Sverko V, Marotti T, Gavella M, Lipovac V, Hrsak I
Department of Experimental Biology and Medicine, Ruder Boskovic Institute, Zagreb, Croatia.
Biomed Pharmacother. 1993;47(1):37-43. doi: 10.1016/0753-3322(93)90036-k.
The unsedimentable activities of acid phosphatase (AP) and beta-glucosidase (BG), from mice liver lysosomes significantly increased 6 h after a single i/p injection of Met-enkephalin (MENK). The activity of AP in the serum at the same time remained unchanged. Multiple injections of MENK (8 x 10 mg/kg) induced a significant decrease in AP activity in the serum and no change in the unsedimentable activities of AP or BG. MENK did not elicit any significant extracellular release of lactate dehydrogenase (LDH) either, indicating that, under the experimental conditions described, the cells remained intact. Other parameters, such as the activities of AP and BG in the liver and total sialic acid content in the serum and spleen remained unaltered. Moreover, MENK in concentrations of 10(-12) M, 10(-8) M, 10(-6) M or 10(-4) M did not change the activities of the lysosomal enzyme markers AP or BG in vitro. These data indicate far less pronounced transient effects of MENK on lysosomal membranes and enzymes compared to Leu-enkephalin which may be relevant for the use of MENK in combined chemo-immunotherapy.
单次腹腔注射甲硫氨酸脑啡肽(MENK)6小时后,小鼠肝脏溶酶体中的酸性磷酸酶(AP)和β-葡萄糖苷酶(BG)的不可沉降活性显著增加。同时血清中AP的活性保持不变。多次注射MENK(8×10毫克/千克)导致血清中AP活性显著降低,而AP或BG的不可沉降活性没有变化。MENK也未引起乳酸脱氢酶(LDH)的任何显著细胞外释放,这表明在所描述的实验条件下,细胞保持完整。其他参数,如肝脏中AP和BG的活性以及血清和脾脏中的总唾液酸含量保持不变。此外,浓度为10^(-12) M、10^(-8) M、10^(-6) M或10^(-4) M的MENK在体外不会改变溶酶体酶标志物AP或BG的活性。这些数据表明,与亮氨酸脑啡肽相比,MENK对溶酶体膜和酶的短暂影响要小得多,这可能与MENK在联合化学免疫治疗中的应用有关。