Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle

Resistance to insulin-induced glucose disposal is associated with hypertension, in accord with recent reports that insulin-induced vasodilation is impaired in men with resistance to insulin-induced glucose disposal. Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished...

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Veröffentlicht in:Hypertension (Dallas, Tex. 1979) Tex. 1979), 1993-11, Vol.22 (5), p.735-742
Hauptverfasser: Kahn, Andrew M, Seidel, Charles L, Allen, Julius C, OʼNeil, Roger G, Shelat, Harnath, Song, Tom
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container_end_page 742
container_issue 5
container_start_page 735
container_title Hypertension (Dallas, Tex. 1979)
container_volume 22
creator Kahn, Andrew M
Seidel, Charles L
Allen, Julius C
OʼNeil, Roger G
Shelat, Harnath
Song, Tom
description Resistance to insulin-induced glucose disposal is associated with hypertension, in accord with recent reports that insulin-induced vasodilation is impaired in men with resistance to insulin-induced glucose disposal. Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P
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Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P &lt;.05). Short-term insulin exposure also attenuated the peak rise of the serotonin-induced intracellular Ca transient and increased the rate constant for intracellular Ca decline. Verapamil and ouabain completely blocked the attenuation of agonist-induced contraction by short-term insulin exposure, indicating the importance of voltage-operated Ca channels and the Na-K pump for this effect. We conclude that a physiological insulin concentration inhibits extracellular K– and agonist-induced contractions at the level of the vascular smooth muscle cell and attenuates the intracellular Ca transient in agonist-stimulated cells. 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The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P &lt;.05). Short-term insulin exposure also attenuated the peak rise of the serotonin-induced intracellular Ca transient and increased the rate constant for intracellular Ca decline. Verapamil and ouabain completely blocked the attenuation of agonist-induced contraction by short-term insulin exposure, indicating the importance of voltage-operated Ca channels and the Na-K pump for this effect. We conclude that a physiological insulin concentration inhibits extracellular K– and agonist-induced contractions at the level of the vascular smooth muscle cell and attenuates the intracellular Ca transient in agonist-stimulated cells. 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Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P &lt;.05). Short-term insulin exposure also attenuated the peak rise of the serotonin-induced intracellular Ca transient and increased the rate constant for intracellular Ca decline. Verapamil and ouabain completely blocked the attenuation of agonist-induced contraction by short-term insulin exposure, indicating the importance of voltage-operated Ca channels and the Na-K pump for this effect. We conclude that a physiological insulin concentration inhibits extracellular K– and agonist-induced contractions at the level of the vascular smooth muscle cell and attenuates the intracellular Ca transient in agonist-stimulated cells. 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subjects Angiotensin II - pharmacology
Animals
Calcium - metabolism
Cells, Cultured
Dogs
Dose-Response Relationship, Drug
Female
Femoral Artery - drug effects
Femoral Artery - metabolism
Femoral Artery - physiology
In Vitro Techniques
Insulin - pharmacology
Kinetics
Male
Muscle Contraction - drug effects
Muscle, Smooth, Vascular - drug effects
Muscle, Smooth, Vascular - metabolism
Muscle, Smooth, Vascular - physiology
Ouabain - pharmacology
Potassium - pharmacology
Serotonin - pharmacology
Vasodilation - drug effects
Verapamil - pharmacology
title Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle
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