Suarez-Kurtz G
Am J Physiol. 1982 May;242(5):C398-403. doi: 10.1152/ajpcell.1982.242.5.C398.
The rate of creatine kinase (CK) release from isolated frog extensor longus digiti IV ("toe") muscle increased on transfer from the control Ringer solution (referred to as 1.0 T) to a hyperosmotic solution (1.0 T plus 400 mM glycerol) or to hypertonic solutions (1.5-2.5 T) prepared by addition of NaCl or sucrose to 1.0 T. On return to 1.0 T, CK release rate was further elevated, reaching peak values (14.4- and 12-fold above the basal value, respectively, with the glycerol treatment and with solution 2.5 T) within 10-15 min and declining subsequently toward base line. Although the stimulation of CK release by changes in external tonicity increased with the magnitude of the osmotic step change, there was no enhancement of release when the tonicity changes were performed gradually in 0.1-T steps at 1-min intervals. The stimulation of CK release by tonicity changes cannot be ascribed to irreversible loss of functional integrity of the surface or tubular membranes or to CK diffusion through aqueous pores. The possibility that an exocytosislike process is involved is discussed.
从离体的青蛙第四趾长伸肌(“趾”肌)释放肌酸激酶(CK)的速率,在从对照任氏液(称为1.0 T)转移至高渗溶液(1.0 T加400 mM甘油)或通过向1.0 T添加氯化钠或蔗糖制备的高渗溶液(1.5 - 2.5 T)时增加。回到1.0 T后,CK释放速率进一步升高,在10 - 15分钟内达到峰值(甘油处理和2.5 T溶液处理分别比基础值高14.4倍和12倍),随后朝着基线下降。尽管外部张力变化对CK释放的刺激随着渗透阶跃变化的幅度而增加,但当以0.1 T步长、1分钟间隔逐渐进行张力变化时,释放并未增强。张力变化对CK释放的刺激不能归因于表面或管状膜功能完整性的不可逆丧失,也不能归因于CK通过水孔的扩散。文中讨论了涉及类似胞吐过程的可能性。