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Sitagliptin

Manufactured by MSD
Sourced in China, Poland

Sitagliptin is a lab equipment product manufactured by MSD. It is a dipeptidyl peptidase-4 (DPP-4) inhibitor, which is a type of enzyme involved in the regulation of blood sugar levels.

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4 protocols using sitagliptin

1

Pharmacological Modulators of Bile Acid Signaling

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The DPP-4 inhibitors diprotin A, FFA-free Bovine Serum Albumine (BSA), Chenodeoxycholic acid (CDCA), TβMCA, Exendin-4(9-39), Phloretin, DMSO and CMC were purchased from Sigma-Aldrich (St Quentin-Fallavier, France). Sitagliptin was purchased from MSD. The synthetic FXR agonist GW4064 was purchased from Tocris (R&D Systems, Lille, France). For in vitro or ex vivo experiments, CDCA, TβMCA and GW4064 were dissolved in dimethylsulfoxide (DMSO) at 0.1% final. For in vivo experiments, GW4064 was dissolved in 1% Carboxymethylcellulose (CMC) and Exendin-4(9-39) was dissolved in NaCl 0.9%. Chow and high fat diets were purchased from UAR (A04, Villemoison/Orge, France). Colesevelam HCl was a kind gift of Daiichi Sankyo.
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2

Insulin Therapy for Glycemic Control

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During the run‐in period, participants were hospitalized, and stopped previous OADs except for MET (no changed dosage), then received short‐term intensive insulin therapy with Gla (Lantus; Sanofi) and bolus insulin glulisine (Apidra; Sanofi). All participants who had an FPG of less than 7.0 mmol/L and 2‐hour postprandial glucose (PPG) of less than 10.0 mmol/L in the last 2 consecutive days of the run‐in period were discharged from hospital and randomly assigned (1:1) to receive once‐daily basal insulin glargine in combination with a dipeptidyl peptidase‐4 inhibitor (DPP4i; either sitagliptin [Januvia; MSD, Beijing, China] or vildagliptin [Galvus; Novartis, Beijing, China]) or twice‐daily premixed insulin aspart (Asp30; Novolog Mix 70/30; Novo Nordisk, Tianjin, China). All participants continued to receive their background MET. Randomization was performed using centralized interactive response technology and was stratified by baseline sulphonylurea/glinide use and HbA1c level at screening (>9.0% or ≤9.0% [>75 or ≤75 mmol/mol]). While participants, investigators and site staff remained unmasked to treatment, the statistician and sponsor were masked to the treatment assignment until after database lock and completion of analyses.
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3

Pharmacological Modulators of Bile Acid Signaling

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The DPP-4 inhibitors diprotin A, FFA-free Bovine Serum Albumine (BSA), Chenodeoxycholic acid (CDCA), TβMCA, Exendin-4(9-39), Phloretin, DMSO and CMC were purchased from Sigma-Aldrich (St Quentin-Fallavier, France). Sitagliptin was purchased from MSD. The synthetic FXR agonist GW4064 was purchased from Tocris (R&D Systems, Lille, France). For in vitro or ex vivo experiments, CDCA, TβMCA and GW4064 were dissolved in dimethylsulfoxide (DMSO) at 0.1% final. For in vivo experiments, GW4064 was dissolved in 1% Carboxymethylcellulose (CMC) and Exendin-4(9-39) was dissolved in NaCl 0.9%. Chow and high fat diets were purchased from UAR (A04, Villemoison/Orge, France). Colesevelam HCl was a kind gift of Daiichi Sankyo.
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4

Pharmacological agents for animal studies

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Sitagliptin (Januvia—tablets 100 mg) was purchased from MSD (Warsaw, Poland), heparin (Heparinum WZF—ampoules 25,000 U/5 mL) from Polfa Warszawa (Warsaw, Poland), ketamine hydrochloride (Bio-ketan) from Vetoquinol Biowet (Gorzów Wlkp, Poland), medetomidine hydrochloride (Domitor, ampoules 1 mg/mL) from Orion Pharma (Warsaw, Poland), butorphanol tartrate (Morphasol, ampoules 4 mg/mL) from aniMedica GmbH (Frankfurt am Main, Germany), Ringer solution from Polfa Lublin S.A. (Lublin, Poland), and solution of 0.9% sodium chloride was obtained from Polpharma S.A. (Starogard Gdański, Poland).
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