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Female sprague dawley rats

Manufactured by Taconic Biosciences
Sourced in United States, United Kingdom, Denmark

Female Sprague-Dawley rats are a widely used laboratory animal model. They are reliable, robust, and well-characterized. These rats are commonly used in a variety of research applications.

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16 protocols using female sprague dawley rats

1

Dietary Iron Impacts Mammary Tumors

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Female Sprague Dawley rats were obtained from Taconic Farms (Germantown, NY, USA) at 21 days of age, housed three per cage, and maintained in an environmentally controlled room at 22 °C with 50% relative humidity and a 12 h light/12 h dark cycle. Rats were fed a purified diet formulation that only varied in the amount of iron that was provided [47 (link)]. Details of the design of each experiment are provided with the presentation of results. The methods for the detection and classification of mammary tumors have been previously described [48 ,49 (link)].
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2

Metabolic Profiling of Lean Rats

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Female Sprague–Dawley rats (104-140 g; 5 weeks of age) possessing a polygenic predisposition for leanness and increased physical activity (lean/activity-prone, LAP) were purchased from Taconic Farms Inc. (Hudson, New York). Rats were housed individually in suspended wire cages at the University of Colorado Anschutz Medical Campus. All rats had free access to water in a temperature (22–25 °C) and humidity (30–40 %) controlled room with a 12 h light–dark cycle (lights off at 1300). All procedures were approved by the institutional animal care and use committee. Rats were allowed to acclimatize for 5 days, during which they had free access to a moderate fat (MF) diet (25 % kcal fat, 21 % kcal protein, 54 % kcal carbohydrate; Research Diets #D07091301, New Brunswick, NJ).
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3

Sprague-Dawley Rat Experiments

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Female Sprague-Dawley rats (200–250g) were purchased from Taconic (Rensselaer, NY). All experiments were performed according to protocols approved by the UPR Medical Sciences Campus Animal Care and Use Committee and conformed to the National Research Council Guide for the Care and Use of Laboratory Animals published by the NIH (2011, eighth edition).
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4

Isolating Rat Cecum Mucosa-Submucosa

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Female Sprague–Dawley rats (190–250 g) were purchased
from Taconic Biosciences (Rensselaer, NY) and housed at 23 ± 1
°C on a 12:12-h lightdark cycle with free access to water and a standard
rodent diet. All animal protocols were approved by the University of California
Riverside Institutional Animal Care and Use Committee. Experiments reported in
this study used rat cecum, the predominant site of microbial fermentation along
the distal intestine. Rats were euthanized by gradual displacement of air with
CO2. The cecum was isolated, opened along the mesenteric border,
and rinsed in an ice-cold Parson’s solution comprised of: 110 mM NaCl,
25 mM NaHCO3, 4 mM KCl, 2 mM Na2HPO4, 1.25 mM
CaCl2, 1 mM MgSO4, and 12 mM glucose, saturated with
5% CO2/95% O2. The osmolarity of all
solutions was adjusted to match that of rat cecal stool fluid (305 mOsm) by the
addition of NaCl or water. The cecum was pinned, mucosal-side down, onto an
ice-cold Sylgard silicone tray and divided into equal halves. To preserve
viability and minimize intrinsic neural influences, the wall of the cecum was
stripped of its outer serosa and muscle layers by dissection under a
stereomicroscope to obtain a conventional mucosasubmucosa preparation.21
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5

Sprague-Dawley Rat SCI Model

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Female Sprague-Dawley rats 1.5 months of age were procured from Taconic Biosciences (Rensselaer, NY) and randomly assigned to sham (n = 7) or SCI (n = 11) groups. Baseline sensorimotor behavioral measures were obtained 1 week before sham or SCI procedures performed at 2 months. Food (standard chow) and water were provided ad libitum during the experiments, and all animal procedures were approved by the Rutgers University and Yale University institutional animal care and use committees in accordance with National Institutes of Health guidelines.
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6

Sprague-Dawley Rat Experiments

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Female Sprague-Dawley rats (200–250g) were purchased from Taconic (Rensselaer, NY). All experiments were performed according to protocols approved by the UPR Medical Sciences Campus Animal Care and Use Committee and conformed to the National Research Council Guide for the Care and Use of Laboratory Animals published by the NIH (2011, eighth edition).
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7

Pharmacological and Optogenetic Modulation of Neuronal Activity in Rat Model

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Female Sprague-Dawley rats (Taconic) were used for all drug treatment experiments. Female transgenic PV-Cre rats with Long-Evans background (NIDA IRP Transgenic Rat Project) were used for optogenetic experiments. Rats were 4-6 weeks old at the time of imaging or behavioral testing. All procedures were conducted in accordance with the institutional Animal Care and Use Committee. N for behavioral data was as follows: SAL group, 13 rats; PCP group, 6 rats; SAL + D-serine group, 5 rats; PCP + D-serine group, 6 rats. N for pharmacological treatment imaging data was as follows: SAL group, 15 movies from 5 rats; PCP group, 15 movies from 5 rats; SAL + D-serine group, 12 movies from 4 rats; PCP + D-serine group, 15 movies from 4 rats, PCP group 2 (baclofen treated), 12 movies from 4 rats, PCP + baclofen group, 12 movies from 4 rats. N for optogenetic stimulation imaging data in PV-Cre rats was as follows: Control (Ctrl) group, 20 movies from 7 rats; LED stimulation, 20 movies from 7 rats. Sample sizes (4–6 animals per group) were chosen based on similar studies19 without biasing for expected effect sizes, in order to obtain statistical significance without overpowering analysis to detect negligibly small effects.
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8

Sprague Dawley Rat Housing Protocols

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Female Sprague Dawley rats weighing 250–300 g were purchased from Taconic Farms. All rats were housed three animals per cage in temperature, humidity and light controlled environments with ad libitum access to food and water. Experimental procedures were approved by the Thomas Jefferson University IACUC and conducted in compliance with Animal Research: Reporting of In Vivo Experiments (ARRIVE) guidelines and the Society for Neuroscience’s Policies on the Use of Animals and Humans in Neuroscience Research.
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9

Dietary Glycemic Load Impact on Carcinogen-Induced Rats

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Female Sprague Dawley rats were obtained from Taconic Farms, Germantown, NY at 19 DOA and injected with 37.5 mg of 1-methyl-1-nitrosourea/kg body weight, intraperitoneally, at 20 DOA as previously described [35 (link)]. All animals were fed purified AIN-93G diet for 1 week post carcinogen injection and were then randomized to one of two dietary groups (n = 50 rats/diet group) and fed either the low or high glycemic load purified diet formulated using corn starch that differed in its content of resistant starch (detailed formulation, Supplementary Table S2).
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10

Sprague-Dawley Rat Husbandry and Approvals

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Female Sprague-Dawley rats weighing 200-250g, (Taconic, Denmark) were used. All rats received food and water ad libitum and were kept in a 12-hour day—night cycle at a constant environmental temperature of 21°C and 65% humidity. All procedures were approved in advance by the Malmö/Lund Animal Ethics Committee on Animal Experiments (registration number M95-11), regulated by the code of regulations of the Swedish Board of Agriculture. These regulations, including directives from the European Union, follow the law on animal welfare legislated by the Swedish parliament. The animals were kept in the animal facilities of the Biomedical Center at Lund University and experiments were carried out at the Section for Neurophysiology.
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