Saito M, Ogawa H, Narama I, Yoshida R
Hamamatsu Seigiken Research Laboratory, Co., Ltd., Shiznoka, Japan.
J Toxicol Sci. 1989 Oct;14 Suppl 2:161-77. doi: 10.2131/jts.14.supplementii_161.
A fertility study was performed in Sprague-Dawley rats by oral administration of propiverine hydrochloride (P-4) at dose levels of 0 (control), 2, 10 and 50 mg/kg/day. Male rats were treated for 9 weeks before mating and following 4 weeks including mating period. Female rats were administered the test substance from 2 weeks before mating to day 7 of pregnancy. The females were sacrificed on day 21 of pregnancy for examination of their fetuses. Toxic signs consisted of mydriasis, salivation and rale were observed in both male and female animals at the dose of 50 mg/kg group and in male animals at the dose of 10 mg/kg group. Body weight gain was supressed and food intake was decreased in the 50 mg/kg group throughout the administration period. Water intake of the 50 mg/kg group was decreased temporarily at the early stage of administration period, although increased thereafter. Autopsy revealed the enlargement of the liver with yellow-brownish coloration in one male rat at the 50 mg/kg group. Fertility and reproductive ability in both sexes were not affected by administration of P-4. There was no lethal effect and no growth-inhibiting or teratogenic effects on the embryos and the fetuses. The results suggest that the non-effective dose level of P-4 was 2 and 10 mg/kg/day for general toxicity in male and female parent animals respectively, 50 mg/kg/day for reproductive ability in parent animals and in embryos and fetuses.
通过对斯普拉格-道利大鼠口服盐酸丙哌维林(P-4)进行生育力研究,剂量水平分别为0(对照)、2、10和50mg/kg/天。雄性大鼠在交配前治疗9周,并在包括交配期在内的后续4周内持续给药。雌性大鼠在交配前2周开始给药,直至怀孕第7天。在怀孕第21天处死雌性大鼠以检查其胎儿。在50mg/kg剂量组的雄性和雌性动物以及10mg/kg剂量组的雄性动物中均观察到了瞳孔散大、流涎和啰音等毒性体征。在整个给药期间,50mg/kg组的体重增加受到抑制,食物摄入量减少。50mg/kg组的水摄入量在给药初期暂时减少,不过之后有所增加。尸检显示,50mg/kg组的一只雄性大鼠肝脏肿大,呈黄棕色。P-4的给药对两性的生育力和生殖能力均无影响。对胚胎和胎儿没有致死作用,也没有生长抑制或致畸作用。结果表明,P-4对雄性和雌性亲代动物一般毒性的无效剂量水平分别为2和10mg/kg/天,对亲代动物以及胚胎和胎儿生殖能力的无效剂量水平为50mg/kg/天。