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缓冲液对脑和脊髓中高亲和力[3H]-哌唑嗪结合的影响。

Buffer effects on high affinity [3H]-prazosin binding in brain and spinal cord.

作者信息

Herr D W, Mailman R B

机构信息

Toxicology Curriculum, University of North Carolina, Chapel Hill 27514.

出版信息

Pharmacol Biochem Behav. 1989 Mar;32(3):831-4. doi: 10.1016/0091-3057(89)90043-9.

Abstract

[3H]-Prazosin binding was characterized in cortical and spinal membranes from Fischer 344N and Sprague-Dawley rats. Estimates of Bmax and Kd values were comparable with earlier studies of these regions in the central nervous system (CNS). However, the Kd obtained using Tris buffer system was greater than when HEPES or phosphate buffer was used. These data indicate that high affinity [3H]-prazosin binding in the homogenates of tissue from the CNS is affected critically by buffer selection.

摘要

在Fischer 344N大鼠和Sprague-Dawley大鼠的皮质和脊髓膜中对[3H]-哌唑嗪结合进行了表征。Bmax和Kd值的估计与先前对中枢神经系统(CNS)这些区域的研究结果相当。然而,使用Tris缓冲系统获得的Kd大于使用HEPES或磷酸盐缓冲液时的Kd。这些数据表明,中枢神经系统组织匀浆中高亲和力的[3H]-哌唑嗪结合受到缓冲液选择的关键影响。

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