Schotte A, Janssen P F, Gommeren W, Luyten W H, Leysen J E
Janssen Research Foundation, Department of Biochemical Pharmacology, Beerse, Belgium.
Eur J Pharmacol. 1992 Aug 6;218(2-3):373-5. doi: 10.1016/0014-2999(92)90196-b.
[125I]Iodosulpride binding was studied in frontal rat brain sections by quantitative autoradiography. Using preincubated (= washed) sections, selective labelling and identification of dopamine D3 receptors was obtained using 0.2 nM [125I]iodosulpride in the presence of 100 nM domperidone for the occlusion of the D2 receptors. A high density of D3 receptors was noticed in the islands of Calleja. When preincubation of the sections was omitted, no D3 receptor labelling could be achieved, indicating tight binding to the receptor of an endogenous inhibitor. Such a tight receptor occupancy was not observed for the D2 receptor and various other neurotransmitter receptors. The occlusion of the D3 receptor could be prevented by tetrabenazine-induced monoamine depletion of the rats. It can be concluded, therefore, that D3 receptors are massively occupied by a monoamine, likely to be dopamine. This observation prompts the question to what extent dopamine D3 receptors can become occupied in vivo by systematically applied exogenous compounds.
通过定量放射自显影法研究了[125I]碘舒必利在大鼠额叶脑切片中的结合情况。使用预孵育(即洗涤)切片,在100 nM多潘立酮存在下,用0.2 nM [125I]碘舒必利进行选择性标记和多巴胺D3受体鉴定,以阻断D2受体。在Calleja岛中发现了高密度的D3受体。若省略切片的预孵育步骤,则无法实现D3受体标记,这表明内源性抑制剂与该受体紧密结合。对于D2受体和其他各种神经递质受体,未观察到如此紧密的受体占据情况。大鼠经丁苯那嗪诱导单胺耗竭后,D3受体的阻断作用可被防止。因此可以得出结论,D3受体被一种单胺大量占据,这种单胺可能是多巴胺。这一观察结果引发了一个问题,即系统性应用外源性化合物时,多巴胺D3受体在体内能被占据到何种程度。