Samuel A, Jago M V
Chem Biol Interact. 1975 Mar;10(3):185-97. doi: 10.1016/0009-2797(75)90112-x.
The antimitotic action of the pyrrolizidine alkaloid lasiocarpine on rat liver parenchyma was investigated using as the experimental model the wave of mitosis produced in liver by a single dose of thioacetamide. A single low dose of lasiocarpine administered two weeks before the thioacetamide, almost completely inhibited the mitotic wave without inhibiting to the same extent the preceding wave of DNA synthesis. By the use of selective inhibitors and radioisotope labelling, the location of the mitotic block was found to be either in the latter half of the DNA synthetic phase, S, or early in G2, the post-synthetic phase. The mitotic wave was similarly inhibited by pretreatment of the rats with a single injection of dehydroheliotridine, a pyrrolic metabolite of heliotridine-based pyrrolizidine alkaloids.
使用硫代乙酰胺单剂量在肝脏中产生的有丝分裂波作为实验模型,研究了吡咯里西啶生物碱阔叶千里光碱对大鼠肝实质的抗有丝分裂作用。在硫代乙酰胺给药前两周给予单一低剂量的阔叶千里光碱,几乎完全抑制了有丝分裂波,但对之前的DNA合成波没有同等程度的抑制。通过使用选择性抑制剂和放射性同位素标记,发现有丝分裂阻滞的位置要么在DNA合成期(S期)的后半段,要么在合成后期(G2期)早期。用基于天芥菜定的吡咯里西啶生物碱的吡咯代谢产物脱氢天芥菜定单次注射预处理大鼠,有丝分裂波也受到类似的抑制。