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mr-compatible small-animal monitoring and gating system  (SA Instruments)

 
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    SA Instruments mr-compatible small-animal monitoring and gating system
    Mr Compatible Small Animal Monitoring And Gating System, supplied by SA Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/small-animal+monitor+system/rectal+temperature+probe/pm40508134-146-9-24
    Average 90 stars, based on 1 article reviews
    mr-compatible small-animal monitoring and gating system - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Cerebral glutamine metabolism under hyperammonemia determined in vivo by localized 1 H and 15 N NMR spectroscopy
    Article Snippet: During the MRS experiments, respiration rate, heart rate, and blood pressure were monitored by a small-animal monitor system (SA Instruments, New York, NY, USA).

    Article Title: A new rat model of creatine transporter deficiency reveals behavioral disorder and altered brain metabolism
    Article Snippet: Body temperature (kept at 37.5 ± 1.0 °C using circulating warm water) and respiration were monitored continuously by a small-animal monitor system (SA Instruments, New York, USA).

    Article Title: In Vivo Longitudinal (1)H MRS Study of Transgenic Mouse Models of Prion Disease in the Hippocampus and Cerebellum at 14.1 T.
    Article Snippet: Respiration rate was monitored by a small-animal monitor system (SA Instruments Inc., New York, NY, USA).

    Article Title: MP-PCA denoising for diffusion MRS data: promises and pitfalls.
    Article Snippet: The respiration rate and body temperature were monitored using a small-animal monitor system (SA Instruments, New York, NY, USA).

    Article Title: Fast High-Resolution Metabolite Mapping in the rat Brain Using 1 H-FID-MRSI at 14.1 T.
    Article Snippet: Magnetic resonance spectroscopic imaging (MRSI) enables the simultaneous noninvasive acquisition of MR spectra from multiple spatial locations inside the brain.. Although 1HMRSI is increasingly used in the human brain, it is not yet widely applied in the preclinical setting, mostly because of difficulties specifically related to very small nominal voxel size in the rat brain and low concentration of brain metabolites, resulting in low signaltonoise ratio (SNR).. In this context, we implemented a free induction decay 1HMRSI sequence (1HFIDMRSI) in the rat brain at 14.1 T. We combined the advantages of 1HFIDMRSI with the ultrahigh magnetic field to achieve higher SNR, coverage, and spatial resolution in the rat brain and developed a custom dedicated processing pipeline with a graphical user interface for Bruker 1HFIDMRSI: MRS4Brain toolbox.



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    Image Search Results


    Efficacy of nebulized hUCMSC-EVs in treating injury-induced lung fibrosis in mice. a A schematic representation of the animal experiments is provided. On day 1, mice were administered intratracheally with bleomycin (BLM; 1.5/2.5 mg/kg body weight) or an equivalent volume of saline solution. After 2 h, three groups of mice challenged with BLM underwent nebulization with hUCMSC-EVs at three different doses (2.5 × 10 7 , 7.5 × 10 7 , 2.25 × 10 8 particles), while one group of BLM-challenged mice and the control group (without BLM challenge) received the same volume of saline treatment. Mice were randomly assigned to 5 groups ( n = 5 per group). b Kaplan-Meier survival curves of mice receiving different interventions (BLM; 2.5 mg/kg body weight). c Micro-CT images of lungs from mice in the experiment. The images were taken at 18th day post-injury. (BLM; 1.5 mg/kg body weight, UC-EVs represents 2.5 × 10 7 , 1 × EVs) d Lung volumes evaluated based on the three-dimensional reconstruction data from micro-CT; n = 5, p values were calculated. e Breath distention and f Oxygen saturation levels were measured by the MouseOx Small Animal Vital Signs Monitor. P values were calculated by two two-tailed t-test; n = 5. g The lung weight histogram depicts the weight of entire lung tissue in each group. h The lung coefficient was determined as wet lung weight (g) divided by total body weight (g). i Representative histological lung sections from mice at 21 days post-injury stained with H&E and Masson’s trichrome. Scale bars, 500 μm or 50 μm. j Quantitative evaluation of fibrotic severity with the Ashcroft score in lungs of mice receiving different interventions. The Ashcroft scores were calculated based on the H&E staining. The severity of fibrotic alterations in each section was assessed as the mean score in the observed microscopic fields. Ten fields per section were selected and the scores were marked by two evaluators and averaged as the final values. Quantitative PCR analyses for the relative mRNA levels of Col1a1 ( k ), Fibronectin ( l ) and Col3a1 ( m ), in the lung tissues of mice. Western blots of Fibronectin ( n ) and Col3a1 ( o ) in the lungs ( n = 3). GAPDH was used as a loading control. Molecular weight was labeled

    Journal: Signal Transduction and Targeted Therapy

    Article Title: Clinical investigation on nebulized human umbilical cord MSC-derived extracellular vesicles for pulmonary fibrosis treatment

    doi: 10.1038/s41392-025-02262-3

    Figure Lengend Snippet: Efficacy of nebulized hUCMSC-EVs in treating injury-induced lung fibrosis in mice. a A schematic representation of the animal experiments is provided. On day 1, mice were administered intratracheally with bleomycin (BLM; 1.5/2.5 mg/kg body weight) or an equivalent volume of saline solution. After 2 h, three groups of mice challenged with BLM underwent nebulization with hUCMSC-EVs at three different doses (2.5 × 10 7 , 7.5 × 10 7 , 2.25 × 10 8 particles), while one group of BLM-challenged mice and the control group (without BLM challenge) received the same volume of saline treatment. Mice were randomly assigned to 5 groups ( n = 5 per group). b Kaplan-Meier survival curves of mice receiving different interventions (BLM; 2.5 mg/kg body weight). c Micro-CT images of lungs from mice in the experiment. The images were taken at 18th day post-injury. (BLM; 1.5 mg/kg body weight, UC-EVs represents 2.5 × 10 7 , 1 × EVs) d Lung volumes evaluated based on the three-dimensional reconstruction data from micro-CT; n = 5, p values were calculated. e Breath distention and f Oxygen saturation levels were measured by the MouseOx Small Animal Vital Signs Monitor. P values were calculated by two two-tailed t-test; n = 5. g The lung weight histogram depicts the weight of entire lung tissue in each group. h The lung coefficient was determined as wet lung weight (g) divided by total body weight (g). i Representative histological lung sections from mice at 21 days post-injury stained with H&E and Masson’s trichrome. Scale bars, 500 μm or 50 μm. j Quantitative evaluation of fibrotic severity with the Ashcroft score in lungs of mice receiving different interventions. The Ashcroft scores were calculated based on the H&E staining. The severity of fibrotic alterations in each section was assessed as the mean score in the observed microscopic fields. Ten fields per section were selected and the scores were marked by two evaluators and averaged as the final values. Quantitative PCR analyses for the relative mRNA levels of Col1a1 ( k ), Fibronectin ( l ) and Col3a1 ( m ), in the lung tissues of mice. Western blots of Fibronectin ( n ) and Col3a1 ( o ) in the lungs ( n = 3). GAPDH was used as a loading control. Molecular weight was labeled

    Article Snippet: Pulse distention, breath distention, and oxygen saturation levels were measured by the MouseOx Small Animal Vital Signs Monitor (STARR, USA) following the manufacturer’s instructions ( https://www.starrlifesciences.com/ ).

    Techniques: Saline, Control, Micro-CT, Two Tailed Test, Staining, Real-time Polymerase Chain Reaction, Western Blot, Molecular Weight, Labeling