Biscoe T J, Fry J P, Rickets C
J Physiol. 1984 Jul;352:509-16. doi: 10.1113/jphysiol.1984.sp015306.
Quantitative light-microscope autoradiography has been used to compare the specific, clonazepam-displaceable binding of [3H]flunitrazepam, a photoaffinity label for the 1,4-benzodiazepine receptor, in different regions of the brain and spinal cord of spastic mice and their unaffected littermates. Specific binding of [3H]flunitrazepam in the central nervous system of the spastic mouse showed significant increases in the anterior colliculus and pretectal area and in all laminae of the grey matter in the lumbar spinal cord. These results confirm homogenate binding assays suggesting an increased number of benzodiazepine receptors in the spinal cord of the spastic mouse. Possible sites are therefore provided at which disorders of function could arise, associated with changes seen at the gamma-aminobutyric acid (GABA)-benzodiazepine receptor complex in spinal cord homogenates from the mutant mouse spastic.
定量光学显微镜放射自显影术已被用于比较[3H]氟硝西泮(一种1,4-苯二氮䓬受体的光亲和标记物)在痉挛小鼠及其未受影响的同窝仔鼠的大脑和脊髓不同区域的特异性、可被氯硝西泮置换的结合情况。[3H]氟硝西泮在痉挛小鼠中枢神经系统中的特异性结合在前丘和顶盖前区以及腰脊髓灰质的所有板层中均显著增加。这些结果证实了匀浆结合试验,表明痉挛小鼠脊髓中苯二氮䓬受体数量增加。因此,可能出现功能障碍的部位得以确定,这些部位与突变型痉挛小鼠脊髓匀浆中γ-氨基丁酸(GABA)-苯二氮䓬受体复合物的变化有关。