Department of Hospital Pharmacy, Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki, Japan.
J Liposome Res. 2009;19(2):141-7. doi: 10.1080/08982100802666514.
In order to elucidate the influence of hepatic disease stage on cationic liposomes-mediated gene delivery, we investigated the cationic liposomes-mediated plasmid DNA delivery with time in murine hepatitis induced by subcutaneous injection of CCl(4). Liver injury after injection of CCl(4) was confirmed by the determination of serum aspartate aminotransferase and alanine aminotransferase activities. Two kinds of liposomes constructed with N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethlylammoniumchloride and dioleylphosphatidylethanolamine (DOTMA-DOPE) or DOTMA and cholesterol (DOTMA-CHOL) were used for the gene-delivery vector. We determined luciferase activities in various organs after the intravenous administration of the lipoplexes. The CCl(4)-treated mice administered with DOTMA-DOPE lipoplexes showed the more significant decreases of transgene expression in the liver and spleen at 18 hours after CCl(4) injection. On the other hand, the CCl(4)-treated mice administered with DOTMA-CHOL lipoplexes showed a significant increase in the liver at 48 hours. In conclusion, our findings demonstrate that murine hepatitis induced by CCl(4) can influence cationic liposomes-mediated plasmid DNA delivery. The extent of influences was also affected by lipid contents. These results indicate the necessity of considering the timing and the formulation for gene therapy according to the disease stage.
为了阐明肝脏疾病阶段对阳离子脂质体介导的基因传递的影响,我们研究了经皮下注射 CCl(4)诱导的小鼠肝炎中阳离子脂质体介导的质粒 DNA 传递随时间的变化。通过测定血清天冬氨酸氨基转移酶和丙氨酸氨基转移酶活性来确认 CCl(4)注射后的肝损伤。使用两种由 N-[1-(2,3-二油酰基)丙基]-N,N,N-三甲基氯化铵和二油酰基磷脂酰乙醇胺(DOTMA-DOPE)或 DOTMA 和胆固醇(DOTMA-CHOL)构建的脂质体作为基因传递载体。我们在静脉给予脂质体后测定了各种器官中的荧光素酶活性。在 CCl(4)注射后 18 小时,给予 DOTMA-DOPE 脂质体的 CCl(4)处理小鼠的肝脏和脾脏中转基因表达明显降低。另一方面,给予 DOTMA-CHOL 脂质体的 CCl(4)处理小鼠在 48 小时时肝脏中的表达显著增加。总之,我们的发现表明 CCl(4)诱导的小鼠肝炎会影响阳离子脂质体介导的质粒 DNA 传递。影响的程度还受到脂质含量的影响。这些结果表明根据疾病阶段,有必要考虑基因治疗的时间和制剂。