Hicks G A, Henderson G
Department of Pharmacology, University of Cambridge, UK.
Neurosci Lett. 1992 Jul 20;141(2):213-7. doi: 10.1016/0304-3940(92)90897-g.
Whole-cell patch clamp recordings were made from neurones in slices of rat substantia nigra zona compacta. The majority exhibited electrophysiological characteristics seen previously with intracellular recordings and were hyperpolarised by dopamine in a sulpiride-reversible manner. The sulphonylureas, tolbutamide and glibenclamide, did not reverse the response to dopamine and had no effect when applied alone. The potassium channel opener, cromakalim, was also without effect on dopaminergic neurones. Under our recording conditions, the potassium conductance activated by dopamine acting through the D2 receptor does not show the pharmacological characteristics of an ATP-sensitive potassium conductance.
采用全细胞膜片钳记录技术,对大鼠黑质致密部切片中的神经元进行记录。大多数神经元表现出先前细胞内记录所见的电生理特性,并且多巴胺以舒必利可逆的方式使其超极化。磺酰脲类药物甲苯磺丁脲和格列本脲不能逆转对多巴胺的反应,单独应用时也无作用。钾通道开放剂克罗卡林对多巴胺能神经元也无作用。在我们的记录条件下,多巴胺通过D2受体激活的钾电导不表现出ATP敏感性钾电导的药理学特性。