Khaw Ban-An, Khudairi Tala
Center for Cardiovascular Targeting, Department of Pharmaceutical Sciences, Northeastern University, Boston, Massachusetts 02115, USA.
J Liposome Res. 2007;17(2):63-77. doi: 10.1080/08982100701375035.
Treatment with Cytoskeketal-antigen Specific ImmunoLiposomes (CSIL) has resulted in the preservation of cell and organ viability and function. The current study investigates whether CSIL-intervention is dose-dependent in Langendorff instrumented adult rat hearts undergoing global ischemia.
Rat hearts undergoing experimental global ischemic insult for 25 minutes were treated with CSIL, IgG-liposomes (IgG-L), plain-liposomes (PL) or placebo. Infarct sizes were assessed by histochemical staining method and quantitated by computer planimetry. Mean infarct size of CSIL treated globally ischemic rat hearts was about 5 times smaller than that of control hearts (P <or= 0.02). Recovery to normal heart function was achieved with CSIL therapy at 1 mg antimyosin antibody dose, where as significant decreases in functional recovery were seen in hearts treated with 0.5 and 0.2 mg antimyosin antibody doses Dose-dependent preservation of cardiac function, and reduction in infarct sizes in CSIL treated hearts were concordant with ultrastructural evidence.
Treatment of globally ischemic rat hearts with CSIL results in significant preservation of function and dramatic decrease in acute myocardial infarct size in a dose dependent process.
细胞骨架抗原特异性免疫脂质体(CSIL)治疗已实现细胞及器官活力与功能的保存。当前研究旨在探究CSIL干预在接受全心缺血的Langendorff灌注成年大鼠心脏中是否呈剂量依赖性。
对经历25分钟实验性全心缺血损伤的大鼠心脏给予CSIL、IgG脂质体(IgG-L)、普通脂质体(PL)或安慰剂治疗。通过组织化学染色法评估梗死面积,并采用计算机图像分析进行定量。接受CSIL治疗的全心缺血大鼠心脏的平均梗死面积约为对照心脏的五分之一(P≤0.02)。在抗肌球蛋白抗体剂量为1mg时,CSIL治疗可使心脏功能恢复正常,而在抗肌球蛋白抗体剂量为0.5mg和0.2mg时,心脏功能恢复显著降低。CSIL治疗心脏中,心脏功能的剂量依赖性保存以及梗死面积的减小与超微结构证据一致。
用CSIL治疗全心缺血大鼠心脏可在剂量依赖性过程中显著保存功能并大幅减小急性心肌梗死面积。