Chlorogenic Acid Improves Late Diabetes through Adiponectin Receptor Signaling Pathways in db/db Mice
Identifieur interne : 000A59 ( Main/Merge ); précédent : 000A58; suivant : 000A60Chlorogenic Acid Improves Late Diabetes through Adiponectin Receptor Signaling Pathways in db/db Mice
Auteurs : Shasha Jin ; Cuiqing Chang ; Lantao Zhang ; Yang Liu ; Xianren Huang ; Zhimin ChenSource :
- PLoS ONE [ 1932-6203 ] ; 2015.
Abstract
The aim of this study was to examine the effects of chlorogenic acid (CGA) on glucose and lipid metabolism in late diabetic
Url:
DOI: 10.1371/journal.pone.0120842
PubMed: 25849026
PubMed Central: 4388831
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PMC:4388831Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Chlorogenic Acid Improves Late Diabetes through Adiponectin Receptor Signaling Pathways in <italic>db/db</italic>
Mice</title>
<author><name sortKey="Jin, Shasha" sort="Jin, Shasha" uniqKey="Jin S" first="Shasha" last="Jin">Shasha Jin</name>
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<author><name sortKey="Liu, Yang" sort="Liu, Yang" uniqKey="Liu Y" first="Yang" last="Liu">Yang Liu</name>
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<author><name sortKey="Huang, Xianren" sort="Huang, Xianren" uniqKey="Huang X" first="Xianren" last="Huang">Xianren Huang</name>
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<author><name sortKey="Chen, Zhimin" sort="Chen, Zhimin" uniqKey="Chen Z" first="Zhimin" last="Chen">Zhimin Chen</name>
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<front><div type="abstract" xml:lang="en"><p>The aim of this study was to examine the effects of chlorogenic acid (CGA) on glucose and lipid metabolism in late diabetic <italic>db/db</italic>
mice, as well as on adiponectin receptors and their signaling molecules, to provide evidence for CGA in the prevention of type 2 diabetes. We randomly divided 16 female <italic>db/db</italic>
mice into <italic>db/db</italic>
-CGA and <italic>db/db</italic>
-control (CON) groups equally; db/m mice were used as control mice. The mice in both the <italic>db/db</italic>
-CGA and db/m-CGA groups were administered 80 mg/kg/d CGA by lavage for 12 weeks, whereas the mice in both CON groups were given equal volumes of phosphate-buffered saline (PBS) by lavage. At the end of the intervention, we assessed body fat and the parameters of glucose and lipid metabolism in the plasma, liver and skeletal muscle tissues as well as the levels of aldose reductase (AR) and transforming growth factor-β1 (TGF-β1) in the kidneys and measured adiponectin receptors and the protein expression of their signaling molecules in liver and muscle tissues. After 12 weeks of intervention, compared with the <italic>db/db</italic>
-CON group, the percentage of body fat, fasting plasma glucose (FPG) and glycosylated hemoglobin (HbA1c) in the <italic>db/db</italic>
-CGA group were all significantly decreased; TGF-β1 protein expression and AR activity in the kidney were both decreased; and the adiponectin level in visceral adipose was increased. The protein expression of adiponectin receptors (ADPNRs), the phosphorylation of AMP-activated protein kinase (AMPK) in the liver and muscle, and the mRNA and protein levels of peroxisome proliferator-activated receptor alpha (PPAR-α) in the liver were all significantly greater. CGA could lower the levels of fasting plasma glucose and HbA1c during late diabetes and improve kidney fibrosis to some extent through the modulation of adiponectin receptor signaling pathways in <italic>db/db</italic>
mice.</p>
</div>
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