PMID- 21783607 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20121002 LR - 20110725 IS - 1382-6689 (Print) IS - 1382-6689 (Linking) VI - 20 IP - 2 DP - 2005 Sep TI - Developmental toxicity evaluation of nerve growth factor for injection in Wistar rats. PG - 321-5 LID - 10.1016/j.etap.2005.03.003 [doi] AB - Nerve growth factor (NGF) for injection is now used as an agent to cure peripheral nerve injury. To assess its potential embryo-lethal and teratogenic toxicity, five groups of pregnant Wistar rats received 0, 40, 200 and 1000U/kg NGF by muscle injection from gestational days (GD) 6 to 17. Maternal body weight was monitored at regular intervals throughout gestation. We selected 7mg/kg body weight cyclophosphamide (CPA) given to positive control group testing the Wistar rats of this study whether sensitive to teratogens or not. The dams were euthanized on GD 20, the day just before expected parturition. All fetuses were removed by cesarean section and examined for external, visceral and skeletal malformations under a dissecting microscope. There were no treatment-related maternal deaths. Our statistical findings were a reduction in maternal body weight and the occurrence of fetal body length shorten in 1000U/(kgday) dose group, which suggesting mild embryotoxicity of NGF. There were no major changes observed in other doses groups such as viable fetuses rate, resorption and dead fetuses rate, external, skeletal, visceral abnormality, fetal weight and length, tail length, indicating no evident maternal toxicity, embryotoxicity and teratogenicity resulted from NGF. Thus, it seems a favorable preclinical safety evaluation profile for NGF. FAU - Liu, Wei AU - Liu W AD - Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Xian Nong Tan Street, Postal code 100050, Beijing, China. FAU - Wang, Aiping AU - Wang A LA - eng PT - Journal Article PL - Netherlands TA - Environ Toxicol Pharmacol JT - Environmental toxicology and pharmacology JID - 9612020 EDAT- 2005/09/01 00:00 MHDA- 2005/09/01 00:01 CRDT- 2011/07/26 06:00 PHST- 2004/09/08 00:00 [received] PHST- 2005/03/11 00:00 [accepted] PHST- 2011/07/26 06:00 [entrez] PHST- 2005/09/01 00:00 [pubmed] PHST- 2005/09/01 00:01 [medline] AID - S1382-6689(05)00071-2 [pii] AID - 10.1016/j.etap.2005.03.003 [doi] PST - ppublish SO - Environ Toxicol Pharmacol. 2005 Sep;20(2):321-5. doi: 10.1016/j.etap.2005.03.003.