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Echomri 100tm

Manufactured by Echo Medical Systems
Sourced in United States

The EchoMRI-100TM is a compact, high-performance medical imaging system designed for laboratory research. It utilizes magnetic resonance imaging (MRI) technology to capture detailed images of small samples and specimens. The system provides accurate and reliable data for a variety of scientific investigations.

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8 protocols using echomri 100tm

1

In Vivo Body Composition Monitoring

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In vivo magnetic resonance imaging (MRI) using EchoMRI-100TM (Echo medical Systems, Houston, Texas) was performed to measure fat mass and lean mass at the beginning of the experiment, after four initial weeks of treatment and at the end point.
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2

Metabolic Regulation in Gadd45b Knockout Mice

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Wild type (WT) and Gadd45b+/– mice14 (link) in the C57BL/6J background were purchased from the Jackson Laboratory (Bar Harbor, ME, USA). Gadd45b–/– knockout (KO) mice were generated by crossbreeding Gadd45b+/– mice (stock number: 013101). Genotyping primers for KO mice are 10936: GCAACCCCAGTAACTTTGGA; 10937: CCTGCAGGAGAGAAGGAGTG; oIMR7996: CTTCCATTTGTCACGTCCTG, provided by the Jackson Laboratory. Eight-week-old male WT and KO mice were subjected to 60% calories high fat diet (ENVIGO #TD.06414, containing 23.5% protein, 27.3% carbohydrate, and 34.3% fat, Harlan Laboratories, Madison, MI, USA) for 17 weeks. Mice received once per week intraperitoneal injections of 1,4-bis[2-(3,5-dichloropyridyloxy)] benzene (TCPOBOP, 0.5 mg/kg) or vehicle (DMSO) as we have previously described10 (link). Body composition was analyzed in live animals using EchoMRI-100TM from Echo Medical Systems (Houston, TX, USA). Mice were sacrificed 24 h after the last dose of drug. The use of animals in the study was approved by the Institutional Animal Care and Use Committee at the University of Pittsburgh (Pittsburgh, PA, USA).
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3

Generation of Liver-specific CA-AHR Mice

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To generate the TetRE-CA-AHR transgenic mice, constitutively activated human AHR (CA-AHR) was constructed by deleting the human AHR region encoding the minimal ligand-binding domain (amino acids 273–432),(2 (link)) and then placed downstream of a minimal cytomegalovirus promoter fused to the tetracycline responsive element (TetRE). Pronuclear microinjection of the transgene into the C57BL/6 embryos was performed at the University of Pittsburgh Transgenic Core Facility. The TetRE-CA-AHR mice were bred with the FABP-tTA mice (16 (link)) to generate liver-specific FABP-CA-AHR mice. AHR knockout (AHRKO) mice in C57BL/6 background were purchased from Taconic (Hudson, NY). Mice were fed with standard chow from PMI Nutrition (St. Louis, MO) or HFD (S3282) from Bio-serv (Frenchtown, NJ). In the HFD model, 6-week-old mice received HFD for 12 weeks in most of the experiments, except that when adenovirus were used, mice were treated with HFD for 6 weeks before viral infection. When necessary, doxycycline (DOX; 1 mg/ml) was given in drinking water. The food intake was measured for 7 days after 10 weeks of HFD feeding. Body composition was analyzed using EchoMRI-100TM from Echo Medical Systems (Houston, TX). The use of mice in this study complied with relevant federal guidelines and institutional policies.
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4

Dietary Cycling Prevents Obesity in Mice

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All procedures performed on animals were approved by the Institutional Animal Care and Use Committee at the University of Georgia and the methods were carried out in accordance with the approved protocol #A2014-07-008-Y1-A0. C57BL/6 mice (male) were purchased from Charles River (Wilmington, MA). For the prevention study, two groups of C57BL/6 mice with a body weight of 25 g were fed an HFD or regular chow continuously for eight weeks, while three groups of mice on an alternating diet (10 per group) were first fed five days of an HFD followed by either one, two, or five days of a regular diet. They were then switched back to five days of HFD feeding to start the second cycle. The repeating feeding cycles were maintained for a total of eight weeks. On day 56, five mice were sacrificed, and the remaining five were placed on the opposite diet to that which they were on at day 56 for one day and then sacrificed. For the treatment study, age-matched obese or normal C57BL/6 mice (male, average 55 g for obese mice) were fed an HFD, a regular diet, or an alternating diet for five weeks and sacrificed on day 36. Body weight and food intake were monitored daily and their body composition was determined using EchoMRI-100TM from Echo Medical Systems (Houston, TX).
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5

NRG4 Gene Delivery in Obese Mice

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All procedures performed on animals were approved by the Institutional Animal Care and Use Committee at the University of Georgia, Athens, Georgia and the methods were carried out in accordance with the approved protocol #A2014-07-008-Y1-A0. For the prevention study, C57BL/6 mice (male, 8-week old) were housed under standard conditions with a 12 h light-dark cycle and fed an HFD for a total of 9 weeks. For the treatment study, mice were first fed an HFD for 25 weeks, reaching a body weight of 56 grams on average. Gene transfer was performed on the obese mice and the treated animals were continued on an HFD for additional 3 weeks. Hydrodynamic gene delivery was performed according to a pre-established procedure10 (link)41 (link)42 (link). Briefly, an appropriate volume of saline solution (equivalent to 8% lean mass) containing 20 μg pLIVE-NRG4 or pLIVE-SEAP was injected through the tail vein within 5–8 sec. The body weight of each mouse was measured on an electronic balance, and body composition was analyzed using an EchoMRI-100TM (Echo Medical Systems, Houston, TX). Food intake per mouse was calculated based on the amount consumed divided by time and the number of mice per cage. Blood was collected at the desired time using a Microvette-CB300-LH. Rectal temperature of the mice was measured at the desired time using a specially designed Thermocouple Meter.
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6

In vivo body composition analysis via MRI

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In vivo MRI using EchoMRI-100TM (Echo Medical Systems, Houston, TX) was performed in order to measure body fat and lean content.
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7

Maternal High-Fat Diet's Impact on Pregnancy

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All studies using mice were approved by an Institutional Animal Care and Use Committee (IACUC) at the University of Kentucky and were conducted in accordance with the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals. Female C57BL/6J mice (8 weeks of age; Jackson Laboratory, Bar Harbor, ME, stock # 000664) were randomly assigned to receive, ad libitum, either a high fat (HF, 60% kcal from fat; D12492, Research Diets Inc, New Brunswick, NJ, USA) or a control low fat (LF, 10% kcal from fat; D12450B, Research Diets Inc, New Brunswick, NJ, USA) diet for 8 weeks (n = 30 mice/diet group). Following quantification of body weight (Ohaus portable digital scale), and fat and lean mass (EchoMRI-100 T M , Echo Medical Systems, Houston, TX, USA), all female mice were crossed with male mice of the same strain and diet (day 0). After 2 days, all females were transferred to single housing for the duration of the study. Mice that did not become pregnant were considered non-pregnant controls. Echocardiography was performed on day 18, making the gestational time frame between day 15 and 17 of the 21-day murine gestational cycle (corresponding with third trimester in humans [9] ).
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8

Mouse Body Composition and Metabolic Efficiency

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Weekly measurements of body weight, food intake, and water intake were made for all mice. Food intake in kJ/day was calculated by dividing weekly food intake by 7 and multiplying by the stated energy density of the chow diet (11.18 kJ/g). The theoretical thermic effect of food was calculated using the thermic effects of fat (2.5%), carbohydrates (7.5%) and protein (25%) (Trumbo et al., 2002) . For mice receiving a two-week vehicle or corticosterone treatment, body composition (EchoMRI-100 TM, Echo Medical Systems, USA) and fecal corticosterone concentrations (see below) were measured before the treatment and after two weeks of treatment. For mice receiving a twelve-week vehicle or corticosterone treatment, body composition, and fecal corticosterone concentrations were measured before the treatment and after 2, 7 and 12 weeks of treatment. Metabolic efficiency (% of energy intake stored in the body) was calculated as follows: ðDfat massðkJÞ + Dlean massðkJÞÞ=food intakeðkJÞ x100, where the energy densities for fat mass and lean mass were 39 kJ/g respectively 5 kJ/g.
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