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α和β肾上腺素能与哇巴因诱导的延迟后去极化的相互作用。

Alpha and beta adrenergic interactions with ouabain-induced delayed afterdepolarizations.

作者信息

Hewett K W, Rosen M R

出版信息

J Pharmacol Exp Ther. 1984 Apr;229(1):188-92.

PMID:6323686
Abstract

Standard microelectrode techniques were used to study the effect of alpha and beta adrenergic agonists and antagonists on ouabain-induced delayed afterdepolarizations (DADs) in isolated canine Purkinje fibers. The Purkinje fibers were superfused with ouabain (2 X 10(-7) M) for approximately 30 min to produce afterdepolarizations before superfusion with appropriate adrenergic agonists and antagonists. Propranolol (2 X 10(-7) M), a beta blocking concentration, had no effect on DAD amplitude; higher concentrations of propranolol (2 X 10(-6) reduced DAD and eliminated triggered rhythms. Isoproterenol (5 X 10(-6) M) increased DAD amplitude and triggered activity, an effect which was abolished by pretreatment with propranolol (2 X 10(-7) M). Neither alpha adrenergic blockade with phentolamine nor superfusion with the alpha adrenergic receptor agonist methoxamine had an effect on DAD amplitude or triggered activity. It is concluded that the beta adrenergic stimulation can enhance DAD amplitude and triggered activity in the ouabain-toxic Purkinje fiber. In contrast, alpha adrenergic agonists and blockers do not appear to have significant effects on DAD amplitude or triggered activity.

摘要

采用标准微电极技术,研究α和β肾上腺素能激动剂及拮抗剂对离体犬浦肯野纤维中哇巴因诱导的延迟后去极化(DADs)的影响。在与适当的肾上腺素能激动剂和拮抗剂进行灌流之前,先用哇巴因(2×10⁻⁷M)对浦肯野纤维进行约30分钟的灌流,以产生后去极化。普萘洛尔(2×10⁻⁷M),一种β受体阻断浓度,对DAD幅度无影响;更高浓度的普萘洛尔(2×10⁻⁶)降低了DAD并消除了触发节律。异丙肾上腺素(5×10⁻⁶M)增加了DAD幅度并引发了活动,这种效应在用普萘洛尔(2×10⁻⁷M)预处理后被消除。酚妥拉明对α肾上腺素能的阻断以及用α肾上腺素能受体激动剂甲氧明进行灌流,对DAD幅度或触发活动均无影响。结论是,β肾上腺素能刺激可增强哇巴因中毒的浦肯野纤维中的DAD幅度和触发活动。相比之下,α肾上腺素能激动剂和阻断剂似乎对DAD幅度或触发活动没有显著影响。

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