊娠的其他阶段、治疗时间更长后、或一旦驹出生并开始承重时是否会显示毒性,仍有待确定。
在妊娠晚期母马中短期给予恩诺沙星可导致胎儿液中检测到恩诺沙星和环丙沙星浓度,且不会导致胎儿出现大体或显微镜下病变。虽然需要进一步研究来解决长期驹的结局问题,但恩诺沙星可能对怀孕母马的某些细菌感染有用。