Inagaki Yoshinori, Matsumoto Yasuhiko, Sekimizu Kazuhisa
Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences, The University of Tokyo.
Drug Discov Ther. 2016 Feb;10(1):40-3. doi: 10.5582/ddt.2016.01023.
Evaluation of tissue injury induced by chemicals is crucial to drug development. Mice and rats, which are effectively used to analyze drug-induced tissue injury, present problems in terms of cost and ethical issues. Although alternative methods have been developed using in vitro techniques or invertebrates, evaluation of ADME and the size of animals are still issues that need to be addressed. Use of silkworms can resolve these problems. Silkworms have pharmacokinetic characteristics similar to those of mammals. Injection of various hepatotoxic chemicals also leads to elevated alanine aminotransferase (ALT) activity in the hemolymph of silkworms. Furthermore, transparent transgenic silkworms expressing GFP have been produced to facilitate continuous analysis without the need to collect hemolymph. Analyses using this silkworm have indicated that the intensity of GFP fluorescence observed on the body surface of the silkworm decreases in a time- and dose-dependent manner when hepatotoxic chemicals are injected. These results suggest that the silkworms can serve as alternative animal model for evaluation of drug-induced tissue injury.
评估化学物质诱导的组织损伤对于药物开发至关重要。小鼠和大鼠虽有效地用于分析药物诱导的组织损伤,但在成本和伦理问题方面存在问题。尽管已开发出使用体外技术或无脊椎动物的替代方法,但药物代谢动力学评价和动物大小仍是需要解决的问题。使用家蚕可以解决这些问题。家蚕具有与哺乳动物相似的药代动力学特征。注射各种肝毒性化学物质也会导致家蚕血淋巴中丙氨酸转氨酶(ALT)活性升高。此外,已培育出表达绿色荧光蛋白(GFP)的透明转基因家蚕,以便无需采集血淋巴就能进行连续分析。使用这种家蚕进行的分析表明,当注射肝毒性化学物质时,在家蚕体表观察到的绿色荧光蛋白荧光强度会以时间和剂量依赖性方式降低。这些结果表明,家蚕可作为评估药物诱导的组织损伤的替代动物模型。