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Sprague dawley ofa rats

Manufactured by Charles River Laboratories
Sourced in France

The Sprague-Dawley OFA rats are a widely used outbred albino rat strain. They are a general-purpose rat model commonly used in research and testing across various fields.

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7 protocols using sprague dawley ofa rats

1

Rat Behavior Experiments Protocol

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All experiments were performed in agreement with the European Community Council Directive of 22nd September (010/63/UE) and the local ethics committee (“Comité d’éthique en matière d’expérimentation animale n°59, ‘Paris Centre et Sud’”, project agreement APAFIS#13363-2018020321116321-V3). Experiments were performed in accordance with these guidelines and regulations previously quoted, and within the strict project agreed by the ethic committee and the French ministry of Research. Experiments required 26 male OFA Sprague Dawley rats (Charles River, Saint-Germain-Nuelles, France) weighing 225–250 g at the beginning of the experiment. Animals arrived in the laboratory two weeks before the experiment. They were kept two per cage at a constant temperature of 22 °C, with a 12-hours alternating light/dark cycle (light 8 AM – 8 PM). Food and water were available ad libitum.
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2

Adjuvant-Induced Arthritis in Sprague Dawley Rats

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Adjuvant-Induced Arthritis (AIA) is a well characterized31 ,32 and clinically-relevant model of polyarthritis induced in male OFA Sprague Dawley rats (Charles River, Saint-Germain-Nuelles, France) by a bilateral injection (50 µl in each hind paw under isoflurane anesthesia) of a mixture of 6 mg of Mycobacterium butyricum (Difco Laboratory, USA) suspended in 1 mL of an emulsion of liquid paraffin/0.9% NaCl/Tween80 (6:4:1 v/v/v). In parallel, control animals received 50 µL of saline. This study required two groups of arthritic rats (N = 9 for the group n°1, required for the main part of the study and N = 8 for the group n°2, required for the validation of the ROC analysis) and one group of control rats (N = 9).
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3

Sprague-Dawley Rat Euthanasia Protocol

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All research procedures were performed according to an experimental protocol following international guidelines (86/609/EEC) and approved by the ethic committee of VetAgro Sup. A total of 97 eight-week old male and female OFA-Sprague-Dawley rats (Charles River, l'Arbresles, France) were used in the present study. All rats were acclimatized for at least five days and housed in the animal facility, four rats per cage as already reported in details 20 (link) . Just before blood sampling, rats were anesthetized with isoflurane and euthanized with CO2 immediately after sampling.
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4

Deep Brain Stimulation for Animal Research

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Efforts were made to minimize the number of animals used, as well as their suffering. In this attempt, in vivo experiments were not replicated for cell proliferation and electrophysiological experiments. However, the same DBS treatment in control has been reproduced several times throughout the manuscript thereby demonstrating the reproducibility of our data. Sample size for each experiment was calculated using an alpha of 0.05 and beta of 0.20. All animals were randomized for each experiment and the experiments were blinded to the experimenter. Experiments were carried out in male Sprague–Dawley OFA rats (Charles Rivers, France) weighing from 260 to 320 g on the day of the experiment. Experiments were performed in compliance with the European Communities Council (86/609 ECC) for the care and use of laboratory animals and ARRIVE guidelines and with the approval of the Regional Animal Care Committees (University Lyon 1, CREEA Côte d'Azur).
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5

Cirrhosis Induction in Rat Models

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In the decompensated chronic liver disease model, cirrhosis was induced by BDL. Male Sprague-Dawley OFA rats (Charles River Laboratories, L’Arbresle, France) weighing 200–220 g were anaesthetized with inhaled isoflurane and the common bile duct was occluded by double ligature with a 4–0 silk thread. The bile duct was then resected between the two ligatures. Animals received weekly intramuscular vitamin k1 to decrease mortality from bleeding56 (link).
To obtain an early cirrhosis model, male Wistar rats (Charles River Laboratories, L’Arbresle, France) weighing 100–120 g followed a CCl4 inhalation protocol43 (link) for 13 weeks. Phenobarbital (0.3 g/L) was added to drinking water one week before the inhalation protocol.
All rats were kept under constant temperature and humidity in a 12 h controlled dark/light cycle and fed ad libitum with a grain-based chow (Teklad 2014, Harlan Laboratories, Indianapolis, IN, USA) containing a fixed formula of ingredients with 0.1% Na+.
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6

Behavioral Neuroscience Protocols in Rats

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A total of 321 adult male rats was used, that is, 144 Wistar rats (Charles River Laboratories, France) for the social recognition memory tests, 69 Sprague Dawley OFA rats (Charles River Laboratories, Saint Germain sur l′Arbresle, France) for the object recognition experiments, 16 Sprague Dawley rats (Harlan Laboratories, Frederick, MD) for the visual signal detection task (VSDT), and 92 Sprague Dawley rats (Charles River Laboratories, Indianapolis, IN) for the in vivo microdialysis, ex vivo receptor occupancy, and pharmacokinetic interaction and exposure time course studies. Additionally, social recognition memory experiments used juvenile Wistar rats as stimulus animals that were not otherwise subjected to any experimental manipulations. All rats were group-housed in plastic cages under temperature- and humidity-controlled conditions, a 12-hour light/dark cycle, and with ad libitum access to food and water, except where noted below. All procedures were performed in a manner consistent with local guidelines on ethical research in animals and were approved by the relevant authority or animal care and use committee prior to the start of experiments.
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7

Embryonic Rat Retinal Tissue Harvesting

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Timed pregnant Sprague-Dawley OFA rats were purchased from Charles River (L'Arbresle, France). The day of vaginal plug corresponded to embryonic day 0 (E0), and the day of birth corresponded to postnatal day 0 (P0). Animals were sacrificed according to the recommendations of our local ethical and animal care committee and eyes were dissected to recover neural retinal tissues (Authorization 75-865 delivered on April 30 2010 by the Minister of Agriculture). The methods used to secure animal tissue complied with the ARVO Statement for the Use of Animals 5/30 in Ophthalmic and Vision Research.
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