Suppr超能文献

经阴道和口服给予[14C]普萘洛尔的大鼠放射性物质的胎盘转运和乳腺转运

Transplacental and mammary passage of radioactivity in rats treated vaginally and orally with [14C]propranolol.

作者信息

Buttar H S, Moffatt J H, Bura C

机构信息

Drug Toxicology Division, Health and Welfare Canada, Ottawa.

出版信息

J Toxicol Environ Health. 1988;24(1):1-18. doi: 10.1080/15287398809531137.

Abstract

The milk transfer, maternal-fetal distribution, and disposition of the antihypertensive/spermicidal agent propranolol were studied in pregnant and lactating rats. Single doses (10 mg/kg) of an aqueous solution of [14C]propranolol were administered either orally (po) or intravaginally (ivg) on gestational d 15, or on postpartum d 7-10. Upon ivg administration, [14C]propranolol was quickly transferred to systemic circulation and the mean blood [14C] concentrations were significantly greater during the first 0.25-2 h than in po dosed counterparts. About 98% of the ivg applied dose was absorbed after 6 h in gravid rats, and the combined 6-h excretions of radioactivity in the urine (ivg = 24.6%; po = 22.9%) and feces (ivg = 16.8%; po = 14.6%) were equivalent in both groups. At the end of 6 h, the levels of [14C] in the urinary bladder, adrenal, uterus, ovary, spleen, skeletal muscle, brain, heart, lung and fat were significantly higher in ivg treated rats than po dosed animals. Compared with the maternal plasma (ivg = 0.76; po = 0.88 microgram/ml), the mean concentrations of [14C] in the placentas were similar in both groups, while the amounts of [14C] were three to five times lower in the amniotic fluids and the fetuses of both po and ivg treated dams. In lactating rats, over 99% of the administered radioactivity was absorbed from the vagina within 6 h. The blood concentrations of [14C] were significantly elevated at 0.5 and 1 h in the per vaginam treated animals, and afterward the disappearance rate of [14C] followed a similar course in both groups. Following ivg application, the milk radioactivity peaked at 0.5 h and declined rapidly. However, the appearance of [14C] in milk was rather slow after oral dosing: the milk [14C] peaked between 2 and 3 h posttreatment and remained steady thereafter. The milk to blood (M/B) [14C] concentration ratios were markedly greater during 0.5 to 1 h in the ivg group than in their po dosed counterparts. At 6 h, the [14C] levels in the whole blood, plasma, milk, and mammary gland were virtually equivalent in the ivg and po treated females. Comparison of the areas under the milk [14C] concentration-time curves (AUCs) indicated that the milk availability of [14C] was about 31% more in dams dosed vaginally. These data suggest that route of administration alters the disposition and milk excretion of [14C]propranolol-derived radioactivity in pregnant and lactating rats.

摘要

在怀孕和哺乳期大鼠中研究了抗高血压/杀精剂普萘洛尔的乳汁转运、母胎分布及处置情况。在妊娠第15天或产后第7 - 10天,经口(po)或经阴道(ivg)给予单剂量(10 mg/kg)的[14C]普萘洛尔水溶液。经阴道给药后,[14C]普萘洛尔迅速转移至体循环,在最初的0.25 - 2小时内,平均血液[14C]浓度显著高于经口给药的对照组。妊娠大鼠经阴道给药后6小时,约98%的给药剂量被吸收,两组尿(经阴道给药 = 24.6%;经口给药 = 22.9%)和粪便(经阴道给药 = 16.8%;经口给药 = 14.6%)中放射性物质的6小时总排泄量相当。6小时末,经阴道给药处理的大鼠膀胱、肾上腺、子宫、卵巢、脾脏、骨骼肌、脑、心脏、肺和脂肪中的[14C]水平显著高于经口给药的动物。与母体血浆(经阴道给药 = 0.76;经口给药 = 0.88微克/毫升)相比,两组胎盘[14C]的平均浓度相似,而经口和经阴道给药母鼠羊水和胎儿中的[14C]量均低三至五倍。在哺乳期大鼠中,超过99%的给药放射性物质在6小时内从阴道吸收。经阴道给药处理的动物在0.5和1小时时血液[14C]浓度显著升高,之后两组[14C]的消失速率相似。经阴道给药后,乳汁放射性在0.5小时达到峰值并迅速下降。然而,经口给药后乳汁中[14C]的出现相当缓慢:乳汁[14C]在给药后2至3小时达到峰值,此后保持稳定。经阴道给药组在0.5至1小时期间乳汁与血液(M/B)[14C]浓度比显著高于经口给药的对照组。6小时时,经阴道和经口给药的雌性大鼠全血、血浆、乳汁和乳腺中的[14C]水平实际上相当。乳汁[14C]浓度 - 时间曲线下面积(AUCs)的比较表明,经阴道给药母鼠中[14C]的乳汁可用性约高31%。这些数据表明,给药途径改变了怀孕和哺乳期大鼠中[14C]普萘洛尔衍生放射性物质的处置和乳汁排泄。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验