1981American Journal of Physiology-Cell PhysiologyRequires access

Insulin does not hyperpolarize rat muscle by means of a ouabain-inhibitable process

Kenneth L. Zierler, Ellen M. Rogus

Open publisher page 18 citations

Abstract

Experiments were designed to test the hypothesis that insulin-induced hyperpolarization of rat skeletal muscle is mediated by stimulation of a ouabain-inhibitable electrogenic pump. Parallel experiments were carried out on rat caudofemoralis with isoproterenol, known to hyperpolarize rat skeletal muscle by stimulation of such a pump. Ouabain (10(-5) M) completely inhibited isoproterenol-induced hyperpolarization within 15 min but had no effect on half-maximal insulin-induced hyperpolarization. Ouabain (10(-6) M) inhibited isoproterenol effect by 60% during a period of 5-15 min. Ouabain (10(-4) M) had no effect on insulin-induced hyperpolarization within 10 min but depolarized during the next 10 min. In a separate series of studies in rat extensor digitorum longus muscle, 10(-5) M ouabain increased intracellular Na+ within 14 min. It is concluded that in rat caudofemoralis muscle, insulin-induced hyperpolarization is not mediated by a ouabain-inhibitable electrogenic pump.

About this research paper

What this paper is about

Experiments were designed to test the hypothesis that insulin-induced hyperpolarization of rat skeletal muscle is mediated by stimulation of a ouabain-inhibitable electrogenic pump. Parallel experiments were carried out on rat caudofemoralis with isoproterenol, known to hyperpolarize rat skeletal muscle by stimulation of such a pump. Ouabain (10(-5) M) completely inhibited isoproterenol-induced hyperpolarization within 15 min but had no effect on half-maximal insulin-induced hyperpolarization. Ouabain (10(-6) M) inhibited isoproterenol effect by 60% during a period of 5-15 min. Ouabain (10(-4) M) had no effect on insulin-induced hyperpolarization within 10 min but depolarized during the next 10 min. In a separate series of studies in rat extensor digitorum longus muscle, 10(-5) M ouabain increased intracellular Na+ within 14 min. It is concluded that in rat caudofemoralis muscle, insulin-induced hyperpolarization is not mediated by a ouabain-inhibitable electrogenic pump.

Why it matters

OpenAlex reports 18 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Experiments were designed to test the hypothesis that insulin-induced hyperpolarization of rat skeletal muscle is mediated by stimulation of a ouabain-inhibitable electrogenic pump. Parallel experiments were carried out on rat caudofemoralis with isoproterenol, known to hyperpolarize rat skeletal muscle by stimulation of such a pump. Ouabain (10(-5) M) completely inhibited isoproterenol-induced hyperpolarization within 15 min but had no effect on half-maximal insulin-induced hyperpolarization. Ouabain (10(-6) M) inhibited isoproterenol effect by 60% during a period of 5-15 min. Ouabain (10(-4) M) had no effect on insulin-induced hyperpolarization within 10 min but depolarized during the next 10 min. In a separate series of studies in rat extensor digitorum longus muscle, 10(-5) M ouabain increased intracellular Na+ within 14 min. It is concluded that in rat caudofemoralis muscle, insulin-induced hyperpolarization is not mediated by a ouabain-inhibitable electrogenic pump.

Key concepts: Ouabain, Insulin, Process (computing), Cell biology, Business, Chemistry, Internal medicine, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Insulin does not hyperpolarize rat muscle by means of a ouabain-inhibitable process — Research Paper | ScholarLens