Young E, Walker J M, Houghten R, Akil H
Life Sci. 1983;33 Suppl 1:287-90. doi: 10.1016/0024-3205(83)90499-x.
[3H] Dynorphin can be shown to bind to the brains of both rat and guinea pigs with approximately 50% specific binding. Characterization of the binding in terms of multiple opiate receptor types supports the kappa selectivity of dynorphin in guinea pig. However, in rat brain, a substantial proportion of the [3H] dynorphin binding is displaced by morphine, suggesting a mu as well as kappa component. Consequently, in rat, dynorphin may show effects at both mu and kappa receptors in vivo.
[3H]强啡肽可被证明能与大鼠和豚鼠的大脑结合,特异性结合率约为50%。从多种阿片受体类型方面对这种结合进行表征,支持强啡肽在豚鼠体内对κ受体的选择性。然而,在大鼠大脑中,[3H]强啡肽结合的很大一部分可被吗啡取代,这表明存在μ受体以及κ受体成分。因此,在大鼠体内,强啡肽可能在μ受体和κ受体上均表现出效应。