期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：1977
卷号：74
期号：8
页码：3607-3611
DOI：10.1073/pnas.74.8.3607
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：This paper compares the transport of Li+ and Na+ in erythrocytes from a patient with mania and from members of his family to that in erythrocytes from normal humans. In normal human erythrocytes, Li+ is transported by at least three operationally distinct pathways: one inhibited by ouabain (ouabain-sensitive), one by phloretin (phloretin-sensitive), and one not inhibited by either compound (insensitive). Li+ can be driven up its electrochemical potential gradient by an oppositely directed electrochemical potential gradient for Na+--i.e., Li+/Na+ counterflow can occur--through the phloretin-sensitive pathway but not through the other two pathways. Because ouabain-sensitive Li+ transport is negligible under physiological conditions, Li+ distribution between erythrocytes and plasma in vivo depends mainly on the balance between Li+/Na+ counterflow and the insensitive pathway(s) of Li+ transport. The steady-state ratio of Li+ concentration in the erythrocytes to that in the plasma of the patient was between 2 and 3 times higher than the comparable ratio in normal persons. The phloretin-sensitive Li+/Na+ counterflow system was almost absent in the erythrocytes of the patient. Furthermore, unlike those from normal individuals, the patient's erythrocytes showed no external Li+-stimulated, phloretin-sensitive, ouabain-insensitive Na+ efflux. The magnitudes of the ouabain-sensitive and insensitive pathways for Li+ transport in the patient's erythrocytes were within normal limits. The decreased Li+/Na+ counterflow in the patient's erythrocytes was probably not due to the presence of an inhibitor in the plasma of the patient but rather to an intrinsic defect in the erythrocytes. Because the father and several siblings of the patient showed a similar abnormality in erythrocyte Li+/Na+ transport, it is probable that this defect is inherited.
