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对照和利血平预处理的兔主动脉对去甲肾上腺素、异丙肾上腺素和乙酰胆碱的张力发展及相关钙内流。

Tension development and associated calcium influx of control and reserpine pretreated rabbit aortae in response to norepinephrine, isoproterenol and acetylcholine.

作者信息

Hester R K, Carrier O

出版信息

Arch Int Pharmacodyn Ther. 1978 May;233(1):21-41.

PMID:686906
Abstract

The influence of reserpine (3mg/kg) pretreatment on phasic and tonic components of the contractile responses of rabbit aortae to maximally effective concentrations of norepinephrine, acetylcholine, and isoproterenol and on agonists-induced movements of 45Ca during these responses were studied. Four hours after reserpine administration, there were no histological changes, in extracellular space, and no change in tissue water, sodium, calcium or magnesium. Potassium contents were slightly decreased and the catecholamine content was depleted by 95%. The responses to the three agonists were enhanced in the reserpine pretreated tissues. The absence of calcium eliminated the slow tonic componenet of the responses. Reserpine induced an increase in lanthanum (La3+) resistant 45Ca uptake. The three agonists induced an increase in La3+ resitant 45Ca uptake of equal magnitude in both reserpine pretreated and control tissues. Lanthanum ion affected 45Ca efflux similarly in both reserpine pretreated and untreated tissues. The results suggest that a major portion of the enhanced responsiveness of rabbit aortic strips following reserpien administration is the result of a change in calcium retention in those tissue stores mobilized by these agonists to initiate the fast, phasic componenet, and is, therefore, a reflection of an increased agonist intrinsic activity.

摘要

研究了利血平(3mg/kg)预处理对兔主动脉对去甲肾上腺素、乙酰胆碱和异丙肾上腺素最大有效浓度收缩反应的时相和张力成分,以及对这些反应过程中激动剂诱导的45Ca移动的影响。给予利血平4小时后,细胞外间隙无组织学变化,组织水分、钠、钙或镁无变化。钾含量略有下降,儿茶酚胺含量减少95%。利血平预处理的组织对三种激动剂的反应增强。去除钙消除了反应的缓慢张力成分。利血平诱导镧(La3+)抗性45Ca摄取增加。三种激动剂在利血平预处理组织和对照组织中诱导的La3+抗性45Ca摄取增加幅度相同。镧离子对利血平预处理组织和未处理组织中的45Ca流出影响相似。结果表明,利血平给药后兔主动脉条反应性增强的主要部分是这些激动剂动员的那些组织储存中钙潴留变化的结果,从而启动快速时相成分,因此,反映了激动剂内在活性的增加。

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