作者: O. Oelz , A. Jakob , E. R. Froesch
DOI: 10.1111/J.1365-2362.1970.TB00596.X
关键词:
摘要: 10 mU of NSILA-S, as determined by the fat pad assay, lowered blood glucose and free fatty acids adrenalectomized rate for a much longer period than crystalline insulin. NSILA-S was not measurably inactivated liver during 2 h cyclical perfusion, whereas insulin rapidly lost activity with half-life 42 min. 6 injected intravenously stimulated incorporation [6-14C] into diaphragm streptozotocin-diabetic rats to greater extent insulin, their effects on carbon 14 were equal. When intraperitoneally in maximal doses normal both agents [U-14C] adipose tissue same extent. There no potentiation either agent other vitro, indicating that they affect transport site cell membrane. Insulin influenced metabolism fasted-refed manner. It is concluded i.v. more effective vivo comparable because it liver. Furthermore, seems have particular affinity receptors muscle This may be an additional factor protecting from inactivation tissues.