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关于MDL 72222及其他拮抗剂对兔迷走传入神经和交感神经节细胞5-羟色胺去极化的阻断作用的进一步研究。

Further studies on the blockade of 5-HT depolarizations of rabbit vagal afferent and sympathetic ganglion cells by MDL 72222 and other antagonists.

作者信息

Round A, Wallis D I

出版信息

Neuropharmacology. 1987 Jan;26(1):39-48. doi: 10.1016/0028-3908(87)90042-6.

Abstract

The blocking action of MDL 72222 (1 alpha H, 3 alpha, 5 alpha H-tropan-3-yl-3, 5-dichlorobenzoate at 5-hydroxytryptamine (5-HT) receptors on nodose (NG) and superior cervical ganglia (SCG) has been investigated further. The sucrose-gap technique was used to record potential changes from populations of neurones. The surmountable blockade induced by small concentrations of the antagonist was quantified and the blocking potency compared with that of a number of other compounds. In nodose ganglia three 4-5 point dose-response (DR) curves were established, using bolus injections of 5-HT (5-80 nmol). The mean amplitude of the response to 80 nmol was 4.18 +/- 0.53 mV and the ED50 was 18.2 nmol. Second and 3rd dose-response curves showed small displacements to the right, indicating a slight reduction in sensitivity. In superior cervical ganglia responsiveness was less. Amounts of 5-HT ranging from 20 to 320 nmol evoked dose-related depolarizations. The mean amplitude of the response evoked by 320 nmol 5-HT was 1.7 +/- 0.14 mV. Three 4-5 point dose-response curves could be elicited from a single ganglion. The ED50 was 55.8 nmol. Initial, 2nd and 3rd dose-response curves could be superimposed, there being no significant rightward shift. The results confirm that MDL 72222 is a potent, selective antagonist at 5-HT receptors in nodose and superior cervical ganglia. In the nodose ganglion, after equilibration for 1 hr with 10(-8) or 10(-7) M MDL 72222, dose-response curves for 5-HT showed rightward, parallel shifts. In contrast, 10(-6) M MDL 72222 or prolonged exposure (3-4 hr) to 10(-8), 10(-7) or 10(-6) M caused larger rightward shifts of the dose-response curves and depressed the maximum responses. In the superior cervical ganglion, equilibration for 1 hr with concentrations of 10(-8) or 10(-7) M produced effects on the dose-response curves similar to those seen in the nodose ganglion, but longer exposures (3-4 hr) did not depress the maximum. Apparent pA2 values were determined from individual experiments on both the nodose and superior cervical ganglia, where MDL 72222 (10(-7) M or less, for 1 hr) caused parallel or near parallel shifts of dose-response curves. In the nodose ganglion the apparent pA2 was 7.7 +/- 0.1, while in the superior cervical ganglion it was 7.8 +/- 0.1 (mean +/- SEM). The nature of the blockade induced by prolonged exposures or by concentrations greater than 10(-7) M is discussed.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

进一步研究了MDL 72222(1αH,3α,5αH-托烷-3-基-3,5-二氯苯甲酸酯)对结节神经节(NG)和颈上神经节(SCG)中5-羟色胺(5-HT)受体的阻断作用。采用蔗糖间隙技术记录神经元群体的电位变化。对小浓度拮抗剂诱导的可克服性阻断进行了定量,并将阻断效力与其他一些化合物进行了比较。在结节神经节中,使用5-HT(5-80 nmol)推注建立了三条4-5点剂量-反应(DR)曲线。对80 nmol反应的平均幅度为4.18±0.53 mV,ED50为18.2 nmol。第二条和第三条剂量-反应曲线向右有小的位移,表明敏感性略有降低。在颈上神经节中反应性较低。20至320 nmol的5-HT量引起剂量相关的去极化。320 nmol 5-HT引起的反应平均幅度为1.7±0.14 mV。从单个神经节可引出三条4-5点剂量-反应曲线。ED50为55.8 nmol。初始、第二条和第三条剂量-反应曲线可叠加,没有明显的向右位移。结果证实MDL 72222是结节神经节和颈上神经节中5-HT受体的强效、选择性拮抗剂。在结节神经节中,用10^(-8)或10^(-7) M MDL 72222平衡1小时后,5-HT的剂量-反应曲线向右平行移动。相比之下,10^(-6) M MDL 72222或长时间暴露(3-4小时)于10^(-8)、10^(-7)或10^(-6) M会导致剂量-反应曲线更大的向右移动并降低最大反应。在颈上神经节中,用10^(-8)或10^(-7) M浓度平衡1小时对剂量-反应曲线产生的影响与在结节神经节中观察到的相似,但更长时间暴露(3-4小时)不会降低最大反应。表观pA2值是通过对结节神经节和颈上神经节的单个实验确定的,其中MDL 72222(10^(-7) M或更低,持续1小时)导致剂量-反应曲线平行或接近平行移动。在结节神经节中表观pA2为7.7±0.1,而在颈上神经节中为7.8±0.1(平均值±标准误)。讨论了长时间暴露或大于10^(-7) M浓度诱导的阻断性质。(摘要截短至400字)

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