Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity

Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity Kazutoshi Miyashita 1 , Hiroshi Itoh 1 , Hirokazu Tsujimoto 2 , Naohisa Tamura 2 , Yasutomo Fukunaga 2 , Masakatsu Sone 2 , Kenichi Yamahara 2 , Daisuke Taura 2 , Megumi Inuzu...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2009-12, Vol.58 (12), p.2880-2892
Hauptverfasser: MIYASHITA, Kazutoshi, ITOH, Hiroshi, NAKAO, Kazuwa, TSUJIMOTO, Hirokazu, TAMURA, Naohisa, FUKUNAGA, Yasutomo, SONE, Masakatsu, YAMAHARA, Kenichi, TAURA, Daisuke, INUZUKA, Megumi, SONOYAMA, Takuhiro
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container_issue 12
container_start_page 2880
container_title Diabetes (New York, N.Y.)
container_volume 58
creator MIYASHITA, Kazutoshi
ITOH, Hiroshi
NAKAO, Kazuwa
TSUJIMOTO, Hirokazu
TAMURA, Naohisa
FUKUNAGA, Yasutomo
SONE, Masakatsu
YAMAHARA, Kenichi
TAURA, Daisuke
INUZUKA, Megumi
SONOYAMA, Takuhiro
description Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity Kazutoshi Miyashita 1 , Hiroshi Itoh 1 , Hirokazu Tsujimoto 2 , Naohisa Tamura 2 , Yasutomo Fukunaga 2 , Masakatsu Sone 2 , Kenichi Yamahara 2 , Daisuke Taura 2 , Megumi Inuzuka 2 , Takuhiro Sonoyama 2 and Kazuwa Nakao 2 1 Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan; 2 Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan. Corresponding author: Hiroshi Itoh, hrith{at}sc.itc.keio.ac.jp . Abstract OBJECTIVE Natriuretic peptides (NPs) have been characterized as vascular hormones that regulate vascular tone via guanylyl cyclase (GC), cyclic GMP (cGMP), and cGMP-dependent protein kinase (cGK). Recent clinical studies have shown that plasma NP levels were lower in subjects with the metabolic syndrome. The present study was conducted to elucidate the roles for NP/cGK cascades in energy metabolism. RESEARCH DESIGN AND METHODS We used three types of genetically engineered mice: brain NP (BNP) transgenic (BNP-Tg), cGK-Tg, and guanylyl cyclase-A (GCA) heterozygous knockout (GCA +/− ) mice and analyzed the metabolic consequences of chronic activation of NP/cGK cascades in vivo. We also examined the effect of NPs in cultured myocytes. RESULTS BNP-Tg mice fed on high-fat diet were protected against diet-induced obesity and insulin resistance, and cGK-Tg mice had reduced body weight even on standard diet; surprisingly, giant mitochondria were densely packed in the skeletal muscle. Both mice showed an increase in muscle mitochondrial content and fat oxidation through upregulation of peroxisome proliferator–activated receptor (PPAR)-γ coactivator (PGC)-1α and PPARδ. The functional NP receptors, GCA and guanylyl cyclase-B, were downregulated by feeding a high-fat diet, while GCA +/− mice showed increases in body weight and glucose intolerance when fed a high-fat diet. NPs directly increased the expression of PGC-1α and PPARδ and mitochondrial content in cultured myocytes. CONCLUSIONS The findings together suggest that NP/cGK cascades can promote muscle mitochondrial biogenesis and fat oxidation, as to prevent obesity and glucose intolerance. The vascular hormone, NP, would contribute to coordinated regulation of oxygen supply and consumption. Footnotes The costs of publication of this article were defrayed in part by the payment of page charges. This article must
doi_str_mv 10.2337/db09-0393
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Corresponding author: Hiroshi Itoh, hrith{at}sc.itc.keio.ac.jp . Abstract OBJECTIVE Natriuretic peptides (NPs) have been characterized as vascular hormones that regulate vascular tone via guanylyl cyclase (GC), cyclic GMP (cGMP), and cGMP-dependent protein kinase (cGK). Recent clinical studies have shown that plasma NP levels were lower in subjects with the metabolic syndrome. The present study was conducted to elucidate the roles for NP/cGK cascades in energy metabolism. RESEARCH DESIGN AND METHODS We used three types of genetically engineered mice: brain NP (BNP) transgenic (BNP-Tg), cGK-Tg, and guanylyl cyclase-A (GCA) heterozygous knockout (GCA +/− ) mice and analyzed the metabolic consequences of chronic activation of NP/cGK cascades in vivo. We also examined the effect of NPs in cultured myocytes. RESULTS BNP-Tg mice fed on high-fat diet were protected against diet-induced obesity and insulin resistance, and cGK-Tg mice had reduced body weight even on standard diet; surprisingly, giant mitochondria were densely packed in the skeletal muscle. Both mice showed an increase in muscle mitochondrial content and fat oxidation through upregulation of peroxisome proliferator–activated receptor (PPAR)-γ coactivator (PGC)-1α and PPARδ. The functional NP receptors, GCA and guanylyl cyclase-B, were downregulated by feeding a high-fat diet, while GCA +/− mice showed increases in body weight and glucose intolerance when fed a high-fat diet. NPs directly increased the expression of PGC-1α and PPARδ and mitochondrial content in cultured myocytes. CONCLUSIONS The findings together suggest that NP/cGK cascades can promote muscle mitochondrial biogenesis and fat oxidation, as to prevent obesity and glucose intolerance. The vascular hormone, NP, would contribute to coordinated regulation of oxygen supply and consumption. Footnotes The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. See accompanying commentary, p. 2726 . . Received March 15, 2009. Accepted July 28, 2009. © 2009 American Diabetes Association</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/db09-0393</identifier><identifier>PMID: 19690065</identifier><identifier>CODEN: DIAEAZ</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Animals ; Biological and medical sciences ; Biosynthesis ; Blood Glucose - metabolism ; Body fat ; Cells, Cultured ; Cyclic GMP - metabolism ; Diabetes ; Diabetes. Impaired glucose tolerance ; Dietary Fats - administration &amp; dosage ; Dietary Fats - adverse effects ; Dietary Fats - metabolism ; Down-Regulation ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Fatty acids ; Genetic Engineering ; Glucose ; Glucose Intolerance - etiology ; Glucose Intolerance - metabolism ; Heart failure ; Hormones ; Insulin Resistance ; Kinases ; Lipid Peroxidation ; Lipids ; Medical sciences ; Metabolic diseases ; Metabolic syndrome ; Mice ; Mice, Knockout ; Mitochondria - metabolism ; Molecular Sequence Data ; Muscle Cells - metabolism ; Muscle, Skeletal - metabolism ; Musculoskeletal system ; Natriuretic Peptide, Brain - metabolism ; Natriuretic Peptides - metabolism ; Obesity ; Obesity - etiology ; Obesity - metabolism ; Obesity - prevention &amp; control ; Original ; Oxidation ; Oxygen Consumption ; Peptides ; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha ; Plasma ; PPAR delta - metabolism ; PPAR gamma - metabolism ; Protein Kinases - metabolism ; Proteins ; Receptors, Atrial Natriuretic Factor - metabolism ; Research design ; Signal transduction ; Trans-Activators - metabolism ; Transcription Factors ; Transgenic animals ; Up-Regulation</subject><ispartof>Diabetes (New York, N.Y.), 2009-12, Vol.58 (12), p.2880-2892</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright American Diabetes Association Dec 2009</rights><rights>2009 American Diabetes Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c534t-3f031db6bed9a9e765e6e62d5bd1b6f42fc8b36b90abfe4fe890f45032957d9e3</citedby><cites>FETCH-LOGICAL-c534t-3f031db6bed9a9e765e6e62d5bd1b6f42fc8b36b90abfe4fe890f45032957d9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780866/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780866/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22204591$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19690065$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MIYASHITA, Kazutoshi</creatorcontrib><creatorcontrib>ITOH, Hiroshi</creatorcontrib><creatorcontrib>NAKAO, Kazuwa</creatorcontrib><creatorcontrib>TSUJIMOTO, Hirokazu</creatorcontrib><creatorcontrib>TAMURA, Naohisa</creatorcontrib><creatorcontrib>FUKUNAGA, Yasutomo</creatorcontrib><creatorcontrib>SONE, Masakatsu</creatorcontrib><creatorcontrib>YAMAHARA, Kenichi</creatorcontrib><creatorcontrib>TAURA, Daisuke</creatorcontrib><creatorcontrib>INUZUKA, Megumi</creatorcontrib><creatorcontrib>SONOYAMA, Takuhiro</creatorcontrib><title>Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity</title><title>Diabetes (New York, N.Y.)</title><addtitle>Diabetes</addtitle><description>Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity Kazutoshi Miyashita 1 , Hiroshi Itoh 1 , Hirokazu Tsujimoto 2 , Naohisa Tamura 2 , Yasutomo Fukunaga 2 , Masakatsu Sone 2 , Kenichi Yamahara 2 , Daisuke Taura 2 , Megumi Inuzuka 2 , Takuhiro Sonoyama 2 and Kazuwa Nakao 2 1 Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan; 2 Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan. Corresponding author: Hiroshi Itoh, hrith{at}sc.itc.keio.ac.jp . Abstract OBJECTIVE Natriuretic peptides (NPs) have been characterized as vascular hormones that regulate vascular tone via guanylyl cyclase (GC), cyclic GMP (cGMP), and cGMP-dependent protein kinase (cGK). Recent clinical studies have shown that plasma NP levels were lower in subjects with the metabolic syndrome. The present study was conducted to elucidate the roles for NP/cGK cascades in energy metabolism. RESEARCH DESIGN AND METHODS We used three types of genetically engineered mice: brain NP (BNP) transgenic (BNP-Tg), cGK-Tg, and guanylyl cyclase-A (GCA) heterozygous knockout (GCA +/− ) mice and analyzed the metabolic consequences of chronic activation of NP/cGK cascades in vivo. We also examined the effect of NPs in cultured myocytes. RESULTS BNP-Tg mice fed on high-fat diet were protected against diet-induced obesity and insulin resistance, and cGK-Tg mice had reduced body weight even on standard diet; surprisingly, giant mitochondria were densely packed in the skeletal muscle. Both mice showed an increase in muscle mitochondrial content and fat oxidation through upregulation of peroxisome proliferator–activated receptor (PPAR)-γ coactivator (PGC)-1α and PPARδ. The functional NP receptors, GCA and guanylyl cyclase-B, were downregulated by feeding a high-fat diet, while GCA +/− mice showed increases in body weight and glucose intolerance when fed a high-fat diet. NPs directly increased the expression of PGC-1α and PPARδ and mitochondrial content in cultured myocytes. CONCLUSIONS The findings together suggest that NP/cGK cascades can promote muscle mitochondrial biogenesis and fat oxidation, as to prevent obesity and glucose intolerance. The vascular hormone, NP, would contribute to coordinated regulation of oxygen supply and consumption. Footnotes The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. See accompanying commentary, p. 2726 . . Received March 15, 2009. Accepted July 28, 2009. © 2009 American Diabetes Association</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biosynthesis</subject><subject>Blood Glucose - metabolism</subject><subject>Body fat</subject><subject>Cells, Cultured</subject><subject>Cyclic GMP - metabolism</subject><subject>Diabetes</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Dietary Fats - administration &amp; dosage</subject><subject>Dietary Fats - adverse effects</subject><subject>Dietary Fats - metabolism</subject><subject>Down-Regulation</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Fatty acids</subject><subject>Genetic Engineering</subject><subject>Glucose</subject><subject>Glucose Intolerance - etiology</subject><subject>Glucose Intolerance - metabolism</subject><subject>Heart failure</subject><subject>Hormones</subject><subject>Insulin Resistance</subject><subject>Kinases</subject><subject>Lipid Peroxidation</subject><subject>Lipids</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Metabolic syndrome</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mitochondria - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Muscle Cells - metabolism</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Musculoskeletal system</subject><subject>Natriuretic Peptide, Brain - metabolism</subject><subject>Natriuretic Peptides - metabolism</subject><subject>Obesity</subject><subject>Obesity - etiology</subject><subject>Obesity - metabolism</subject><subject>Obesity - prevention &amp; 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ITOH, Hiroshi ; NAKAO, Kazuwa ; TSUJIMOTO, Hirokazu ; TAMURA, Naohisa ; FUKUNAGA, Yasutomo ; SONE, Masakatsu ; YAMAHARA, Kenichi ; TAURA, Daisuke ; INUZUKA, Megumi ; SONOYAMA, Takuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-3f031db6bed9a9e765e6e62d5bd1b6f42fc8b36b90abfe4fe890f45032957d9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biosynthesis</topic><topic>Blood Glucose - metabolism</topic><topic>Body fat</topic><topic>Cells, Cultured</topic><topic>Cyclic GMP - metabolism</topic><topic>Diabetes</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Dietary Fats - administration &amp; dosage</topic><topic>Dietary Fats - adverse effects</topic><topic>Dietary Fats - metabolism</topic><topic>Down-Regulation</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Fatty acids</topic><topic>Genetic Engineering</topic><topic>Glucose</topic><topic>Glucose Intolerance - etiology</topic><topic>Glucose Intolerance - metabolism</topic><topic>Heart failure</topic><topic>Hormones</topic><topic>Insulin Resistance</topic><topic>Kinases</topic><topic>Lipid Peroxidation</topic><topic>Lipids</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Metabolic syndrome</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Mitochondria - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Muscle Cells - metabolism</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Musculoskeletal system</topic><topic>Natriuretic Peptide, Brain - metabolism</topic><topic>Natriuretic Peptides - metabolism</topic><topic>Obesity</topic><topic>Obesity - etiology</topic><topic>Obesity - metabolism</topic><topic>Obesity - prevention &amp; control</topic><topic>Original</topic><topic>Oxidation</topic><topic>Oxygen Consumption</topic><topic>Peptides</topic><topic>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha</topic><topic>Plasma</topic><topic>PPAR delta - metabolism</topic><topic>PPAR gamma - metabolism</topic><topic>Protein Kinases - metabolism</topic><topic>Proteins</topic><topic>Receptors, Atrial Natriuretic Factor - metabolism</topic><topic>Research design</topic><topic>Signal transduction</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription Factors</topic><topic>Transgenic animals</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MIYASHITA, Kazutoshi</creatorcontrib><creatorcontrib>ITOH, Hiroshi</creatorcontrib><creatorcontrib>NAKAO, Kazuwa</creatorcontrib><creatorcontrib>TSUJIMOTO, Hirokazu</creatorcontrib><creatorcontrib>TAMURA, Naohisa</creatorcontrib><creatorcontrib>FUKUNAGA, Yasutomo</creatorcontrib><creatorcontrib>SONE, Masakatsu</creatorcontrib><creatorcontrib>YAMAHARA, Kenichi</creatorcontrib><creatorcontrib>TAURA, Daisuke</creatorcontrib><creatorcontrib>INUZUKA, Megumi</creatorcontrib><creatorcontrib>SONOYAMA, Takuhiro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MIYASHITA, Kazutoshi</au><au>ITOH, Hiroshi</au><au>NAKAO, Kazuwa</au><au>TSUJIMOTO, Hirokazu</au><au>TAMURA, Naohisa</au><au>FUKUNAGA, Yasutomo</au><au>SONE, Masakatsu</au><au>YAMAHARA, Kenichi</au><au>TAURA, Daisuke</au><au>INUZUKA, Megumi</au><au>SONOYAMA, Takuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><addtitle>Diabetes</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>58</volume><issue>12</issue><spage>2880</spage><epage>2892</epage><pages>2880-2892</pages><issn>0012-1797</issn><eissn>1939-327X</eissn><coden>DIAEAZ</coden><abstract>Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity Kazutoshi Miyashita 1 , Hiroshi Itoh 1 , Hirokazu Tsujimoto 2 , Naohisa Tamura 2 , Yasutomo Fukunaga 2 , Masakatsu Sone 2 , Kenichi Yamahara 2 , Daisuke Taura 2 , Megumi Inuzuka 2 , Takuhiro Sonoyama 2 and Kazuwa Nakao 2 1 Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan; 2 Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan. Corresponding author: Hiroshi Itoh, hrith{at}sc.itc.keio.ac.jp . Abstract OBJECTIVE Natriuretic peptides (NPs) have been characterized as vascular hormones that regulate vascular tone via guanylyl cyclase (GC), cyclic GMP (cGMP), and cGMP-dependent protein kinase (cGK). Recent clinical studies have shown that plasma NP levels were lower in subjects with the metabolic syndrome. The present study was conducted to elucidate the roles for NP/cGK cascades in energy metabolism. RESEARCH DESIGN AND METHODS We used three types of genetically engineered mice: brain NP (BNP) transgenic (BNP-Tg), cGK-Tg, and guanylyl cyclase-A (GCA) heterozygous knockout (GCA +/− ) mice and analyzed the metabolic consequences of chronic activation of NP/cGK cascades in vivo. We also examined the effect of NPs in cultured myocytes. RESULTS BNP-Tg mice fed on high-fat diet were protected against diet-induced obesity and insulin resistance, and cGK-Tg mice had reduced body weight even on standard diet; surprisingly, giant mitochondria were densely packed in the skeletal muscle. Both mice showed an increase in muscle mitochondrial content and fat oxidation through upregulation of peroxisome proliferator–activated receptor (PPAR)-γ coactivator (PGC)-1α and PPARδ. The functional NP receptors, GCA and guanylyl cyclase-B, were downregulated by feeding a high-fat diet, while GCA +/− mice showed increases in body weight and glucose intolerance when fed a high-fat diet. NPs directly increased the expression of PGC-1α and PPARδ and mitochondrial content in cultured myocytes. CONCLUSIONS The findings together suggest that NP/cGK cascades can promote muscle mitochondrial biogenesis and fat oxidation, as to prevent obesity and glucose intolerance. The vascular hormone, NP, would contribute to coordinated regulation of oxygen supply and consumption. Footnotes The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. See accompanying commentary, p. 2726 . . Received March 15, 2009. Accepted July 28, 2009. © 2009 American Diabetes Association</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>19690065</pmid><doi>10.2337/db09-0393</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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issn 0012-1797
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language eng
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Animals
Biological and medical sciences
Biosynthesis
Blood Glucose - metabolism
Body fat
Cells, Cultured
Cyclic GMP - metabolism
Diabetes
Diabetes. Impaired glucose tolerance
Dietary Fats - administration & dosage
Dietary Fats - adverse effects
Dietary Fats - metabolism
Down-Regulation
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Fatty acids
Genetic Engineering
Glucose
Glucose Intolerance - etiology
Glucose Intolerance - metabolism
Heart failure
Hormones
Insulin Resistance
Kinases
Lipid Peroxidation
Lipids
Medical sciences
Metabolic diseases
Metabolic syndrome
Mice
Mice, Knockout
Mitochondria - metabolism
Molecular Sequence Data
Muscle Cells - metabolism
Muscle, Skeletal - metabolism
Musculoskeletal system
Natriuretic Peptide, Brain - metabolism
Natriuretic Peptides - metabolism
Obesity
Obesity - etiology
Obesity - metabolism
Obesity - prevention & control
Original
Oxidation
Oxygen Consumption
Peptides
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
Plasma
PPAR delta - metabolism
PPAR gamma - metabolism
Protein Kinases - metabolism
Proteins
Receptors, Atrial Natriuretic Factor - metabolism
Research design
Signal transduction
Trans-Activators - metabolism
Transcription Factors
Transgenic animals
Up-Regulation
title Natriuretic Peptides/cGMP/cGMP-Dependent Protein Kinase Cascades Promote Muscle Mitochondrial Biogenesis and Prevent Obesity
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