静脉注射枸橼酸克罗米芬在健康母马体内的药代动力学:用于生殖的第一步。

IF 1.4 3区 农林科学 Q2 VETERINARY SCIENCES
Hayley L Moore, Jessica L Klabnik, Dawn M Boothe, Crisanta Cruz-Espindola, Nur Mita, Kamoltip Thungrat, R Jayachandra Babu, Candace C Lyman
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引用次数: 0

摘要

目的:研究选择性雌激素受体调节剂柠檬酸克罗米芬(CC)在马体内的静脉药动学参数。方法:采用实验方法研究CC在马体内的药动学参数。八匹母马接受了单次2000毫克剂量的静脉注射CC,以确定336小时内的血浆浓度。在此之后,6匹母马接受多剂量静脉注射CC (2000 mg, q 24 h),连续5天,每天确定血药谷底浓度。结果:CC耐受性良好,消除半衰期(4.95±1.10小时)短,平均停留时间(7.14±1.59小时),并达到被认为对女性有治疗作用的血浆药物浓度。测定血药浓度峰谷。结论:2000mg静脉注射CC达到假定的治疗浓度。根据多剂量试验,静脉注射2000毫克CC可能需要每12至24小时给药一次。临床相关性:IV CC似乎在母马中耐受性良好。未来的生育试验有必要评估CC在提高马体外胚胎生产效率方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravenous clomiphene citrate pharmacokinetics in healthy mares as a first step toward use in reproduction.

Objective: To investigate the IV pharmacokinetic parameters of clomiphene citrate (CC), a selective estrogen receptor modulator, in mares.

Methods: This was an experimental study to assess the pharmacokinetic parameters of CC in the mare. Eight mares received a single 2,000-mg dose of IV CC to identify plasma concentrations over 336 hours. Following this, 6 mares received a multidose regimen of IV CC (2,000 mg, q 24 h) for 5 days to identify trough plasma concentration each day.

Results: CC was well tolerated, demonstrated a short elimination half-life of 4.95 ± 1.10 hours and a mean residence time of 7.14 ± 1.59 hours, and reached plasma drug concentrations considered to be therapeutic in women. Peak and trough plasma concentrations were determined.

Conclusions: IV CC at 2,000 mg reaches presumed therapeutic concentrations in the mare. Based on the multidose trial, 2,000 mg of IV CC may require administration every 12 to 24 hours.

Clinical relevance: IV CC appears to be well tolerated in the mare. Future fertility trials are warranted to assess the potential that CC may have in increasing the efficiency of equine in vitro embryo production.

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来源期刊
CiteScore
1.70
自引率
10.00%
发文量
186
审稿时长
3 months
期刊介绍: The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.
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