Millington W R, Aizenman E, Bierkamper G G, Zarbin M A, Kuhar M J
Brain Res. 1985 Aug 12;340(2):269-76. doi: 10.1016/0006-8993(85)90923-0.
[125I]alpha-Bungarotoxin (alpha-BuTX) binding sites accumulate both proximal and distal to a ligature positioned around the sciatic nerve of rats. [125I]alpha-BuTX binding sites, localized using quantitative receptor autoradiography, were found to accumulate at nerve ligatures at a relatively constant rate which suggests that they undergo both anterograde and retrograde axonal transport. [125I]alpha-BuTX binding to sections of ligated sciatic nerve was saturable with apparent dissociation constants of 0.97 nM proximal and 0.53 nM distal to the ligature. D-Tubocurarine, nicotine, decamethonium and atropine displaced [125]alpha-BuTX from sciatic nerve sections with affinities comparable to those previously reported for the toxin binding component of rat brain. These data indicate that [125I]alpha-BuTX binding sites pharmacologically similar to those of rat brain are transported in sciatic nerve. Axonally transported toxin binding sites may correspond to those previously localized to the plasma membrane of peripheral nerve axons and on the terminals of motor neurons.
[125I]α-银环蛇毒素(α-BuTX)结合位点在围绕大鼠坐骨神经结扎部位的近端和远端均有累积。利用定量受体放射自显影定位的[125I]α-BuTX结合位点,被发现以相对恒定的速率在神经结扎处累积,这表明它们经历顺行和逆行轴突运输。[125I]α-BuTX与结扎坐骨神经切片的结合是可饱和的,结扎近端的表观解离常数为0.97 nM,远端为0.53 nM。筒箭毒碱、尼古丁、十烃季铵和阿托品从坐骨神经切片上取代[125]α-BuTX的亲和力与先前报道的大鼠脑毒素结合成分的亲和力相当。这些数据表明,[125I]α-BuTX结合位点在药理学上与大鼠脑的相似,在坐骨神经中运输。轴突运输的毒素结合位点可能与先前定位于周围神经轴突质膜和运动神经元终末的位点相对应。