Sunderman F W, Maenza R M, Alpass P R, Mitchell J M, Damjanov I, Goldblatt P J
Adv Exp Med Biol. 1977;91:57-67. doi: 10.1007/978-1-4684-0796-9_4.
In an endeavor to expand the variety of experimental models for study of nickel carcinogenesis, nickel subsulfide (Ni3S2) was administered to rodents by five previously untested routes. In two groups of Syrian hamsters, Ni3S2 induced multiple sarcomas at the sites of single im injections (5 or 10 mg of Ni3S2). In contrast, Ni3S2 did not induce any malignant tumors of the cheek pouches, oral cavity or gastrointestinal tract, despite multiple local applications to the cheek pouches of several groups of hamsters in total dosages as large as 1.1 g of Ni3S2. In a group of Fischer rats, single intratesticular injections of Ni3S2 (10 mg) induced many testicular sarcomas. In contrast, no malignant tumors developed in two groups of rats that received single injections into the submaxillary gland (2.5 mg of Ni3S2) or into the liver (5 mg of Ni3S2 via the portal venous system).
为了扩大用于镍致癌作用研究的实验模型种类,通过五种之前未测试过的途径给啮齿动物施用硫化镍(Ni3S2)。在两组叙利亚仓鼠中,单次肌肉注射(5或10毫克Ni3S2)后,Ni3S2在注射部位诱发了多个肉瘤。相比之下,尽管对几组仓鼠的颊囊进行了多次局部应用,总剂量高达1.1克Ni3S2,但Ni3S2并未诱发颊囊、口腔或胃肠道的任何恶性肿瘤。在一组Fischer大鼠中,单次睾丸内注射Ni3S2(10毫克)诱发了许多睾丸肉瘤。相比之下,在两组接受单次注射到颌下腺(2.5毫克Ni3S2)或肝脏(通过门静脉系统注射5毫克Ni3S2)的大鼠中未发生恶性肿瘤。