Hattori T, Nishimura Y, Sakai N, Yamada H, Kameyama Y, Banno Y, Nozawa Y
Department of Neurosurgery, Gifu University School of Medicine, Japan.
Neurol Res. 1987 Sep;9(3):164-8. doi: 10.1080/01616412.1987.11739789.
Ischaemic rat brains were examined for temporal changes in phospholipase C activity with phosphatidylinositol; the effects of pentobarbital on the activity also were investigated. Ischaemia was produced by decapitation. Pentobarbital (60 mg/kg) was administered i.p. for 15 min before decapitation. The removed heads were incubated at 37 degrees C for 1, 5, 15 or 30 min and then quickly frozen in liquid nitrogen. After isolation of subcellular fractions from the brains, phospholipase C activity was measured for cytosol and microsomes, using radioactive phosphatidylinositol as a substrate. The results demonstrated that brain phospholipase C predominantly localized in the cytosol was dependent on Ca2+ for full activity and had neutral pH optima. Although the enzyme activity did not increase during ischaemia, pentobarbital inhibited phospholipase C activity in the cytosol but not in the microsomes. These observations suggest that pentobarbital may exert a cerebral protective action due to, at least in part, the repression of phospholipase C followed by a reduction of phosphatidylinositol breakdown, preventing perturbation to the integrity of membranes, during ischaemia.
研究了缺血大鼠脑内磷脂酶C对磷脂酰肌醇的活性随时间的变化;还研究了戊巴比妥对该活性的影响。通过断头造成缺血。在断头前15分钟腹腔注射戊巴比妥(60mg/kg)。将取下的头部在37℃孵育1、5、15或30分钟,然后迅速在液氮中冷冻。从脑中分离出亚细胞组分后,以放射性磷脂酰肌醇为底物,测定细胞溶质和微粒体中的磷脂酶C活性。结果表明,脑磷脂酶C主要定位于细胞溶质中,其充分活性依赖于Ca2+,最适pH为中性。虽然缺血期间酶活性没有增加,但戊巴比妥抑制了细胞溶质中的磷脂酶C活性,而对微粒体中的磷脂酶C活性没有影响。这些观察结果表明,戊巴比妥可能至少部分地通过抑制磷脂酶C,随后减少磷脂酰肌醇的分解,防止缺血期间对膜完整性的干扰,从而发挥脑保护作用。