Witt K L, Gudi R, Bishop J B
Oak Ridge Associated Universities, TN.
Mutat Res. 1992 Sep;283(1):53-7. doi: 10.1016/0165-7992(92)90121-w.
Salicylazosulfapyridine (SASP) and its major metabolite sulfapyridine (SP) have been shown to induce chromosomal damage in vivo. Both chemicals were tested in the micronucleus (MN)/kinetochore (KC) staining test to gain insight into the question of whether chromosomal breakage, aneuploidy-inducing events, or both were important to the observed production of MN in bone marrow cells of mice. In this test, both SASP and SP were shown to be strong inducers of kinetochore positive (KC+) MN. Although small increases in kinetochore negative (KC-) MN were also observed in SP treated mice, as well as in mice receiving the highest dose of SASP tested, the results suggest that both chemicals induce predominantly aneuploidogenic type damage.
柳氮磺胺吡啶(SASP)及其主要代谢产物磺胺吡啶(SP)已被证明在体内可诱导染色体损伤。这两种化学物质都在微核(MN)/动粒(KC)染色试验中进行了测试,以深入了解染色体断裂、非整倍体诱导事件,或两者对在小鼠骨髓细胞中观察到的微核产生是否重要的问题。在该试验中,SASP和SP均被证明是动粒阳性(KC+)微核的强诱导剂。虽然在SP处理的小鼠以及接受测试的最高剂量SASP的小鼠中也观察到动粒阴性(KC-)微核略有增加,但结果表明这两种化学物质主要诱导非整倍体形成型损伤。