Cozens D D, Barton S J, Clark R, Gibson W A, Hughes E W, Masters R E, Offer J M, Perkin C J, Stramentinoli G
Huntingdon Research Centre Ltd., Cambridgeshire, England.
Arzneimittelforschung. 1988 Nov;38(11):1625-9.
S-Adenosyl-L-methionine sulphate-p-toluene sulphonate (ademetionine, SAMe), a donor of methyl groups, was examined for effects upon embryofoetal toxicity following both premating treatment and treatment during pregnancy and for peri- and post-natal toxicity in the rat at dosages of 0, 100, 200 and 400 mg/kg/d SAMe ion by subcutaneous or intravenous administration. Embryofoetal toxicity was also examined in the New Zealand White rabbit at dosages of 0, 10, 20 and 40 mg/kg/d SAMe by intravenous administration. Treatment was considered to be without adverse effect upon any of the reproductive parameters examined on either F0 or on the untreated F1 generations. There was no indication that treatment adversely affected the litter parameters including the incidences of malformations, anomalies and skeletal variants. Some slight changes in the activity of the F1 females derived from F0 animals given 400 mg/kg/d were considered to be of minimal importance. In contrast to the above, adverse effects upon the parents were noted at 400 mg/kg/d including local tissue reaction at the injection sites and retardation of body weight gain. In the intravenous studies some rigidity and dyspnoea were noted following administration. Following subcutaneous premating treatment there was also evidence of histopathological change to the kidney of the female rat. Increased water consumption was noted in this latter study and amongst females rearing offspring in the embryo foetal toxicity study in which the compound was administered intravenously. At the lower dosages administered to the rat some local tissue reaction was evident as was some retardation of body weight gain, minimal at the lowest intravenous dose.(ABSTRACT TRUNCATED AT 250 WORDS)
S-腺苷-L-蛋氨酸硫酸对甲苯磺酸盐(腺苷蛋氨酸,SAMe)作为一种甲基供体,在大鼠交配前及孕期给药后,对胚胎-胎儿毒性以及围产期和产后毒性进行了研究,给药剂量分别为0、100、200和400mg/kg/d SAMe离子,给药途径为皮下或静脉注射。还通过静脉注射,以0、10、20和40mg/kg/d SAMe的剂量,在新西兰白兔中研究了胚胎-胎儿毒性。研究认为,该治疗对F0代或未治疗的F1代所检测的任何生殖参数均无不良影响。没有迹象表明该治疗会对包括畸形、异常和骨骼变异发生率在内的窝仔参数产生不利影响。来自给予400mg/kg/d的F0动物的F1代雌性动物的活动有一些轻微变化,被认为重要性极小。与上述情况相反,在400mg/kg/d时观察到对亲本有不良影响,包括注射部位的局部组织反应和体重增加迟缓。在静脉注射研究中,给药后观察到一些僵硬和呼吸困难。皮下交配前治疗后,也有证据表明雌性大鼠肾脏出现组织病理学变化。在后者的研究中以及在胚胎-胎儿毒性研究中静脉注射该化合物的雌性动物养育后代时,观察到饮水量增加。在给予大鼠较低剂量时,有一些局部组织反应明显,体重增加也有一些迟缓,最低静脉注射剂量时最小。(摘要截断于250字)