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Minispec mq7

Manufactured by Bruker
Sourced in United States

The Minispec mq7.5 is a compact, benchtop nuclear magnetic resonance (NMR) analyzer developed by Bruker. It is designed for rapid, non-invasive analysis of various materials and samples. The Minispec mq7.5 provides quantitative measurements without the need for sample preparation.

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7 protocols using minispec mq7

1

Comprehensive Metabolic Phenotyping of Mice

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At 4, 8 and 16 wk post-surgery the mice were analyzed for body composition using an NMR-based instrument (Minispec mq7.5, Bruker Optics). At 4 and 16 wk post-surgery, mice were placed in TSE cages for metabolic phenotyping (PhenoMaster, TSE Systems). After 24 hours of acclimation, mice were continuously monitored for food and water intake, locomotor activity, and energy expenditure over 4 days. Ambient temperature was maintained at 20–23°C and the airflow rate through the chambers was adjusted to maintain an oxygen differential around 0.3% at resting conditions. Metabolic parameters including VO2, respiratory exchange ratio, and energy expenditure were assessed via indirect calorimetry by comparing O2 and CO2 concentrations relative to a reference cage.
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2

Body Composition and Metabolic Profiling

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Body composition was measured 12 weeks post-surgery using a nuclear magnetic resonance-based instrument (Minispec mq7.5, Bruker Optics, Billerica, MA, USA). Mice were then acclimated in TSE Cages (PhenoMaster, TSE Systems, Chesterfield, MT, USA) for 24 h, followed by 3 days of continuous measurement of food and water intake, locomotor activity, energy expenditure and respiratory exchange ratio (RER). The final 24-h cycle was used for data analysis. Ambient temperature was maintained at 20–23 °C and the airflow rate through the chambers was adjusted to maintain an oxygen differential around 0.3% at resting conditions.
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3

Metabolic Phenotyping in Mice

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Body weight was measured weekly in a single-occupant cage with ALPHA-dri bedding. Body composition in 4 month old mice was assessed by nuclear magnetic resonance (minispec mq7.5, Bruker Optics, Billerica, Massachusetts) to determine the percentage of fat mass, as previously described [55 (link)]. Glucose tolerance tests (GTT) and insulin tolerance tests (ITT) were done as previously described[46 (link)]. Briefly, following overnight fast, tail blood glucose was measured using a mouse-specific glucometer (AlphaTRAK, Abbott, Abbott Park, Illinois) before and 15, 30, 60, 90 and 120 min after dextrose (2g/kg, i.p.) injection. For ITT, following a 4 hour fast, mice were injected with recombinant insulin (0.75U/kg, i.p.). Tail blood glucose was measured again at specified time points. Food intake was measured every week until mice were 4 months old.
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4

Obesity Induction and BAPSP1 Treatment

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Male mice on a C57BL/6 background were purchased from the Animal Core Facility of Nanjing Medical University and housed on a 12/12 h light/dark cycle with free access to food and water. Mice were maintained in cages exposed to room air (25 °C) or in cages inside temperature-controlled chambers (16 °C) as indicated in the figure legend. After acclimation to the facility (1 week), mice were fed a high-fat diet with 60% of the calories from fat (Research Diets) starting at 7–8 weeks of age to induce obesity. Synthesized BAPSP1 or vehicle (saline) was administered by intraperitoneal (i.p.) injection twice a week for 16 weeks. Body weight and food intake were monitored daily. The total amounts of fat and lean mass in HFD-fed mice were assessed with a nuclear magnetic resonance imaging (MRI) system (Minispec mq 7.5, Bruker Optics).
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5

Evaluating Body Composition and Metabolism

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Body composition was determined in vivo with a nuclear magnetic resonance analyzer (minispec mq7.5, Bruker). For metabolic measurements, mice were acclimated for 1–2 days and then monitored for 48 h using a PhenoMaster System (TSE Systems) fitted with indirect calorimetry and activity monitors to measure activity and energy expenditure. Due to locomotor dysfunction of NYKO mice, food was provided from the bottom of the cage during the measurements for both genotypes.
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6

Comprehensive Metabolic and Physiological Assessment in Mice

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The body weight of the mice was assessed weekly. Naso-anal length and body weight after 25 weeks of treatment were calculated to evaluate BMI. The body composition of lean and fat mass was assessed by NMR spectroscopy using the Minispec-mq7.5 (Bruker Corporation, Billerica, MA, USA). An oral glucose tolerance test was performed after 8 weeks of treatment. Mice were fasted for 6 h and fasting blood glucose values were assessed. Then animals received a 40% glucose solution to a final dose of 1 mg glucose/g body weight. Blood glucose values were measured after 0, 5, 15, 30, 60 and 120 min after glucose application using an ACCU-CHEK glucometer (Roche Diabetes Care Deutschland, Germany).
Blood pressure and heart rate were measured using a non-invasive, photoplethysmographic method (BP-2000 Blood Pressure Analysis System, version 2015.1.29, Visitech Systems, Apex, USA). The measurements were performed for 10 days in a row at the same time of day. There were three single measurements each day. For statistical analysis with the manufacturer’s software (BP-2000 Analysis Software) the mean values of the previous 3 days were used since the mice needed to become accustomed to the method in order to generate valid values. The systolic blood pressure was measured by a non-invasive computerised tail cuff system (Visitech System BP-2000, Apex, USA) as described previously [20 (link)].
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7

Nfatc3 Knockout Mice for Diet-Induced Obesity

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Nfatc3-/-mice that were backcrossed to C57BL/6 mice as described before (Oukka et al. 1998) (link) were obtained from Jackson Laboratory (Stock number 010589). Nfatc3+/heterozygous mice were bred to generate age-matched Nfatc3-/-and WT littermates. All mice were maintained in the Specific Pathogen Free (SPF) mice facility of Second Xiangya Hospital under a 12-h light/darkness cycle. At age 6 weeks, male mice were fed either a normal diet (ND, SLA-COM) containing 4% (wt/wt) total lipids or a HFD (Research Diets) containing 60% kcal fat for different weeks. Total body fat content was measured by nuclear magnetic resonance with the Minispec Mq7.5 (Bruker, Karlsruhe, Germany). All animal experiments were performed according to the protocols approved by the Animal Care Research Committee of Second Xiangya Hospital of Central South University. Anti-phospho-Akt (S473) and anti-beta-actin antibody were from Cell Signaling Technology.
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