Kopp J, Hall H, Persson A, Sedvall G
Department of Psychiatry and Psychology, Karolinska Hospital, Stockholm, Sweden.
J Neurochem. 1990 Oct;55(4):1310-5. doi: 10.1111/j.1471-4159.1990.tb03140.x.
The temperature dependence of in vitro binding of [3H]Ro 15-1788 to benzodiazepine receptors in human postmortem neocortex and neocerebellum homogenates was studied. An increase of the equilibrium dissociation constants (KD) from 1.40 nmol/L and 1.04 nmol/L at 4 degrees C to 6.10 nmol/L and 8.91 nmol/L at 37 degrees C was found for neocortex and neocerebellum, respectively. In contrast, maximal binding (Bmax) remained in the range of 30-35 fmol/mg for neocortex and 24-27 fmol/mg of tissue (wet weight) for neocerebellum at all the temperatures. The KD of 6.10 nmol/L for neocortex at 37 degrees C in vitro is of the same order as the KD of 10 nmol/L obtained by positron emission tomography for [11C]Ro 15-1788 binding to benzodiazepine receptors in the human neocortex in vivo. The differences in KD between in vitro and in vivo benzodiazepine receptor binding to human neocortex and cerebellum seem to be due at least partially to temperature differences of in vitro and in vivo studies.
研究了[3H]Ro 15 - 1788与人死后新皮质和新小脑匀浆中苯二氮䓬受体的体外结合对温度的依赖性。新皮质和新小脑的平衡解离常数(KD)分别从4℃时的1.40 nmol/L和1.04 nmol/L增加到37℃时的6.10 nmol/L和8.91 nmol/L。相反,在所有温度下,新皮质的最大结合量(Bmax)保持在30 - 35 fmol/mg范围内,新小脑的最大结合量保持在24 - 27 fmol/mg组织(湿重)范围内。体外37℃时新皮质的KD为6.10 nmol/L,与通过正电子发射断层扫描获得的[11C]Ro 15 - 1788在体内与人新皮质中苯二氮䓬受体结合的KD为10 nmol/L处于同一数量级。体外和体内苯二氮䓬受体与人新皮质和小脑结合的KD差异似乎至少部分归因于体外和体内研究的温度差异。