Müller L J, Moorer-van Delft C M, Zijl R, Roubos E W
Department of Biology, Vrije Universiteit, Amsterdam, The Netherlands.
Cancer Res. 1990 Mar 15;50(6):1924-8.
The central nervous system of the snail Lymnaea stagnalis was studied in order to develop a test system to predict the neurotoxic side effects of the three cytostatic Vinca alkaloids, vincristine (VCR), vindesine (VDS), and vinblastine (VLB). Vinca alkaloids appear to interfere with microtubule formation by the induction of paracrystalline inclusions. After in vitro incubation the numbers of these inclusions were counted in cross-sections of the cerebral commissure using electron microscopy. For each compound the number of paracrystalline profiles increases with increasing concentrations and incubation times. At equimolar concentrations (0.15 mM), VCR induces more paracrystals than VDS, and VDS induces more than VLB. These effects are clear after short periods of incubation (e.g., after 2 h, VCR:VDS:VLB = 5:2:1). Equitoxic concentrations of VCR, VDS, and VLB induce similar numbers of paracrystals. Furthermore, morphological changes in the cell bodies of identified neurons (light green cells) in the cerebral ganglia were observed. Quantitative analysis shows that at equimolar concentrations the surface area of nuclear chromatin of all Vinca alkaloid-treated cells is approximately 30% lower than that of the controls. The lamellae of the rough endoplasmic reticulum are swollen and have lost their regular arrangement. For VDS and VLB this swelling is accompanied by a strong increase (about 3-fold) in the total surface area of the rough endoplasmic reticulum. No increase was observed for VCR. The compounds do not affect the number of secretory granules. In contrast to the controls, all Vinca-treated cells show lipid droplets. After VCR treatment they are about 5-fold as numerous as after treatment with VDS or VLB. The total surface area of lysosomes increases about 1.3-fold by VDS and VLB treatment and about 3-fold by VCR treatment. From these quantitative data it is concluded that VCR is more neurotoxic than VDS and VLB. VDS appears to be more neurotoxic than VLB as judged from the data on paracrystal induction. On the basis of a comparison of these data with clinical data on Vinca-induced neurotoxicities, it is proposed that neurons of the snail L. stagnalis may be suitable for the development of a test system to predict the degree of clinical neurotoxicity induced by Vinca antitumor drugs.
为了开发一种测试系统来预测三种细胞毒性长春花生物碱(长春新碱(VCR)、长春地辛(VDS)和长春碱(VLB))的神经毒性副作用,对椎实螺的中枢神经系统进行了研究。长春花生物碱似乎通过诱导副晶状内含物来干扰微管形成。体外孵育后,使用电子显微镜在脑 commissure 的横切面上对这些内含物的数量进行计数。对于每种化合物,副晶状轮廓的数量随着浓度和孵育时间的增加而增加。在等摩尔浓度(0.15 mM)下,VCR 诱导的副晶比 VDS 多,VDS 诱导的比 VLB 多。在短时间孵育后(例如,2 小时后,VCR:VDS:VLB = 5:2:1)这些效应就很明显。VCR、VDS 和 VLB 的等毒性浓度诱导的副晶数量相似。此外,观察到脑神经节中已鉴定神经元(浅绿色细胞)的细胞体有形态变化。定量分析表明,在等摩尔浓度下,所有长春花生物碱处理细胞的核染色质表面积比对照细胞大约低 30%。粗面内质网的片层肿胀且失去了规则排列。对于 VDS 和 VLB,这种肿胀伴随着粗面内质网总表面积的强烈增加(约 3 倍)。VCR 未观察到增加。这些化合物不影响分泌颗粒的数量。与对照相比,所有长春花生物碱处理的细胞都显示有脂滴。VCR 处理后的脂滴数量是 VDS 或 VLB 处理后的约 5 倍。VDS 和 VLB 处理使溶酶体的总表面积增加约 1.3 倍,VCR 处理使其增加约 3 倍。从这些定量数据得出结论,VCR 的神经毒性比 VDS 和 VLB 更强。从副晶诱导数据判断,VDS 的神经毒性似乎比 VLB 更强。基于将这些数据与长春花生物碱诱导的神经毒性的临床数据进行比较,提出椎实螺的神经元可能适合开发一种测试系统来预测长春花抗肿瘤药物诱导的临床神经毒性程度。