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洛苏拉嗪对大鼠生殖与发育的影响。

Effects of losulazine on rat reproduction and development.

作者信息

Morris D F, Marks T A, Mesfin G M

机构信息

Reproductive and Developmental Toxicology Research, Upjohn Company, Kalamazoo, Michigan 49001.

出版信息

Fundam Appl Toxicol. 1987 Oct;9(3):573-87. doi: 10.1016/0272-0590(87)90038-8.

Abstract

Losulazine, a hypotensive agent, was given orally by gastric intubation to Sprague-Dawley rats in doses of 0, 2, 4, or 8 mg/kg/day in a study of fertility and general reproductive performance. Eighteen males per group were treated for 67 days before cohabitation, then daily until killed. Thirty-six females per group were treated for only 14 days because estrous cycles had been disrupted. Females remained untreated for 7 days before cohabitation; treatment was resumed after insemination was confirmed or when the cohabitation period ended. Males were cohabited on a 1:2 basis with females from the same treatment group for up to 14 days, then for 14 days with untreated females. The conception rate of both treated and untreated females was statistically significantly decreased as the dose increased. Mean body weights were statistically significantly greater and mean gestation periods were statistically significantly longer in losulazine-treated females than in females of the vehicle control group. Throughout the preweaning period mean body weights were significantly less in offspring from treated dams than in offspring of dams in the vehicle control group. This adverse effect on weight gain continued in male offspring until at least postpartum day 79. Functional development was significantly delayed in the offspring of losulazine-treated dams tested for pinna detachment, auditory startle, negative geotaxis, eye opening, and learning (swimming M-maze). Delays in development were generally greater in offspring of dams and sires treated with higher doses of losulazine. Fertility of male offspring from dams and sires treated with losulazine at 4 and 8 mg/kg/day was also affected adversely.

摘要

在一项关于生育力和一般生殖性能的研究中,给斯普拉格 - 道利大鼠经胃管口服给予降压药洛苏拉嗪,剂量为0、2、4或8毫克/千克/天。每组18只雄性大鼠在交配前接受67天治疗,然后每天给药直至处死。每组36只雌性大鼠仅接受14天治疗,因为其发情周期已被打乱。雌性大鼠在交配前7天不接受治疗;在确认受孕或同居期结束后恢复治疗。雄性大鼠与来自同一治疗组的雌性大鼠按1:2的比例同居长达14天,然后与未治疗的雌性大鼠同居14天。随着剂量增加,治疗组和未治疗组雌性大鼠的受孕率均有统计学显著下降。洛苏拉嗪治疗组雌性大鼠的平均体重在统计学上显著高于溶媒对照组雌性大鼠,平均妊娠期在统计学上显著更长。在整个断奶前期,经治疗母鼠的后代平均体重显著低于溶媒对照组母鼠的后代。这种对体重增加的不利影响在雄性后代中至少持续到产后第79天。对经洛苏拉嗪治疗的母鼠后代进行耳廓分离、听觉惊吓、负趋地性、睁眼和学习(游泳M迷宫)测试,发现其功能发育明显延迟。用较高剂量洛苏拉嗪治疗的母鼠和父鼠的后代发育延迟通常更大。以4和8毫克/千克/天的剂量给母鼠和父鼠使用洛苏拉嗪,雄性后代的生育力也受到不利影响。

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