Bothmer J, Mommers M, Markerink M, Jolles J
Department of Neuropsychology and Psychobiology, University of Limburg, Maastricht, The Netherlands.
Growth Dev Aging. 1994 Summer;58(2):67-73.
A previous study, in which a lysed fraction was used with endogenous phospholipids as substrate, revealed age-related changes in PA and PIP2 formation but not in PIP formation (Bothmer et al., Neurochem. Int. 21, 223-228, 1992). To rule out the influence of substrate availability in the present study, the effect of age on PI kinase, PIP kinase and DAG kinase activities was studied with exogenous phospholipids as substrate in the cerebral cortex from 8-month-old, 14-month-old and 26-month-old Brown Norway rats. PI kinase activity was predominantly located in a tight membrane-bound protein fraction, DAG kinase activity in cytosolic and loosely membrane-bound protein fractions, and PIP kinase activity was present in all three protein preparations. The effects of age were limited to a small increase in kinase activity in the tight membrane-bound protein fraction in 14-month-old and 26-month-old rats compared to 8-month-old rats, and a 10% decrease in PIP kinase activity in the cytosolic protein fraction in 14-month-old and 26-month-old rats compared to 8-month-old rats. DAG kinase activity showed no age-related changes. In conclusion, one should take care in comparing rat aging with human aging as PI kinase activity shows an age-related decline in human brain cortex (Jolles et al., J. Neurochem. 58, 2326-2329, 1992). Furthermore, previously reported decreases in PA formation rates in rat brain are probably not due to changes in DAG kinase itself but to changes in DAG availability, although further experimental evidence is needed to confirm this conclusion.
先前一项研究使用裂解物与内源性磷脂作为底物,揭示了PA和PIP2形成过程中与年龄相关的变化,但PIP形成过程中未出现这种变化(博特默等人,《神经化学国际》21卷,223 - 228页,1992年)。为排除本研究中底物可用性的影响,以8月龄、14月龄和26月龄的挪威棕色大鼠大脑皮层中的外源性磷脂作为底物,研究了年龄对PI激酶、PIP激酶和DAG激酶活性的影响。PI激酶活性主要位于紧密膜结合蛋白组分中,DAG激酶活性位于胞质和松散膜结合蛋白组分中,PIP激酶活性则存在于所有三种蛋白制剂中。年龄的影响仅限于与8月龄大鼠相比,14月龄和26月龄大鼠紧密膜结合蛋白组分中的激酶活性略有增加,以及与8月龄大鼠相比,14月龄和26月龄大鼠胞质蛋白组分中的PIP激酶活性降低10%。DAG激酶活性未显示出与年龄相关的变化。总之,在将大鼠衰老与人类衰老进行比较时应谨慎,因为PI激酶活性在人类大脑皮层中显示出与年龄相关的下降(约勒斯等人,《神经化学杂志》58卷,2326 - 2329页,1992年)。此外,先前报道的大鼠大脑中PA形成速率的降低可能并非由于DAG激酶本身的变化,而是由于DAG可用性的变化,尽管需要进一步的实验证据来证实这一结论。