Edlund C, Brunk U, Chojnacki T, Dallner G
Department of Biochemistry, Arrhenius Laboratory, University of Stockholm, Sweden.
Biosci Rep. 1988 Apr;8(2):139-46. doi: 10.1007/BF01116458.
Rat liver dolichol and dolichyl-P were labeled by injection of [3H]mevalonate into the portal vein and their rates of synthesis and breakdown determined. In the initial phase the radioactivity appeared in alpha-unsaturated polyprenols. Subsequent saturation required 90 min. The half-lives of dolichols in microsomes were between 80 and 118 h, and shorter dolichols had shorter values of T1/2. The half-lives of dolichols in lysosomes were between 115 and 137 h, while microsomal dolichyl-P exhibited a T1/2 of 32 h. Injected dolichol was recovered in the lysosomes of hepatocytes and exhibited a rate of breakdown which was slower than that of the endogenous compound. These results indicate differences in the catabolism of dolichol at different subcellular locations, as well as differences between the catabolism of dolichol and dolichyl-P.
通过将[3H]甲羟戊酸注入门静脉来标记大鼠肝脏中的多萜醇和多萜醇磷酸,并测定它们的合成和分解速率。在初始阶段,放射性出现在α-不饱和聚戊烯醇中。随后达到饱和需要90分钟。微粒体中多萜醇的半衰期在80至118小时之间,较短的多萜醇半衰期值较短。溶酶体中多萜醇的半衰期在115至137小时之间,而微粒体多萜醇磷酸的半衰期为32小时。注入的多萜醇在肝细胞的溶酶体中被回收,其分解速率比内源性化合物慢。这些结果表明多萜醇在不同亚细胞位置的分解代谢存在差异,以及多萜醇和多萜醇磷酸的分解代谢之间存在差异。