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阿托品对Triton X-100所致中枢毒蕈碱受体抑制的保护作用。

Protection by atropine of the inhibition caused by Triton X-100 on central muscarinic receptors.

作者信息

Aguilar J S, Criado M, De Robertis E

出版信息

Eur J Pharmacol. 1980 May 16;63(4):251-7. doi: 10.1016/0014-2999(80)90252-6.

Abstract

Synaptosomal membranes from cat cerebral cortex were labelled with [3H]-quinuclidinyl benzylate ([3H]QNB). There was shown to be a single type of binding site with Kd = 0.34 nM, Bmax = 2.2 nmol/g protein and Hill No. = 1.01. Triton X-100 at 5 x 10(-4)% inhibited the specific binding of [3H]QNB and the inhibition was almost complete at 10(-2)%. Treatment with 2.5 x 10(-6) M atropine, followed by centrifugation washings protected the receptor site from the inhibitory action of the detergent. The protection afforded by other cholinergic drugs was less effective. The use of this technique has confirmed the results of our previous work on the possible pre- and postsynaptic location of central muscarinic receptors. These findings open the possibility for protection of other detergent-sensitive receptors and for their isolation and purification as well-defined macromolecules.

摘要

用[3H]-喹核醇基苯甲酸酯([3H]QNB)标记猫大脑皮层的突触体膜。结果显示存在一种单一类型的结合位点,其解离常数(Kd)为0.34 nM,最大结合容量(Bmax)为2.2 nmol/g蛋白质,希尔系数(Hill No.)为1.01。5×10(-4)%的 Triton X-100可抑制[3H]QNB的特异性结合,在10(-2)%时抑制几乎完全。用2.5×10(-6) M阿托品处理,随后进行离心洗涤,可保护受体位点免受去污剂的抑制作用。其他胆碱能药物提供的保护效果较差。该技术的应用证实了我们先前关于中枢毒蕈碱受体可能的突触前和突触后定位的研究结果。这些发现为保护其他对去污剂敏感的受体以及将它们作为明确的大分子进行分离和纯化开辟了可能性。

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