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macrophage mRNA expression of TNF-α and IL-18 was significantly upregulated, while M2 macrophage mRNA expression of Arg1 and IL-10 was downregulated in db/db mice. Kaempferol administration effectively reversed the M1-specific macrophage and M2-specific
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concentration and purity of RNA were detected, and the extracted RNA was reverse transcribed into cDNA by Takara reverse transcription kit (RR037A, Takara Bio). Then, the mRNA expression was quantitatively detected using the Takara quantitative kit (RR014A
Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark
Danish Diabetes Academy, Odense University Hospital, Odense, Denmark
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Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark
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Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark
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Department of Biomedicine, Aarhus University, Aarhus, Denmark
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Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark
Danish Diabetes Academy, Odense University Hospital, Odense, Denmark
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LightCycler SYBR Green master mix. mRNA levels of GLUT4, G0S2, CIDEC, PDE3B, ATGL, HSL, PLIN1, ANGPTL4, LPL, IL6, PTEN, PGC1A and PIK3R1 were analyzed. Beta 2 microglobulin was used as the housekeeping gene and β2 microglobulin mRNA levels were similar in both
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mainly in muscle tissue. Therefore, the expression of BCAAs-metabolizing enzymes in rat skeletal hindlimb muscles was investigated. Branched-chain α-keto acid dehydrogenase (BCKDH) and ACAD are the two rate-limiting enzymes of BCAA catabolism. The mRNA
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(Applied Biosystems ). Thereafter, an RT-PCR kit (Promega) was used to determine the target mRNA content using an RT-PCR system (Applied Biosystems), according to the manufacturer’s instructions. The primers used in this study were as follows: Pgc1a , 5
Department of Anatomy, Shanxi Medical University, Taiyuan, China
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mice (KO, catalog number: ENSMUST00000074519.12) were originally generated by GemPharmatech Co., Ltd (Nanjing, China) using CRISPR/Cas9 technology. In brief, Cas9 mRNA and gRNA (sequence, S1: 5’-ACACGGTGTGCTCCTAGCG-3’; S2: 5’-CAACCAATCAGCGAGGCCGC-3’; S3
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. Insulin signaling was impaired in skeletal muscle of male CG-IUGR To investigate the insulin signaling in skeletal muscle of male CG-IUGR, the protein and mRNA level of insulin receptor (IR)-β and insulin receptor substrate (IRS)-1, two canonical
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) and chemerin (−/−) mice at DNA level. The mRNA levels of chemerin in (C) gastrocnemius and (D) liver of WT and chemerin (−/−) mice. (E) The protein levels of chemerin in multiply organs of WT and chemerin (−/−) mice. eWAT, epididymal white adipose
Department of Endocrinology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
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protein expression levels ( Fig. 2C , D and E ). Figure 2 Effects of palmitate and oleate on mRNA and total protein expressions of K ATP channels. Cells were exposed to 0.5 mM PA or OA for 48 h and then washed out for 24 h with vehicle. qRT
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, HFD, and HGD groups ( Fig. 4C , D and E , P < 0.05). These data suggested that inhibitory neurotransmitters (NO) played a critical role in colonic neuromuscular relaxation in the HGD group. Next, the mRNA and protein expression levels of nNOS were