Frederiks W M, Marx F
Laboratory of Cell Biology and Histology, University of Amsterdam, The Netherlands.
Anal Cell Pathol. 1990 Oct;2(6):347-55.
The effects of ischemia in vitro for 0-60 min at 37 degrees C on glycogen phosphorylase activity in rat liver have been studied under different feeding conditions. Glycogen phosphorylase activity was demonstrated with a recently developed quantitative histochemical method using a semipermeable membrane and the PAS-reaction. The cytophotometrically measured glycogen phosphorylase activity in livers from 24 h-fasted rats was approximately five times the activity in livers from normally fed rats. The activity in periportal areas was about 1.5 times higher than the activity in pericentral areas in livers from starved rats, but more or less evenly distributed in livers from fed rats. Enzyme activity in pericentral areas of livers from 24 h-fasted rats started to decrease after 20 min of ischemia. After 50-60 min of ischemia, the activity was decreased to approximately 25% of the control activity. Livers from normally fed rats showed unchanged activity in periportal and pericentral areas after 10-60 min of ischemia. It has been assumed that the activation of the enzyme was disturbed by ischemia, possibly as a consequence of plasma membrane damage.
在不同喂养条件下,研究了37℃体外缺血0 - 60分钟对大鼠肝脏糖原磷酸化酶活性的影响。采用一种新开发的使用半透膜和PAS反应的定量组织化学方法来检测糖原磷酸化酶活性。通过细胞光度法测定,禁食24小时大鼠肝脏中的糖原磷酸化酶活性约为正常喂养大鼠肝脏活性的五倍。在饥饿大鼠的肝脏中,门静脉周围区域的活性比中央静脉周围区域的活性高约1.5倍,但在喂食大鼠的肝脏中,活性分布或多或少较为均匀。禁食24小时大鼠肝脏中央静脉周围区域的酶活性在缺血20分钟后开始下降。缺血50 - 60分钟后,活性降至对照活性的约25%。正常喂养大鼠的肝脏在缺血10 - 60分钟后,门静脉周围和中央静脉周围区域的活性没有变化。据推测,缺血可能由于质膜损伤而干扰了该酶的激活。