The effects of muscarinic receptor agonists on the electrically-evoked surface-negative field potential (N-wave) were measured in the guinea-pig olfactory cortex slice maintained in vitro. 2. Bath-superfusion of (+/-)-muscarine, acetylcholine (ACh), carbachol (CCh), or methacholine (MCh) (10-200 microM) produced reversible, dose-dependent depressions of the N-wave (ACh and MCh effects were observed in the presence of 10 microM neostigmine). The order of potencies (based on agonist dose causing 50% field depression: IC50) was: ACh greater than or equal to muscarine greater than CCh greater than MCh. All four agonists depressed the field potential by 100% at doses greater than 500 microM. 3. Pilocarpine and bethanechol were weak agonists and only produced measurable effects at high doses (1-2 mM). Neither agonist evoked a maximum response at doses up to 10 mM. 4. The muscarinic ganglion stimulant, McN-A-343 yielded inconsistent results, depressing the field potential in some slices, but having no effect in others. Pre-application of a conditioning dose (100 microM) of McN-A-343 reduced subsequent responses to CCh, suggesting possible partial agonist properties. 5. Oxotremorine (up to 100 microM) did not depress the field potential, but it reversibly antagonized the effects of CCh. 6. It is concluded that reproducible, quantifiable responses to muscarinic agonists can be evoked in the olfactory cortex slice. We suggest this preparation may be useful for conducting pharmacological studies of 'intact' central muscarinic receptors.
摘要
在体外维持的豚鼠嗅皮质切片中,测量了毒蕈碱受体激动剂对电诱发的表面负向场电位(N波)的影响。2. 用(±)-毒蕈碱、乙酰胆碱(ACh)、卡巴胆碱(CCh)或醋甲胆碱(MCh)(10 - 200微摩尔)进行浴槽灌注,可产生可逆的、剂量依赖性的N波抑制(在存在10微摩尔新斯的明的情况下观察到ACh和MCh的作用)。效价顺序(基于引起50%场抑制的激动剂剂量:半数抑制浓度)为:ACh≥毒蕈碱>CCh>MCh。所有四种激动剂在剂量大于500微摩尔时可将场电位抑制100%。3. 毛果芸香碱和氨甲酰甲胆碱是弱激动剂,仅在高剂量(1 - 2毫摩尔)时产生可测量的作用。在剂量高达10毫摩尔时,两种激动剂均未引起最大反应。4. 毒蕈碱型神经节兴奋剂McN - A - 343产生的结果不一致,在一些切片中抑制场电位,但在其他切片中无作用。预先给予100微摩尔的预处理剂量的McN - A - 343可降低随后对CCh的反应,提示可能具有部分激动剂特性。5. 氧化震颤素(高达100微摩尔)未抑制场电位,但可可逆地拮抗CCh的作用。6. 得出结论,在嗅皮质切片中可诱发对毒蕈碱激动剂的可重复、可量化的反应。我们认为该制剂可能有助于进行“完整”中枢毒蕈碱受体的药理学研究。