Sarah J Blackwood, Dominik Tischer, Myrthe P F van de Ven, Marjan Pontén, Sebastian Edman, Oscar Horwath, William Apró, Julia Röja, Maria M Ekblom, Marcus Moberg, Abram Katz
{"title":"在胰岛素抵抗的早期发展过程中,心率升高和肌肉内皮一氧化氮合酶减少。","authors":"Sarah J Blackwood, Dominik Tischer, Myrthe P F van de Ven, Marjan Pontén, Sebastian Edman, Oscar Horwath, William Apró, Julia Röja, Maria M Ekblom, Marcus Moberg, Abram Katz","doi":"10.1152/ajpendo.00148.2024","DOIUrl":null,"url":null,"abstract":"<p><p>Insulin resistance (IR) is a risk factor for the development of several major metabolic diseases. Muscle fiber composition is established early in life and is associated with insulin sensitivity. Hence, muscle fiber composition was used to identify early defects in the development of IR in healthy young individuals in the absence of clinical manifestations. Biopsies were obtained from the thigh muscle, followed by an intravenous glucose tolerance test. Indices of insulin action were calculated and cardiovascular measurements, analyses of blood and muscle were performed. Whole body insulin sensitivity (SI<sub>galvin</sub>) was positively related to expression of type I muscle fibers (<i>r</i> = 0.49; <i>P</i> < 0.001) and negatively related to resting heart rate (HR, <i>r</i> = -0.39; <i>P</i> < 0.001), which was also negatively related to expression of type I muscle fibers (<i>r</i> = -0.41; <i>P</i> < 0.001). Muscle protein expression of endothelial nitric oxide synthase (eNOS), whose activation results in vasodilation, was measured in two subsets of subjects expressing a high percentage of type I fibers (59 ± 6%; HR = 57 ± 9 beats/min; SI<sub>galvin</sub> = 1.8 ± 0.7 units) or low percentage of type I fibers (30 ± 6%; HR = 71 ± 11; SI<sub>galvin</sub> = 0.8 ± 0.3 units; <i>P</i> < 0.001 for all variables vs. first group). eNOS expression was <i>1</i>) higher in subjects with high type I expression; <i>2</i>) almost twofold higher in pools of type I versus II fibers; <i>3</i>) only detected in capillaries surrounding muscle fibers; and <i>4</i>) linearly associated with SI<sub>galvin</sub>. These data demonstrate that an altered function of the autonomic nervous system and a compromised capacity for vasodilation in the microvasculature occur early in the development of IR.<b>NEW & NOTEWORTHY</b> Insulin resistance (IR) is a risk factor for the development of several metabolic diseases. In healthy young individuals, an elevated heart rate (HR) correlates with low insulin sensitivity and high expression of type II skeletal muscle fibers, which express low levels of endothelial nitric oxide synthase (eNOS) and, hence, a limited capacity to induce vasodilation in response to insulin. Early targeting of the autonomic nervous system and microvasculature may attenuate development of diseases stemming from insulin resistance.</p>","PeriodicalId":7594,"journal":{"name":"American journal of physiology. Endocrinology and metabolism","volume":" ","pages":"E172-E182"},"PeriodicalIF":4.2000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Elevated heart rate and decreased muscle endothelial nitric oxide synthase in early development of insulin resistance.\",\"authors\":\"Sarah J Blackwood, Dominik Tischer, Myrthe P F van de Ven, Marjan Pontén, Sebastian Edman, Oscar Horwath, William Apró, Julia Röja, Maria M Ekblom, Marcus Moberg, Abram Katz\",\"doi\":\"10.1152/ajpendo.00148.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Insulin resistance (IR) is a risk factor for the development of several major metabolic diseases. Muscle fiber composition is established early in life and is associated with insulin sensitivity. Hence, muscle fiber composition was used to identify early defects in the development of IR in healthy young individuals in the absence of clinical manifestations. Biopsies were obtained from the thigh muscle, followed by an intravenous glucose tolerance test. Indices of insulin action were calculated and cardiovascular measurements, analyses of blood and muscle were performed. Whole body insulin sensitivity (SI<sub>galvin</sub>) was positively related to expression of type I muscle fibers (<i>r</i> = 0.49; <i>P</i> < 0.001) and negatively related to resting heart rate (HR, <i>r</i> = -0.39; <i>P</i> < 0.001), which was also negatively related to expression of type I muscle fibers (<i>r</i> = -0.41; <i>P</i> < 0.001). Muscle protein expression of endothelial nitric oxide synthase (eNOS), whose activation results in vasodilation, was measured in two subsets of subjects expressing a high percentage of type I fibers (59 ± 6%; HR = 57 ± 9 beats/min; SI<sub>galvin</sub> = 1.8 ± 0.7 units) or low percentage of type I fibers (30 ± 6%; HR = 71 ± 11; SI<sub>galvin</sub> = 0.8 ± 0.3 units; <i>P</i> < 0.001 for all variables vs. first group). eNOS expression was <i>1</i>) higher in subjects with high type I expression; <i>2</i>) almost twofold higher in pools of type I versus II fibers; <i>3</i>) only detected in capillaries surrounding muscle fibers; and <i>4</i>) linearly associated with SI<sub>galvin</sub>. These data demonstrate that an altered function of the autonomic nervous system and a compromised capacity for vasodilation in the microvasculature occur early in the development of IR.<b>NEW & NOTEWORTHY</b> Insulin resistance (IR) is a risk factor for the development of several metabolic diseases. In healthy young individuals, an elevated heart rate (HR) correlates with low insulin sensitivity and high expression of type II skeletal muscle fibers, which express low levels of endothelial nitric oxide synthase (eNOS) and, hence, a limited capacity to induce vasodilation in response to insulin. Early targeting of the autonomic nervous system and microvasculature may attenuate development of diseases stemming from insulin resistance.</p>\",\"PeriodicalId\":7594,\"journal\":{\"name\":\"American journal of physiology. Endocrinology and metabolism\",\"volume\":\" \",\"pages\":\"E172-E182\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of physiology. 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Elevated heart rate and decreased muscle endothelial nitric oxide synthase in early development of insulin resistance.
Insulin resistance (IR) is a risk factor for the development of several major metabolic diseases. Muscle fiber composition is established early in life and is associated with insulin sensitivity. Hence, muscle fiber composition was used to identify early defects in the development of IR in healthy young individuals in the absence of clinical manifestations. Biopsies were obtained from the thigh muscle, followed by an intravenous glucose tolerance test. Indices of insulin action were calculated and cardiovascular measurements, analyses of blood and muscle were performed. Whole body insulin sensitivity (SIgalvin) was positively related to expression of type I muscle fibers (r = 0.49; P < 0.001) and negatively related to resting heart rate (HR, r = -0.39; P < 0.001), which was also negatively related to expression of type I muscle fibers (r = -0.41; P < 0.001). Muscle protein expression of endothelial nitric oxide synthase (eNOS), whose activation results in vasodilation, was measured in two subsets of subjects expressing a high percentage of type I fibers (59 ± 6%; HR = 57 ± 9 beats/min; SIgalvin = 1.8 ± 0.7 units) or low percentage of type I fibers (30 ± 6%; HR = 71 ± 11; SIgalvin = 0.8 ± 0.3 units; P < 0.001 for all variables vs. first group). eNOS expression was 1) higher in subjects with high type I expression; 2) almost twofold higher in pools of type I versus II fibers; 3) only detected in capillaries surrounding muscle fibers; and 4) linearly associated with SIgalvin. These data demonstrate that an altered function of the autonomic nervous system and a compromised capacity for vasodilation in the microvasculature occur early in the development of IR.NEW & NOTEWORTHY Insulin resistance (IR) is a risk factor for the development of several metabolic diseases. In healthy young individuals, an elevated heart rate (HR) correlates with low insulin sensitivity and high expression of type II skeletal muscle fibers, which express low levels of endothelial nitric oxide synthase (eNOS) and, hence, a limited capacity to induce vasodilation in response to insulin. Early targeting of the autonomic nervous system and microvasculature may attenuate development of diseases stemming from insulin resistance.
期刊介绍:
The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.