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 |
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Zusammenfassung: | 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 |
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ISSN: | 0012-1797 1939-327X |
DOI: | 10.2337/db09-0393 |